[ { "uniprot_canonical_ac": "Q3UT54-1", "uniprot_id": "OBOX3_MOUSE", "mass": 37777.0, "length": 335, "protein_name": "Oocyte-specific homeobox protein 3", "gene_name": "Obox3", "organism": "Mouse", "refseq_name": "oocyte-specific homeobox protein 3", "refseq_ac": "NP_663753", "gene_names_uniprotkb": "Obox3; Ohx", "gene_names_refseq": "Obox3; Ohx", "protein_names_uniprotkb": "Oocyte-specific homeobox protein 3; Oocyte-specific homeobox", "protein_names_refseq": "oocyte-specific homeobox protein 3; oocyte-specific homeobox", "tax_id": 10090, "disease": "", "pathway": " (mmu:246791)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "11991721;12204267;21750661;37459895;38619966", "class_list": "", "function": "Detection of newly synthesized RNA reveals transcriptional reprogramming during ZGA and a role of Obox3 in totipotency acquisition., [RefSeq, PubMed]; Transcription factor required for zygotic genome activation (ZGA), a critical event in early embryonic development during which the developmental control passes from maternally provided mRNAs to the expression of the zygotic genome after fertilization (PubMed:37459895). Together with other Obox family members, required in early two-cell stage embryos to kick-start the major ZGA wave by facilitating RNA Polymerase II 'pre-configuration', during which RNA Polymerase II relocates from the initial one-cell stage binding targets to ZGA gene promoters and distal enhancers (PubMed:37459895). Mechanistically, promotes recruitment of RNA Polymerase II from (CG-rich) non-ZGA genes to (CG-poor) ZGA genes at the two-cell stage (PubMed:37459895). Binds to regulatory DNA sequences containing a 5'-ACNCCTTTAATCCCAG-3' sequence motif (PubMed:37459895). Most maternal and zygotic Obox family proteins can compensate for one another (PubMed:37459895)., [UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "D3YXK4;G3UXQ8;G3UXT3;G3UZJ7;Q8JZN9;Q8VHG6", "ec_number_list": "", "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0003677 DNA binding", "go_cellular_component": "GO:0005634 nucleus", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0030154 cell differentiation;GO:0048706 embryonic skeletal system development;GO:0160021 maternal-to-zygotic transition of gene expression", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "Q3UT54-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A1W2P728-1", "uniprot_id": "A0A1W2P728_MOUSE", "mass": 22894.0, "length": 225, "protein_name": "Keratin associated protein 10-31", "gene_name": "Krtap10-31", "organism": "Mouse", "refseq_name": "keratin associated protein 10-4-like", "refseq_ac": "NP_001156416", "gene_names_uniprotkb": "Krtap10-31; Gm10318", "gene_names_refseq": "EG622629; Gm10318; Krtap10-31", "protein_names_uniprotkb": "Keratin associated protein 10-31", "protein_names_refseq": "keratin associated protein 10-4-like", "tax_id": 10090, "disease": "", "pathway": " (mmu:622629); (R-MMU-6805567)", "pathway_count": 2, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "In the hair cortex, hair keratin intermediate filaments are embedded in an interfilamentous matrix, consisting of hair keratin-associated proteins (KRTAP), which are essential for the formation of a rigid and resistant hair shaft through their extensive disulfide bond cross-linking with abundant cysteine residues of hair keratins. The matrix proteins include the high-sulfur and high-glycine-tyrosine keratins., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0042802 identical protein binding", "go_cellular_component": "GO:0005829 cytosol;GO:0045095 keratin filament", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A1W2P728-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9DBK7-1", "uniprot_id": "UBA7_MOUSE", "mass": 108679.0, "length": 977, "protein_name": "Ubiquitin-like modifier-activating enzyme 7", "gene_name": "Uba7", "organism": "Mouse", "refseq_name": "ubiquitin-like modifier-activating enzyme 7", "refseq_ac": "NP_076227", "gene_names_uniprotkb": "Uba7; Ube1l", "gene_names_refseq": "1300004C08Rik; Uba7; Ube1l", "protein_names_uniprotkb": "Ubiquitin-like modifier-activating enzyme 7; 6.2.1.-; Ubiquitin-activating enzyme 7; Ubiquitin-activating enzyme E1 homolog", "protein_names_refseq": "ubiquitin-activating enzyme 7; ubiquitin-activating enzyme E1 homolog; ubiquitin-like modifier-activating enzyme 7", "tax_id": 10090, "disease": "", "pathway": " (mmu:74153); (R-MMU-1169408); (R-MMU-5656169); (R-MMU-983168); (R-MMU-9909505)", "pathway_count": 5, "publication_count": 5, "publication_id_list": "16382139;18571763;19004958;21750661;31974171", "class_list": "", "function": "E1-activating enzyme that catalyzes the covalent conjugation of the ubiquitin-like protein product of ISG15 to additional interferons stimulated proteins (ISGs) as well as other cellular proteins such as P53 in a process termed protein ISGylation. Plays an essential role in antiviral immunity together with ISG15 by restricting the replication of many viruses including rabies virus, influenza virus, sindbis virus or rotavirus (PubMed:19004958, PubMed:31974171)., [UniProtKB, PubMed, PubMed, UniProtKB]; UBE1L and protein ISGylation are not critical for IFN-alpha/beta signaling via JAK/STAT activation., [RefSeq, PubMed]; Ube1l is not a tumor suppressor gene in K-ras(LA2) lung cancer mouse model., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "2.3.2.26;2.3.2.31;2.3.2.27;2.3.2.-;3.6.4.-;2.3.2.24;2.3.2.23;2.3.2.34;2.3.2.32;6.2.1.45;6.3.2.n3;3.6.4.13;2.7.7.7;2.7.11.1;6.2.1.64;2.3.2.36;2.3.2.25;2.7.7.-;6.2.1.-", "go_molecular_function": "GO:0004842 ubiquitin-protein transferase activity;GO:0019782 ISG15 activating enzyme activity;GO:0008641 ubiquitin-like modifier activating enzyme activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm", "go_biological_process": "GO:0045087 innate immune response;GO:0006974 DNA damage response;GO:0016567 protein ubiquitination;GO:0019941 modification-dependent protein catabolic process;GO:0032020 ISG15-protein conjugation", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "Q9DBK7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TRD9-1", "uniprot_id": "Q7TRD9_MOUSE", "mass": 35485.0, "length": 314, "protein_name": "Olfactory receptor family 8 subfamily B member 41", "gene_name": "Or8b41", "organism": "Mouse", "refseq_name": "olfactory receptor 890", "refseq_ac": "NP_666692", "gene_names_uniprotkb": "Or8b41; Olfr890", "gene_names_refseq": "MOR162-3; Olfr890; Or8b41", "protein_names_uniprotkb": "Olfactory receptor family 8 subfamily B member 41", "protein_names_refseq": "GA_x6K02T2PVTD-31822365-31823309; MOR162-15_p; olfactory receptor 890; olfactory receptor MOR162-3", "tax_id": 10090, "disease": "", "pathway": " (mmu:258474)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Odorant receptor., [UniProtKB, UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q7TRD9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "D3YWC7-1", "uniprot_id": "D3YWC7_MOUSE", "mass": 46451.0, "length": 402, "protein_name": "Family with sequence similarity 47, member E", "gene_name": "Fam47e", "organism": "Mouse", "refseq_name": "protein FAM47E isoform 3", "refseq_ac": "NP_001361643", "gene_names_uniprotkb": "Fam47e", "gene_names_refseq": "C730043O17; Fam47e; Gm1381", "protein_names_uniprotkb": "Family with sequence similarity 47, member E", "protein_names_refseq": "protein FAM47E isoform 3", "tax_id": 10090, "disease": "", "pathway": " (mmu:384198)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0008047 enzyme activator activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0000785 chromatin", "go_biological_process": "GO:0045815 transcription initiation-coupled chromatin remodeling;GO:0071168 protein localization to chromatin", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "D3YWC7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9PYJ0-1", "uniprot_id": "E9PYJ0_MOUSE", "mass": 49361.0, "length": 438, "protein_name": "T-complex protein 10b", "gene_name": "Tcp10b", "organism": "Mouse", "refseq_name": "t-complex protein 10b", "refseq_ac": "NP_033367", "gene_names_uniprotkb": "Tcp10b; Gm10326; Tcp10a", "gene_names_refseq": "D17Leh66B; D17Leh66ba; T66B-a; Tcp-10bt; Tcp-10b; Tcp10b", "protein_names_uniprotkb": "T-complex protein 10b", "protein_names_refseq": "t-complex protein 10b", "tax_id": 10090, "disease": "primary autosomal recessive microcephaly 6 (Disease Ontology:DOID:0070290); microcephaly (Disease Ontology:DOID:10907)", "pathway": " (mmu:21462)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "F6SKG2", "ec_number_list": "", "go_molecular_function": "GO:0042802 identical protein binding;GO:0003714 transcription corepressor activity;GO:0140297 DNA-binding transcription factor binding", "go_cellular_component": "GO:0005634 nucleus", "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "E9PYJ0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8K004-1", "uniprot_id": "SPAT2_MOUSE", "mass": 57812.0, "length": 515, "protein_name": "Spermatogenesis-associated protein 2", "gene_name": "Spata2", "organism": "Mouse", "refseq_name": "spermatogenesis-associated protein 2 isoform 1", "refseq_ac": "NP_739562", "gene_names_uniprotkb": "Spata2", "gene_names_refseq": "Spata2; mKIAA0757", "protein_names_uniprotkb": "Spermatogenesis-associated protein 2", "protein_names_refseq": "spermatogenesis-associated protein 2 isoform 1; spermatogenesis-associated protein 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:263876); (R-MMU-5357786); (R-MMU-5357905); (R-MMU-5357956)", "pathway_count": 4, "publication_count": 6, "publication_id_list": "27458237;27545878;28701375;29025062;36640323;40885482", "class_list": "", "function": "Bridging factor that mediates the recruitment of CYLD to the LUBAC complex, thereby regulating TNF-induced necroptosis (By similarity). Acts as a direct binding intermediate that bridges RNF31/HOIP, the catalytic subunit of the LUBAC complex, and the deubiquitinase (CYLD), thereby recruiting CYLD to the TNF-R1 signaling complex (TNF-RSC) (By similarity). Required to activate the 'Met-1'- (linear) and 'Lys-63'-linked deubiquitinase activities of CYLD (PubMed:28701375). Controls the kinase activity of RIPK1 and TNF-induced necroptosis by promoting 'Met-1'-linked deubiquitination of RIPK1 by CYLD (PubMed:28701375)., [UniProtKB, UniProtKB, PubMed]; Our data revealed the impact of SPATA2 on male fertility and suggested that SPATA2 ensures the normal secretory function of Sertoli cells, [RefSeq, PubMed]; SPATA2 has been described as a previously unrecognized factor in the linear ubiquitin chain assembly complex-dependent signaling pathways that serves as an adaptor between HOIP and CYLD, thereby enabling recruitment of CYLD to signaling complexes., [RefSeq, PubMed]; SPATA2 restricts OTULIN-dependent LUBAC activity independently of CYLD., [RefSeq, PubMed]; Spata2 can regulate inflammatory response and cell death in both RIPK1-dependent and RIPK1-independent manners Erratum:[Genes Dev. 2018 Dec 1;32(23-24):1591. doi: 10.1101/gad.321075.118. PMID: 30509949], [RefSeq, PubMed]; This study identifies SPATA2 as an important factor in the TNF signaling pathway with a substantial role for the effects mediated by the cytokine., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 3, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 3, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 3, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "Q3TAH0;Q3UML2", "ec_number_list": "", "go_molecular_function": "GO:0044877 protein-containing complex binding;GO:1990381 ubiquitin-specific protease binding;GO:0030159 signaling receptor complex adaptor activity", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0001650 fibrillar center", "go_biological_process": "GO:0007283 spermatogenesis;GO:0070536 protein K63-linked deubiquitination;GO:0050727 regulation of inflammatory response;GO:0072520 seminiferous tubule development;GO:0010803 regulation of tumor necrosis factor-mediated signaling pathway", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q8K004-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A2AK42-1", "uniprot_id": "A2AK42_MOUSE", "mass": 95672.0, "length": 830, "protein_name": "Pre-mRNA-splicing factor CWC22 homolog", "gene_name": "Cwc22rt4; Cwc22rt5", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Cwc22rt4; Cwc22rt5; Cwc22rt1; Cwc22rt2; Cwc22rt4; Cwc22rt5; Cwc22rt6; Cwc22rt7", "gene_names_refseq": "", "protein_names_uniprotkb": "Pre-mRNA-splicing factor CWC22 homolog; Nucampholin homolog", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 2, "publication_id_list": "21750661;37507081", "class_list": "", "function": "Required for pre-mRNA splicing as component of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs. Promotes exon-junction complex (EJC) assembly. Hinders EIF4A3 from non-specifically binding RNA and escorts it to the splicing machinery to promote EJC assembly on mature mRNAs. Through its role in EJC assembly, required for nonsense-mediated mRNA decay., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003723 RNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0016607 nuclear speck;GO:0005681 spliceosomal complex;GO:0071013 catalytic step 2 spliceosome;GO:0071006 U2-type catalytic step 1 spliceosome", "go_biological_process": "GO:0000398 mRNA splicing, via spliceosome", "synthesized_glycan_count": 0, "hit_score": 0.5, "record_id": "A2AK42-1", "record_type": "protein" }, { "uniprot_canonical_ac": "J3QNB7-1", "uniprot_id": "J3QNB7_MOUSE", "mass": 31868.0, "length": 292, "protein_name": "Family with sequence similarity 181, member A", "gene_name": "Fam181a", "organism": "Mouse", "refseq_name": "protein FAM181A", "refseq_ac": "NP_001182655", "gene_names_uniprotkb": "Fam181a", "gene_names_refseq": "EG544888; Fam181a", "protein_names_uniprotkb": "Family with sequence similarity 181, member A", "protein_names_refseq": "protein FAM181A", "tax_id": 10090, "disease": "", "pathway": " (mmu:100504156)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21750661;26407640", "class_list": "", "function": "Data show that Fam181a presents partially overlapping mRNA expression with Fam181b during embryonic development and encodes for protein containing highly-conserved motifs with mainly nuclear localization., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005737 cytoplasm", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "J3QNB7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G3X9I0-1", "uniprot_id": "G3X9I0_MOUSE", "mass": 58421.0, "length": 524, "protein_name": "Zinc finger protein 105", "gene_name": "Zfp105", "organism": "Mouse", "refseq_name": "zinc finger protein 35", "refseq_ac": "NP_033570", "gene_names_uniprotkb": "Zfp105", "gene_names_refseq": "Zfp105", "protein_names_uniprotkb": "Zinc finger protein 105", "protein_names_refseq": "zinc finger protein 35", "tax_id": 10090, "disease": "", "pathway": " (mmu:22646)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "20186958;21750661", "class_list": "", "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]; Results suggest that ZFP105 is a male germ-cell factor and plays a role in male reproduction., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0043565 sequence-specific DNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0048471 perinuclear region of cytoplasm", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "G3X9I0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A2ART0-1", "uniprot_id": "A2ART0_MOUSE", "mass": 64075.0, "length": 554, "protein_name": "Predicted gene 14391; Predicted gene 6710", "gene_name": "Gm14391; Gm6710", "organism": "Mouse", "refseq_name": "KRAB box and zinc finger, C2H2 type domain containing isoform 1", "refseq_ac": "NP_001092778", "gene_names_uniprotkb": "Gm14391; Gm6710; Gm14391", "gene_names_refseq": "Gm14391", "protein_names_uniprotkb": "Predicted gene 14391; Predicted gene 6710", "protein_names_refseq": "KRAB box and zinc finger, C2H2 type domain containing isoform 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:626832); (mmu:665001); (R-MMU-212436); (R-MMU-9843940)", "pathway_count": 4, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "F7CJX1", "ec_number_list": "", "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific", "go_cellular_component": "GO:0005634 nucleus", "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A2ART0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TNC9-1", "uniprot_id": "I5P1_MOUSE", "mass": 47622.0, "length": 412, "protein_name": "Inositol polyphosphate-5-phosphatase A", "gene_name": "Inpp5a", "organism": "Mouse", "refseq_name": "inositol polyphosphate-5-phosphatase A isoform b", "refseq_ac": "NP_898967", "gene_names_uniprotkb": "Inpp5a", "gene_names_refseq": "Inpp5a", "protein_names_uniprotkb": "Inositol polyphosphate-5-phosphatase A; 3.1.3.56; 5PTase; Type I inositol 1,4,5-trisphosphate 5-phosphatase", "protein_names_refseq": "5PTase; inositol polyphosphate-5-phosphatase A isoform b; type I inositol 1,4,5-trisphosphate 5-phosphatase", "tax_id": 10090, "disease": "", "pathway": " (mmu:212111); (R-MMU-1855183)", "pathway_count": 2, "publication_count": 4, "publication_id_list": "26051944;31112734;32107387;33720513", "class_list": "", "function": "A novel microduplication in INPP5A segregates with schizophrenia spectrum disorder in the family of a patient with both childhood onset schizophrenia and autism spectrum disorder., [RefSeq, PubMed]; Phosphatase that specifically hydrolyzes the 5-phosphate of inositol 1,4,5-trisphosphate to inositol 1,4-bisphosphate, and inositol 1,3,4,5-tetrasphosphate to inositol 1,3,4-trisphosphate (PubMed:26051944). Plays a crucial role in the survival of cerebellar Purkinje cells (PubMed:26051944)., [UniProtKB, PubMed]; Using SCA17 knock-in mice that endogenously express mutant TATA box-binding protein (TBP), study found that Inpp5a, a protein that is highly abundant in the cerebellum and functions as a terminator of the inositol 1,4,5-trisphosphate (IP3) second messenger, is downregulated. This was caused by the abnormal binding of mutant TBP to the transcription factor SP1, leading to reduced Inpp5a transcription. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "E9QAS7;Q8BNK3", "ec_number_list": "3.1.3.56;3.1.3.36;3.1.3.86;3.1.3.-;3.1.3.95", "go_molecular_function": "GO:0042731 PH domain binding;GO:0004445 inositol-polyphosphate 5-phosphatase activity;GO:0052658 inositol-1,4,5-trisphosphate 5-phosphatase activity;GO:0052659 inositol-1,3,4,5-tetrakisphosphate 5-phosphatase activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0030425 dendrite", "go_biological_process": "GO:0050849 negative regulation of calcium-mediated signaling;GO:0046856 phosphatidylinositol dephosphorylation;GO:1900737 negative regulation of phospholipase C-activating G protein-coupled receptor signaling pathway;GO:0043647 inositol phosphate metabolic process", "synthesized_glycan_count": 0, "hit_score": 0.5, "record_id": "Q7TNC9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8CIH9-1", "uniprot_id": "PUR1_MOUSE", "mass": 57403.0, "length": 517, "protein_name": "Amidophosphoribosyltransferase", "gene_name": "Ppat", "organism": "Mouse", "refseq_name": "amidophosphoribosyltransferase", "refseq_ac": "NP_742158", "gene_names_uniprotkb": "Ppat", "gene_names_refseq": "5730454C12Rik; GPAT; Ppat", "protein_names_uniprotkb": "Amidophosphoribosyltransferase; 2.4.2.14; ATase; GPAT; Glutamine phosphoribosylpyrophosphate amidotransferase", "protein_names_refseq": "ATase; amidophosphoribosyltransferase; glutamine phosphoribosylpyrophosphate amidotransferase", "tax_id": 10090, "disease": "renal cell carcinoma (Disease Ontology:DOID:4450); hepatocellular carcinoma (Disease Ontology:DOID:684)", "pathway": " (mmu:231327); (R-MMU-73817)", "pathway_count": 2, "publication_count": 3, "publication_id_list": "21750661;23806337;28135057", "class_list": "", "function": "Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q3TKC5;Q3TUW2;Q3UGU3", "ec_number_list": "2.4.2.14", "go_molecular_function": "GO:0042802 identical protein binding;GO:0046872 metal ion binding;GO:0051539 4 iron, 4 sulfur cluster binding;GO:0004044 amidophosphoribosyltransferase activity", "go_cellular_component": "", "go_biological_process": "GO:0006177 GMP biosynthetic process;GO:0009113 purine nucleobase biosynthetic process;GO:0006164 purine nucleotide biosynthetic process;GO:0006189 'de novo' IMP biosynthetic process;GO:0044208 'de novo' AMP biosynthetic process", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "Q8CIH9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "F8VPK8-1", "uniprot_id": "F8VPK8_MOUSE", "mass": 136145.0, "length": 1237, "protein_name": "Protocadherin 9", "gene_name": "Pcdh9", "organism": "Mouse", "refseq_name": "protocadherin-9 isoform a precursor", "refseq_ac": "NP_001074846", "gene_names_uniprotkb": "Pcdh9", "gene_names_refseq": "Pcdh9", "protein_names_uniprotkb": "Protocadherin 9", "protein_names_refseq": "protocadherin-9 isoform a precursor", "tax_id": 10090, "disease": "prostate cancer (Disease Ontology:DOID:10283); cancer (Disease Ontology:DOID:162)", "pathway": " (mmu:211712)", "pathway_count": 1, "publication_count": 4, "publication_id_list": "10.1101/2023.09.13.557529;21750661;25428506;30899004", "class_list": "", "function": "Potential calcium-dependent cell-adhesion protein., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; This gene encodes a member of the protocadherin family, and cadherin superfamily, of transmembrane proteins containing cadherin domains. These proteins mediate cell adhesion in neural tissues in the presence of calcium. The encoded protein may be involved in signaling at neuronal synaptic junctions. Sharing a characteristic with other protocadherin genes, this gene has a notably large exon that encodes multiple cadherin domains and a transmembrane region. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2012]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 13, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 13, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 13, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 9015, "biomarker_type": "", "glycan_count": 24, "disease_count": 2, "glyco_site_count": 13, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005509 calcium ion binding;GO:0050839 cell adhesion molecule binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0098978 glutamatergic synapse;GO:0030426 growth cone;GO:0097060 synaptic membrane;GO:0044291 cell-cell contact zone", "go_biological_process": "GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules;GO:0007155 cell adhesion;GO:0030900 forebrain development", "synthesized_glycan_count": 0, "hit_score": 4.2, "record_id": "F8VPK8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "B1AUS6-1", "uniprot_id": "B1AUS6_MOUSE", "mass": 53350.0, "length": 473, "protein_name": "Mitochondrial adenyl nucleotide antiporter SLC25A24", "gene_name": "Slc25a54", "organism": "Mouse", "refseq_name": "solute carrier family 25, member 54", "refseq_ac": "NP_083330", "gene_names_uniprotkb": "Slc25a54; 4930443G12Rik", "gene_names_refseq": "4930443G12Rik; SCaMC-1like; Slc25a54", "protein_names_uniprotkb": "Mitochondrial adenyl nucleotide antiporter SLC25A24; Small calcium-binding mitochondrial carrier protein 1; Solute carrier family 25 member 24", "protein_names_refseq": "solute carrier family 25 member 24; solute carrier family 25, member 54", "tax_id": 10090, "disease": "", "pathway": " (mmu:74686)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21750661;22792342", "class_list": "", "function": "Electroneutral antiporter that mediates the transport of adenyl nucleotides through the inner mitochondrial membrane. Originally identified as an ATP-magnesium/inorganic phosphate antiporter, it also acts as a broad specificity adenyl nucleotide antiporter. By regulating the mitochondrial matrix adenyl nucleotide pool, could adapt to changing cellular energetic demands and indirectly regulate adenyl nucleotide-dependent metabolic pathways. In vitro, a low activity is also observed with guanyl and pyrimidine nucleotides. May play a role in protecting cells against oxidative stress-induced cell death, by buffering calcium levels in the mitochondrial matrix through the formation of calcium-phosphate precipitates., [UniProtKB, UniProtKB]; SCaMC-1L expression is restricted to male germ cells and regulated during spermatogenesis but unexpectedly its localization is not limited to mitochondrial structures., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005509 calcium ion binding;GO:0015297 antiporter activity;GO:0005347 ATP transmembrane transporter activity", "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0005829 cytosol;GO:0005815 microtubule organizing center;GO:0033391 chromatoid body", "go_biological_process": "GO:0015866 ADP transport;GO:0015867 ATP transport", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "B1AUS6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9QA35-1", "uniprot_id": "E9QA35_MOUSE", "mass": 144842.0, "length": 1336, "protein_name": "Spermatogenesis associated 31 subfamily D, member 1A", "gene_name": "Spata31d1a", "organism": "Mouse", "refseq_name": "spermatogenesis-associated protein 31D1", "refseq_ac": "NP_082433", "gene_names_uniprotkb": "Spata31d1a; Fam75d1a", "gene_names_refseq": "1700013B16Rik; Fam75d1a; Fam75d3; Spata31d1a", "protein_names_uniprotkb": "Spermatogenesis associated 31 subfamily D, member 1A", "protein_names_refseq": "family with sequence similarity 75, member D1A; family with sequence similarity 75, member D3; spermatogenesis-associated protein 31D1", "tax_id": 10090, "disease": "", "pathway": " (mmu:72219)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0016020 membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "E9QA35-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VG88-1", "uniprot_id": "Q8VG88_MOUSE", "mass": 34786.0, "length": 311, "protein_name": "Olfactory receptor", "gene_name": "Or7d9", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Or7d9; Olfr39", "gene_names_refseq": "", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": " (mmu:258822); (R-MMU-381753)", "pathway_count": 2, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007165 signal transduction;GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q8VG88-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VG76-1", "uniprot_id": "Q8VG76_MOUSE", "mass": 34803.0, "length": 310, "protein_name": "Olfactory receptor", "gene_name": "Or8b46", "organism": "Mouse", "refseq_name": "olfactory receptor 910", "refseq_ac": "NP_667022", "gene_names_uniprotkb": "Or8b46; Olfr910", "gene_names_refseq": "MOR165-3; Olfr910; Or8b46", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2PVTD-32239063-32239995; olfactory receptor 910; olfactory receptor MOR165-3", "tax_id": 10090, "disease": "", "pathway": " (mmu:258807)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q8VG76-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VEV7-1", "uniprot_id": "Q8VEV7_MOUSE", "mass": 35181.0, "length": 312, "protein_name": "Olfactory receptor", "gene_name": "Or5b107", "organism": "Mouse", "refseq_name": "olfactory receptor family 5 subfamily B member 107", "refseq_ac": "NP_666414", "gene_names_uniprotkb": "Or5b107; Olfr1461", "gene_names_refseq": "MOR202-35; Olfr1461; Or5b107", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2RE5P-3491834-3492772; olfactory receptor 1461; olfactory receptor MOR202-35; olfactory receptor family 5 subfamily B member 107", "tax_id": 10090, "disease": "", "pathway": " (mmu:258299)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q8VEV7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A087WQA3-1", "uniprot_id": "A0A087WQA3_MOUSE", "mass": 25715.0, "length": 222, "protein_name": "Predicted gene, 20843; Predicted gene, 20888; Predicted gene, 20937; Predicted gene, 21209; Predicted gene, 21518", "gene_name": "Gm21209; Gm21518; Gm21650", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Gm21209; Gm21518; Gm21650; Gm20843; Gm20888; Gm20937; Gm21209; Gm21518; Gm21650", "gene_names_refseq": "", "protein_names_uniprotkb": "Predicted gene, 20843; Predicted gene, 20888; Predicted gene, 20937; Predicted gene, 21209; Predicted gene, 21518", "protein_names_refseq": "", "tax_id": 10090, "disease": "spermatogenic failure 4 (Disease Ontology:DOID:0070176)", "pathway": " (mmu:108168515); (mmu:108168520); (mmu:108168524); (mmu:108168525); (mmu:108168527); (mmu:108168530); (mmu:108168532); (mmu:108168533); (mmu:108168595)", "pathway_count": 9, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005634 nucleus;GO:0000795 synaptonemal complex", "go_biological_process": "GO:0007286 spermatid development;GO:0051321 meiotic cell cycle;GO:0035092 sperm DNA condensation", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A087WQA3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q80WM9-1", "uniprot_id": "TNR14_MOUSE", "mass": 30171.0, "length": 275, "protein_name": "Tumor necrosis factor receptor superfamily member 14", "gene_name": "Tnfrsf14", "organism": "Mouse", "refseq_name": "tumor necrosis factor receptor superfamily member 14 precursor", "refseq_ac": "NP_849262", "gene_names_uniprotkb": "Tnfrsf14; hvem", "gene_names_refseq": "Atar; HveA; Hvem; TR2; Tnfrs14; Tnfrsf14", "protein_names_uniprotkb": "Tumor necrosis factor receptor superfamily member 14; Herpes virus entry mediator A; Herpesvirus entry mediator A; HveA; TR2; Tumor necrosis factor receptor-like 2", "protein_names_refseq": "herpes virus entry mediator A; herpesvirus entry mediator A; tumor necrosis factor receptor superfamily member 14 precursor; tumor necrosis factor receptor superfamily member 14; tumor necrosis factor receptor-like 2", "tax_id": 10090, "disease": "arteriosclerosis (Disease Ontology:DOID:2349); myocardial infarction (Disease Ontology:DOID:5844)", "pathway": " (mmu:230979); (R-MMU-5669034); (R-MMU-9927353)", "pathway_count": 3, "publication_count": 12, "publication_id_list": "15016549;15178556;15568026;18193050;19915044;21750661;22801499;25711213;36654880;37000475;37033927;38831106", "class_list": "", "function": "Exerts a significant antiviral effect against HSV-1 infection in vivo., [RefSeq, PubMed]; Genetic deletion of HVEM in a leukemia B cell line promotes a preferential increase of PD-1[-] stem cell-like T cells over PD-1[+] T cells curbing tumor progression. Publication Status: Online-Only, [RefSeq, PubMed]; In graft arterial disease, HVEM was detected in SMCs stimulated by IFN-gamma. The LIGHT pathway plays important roles in the regulation not only of T-cell activation but also of SMC proliferation., [RefSeq, PubMed]; LIGHT Amplification by NF-kappaB Contributes to TLR3 Signaling Pathway-Induced Acute Hepatitis. Publication Status: Online-Only, [RefSeq, PubMed]; Lack of Herpes Virus Entry Mediator Signals in Thymocytes Impairs Conventional CD8 T Cell Selection and Promotes Memory-like CD8 T Cell Development., [RefSeq, PubMed]; Receptor for four distinct ligands: The TNF superfamily members TNFSF14/LIGHT and homotrimeric LTA/lymphotoxin-alpha and the immunoglobulin superfamily members BTLA and CD160, altogether defining a complex stimulatory and inhibitory signaling network (By similarity). Signals via the TRAF2-TRAF3 E3 ligase pathway to promote immune cell survival and differentiation (PubMed:19915044). Participates in bidirectional cell-cell contact signaling between antigen presenting cells and lymphocytes. In response to ligation of TNFSF14/LIGHT, delivers costimulatory signals to T cells, promoting cell proliferation and effector functions (By similarity). Interacts with CD160 on NK cells, enhancing IFNG production and anti-tumor immune response (PubMed:25711213). In the context of bacterial infection, acts as a signaling receptor on epithelial cells for CD160 from intraepithelial lymphocytes, triggering the production of antimicrobial proteins and pro-inflammatory cytokines (PubMed:22801499). Upon binding to CD160 on activated CD4+ T cells, down-regulates CD28 costimulatory signaling, restricting memory and alloantigen-specific immune response (By similarity). May interact in cis (on the same cell) or in trans (on other cells) with BTLA (PubMed:15568026, PubMed:19915044). In cis interactions, appears to play an immune regulatory role inhibiting in trans interactions in naive T cells to maintain a resting state. In trans interactions, can predominate during adaptive immune response to provide survival signals to effector T cells (PubMed:15568026, PubMed:19915044)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed, PubMed]; The BTLA-HVEM axis restricts CAR T cell efficacy in cancer., [RefSeq, PubMed]", "predicted_glycosites": 2, "predicted_n_glycosites": 2, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0031625 ubiquitin protein ligase binding;GO:0001618 virus receptor activity;GO:0048018 receptor ligand activity;GO:0019955 cytokine binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0009897 external side of plasma membrane;GO:0098797 plasma membrane protein complex;GO:0002947 tumor necrosis factor receptor superfamily complex", "go_biological_process": "GO:0045087 innate immune response;GO:0050829 defense response to Gram-negative bacterium;GO:0050830 defense response to Gram-positive bacterium;GO:2000406 positive regulation of T cell migration;GO:0031295 T cell costimulation", "synthesized_glycan_count": 0, "hit_score": 1.3, "record_id": "Q80WM9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8CGR6-1", "uniprot_id": "Q8CGR6_MOUSE", "mass": 30360.0, "length": 276, "protein_name": "Kallikrein related-peptidase 13", "gene_name": "Klk13", "organism": "Mouse", "refseq_name": "kallikrein-13 precursor", "refseq_ac": "NP_001034131", "gene_names_uniprotkb": "Klk13", "gene_names_refseq": "Egfbp-2; Klk13; mGk-13", "protein_names_uniprotkb": "Kallikrein related-peptidase 13", "protein_names_refseq": "kallikrein 13; kallikrein-13 precursor", "tax_id": 10090, "disease": "prostate cancer (Disease Ontology:DOID:10283); ovarian carcinoma (Disease Ontology:DOID:4001)", "pathway": " (mmu:626834); (R-MMU-6809371)", "pathway_count": 2, "publication_count": 2, "publication_id_list": "16423834;21750661", "class_list": "", "function": "Kallikrein mK13 is a plausible candidate for the processing enzyme for pro-IL-1beta in the submandibular gland of mice, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004252 serine-type endopeptidase activity;GO:0004175 endopeptidase activity;GO:0016787 hydrolase activity", "go_cellular_component": "GO:0005615 extracellular space;GO:0005737 cytoplasm;GO:0030141 secretory granule", "go_biological_process": "GO:0006508 proteolysis;GO:0016485 protein processing;GO:0051604 protein maturation", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "Q8CGR6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A2A7F4-1", "uniprot_id": "A2A7F4_MOUSE", "mass": 217389.0, "length": 1918, "protein_name": "Rearranged L-myc fusion sequence", "gene_name": "Rlf", "organism": "Mouse", "refseq_name": "zinc finger protein Rlf", "refseq_ac": "NP_001333589", "gene_names_uniprotkb": "Rlf", "gene_names_refseq": "9230110M18Rik; MommeD8; Rlf", "protein_names_uniprotkb": "Rearranged L-myc fusion sequence", "protein_names_refseq": "zinc finger protein Rlf", "tax_id": 10090, "disease": "", "pathway": " (mmu:109263)", "pathway_count": 1, "publication_count": 4, "publication_id_list": "21750661;25428506;25857663;27930960", "class_list": "", "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]; Our study highlights the importance of RLF-dependent epigenetic modifications to DNA for maintaining correct gene regulatory network and intercellular signalling interactions during heart chamber and septal development., [RefSeq, PubMed]; This study provides the first evidence that the epigenetic modifier Rlf is involved in the maintenance of DNA methylation at enhancers and CpG island shores across the genome. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific", "go_cellular_component": "GO:0005634 nucleus", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0031452 negative regulation of heterochromatin formation", "synthesized_glycan_count": 0, "hit_score": 0.5, "record_id": "A2A7F4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A2ANE1-1", "uniprot_id": "A2ANE1_MOUSE", "mass": 24710.0, "length": 215, "protein_name": "Reproductive homeobox 3F", "gene_name": "Rhox3f", "organism": "Mouse", "refseq_name": "reproductive homeobox 3F", "refseq_ac": "NP_001035178", "gene_names_uniprotkb": "Rhox3f", "gene_names_refseq": "Rhox3.6; Rhox3e; Rhox3f", "protein_names_uniprotkb": "Reproductive homeobox 3F", "protein_names_refseq": "PEPP subfamily member; reproductive homeobox 3E; reproductive homeobox 3F", "tax_id": 10090, "disease": "", "pathway": " (mmu:621852)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "F7BKG6", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific", "go_cellular_component": "GO:0005634 nucleus", "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A2ANE1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G3UY57-1", "uniprot_id": "G3UY57_MOUSE", "mass": 33629.0, "length": 292, "protein_name": "Tripartite motif-containing 15", "gene_name": "Trim15", "organism": "Mouse", "refseq_name": "E3 ubiquitin-protein ligase TRIM15 isoform 1", "refseq_ac": "NP_001171343", "gene_names_uniprotkb": "Trim15", "gene_names_refseq": "1810012B10Rik; Trim15", "protein_names_uniprotkb": "Tripartite motif-containing 15", "protein_names_refseq": "E3 ubiquitin-protein ligase TRIM15 isoform 1; tripartite motif protein 15", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 2, "publication_id_list": "21750661;25015296", "class_list": "", "function": "TRIM15-depleted cells display impaired cell migration and reduced focal adhesion disassembly rates., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity;GO:0140313 molecular sequestering activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm", "go_biological_process": "GO:0044790 suppression of viral release by host;GO:0045087 innate immune response;GO:1901223 negative regulation of non-canonical NF-kappaB signal transduction;GO:1900246 positive regulation of RIG-I signaling pathway;GO:0032481 positive regulation of type I interferon production", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "G3UY57-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A087WQC7-1", "uniprot_id": "A0A087WQC7_MOUSE", "mass": 25666.0, "length": 222, "protein_name": "Predicted gene, 20736; Predicted gene, 21258", "gene_name": "Gm20736; Gm21258", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Gm20736; Gm21258; Gm20736; Gm21258", "gene_names_refseq": "", "protein_names_uniprotkb": "Predicted gene, 20736; Predicted gene, 21258", "protein_names_refseq": "", "tax_id": 10090, "disease": "spermatogenic failure 4 (Disease Ontology:DOID:0070176)", "pathway": " (mmu:380994)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005634 nucleus;GO:0000795 synaptonemal complex", "go_biological_process": "GO:0007286 spermatid development;GO:0051321 meiotic cell cycle;GO:0035092 sperm DNA condensation", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A087WQC7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G5E8P1-1", "uniprot_id": "BRD1_MOUSE", "mass": 119714.0, "length": 1058, "protein_name": "Bromodomain-containing protein 1", "gene_name": "Brd1", "organism": "Mouse", "refseq_name": "bromodomain-containing protein 1", "refseq_ac": "NP_001028446", "gene_names_uniprotkb": "Brd1; Brpf2; Kiaa4191", "gene_names_refseq": "1110059H06Rik; Brd1; mKIAA4191", "protein_names_uniprotkb": "Bromodomain-containing protein 1; Bromodomain and PHD finger-containing protein 2", "protein_names_refseq": "bromodomain and PHD finger-containing protein 2; bromodomain-containing protein 1", "tax_id": 10090, "disease": "bipolar disorder (Disease Ontology:DOID:3312); schizophrenia (Disease Ontology:DOID:5419)", "pathway": " (mmu:223770); (R-MMU-3214847); (R-MMU-6804758)", "pathway_count": 3, "publication_count": 6, "publication_id_list": "17242355;21753189;23806337;28341151;32681022;34056693", "class_list": "", "function": "Brd1(+/-) mice exhibit relational encoding deficits, compromised working and long term memory, as well as impaired executive cognitive functioning with cognitive behaviors relying on medial prefrontal cortex being particularly affected. Akin to patients with schizophrenia, the cognitive deficits displayed by Brd1(+/)(-) mice are not global, but selective., [RefSeq, PubMed]; Inactivation of the Schizophrenia-associated BRD1 gene in Brain Causes Failure-to-thrive, Seizure Susceptibility and Abnormal Histone H3 Acetylation and N-tail Clipping., [RefSeq, PubMed]; Reduced Brd1 expression leads to reversible depression-like behaviors and gene-expression changes in female mice. Publication Status: Online-Only, [RefSeq, PubMed]; Scaffold subunit of various histone acetyltransferase (HAT) complexes, such as the MOZ/MORF and HBO1 complexes, that acts as a regulator of hematopoiesis (PubMed:21753189). Plays a key role in HBO1 complex by directing KAT7/HBO1 specificity towards histone H3 'Lys-14' acetylation (H3K14ac), thereby promoting erythroid differentiation (PubMed:21753189)., [UniProtKB, PubMed]; The Hbo1-Brd1 complex is the major H3K14 HAT required for transcriptional activation of erythroid developmental regulator genes., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "E9PZ26;Q571F6;Q8BU83", "ec_number_list": "", "go_molecular_function": "GO:0043997 histone H4K12 acetyltransferase activity;GO:0008270 zinc ion binding;GO:0043995 histone H4K5 acetyltransferase activity;GO:0043996 histone H4K8 acetyltransferase activity;GO:0036408 histone H3K14 acetyltransferase activity", "go_cellular_component": "GO:0005634 nucleus;GO:0016607 nuclear speck;GO:0030425 dendrite;GO:0043204 perikaryon;GO:0070776 MOZ/MORF histone acetyltransferase complex", "go_biological_process": "GO:0050793 regulation of developmental process;GO:0043249 erythrocyte maturation;GO:0006338 chromatin remodeling;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription", "synthesized_glycan_count": 0, "hit_score": 0.7, "record_id": "G5E8P1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9PW10-1", "uniprot_id": "E9PW10_MOUSE", "mass": 47808.0, "length": 424, "protein_name": "Tripartite motif family-like 2", "gene_name": "Triml2", "organism": "Mouse", "refseq_name": "probable E3 ubiquitin-protein ligase TRIML2", "refseq_ac": "NP_001153884", "gene_names_uniprotkb": "Triml2", "gene_names_refseq": "EG622117; Triml2; Tu4", "protein_names_uniprotkb": "Tripartite motif family-like 2", "protein_names_refseq": "probable E3 ubiquitin-protein ligase TRIML2", "tax_id": 10090, "disease": "", "pathway": " (mmu:622117)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21750661;25256710", "class_list": "", "function": "Data indicate that TRIML2 is part of a feed-forward loop that activates p53 in cells expressing the R72 variant, particularly after prolonged stress., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0042802 identical protein binding;GO:0061630 ubiquitin protein ligase activity", "go_cellular_component": "GO:0005737 cytoplasm", "go_biological_process": "GO:0045087 innate immune response;GO:0032526 response to retinoic acid", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "E9PW10-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A8DUK4-1", "uniprot_id": "A8DUK4_MOUSE", "mass": 15748.0, "length": 147, "protein_name": "Hemoglobin, beta adult s chain; Hemoglobin, beta adult t chain", "gene_name": "Hbb-bs", "organism": "Mouse", "refseq_name": "hemoglobin, beta adult s chain", "refseq_ac": "NP_001188320", "gene_names_uniprotkb": "Hbb-bs; Hbb-bt", "gene_names_refseq": "Beta-s; Hbb-bs; Hbbt1; Hbbt2", "protein_names_uniprotkb": "Hemoglobin, beta adult s chain; Hemoglobin, beta adult t chain", "protein_names_refseq": "beta s; beta-globin; beta-single; hemoglobin subunit beta-1-like; hemoglobin, beta adult s chain", "tax_id": 10090, "disease": "autosomal dominant beta thalassemia (Disease Ontology:DOID:0080770); delta beta-thalassemia (Disease Ontology:DOID:0080773); sickle cell disease (Disease Ontology:DOID:0081445); Heinz body anemia (Disease Ontology:DOID:0111363); familial erythrocytosis 6 (Disease Ontology:DOID:0111632); sickle cell anemia (Disease Ontology:DOID:10923); alpha thalassemia (Disease Ontology:DOID:1099); beta thalassemia (Disease Ontology:DOID:12241); malaria (Disease Ontology:DOID:12365); Parkinson's disease (Disease Ontology:DOID:14330); acute chest syndrome (Disease Ontology:DOID:1584); anemia (Disease Ontology:DOID:2355); hemoglobin C disease (Disease Ontology:DOID:2859); hemoglobinopathy (Disease Ontology:DOID:2860); congenital hemolytic anemia (Disease Ontology:DOID:589); polycythemia (Disease Ontology:DOID:8432)", "pathway": " (mmu:100503605); (mmu:101488143); (R-MMU-1237044); (R-MMU-1247673); (R-MMU-2168880); (R-MMU-6798695); (R-MMU-9707564); (R-MMU-9707616)", "pathway_count": 8, "publication_count": 3, "publication_id_list": "21750661;23040355;37507081", "class_list": "", "function": "ENU mutagenesis generated mouse lines with dominant beta-thalassemia mutations resembling those in the human disease: a nonsense mutation at codon 40 in exon 2 and a mutation at the polyadenylation signal of the beta-major gene., [RefSeq, PubMed]; Involved in oxygen transport from the lung to the various peripheral tissues., [UniProtKB, UniProtKB, UniProtKB]; This gene encodes a beta polypeptide chain found in adult hemoglobin, which consists of a tetramer of two alpha chains and two beta chains, and which functions in the transport of oxygen to various peripheral tissues. This gene is one of a cluster of beta-hemoglobin genes that are distally regulated by a locus control region, and which are organized along the chromosome in the order of their developmental expression. In mouse, two major strain-specific haplotypes of the beta-globin gene cluster are found - a 'single' haplotype found in C57BL/-type strains, which includes two highly similar adult beta-globin genes, beta s and beta t, and a 'diffuse' haplotype found in strains such as BALB/c and 129Sv, which includes two somewhat diverse adult beta-globin genes, beta-major and beta-minor. This gene represents the beta s adult gene found in the 'single' haplotype. Primary chromosome 7 of the mouse reference genome assembly, which is derived from C57BL/6 strain mice, represents the 'single' haplotype, while the 'diffuse' haplotype is represented in the reference genome collection by the BALB/c strain alternate contig, NT_095534.1. [provided by RefSeq, May 2013]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 16, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0046872 metal ion binding;GO:0044877 protein-containing complex binding;GO:0030492 hemoglobin binding;GO:0020037 heme binding;GO:0031721 hemoglobin alpha binding", "go_cellular_component": "GO:0005615 extracellular space;GO:0005833 hemoglobin complex;GO:0031838 haptoglobin-hemoglobin complex", "go_biological_process": "GO:0048821 erythrocyte development;GO:0098869 cellular oxidant detoxification;GO:0015671 oxygen transport", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "A8DUK4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "D3YX29-1", "uniprot_id": "D3YX29_MOUSE", "mass": 14105.0, "length": 119, "protein_name": "Oocyte maturation, beta", "gene_name": "Omt2b", "organism": "Mouse", "refseq_name": "oocyte maturation, beta", "refseq_ac": "NP_991391", "gene_names_uniprotkb": "Omt2b", "gene_names_refseq": "Mosg; OM2b; Omt2b", "protein_names_uniprotkb": "Oocyte maturation, beta", "protein_names_refseq": "oocyte maturation, beta", "tax_id": 10090, "disease": "", "pathway": " (mmu:382088)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005829 cytosol", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "D3YX29-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G5E8K1-1", "uniprot_id": "G5E8K1_MOUSE", "mass": 30016.0, "length": 270, "protein_name": "RIKEN cDNA 2610028H24 gene", "gene_name": "2610028H24Rik", "organism": "Mouse", "refseq_name": "uncharacterized protein C21orf58 homolog", "refseq_ac": "NP_084092", "gene_names_uniprotkb": "2610028H24Rik", "gene_names_refseq": "2610028H24Rik; ORF67", "protein_names_uniprotkb": "RIKEN cDNA 2610028H24 gene", "protein_names_refseq": "uncharacterized protein C21orf58 homolog", "tax_id": 10090, "disease": "", "pathway": " (mmu:76964)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "G5E8K1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3UU43-1", "uniprot_id": "CHPF2_MOUSE", "mass": 85656.0, "length": 768, "protein_name": "Chondroitin polymerizing factor 2, non-catalytic subunit", "gene_name": "Chpf2", "organism": "Mouse", "refseq_name": "chondroitin sulfate glucuronyltransferase", "refseq_ac": "NP_598674", "gene_names_uniprotkb": "Chpf2", "gene_names_refseq": "2010209O12Rik; Chpf2; Gm42230; mKIAA1402; mir-671", "protein_names_uniprotkb": "Chondroitin polymerizing factor 2, non-catalytic subunit", "protein_names_refseq": "chondroitin sulfate glucuronyltransferase", "tax_id": 10090, "disease": "", "pathway": " (mmu:100910); (R-MMU-2022870)", "pathway_count": 2, "publication_count": 3, "publication_id_list": "10.1101/2023.09.13.557529;21750661;30059200", "class_list": "glycogene;glycosyltransferase", "function": "Non-catalytic component of CHSY1-CHPF2 and CHSY3-CHPF2 chondroitin sulfate synthase complexes. CHPF2 associates with catalytically active chondroitin synthases (CHSY1/3) within heterodimeric complexes. Plays an essential role for the formation of a stable and functional chondroitin sulfate polymerase complexes., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 1, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 1, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 28, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0050510 N-acetylgalactosaminyl-proteoglycan 3-beta-glucuronosyltransferase activity;GO:0047238 glucuronosyl-N-acetylgalactosaminyl-proteoglycan 4-beta-N-acetylgalactosaminyltransferase activity", "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0032580 Golgi cisterna membrane", "go_biological_process": "GO:0050650 chondroitin sulfate proteoglycan biosynthetic process", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q3UU43-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TQQ6-1", "uniprot_id": "Q7TQQ6_MOUSE", "mass": 35086.0, "length": 315, "protein_name": "Olfactory receptor", "gene_name": "Or5b121", "organism": "Mouse", "refseq_name": "olfactory receptor family 5 subfamily B member 121", "refseq_ac": "NP_997458", "gene_names_uniprotkb": "Or5b121; Olfr1480; Olfr1484", "gene_names_refseq": "MOR202-44; Olfr1480; Or5b121", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2RE5P-3862389-3863336; olfactory receptor 1480; olfactory receptor family 5 subfamily B member 121", "tax_id": 10090, "disease": "", "pathway": " (mmu:404339)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21750661;32061665", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]; This odorant receptor, Olfr1480, responds to the odorant isoamyl acetate in vivo., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "Q7TQQ6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q61243-1", "uniprot_id": "Q61243_MOUSE", "mass": 13400.0, "length": 123, "protein_name": "V-set pre-B cell surrogate light chain 3", "gene_name": "Vpreb3", "organism": "Mouse", "refseq_name": "pre-B lymphocyte protein 3 isoform 1 precursor", "refseq_ac": "NP_033540", "gene_names_uniprotkb": "Vpreb3", "gene_names_refseq": "8HS-20; Vpreb-3; Vpreb3", "protein_names_uniprotkb": "V-set pre-B cell surrogate light chain 3", "protein_names_refseq": "pre-B lymphocyte gene 3; pre-B lymphocyte protein 3 isoform 1 precursor", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 3, "publication_id_list": "12165522;17681603;21750661", "class_list": "", "function": "Detection of functional V(H)81X heavy chains in adult mice with an assessment of complementarity-determining region 3 diversity and capacity to form pre-B cell receptor., [RefSeq, PubMed]; Pre-B cell receptor (BCR) signals establish the molecular network for BCR signaling even before the production of an IgL Chain and induce the expression of KLF2, a candidate for controlling clonal expansion and migration of functional pre-B cells., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0019814 immunoglobulin complex;GO:0005783 endoplasmic reticulum", "go_biological_process": "GO:0006955 immune response;GO:0002638 negative regulation of immunoglobulin production", "synthesized_glycan_count": 0, "hit_score": 0.4, "record_id": "Q61243-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9EPG6-1", "uniprot_id": "Q9EPG6_MOUSE", "mass": 35438.0, "length": 314, "protein_name": "Olfactory receptor", "gene_name": "Or2d36", "organism": "Mouse", "refseq_name": "olfactory receptor 716", "refseq_ac": "NP_666815", "gene_names_uniprotkb": "Or2d36; Olfr716", "gene_names_refseq": "MOR260-2; Olfr716; Or2d36", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "B1 olfactory receptor; GA_x6K02T2PBJ9-9497411-9498355; olfactory receptor 716; olfactory receptor MOR260-2", "tax_id": 10090, "disease": "", "pathway": " (mmu:258597)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0016020 membrane;GO:0005886 plasma membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell;GO:0050911 detection of chemical stimulus involved in sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q9EPG6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G5E845-1", "uniprot_id": "KCNKG_MOUSE", "mass": 32462.0, "length": 292, "protein_name": "Potassium channel, subfamily K, member 16", "gene_name": "Kcnk16", "organism": "Mouse", "refseq_name": "potassium channel, subfamily K, member 16", "refseq_ac": "NP_083282", "gene_names_uniprotkb": "Kcnk16", "gene_names_refseq": "4731413G05Rik; Kcnk16; TALK-1; TALK1", "protein_names_uniprotkb": "Potassium channel, subfamily K, member 16; 2P domain potassium channel Talk-1; Potassium channel subfamily K member 16; TALK-1; TWIK-related alkaline pH-activated K(+) channel 1", "protein_names_refseq": "2P domain potassium channel Talk-1; TWIK-related alkaline pH-activated K(+) channel 1; potassium channel, subfamily K, member 16", "tax_id": 10090, "disease": "heart conduction disease (Disease Ontology:DOID:10273)", "pathway": " (mmu:74571); (R-MMU-1299361); (R-MMU-5576886)", "pathway_count": 3, "publication_count": 7, "publication_id_list": "21750661;26239056;28928238;29348619;29402588;38206814;38700926", "class_list": "", "function": "Data establish TALK-1 channels as key regulators of beta cell ER Ca(2+) and suggest that TALK-1 may be a therapeutic target to reduce ER Ca(2+) handling defects in beta cells during the pathogenesis of diabetes. Publication Status: Online-Only, [RefSeq, PubMed]; K(+) channel that conducts voltage-dependent outward rectifying currents upon membrane depolarization. Voltage sensing is coupled to K(+) electrochemical gradient in an 'ion flux gating' mode where outward but not inward ion flow opens the gate (By similarity). Homo- and heterodimerizes to form functional channels with distinct regulatory and gating properties (By similarity). In pancreatic islets, conducts K(+) countercurrents for Ca(2+) release from the endoplasmic reticulum (ER) and regulates the frequency and duration of cytosolic Ca(2+) oscillations coupled to secretion of pancreatic hormones (PubMed:26239056, PubMed:28928238, PubMed:29402588). In pancreatic beta cells, drives ER Ca(2+) efflux, which in turn activates Ca(2+)-dependent plasma membrane K(+) slow currents and cytosolic Ca(2+) influx, overall contributing to synchronous cytosolic Ca(2+) oscillations. Limits glucose-induced cytosolic Ca(2+) oscillations coupled to second-phase INS secretion (PubMed:26239056, PubMed:28928238, PubMed:29348619). Contributes to beta cell adaptation to acute inflammation by maintaining normal cytosolic Ca(2+) levels and INS secretion (PubMed:29348619). May regulate beta cell mitochondrial Ca(2+) levels either indirectly via ER Ca(2+) efflux or directly by hyperpolarizing the mitochondrial membrane potential. Limits mitochondrial Ca(2+) oscillations and ATP production involved in glucose homeostasis upon metabolic stress (PubMed:26239056). In pancreatic delta cells, limits Ca(2+)-induced Ca(2+)-release involved in somatostatin secretion and modulates islet paracrine signaling involved in glucagon secretion (PubMed:29402588). Permeable to other monovalent cations such as Rb(+) and Cs(+) (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed, UniProtKB, PubMed]; TALK-1 reduces delta-cell cytosolic Ca2+ elevations and somatostatin release by limiting delta-cell Ca2+-induced Ca2+ release., [RefSeq, PubMed]; TALK-1-mediated alterations of beta-cell mitochondrial function and insulin secretion impair glucose homeostasis on a diabetogenic diet., [RefSeq, PubMed]; The MODY-associated KCNK16 L114P mutation increases islet glucagon secretion and limits insulin secretion resulting in transient neonatal diabetes and glucose dyshomeostasis in adults. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "1.8.-.-", "go_molecular_function": "GO:0015271 outward rectifier potassium channel activity;GO:0022841 potassium ion leak channel activity;GO:0042802 identical protein binding;GO:0046872 metal ion binding;GO:0046982 protein heterodimerization activity", "go_cellular_component": "GO:0005743 mitochondrial inner membrane;GO:0005886 plasma membrane;GO:0005789 endoplasmic reticulum membrane;GO:0016020 membrane", "go_biological_process": "GO:0086011 membrane repolarization during action potential;GO:0098900 regulation of action potential;GO:0006813 potassium ion transport;GO:0061178 regulation of insulin secretion involved in cellular response to glucose stimulus;GO:0051279 regulation of release of sequestered calcium ion into cytosol", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "G5E845-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9R0K4-1", "uniprot_id": "Q9R0K4_MOUSE", "mass": 34980.0, "length": 310, "protein_name": "Olfactory receptor", "gene_name": "Or4e1", "organism": "Mouse", "refseq_name": "odorant receptor MOR10", "refseq_ac": "NP_065259", "gene_names_uniprotkb": "Or4e1; Olfr1508", "gene_names_refseq": "MOR244-2; MOR244-4; Mor10; Olfr1508; Or10; Or4e1", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2RJGY-520647-521579; gene for odorant receptor MOR10; odorant receptor MOR10; olfactory receptor 1508; olfactory receptor MOR244-2", "tax_id": 10090, "disease": "", "pathway": " (mmu:57270)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell;GO:0050911 detection of chemical stimulus involved in sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q9R0K4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G5E8V9-1", "uniprot_id": "ARFP1_MOUSE", "mass": 41518.0, "length": 373, "protein_name": "Arfaptin-1", "gene_name": "Arfip1", "organism": "Mouse", "refseq_name": "arfaptin-1 isoform 1", "refseq_ac": "NP_001074562", "gene_names_uniprotkb": "Arfip1", "gene_names_refseq": "2310030I10Rik; Arfaptin; Arfip1; D3Ertd598e", "protein_names_uniprotkb": "Arfaptin-1; ADP-ribosylation factor-interacting protein 1", "protein_names_refseq": "ADP-ribosylation factor interacting protein 1; arfaptin-1 isoform 1; arfaptin-1", "tax_id": 10090, "disease": "", "pathway": " (mmu:99889)", "pathway_count": 1, "publication_count": 0, "publication_id_list": "", "class_list": "", "function": "Plays a role in controlling biogenesis of secretory granules at the trans-Golgi network. Mechanistically, binds ARF-GTP at the neck of a growing secretory granule precursor and forms a protective scaffold. Once the granule precursor has been completely loaded, active PRKD1 phosphorylates ARFIP1 and releases it from ARFs. In turn, ARFs induce fission. Through this mechanism, ensures proper secretory granule formation at the Golgi of pancreatic beta cells., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 7, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "A2RSX9;E9Q3G5", "ec_number_list": "", "go_molecular_function": "GO:0005543 phospholipid binding;GO:0019904 protein domain specific binding;GO:0070273 phosphatidylinositol-4-phosphate binding", "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus;GO:0005829 cytosol;GO:0032588 trans-Golgi network membrane", "go_biological_process": "GO:1905280 negative regulation of retrograde transport, endosome to Golgi;GO:0006886 intracellular protein transport;GO:0050708 regulation of protein secretion;GO:0034315 regulation of Arp2/3 complex-mediated actin nucleation", "synthesized_glycan_count": 0, "hit_score": 0.1, "record_id": "G5E8V9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A2BI50-1", "uniprot_id": "A2BI50_MOUSE", "mass": 27193.0, "length": 236, "protein_name": "X-linked lymphocyte-regulated 5B", "gene_name": "Xlr5b", "organism": "Mouse", "refseq_name": "X-linked lymphocyte-regulated 5B", "refseq_ac": "NP_001104763", "gene_names_uniprotkb": "Xlr5b", "gene_names_refseq": "Xlr5b", "protein_names_uniprotkb": "X-linked lymphocyte-regulated 5B", "protein_names_refseq": "X-linked lymphocyte-regulated 5B", "tax_id": 10090, "disease": "", "pathway": " (mmu:627081)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0000795 synaptonemal complex", "go_biological_process": "GO:0007286 spermatid development;GO:0051321 meiotic cell cycle", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A2BI50-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q78TU8-1", "uniprot_id": "F107A_MOUSE", "mass": 17510.0, "length": 144, "protein_name": "Actin-associated protein FAM107A", "gene_name": "Fam107a", "organism": "Mouse", "refseq_name": "actin-associated protein FAM107A isoform 1", "refseq_ac": "NP_899010", "gene_names_uniprotkb": "Fam107a", "gene_names_refseq": "DRR1; Fam107a", "protein_names_uniprotkb": "Actin-associated protein FAM107A", "protein_names_refseq": "actin-associated protein FAM107A isoform 1; actin-associated protein FAM107A; protein FAM107A", "tax_id": 10090, "disease": "", "pathway": " (mmu:268709)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "21750661;21969592;25637808;33878327;33965500", "class_list": "", "function": "Downregulated in renal carcinoma 1 (DRR1) mediates the differentiation of neural stem cells through transcriptional regulation., [RefSeq, PubMed]; Endogenous DRR1 localizes to some, but not all, synapses, with preference for the presynaptic region. Enhancement of DRR1 expression reduced spine density, diminished the probability of synaptic glutamate release, and altered cognitive performance., [RefSeq, PubMed]; Loss of family with sequence similarity 107, member A (FAM107A) induces browning in 3T3-L1 adipocytes., [RefSeq, PubMed]; Stress-inducible actin-binding protein that plays a role in synaptic and cognitive functions by modulating actin filamentous (F-actin) dynamics (PubMed:21969592). Mediates polymerization of globular actin to F-actin (PubMed:21969592). Also binds to, stabilizes and bundles F-actin (PubMed:21969592). Involved in synaptic function by regulating neurite outgrowth in an actin-dependent manner and for the acquisition of hippocampus-dependent cognitive function, such as learning and long-term memory (PubMed:21969592). Plays a role in the actin and microtubule cytoskeleton organization; negatively regulates focal adhesion (FA) assembly promoting malignant glial cell migration in an actin-, microtubule- and MAP1A-dependent manner. Also involved in neuroblastoma G1/S phase cell cycle progression and cell proliferation inhibition by stimulating ubiquitination of NF-kappa-B subunit RELA and NF-kappa-B degradation in a COMMD1- and actin-dependent manner. May play a role in tumor development (By similarity)., [UniProtKB, UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003779 actin binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0098871 postsynaptic actin cytoskeleton;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005925 focal adhesion", "go_biological_process": "GO:0030335 positive regulation of cell migration;GO:0032956 regulation of actin cytoskeleton organization;GO:0050890 cognition;GO:1900272 negative regulation of long-term synaptic potentiation;GO:0051017 actin filament bundle assembly", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "Q78TU8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q63953-1", "uniprot_id": "Q63953_MOUSE", "mass": 37471.0, "length": 332, "protein_name": "Interferon gamma receptor 2", "gene_name": "Ifngr2", "organism": "Mouse", "refseq_name": "interferon gamma receptor 2 precursor", "refseq_ac": "NP_032364", "gene_names_uniprotkb": "Ifngr2", "gene_names_refseq": "Ifgr2; Ifgt; Ifngr2", "protein_names_uniprotkb": "Interferon gamma receptor 2", "protein_names_refseq": "interferon gamma receptor 2 precursor", "tax_id": 10090, "disease": "immunodeficiency 28 (Disease Ontology:DOID:0111995); congenital heart disease (Disease Ontology:DOID:1682); pulmonary tuberculosis (Disease Ontology:DOID:2957); acute myocardial infarction (Disease Ontology:DOID:9408); allergic asthma (Disease Ontology:DOID:9415); type 1 diabetes mellitus (Disease Ontology:DOID:9744)", "pathway": " (mmu:15980); (R-MMU-877300); (R-MMU-877312); (R-MMU-9732724)", "pathway_count": 4, "publication_count": 4, "publication_id_list": "10.1101/2023.09.13.557529;21750661;30779550;30899004", "class_list": "", "function": "", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 4, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 4, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 4, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 9015, "biomarker_type": "", "glycan_count": 5, "disease_count": 6, "glyco_site_count": 5, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004906 type II interferon receptor activity;GO:0004896 cytokine receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0001774 microglial cell activation;GO:0051607 defense response to virus;GO:0019221 cytokine-mediated signaling pathway;GO:1900451 positive regulation of glutamate receptor signaling pathway;GO:0038196 type III interferon-mediated signaling pathway", "synthesized_glycan_count": 0, "hit_score": 1.4, "record_id": "Q63953-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TRW8-1", "uniprot_id": "Q7TRW8_MOUSE", "mass": 34354.0, "length": 315, "protein_name": "Olfactory receptor", "gene_name": "Or3a1d", "organism": "Mouse", "refseq_name": "olfactory receptor 411", "refseq_ac": "NP_666920", "gene_names_uniprotkb": "Or3a1d; Olfr410; Olfr411", "gene_names_refseq": "MOR255-3; Olfr411; Or3a1d", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2P1NL-4481525-4480578; olfactory receptor 411; olfactory receptor MOR255-3; olfactory receptor MOR255-6", "tax_id": 10090, "disease": "", "pathway": " (mmu:258704)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007165 signal transduction;GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q7TRW8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "D3Z1A5-1", "uniprot_id": "D3Z1A5_MOUSE", "mass": 125059.0, "length": 1117, "protein_name": "ADAM metallopeptidase with thrombospondin type 1 motif 6", "gene_name": "Adamts6", "organism": "Mouse", "refseq_name": "A disintegrin and metalloproteinase with thrombospondin motifs 6 precursor", "refseq_ac": "NP_001074489", "gene_names_uniprotkb": "Adamts6", "gene_names_refseq": "A930019D11Rik; ADAM-TS6; Adamts6; b2b1879.1Clo; b2b2029Clo; b2b2182Clo; b2b2187.1Clo; b2b2228Clo", "protein_names_uniprotkb": "ADAM metallopeptidase with thrombospondin type 1 motif 6", "protein_names_refseq": "A disintegrin and metalloproteinase with thrombospondin motifs 6 precursor; a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 6; a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 6", "tax_id": 10090, "disease": "", "pathway": " (mmu:108154); (R-MMU-5173214)", "pathway_count": 2, "publication_count": 2, "publication_id_list": "21750661;25428506", "class_list": "", "function": "", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004222 metalloendopeptidase activity;GO:0046872 metal ion binding;GO:0008237 metallopeptidase activity", "go_cellular_component": "GO:0031012 extracellular matrix", "go_biological_process": "GO:0006508 proteolysis;GO:0007507 heart development;GO:0030198 extracellular matrix organization;GO:0001822 kidney development;GO:0035904 aorta development", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "D3Z1A5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9EQB6-1", "uniprot_id": "Q9EQB6_MOUSE", "mass": 35073.0, "length": 314, "protein_name": "Olfactory receptor", "gene_name": "Or8g34", "organism": "Mouse", "refseq_name": "olfactory receptor family 8 subfamily G member 34", "refseq_ac": "NP_666443", "gene_names_uniprotkb": "Or8g34; Olfr954", "gene_names_refseq": "MOR171-42; MOR171-53; Olfr954; Or8g34", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2PVTD-33158015-33158950; olfactory receptor 954; olfactory receptor MOR171-42; olfactory receptor family 8 subfamily G member 34", "tax_id": 10090, "disease": "", "pathway": " (mmu:258328)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. 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The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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Publication Status: Online-Only, [RefSeq, PubMed]; Host versus cell-dependent effects of beta-arrestin 1 expression in prostate tumorigenesis., [RefSeq, PubMed]; Identification of a novel role for TL1A/DR3 deficiency in acute respiratory distress syndrome that exacerbates alveolar epithelial disruption. Publication Status: Online-Only, [RefSeq, PubMed]; The cytokine receptor DR3 identifies and promotes the activation of thymic NKT17 cells. 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The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q7TR95-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TRA0-1", "uniprot_id": "Q7TRA0_MOUSE", "mass": 35133.0, "length": 314, "protein_name": "Olfactory receptor", "gene_name": "Or5g27", "organism": "Mouse", "refseq_name": "olfactory receptor 996", "refseq_ac": "NP_666648", "gene_names_uniprotkb": "Or5g27; Olfr996", "gene_names_refseq": "MOR175-4; Olfr996; Or5g27", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2Q125-47058060-47059004; olfactory receptor 996; olfactory receptor MOR175-4", "tax_id": 10090, "disease": "", "pathway": " (mmu:258429)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q7TRA0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TRI2-1", "uniprot_id": "Q7TRI2_MOUSE", "mass": 35794.0, "length": 314, "protein_name": "Olfactory receptor", "gene_name": "Or6c6", "organism": "Mouse", "refseq_name": "olfactory receptor family 6 subfamily C member 6", "refseq_ac": "NP_001011797", "gene_names_uniprotkb": "Or6c6; Olfr782; Olfr804", "gene_names_refseq": "MOR110-8; Olfr782; Or6c6", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2PULF-11031172-11032116; olfactory receptor 782; olfactory receptor MOR110-8; olfactory receptor family 6 subfamily C member 6", "tax_id": 10090, "disease": "", "pathway": " (mmu:257985)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q7TRI2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TRI8-1", "uniprot_id": "Q7TRI8_MOUSE", "mass": 34977.0, "length": 313, "protein_name": "Olfactory receptor", "gene_name": "Or2h15", "organism": "Mouse", "refseq_name": "olfactory receptor family 2 subfamily H member 15", "refseq_ac": "NP_001005481", "gene_names_uniprotkb": "Or2h15; Olfr132", "gene_names_refseq": "MOR256-49; Olfr132; Or2h15", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2PSCP-2579687-2578746; olfactory receptor 132; olfactory receptor MOR256-49; olfactory receptor family 2 subfamily H member 15", "tax_id": 10090, "disease": "", "pathway": " (mmu:257889)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell;GO:0050911 detection of chemical stimulus involved in sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q7TRI8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TRV7-1", "uniprot_id": "Q7TRV7_MOUSE", "mass": 35494.0, "length": 317, "protein_name": "Olfactory receptor", "gene_name": "Or2f1", "organism": "Mouse", "refseq_name": "olfactory receptor family 2 subfamily F member 1", "refseq_ac": "NP_001011799", "gene_names_uniprotkb": "Or2f1; Olfr453", "gene_names_refseq": "MOR257-8P; Olfr453; Or2f1", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2P3E9-4815856-4814903; olfactory receptor 453; olfactory receptor MOR257-8P; olfactory receptor family 2 subfamily F member 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:258016); (R-MMU-381753)", "pathway_count": 2, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell;GO:0050911 detection of chemical stimulus involved in sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q7TRV7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TRY5-1", "uniprot_id": "Q7TRY5_MOUSE", "mass": 36802.0, "length": 330, "protein_name": "Olfactory receptor", "gene_name": "Or12k5", "organism": "Mouse", "refseq_name": "olfactory receptor family 12 subfamily K member 5", "refseq_ac": "NP_997118", "gene_names_uniprotkb": "Or12k5; Olfr358", "gene_names_refseq": "GA_x6K02T2NLDC-33697309-33696317; MOR159-4; Olfr358; Or12k5", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "olfactory receptor 358; olfactory receptor GA_x6K02T2NLDC-33697309-33696317; olfactory receptor family 12 subfamily K member 5", "tax_id": 10090, "disease": "", "pathway": " (mmu:227789)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]; Possible taste receptor., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell;GO:0050911 detection of chemical stimulus involved in sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q7TRY5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TS13-1", "uniprot_id": "Q7TS13_MOUSE", "mass": 35274.0, "length": 315, "protein_name": "Olfactory receptor", "gene_name": "Or5ae1", "organism": "Mouse", "refseq_name": "olfactory receptor 290", "refseq_ac": "NP_666528", "gene_names_uniprotkb": "Or5ae1; Olfr290", "gene_names_refseq": "MOR254-1; Olfr290; Or5ae1", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2NHDJ-11170115-11169168; olfactory receptor 290; olfactory receptor MOR254-1", "tax_id": 10090, "disease": "", "pathway": " (mmu:258411)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q7TS13-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BJT9-1", "uniprot_id": "EDEM2_MOUSE", "mass": 64610.0, "length": 577, "protein_name": "ER degradation-enhancing alpha-mannosidase-like protein 2", "gene_name": "Edem2", "organism": "Mouse", "refseq_name": "ER degradation-enhancing alpha-mannosidase-like protein 2 precursor", "refseq_ac": "NP_663512", "gene_names_uniprotkb": "Edem2", "gene_names_refseq": "9530090G24Rik; Edem2", "protein_names_uniprotkb": "ER degradation-enhancing alpha-mannosidase-like protein 2", "protein_names_refseq": "ER degradation-enhancing alpha-mannosidase-like protein 2 precursor; ER degradation-enhancing alpha-mannosidase-like protein 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:108687)", "pathway_count": 1, "publication_count": 6, "publication_id_list": "15579471;20485683;24200403;25655076;34428180;35820727", "class_list": "glycogene;glycosylhydrolase", "function": "Data suggest Edem1/Edem2 participate in ricin translocation; overexpression of Edem2, in contrast to Edem1, directly promotes ricin subunit A transport from endoplasmic reticulum (ER) to cytosol; this translocation is not dependent on ER translocon., [RefSeq, PubMed]; Involved in the endoplasmic reticulum-associated degradation (ERAD) pathway that targets misfolded glycoproteins for degradation in an N-glycan-dependent manner (PubMed:15579471, PubMed:25655076). May initiate ERAD by promoting the first mannose trimming step of ERAD substrates, from Man9GlcNAc2 to Man8GlcNAc2 (By similarity). Seems to recognize and bind to exposed hydrophobic regions in target proteins (PubMed:25655076)., [UniProtKB, PubMed, UniProtKB, PubMed]", "predicted_glycosites": 4, "predicted_n_glycosites": 4, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 32, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 4, "binding_glycan_count": 0, "secondary_ac_list": "Q8BJR2;Q8BK85;Q91VV3", "ec_number_list": "", "go_molecular_function": "GO:0005509 calcium ion binding;GO:0004571 mannosyl-oligosaccharide 1,2-alpha-mannosidase activity", "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005788 endoplasmic reticulum lumen;GO:0016020 membrane;GO:0044322 endoplasmic reticulum quality control compartment", "go_biological_process": "GO:0005975 carbohydrate metabolic process;GO:0030968 endoplasmic reticulum unfolded protein response;GO:0036503 ERAD pathway;GO:1904380 endoplasmic reticulum mannose trimming;GO:1904154 positive regulation of retrograde protein transport, ER to cytosol", "synthesized_glycan_count": 0, "hit_score": 0.7, "record_id": "Q8BJT9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8R2D0-1", "uniprot_id": "Q8R2D0_MOUSE", "mass": 34754.0, "length": 302, "protein_name": "Vomeronasal type-1 receptor", "gene_name": "Vmn1r23", "organism": "Mouse", "refseq_name": "vomeronasal 1 receptor 23", "refseq_ac": "NP_598940", "gene_names_uniprotkb": "Vmn1r23", "gene_names_refseq": "V1rc24; Vmn1r23", "protein_names_uniprotkb": "Vomeronasal type-1 receptor", "protein_names_refseq": "vomernasal 1 receptor Vmn1r23; vomeronasal 1 receptor 23; vomeronasal 1 receptor, C24", "tax_id": 10090, "disease": "", "pathway": " (mmu:171197)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005550 pheromone binding;GO:0016503 pheromone receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0019236 response to pheromone;GO:0007606 sensory perception of chemical stimulus", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q8R2D0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8R2D4-1", "uniprot_id": "Q8R2D4_MOUSE", "mass": 35231.0, "length": 303, "protein_name": "Vomeronasal type-1 receptor", "gene_name": "Vmn1r6", "organism": "Mouse", "refseq_name": "vomeronasal 1 receptor 6", "refseq_ac": "NP_598936", "gene_names_uniprotkb": "Vmn1r6", "gene_names_refseq": "V1rc20; Vmn1r6", "protein_names_uniprotkb": "Vomeronasal type-1 receptor", "protein_names_refseq": "vomernasal 1 receptor Vmn1r6; vomeronasal 1 receptor 6; vomeronasal 1 receptor, C20", "tax_id": 10090, "disease": "", "pathway": " (mmu:171193)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005550 pheromone binding;GO:0016503 pheromone receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0019236 response to pheromone;GO:0007606 sensory perception of chemical stimulus", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q8R2D4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VEU4-1", "uniprot_id": "Q8VEU4_MOUSE", "mass": 34884.0, "length": 312, "protein_name": "Olfactory receptor", "gene_name": "Or14j2", "organism": "Mouse", "refseq_name": "olfactory receptor family 14 subfamily J member 2", "refseq_ac": "NP_666401", "gene_names_uniprotkb": "Or14j2; Olfr113", "gene_names_refseq": "MOR218-9; Olfr113; Or14j2", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2PSCP-2034880-2033942; olfactory receptor 113; olfactory receptor MOR218-9; olfactory receptor family 14 subfamily J member 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:258286)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q8VEU4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VF05-1", "uniprot_id": "Q8VF05_MOUSE", "mass": 35537.0, "length": 312, "protein_name": "Olfactory receptor", "gene_name": "Or2l13b", "organism": "Mouse", "refseq_name": "olfactory receptor family 2 subfamily L member 13B", "refseq_ac": "NP_666469", "gene_names_uniprotkb": "Or2l13b; Olfr168", "gene_names_refseq": "MOR271-1; Olfr168; Or2l13b", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x54KRFPKG5P-15979009-15978071; olfactory receptor 168; olfactory receptor MOR271-1; olfactory receptor family 2 subfamily L member 13B", "tax_id": 10090, "disease": "", "pathway": " (mmu:258354)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0005789 endoplasmic reticulum membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell;GO:0050911 detection of chemical stimulus involved in sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q8VF05-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VF10-1", "uniprot_id": "Q8VF10_MOUSE", "mass": 35944.0, "length": 317, "protein_name": "Olfactory receptor", "gene_name": "Or4f59", "organism": "Mouse", "refseq_name": "olfactory receptor 1312", "refseq_ac": "NP_666474", "gene_names_uniprotkb": "Or4f59; Olfr1312", "gene_names_refseq": "MOR245-20; Olfr1312; Or4f59", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2Q125-73090482-73089529; olfactory receptor 1312; olfactory receptor MOR245-20", "tax_id": 10090, "disease": "", "pathway": " (mmu:258359)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q8VF10-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VF73-1", "uniprot_id": "Q8VF73_MOUSE", "mass": 35314.0, "length": 314, "protein_name": "Olfactory receptor", "gene_name": "Or5ak24", "organism": "Mouse", "refseq_name": "olfactory receptor family 5 subfamily AK member 24", "refseq_ac": "NP_666644", "gene_names_uniprotkb": "Or5ak24; Olfr994", "gene_names_refseq": "MOR203-4; Olfr994; Or5ak24", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2Q125-46907515-46906571; olfactory receptor 994; olfactory receptor MOR203-4; olfactory receptor family 5 subfamily AK member 24", "tax_id": 10090, "disease": "", "pathway": " (mmu:258425)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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Gm4175; Gm4214; Vmn1r247", "gene_names_refseq": "100043079; Gm4214; Vmn1r161; Vmn1r258", "protein_names_uniprotkb": "Vomeronasal type-1 receptor", "protein_names_refseq": "vomeronasal 1 receptor Vmn1r161", "tax_id": 10090, "disease": "", "pathway": " (mmu:100043019); (mmu:100043079)", "pathway_count": 2, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "D3YTX7;D3YTX8;E9Q2L6;E9Q8L4;E9Q8L5;G3UYH3", "ec_number_list": "", "go_molecular_function": "GO:0005550 pheromone binding;GO:0016503 pheromone receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0019236 response to pheromone;GO:0007606 sensory perception of chemical stimulus", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "D3YTW8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "D3YUI0-1", "uniprot_id": "D3YUI0_MOUSE", "mass": 95915.0, "length": 854, "protein_name": "Parathyroid cell calcium-sensing receptor", "gene_name": "Vmn2r24", "organism": "Mouse", "refseq_name": "vomeronasal receptor Vmn2r24", "refseq_ac": "NP_001098109", "gene_names_uniprotkb": "Vmn2r24", "gene_names_refseq": "EG243628; Vmn2r24", "protein_names_uniprotkb": "Parathyroid cell calcium-sensing receptor", "protein_names_refseq": "vomeronasal receptor Vmn2r24", "tax_id": 10090, "disease": "", "pathway": " (mmu:243628)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0051924 regulation of calcium ion transport", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "D3YUI0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9PW59-1", "uniprot_id": "E9PW59_MOUSE", "mass": 35639.0, "length": 316, "protein_name": "Olfactory receptor", "gene_name": "Or8b50", "organism": "Mouse", "refseq_name": "olfactory receptor 914", "refseq_ac": "NP_666997", "gene_names_uniprotkb": "Or8b50; Olfr914", "gene_names_refseq": "MOR165-7; Olfr914; Or8b50", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2PVTD-32308823-32309773; olfactory receptor 914; olfactory receptor MOR165-7", "tax_id": 10090, "disease": "", "pathway": " (mmu:258782)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21750661;25428506", "class_list": "", "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "E9PWI5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9PX47-1", "uniprot_id": "E9PX47_MOUSE", "mass": 37201.0, "length": 334, "protein_name": "Olfactory receptor", "gene_name": "Or55b4", "organism": "Mouse", "refseq_name": "olfactory receptor 544", "refseq_ac": "NP_064685", "gene_names_uniprotkb": "Or55b4; Olfr544", "gene_names_refseq": "MOR42-3; Olfr544; Or55b4; Ors6", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "G-protein-coupled receptor; GA_x6K02T2PBJ9-5206624-5205620; odorant receptor S6; odorant receptor S79; olfactory receptor 544; olfactory receptor MOR42-3", "tax_id": 10090, "disease": "", "pathway": " (mmu:257926)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "17114180;21750661;28235481;28990936;34674602", "class_list": "", "function": "A network of 8 residues in transmembrane domains III, V, and VI was identified forming part of the ligand binding pocket of MOR42-3, [RefSeq, PubMed]; Activation of ectopic olfactory receptor 544 induces GLP-1 secretion and regulates gut inflammation., [RefSeq, PubMed]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]; Olfr544 orchestrates the metabolic interplay between the liver and adipose tissue, mobilizing stored fats from adipose tissue and shifting the fuel preference to fats in the liver and brown adipose tissue., [RefSeq, PubMed]; These data indicated that a hydrogen bond between Y109 residue and azelaic acid is a major determinant of the Olfr544-azelaic acid interaction and activation., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "E9PX47-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9PXC0-1", "uniprot_id": "E9PXC0_MOUSE", "mass": 55816.0, "length": 504, "protein_name": "Signal recognition particle 54 kDa protein", "gene_name": "Srp54c", "organism": "Mouse", "refseq_name": "signal recognition particle 54C isoform 1", "refseq_ac": "NP_001093580", "gene_names_uniprotkb": "Srp54c", "gene_names_refseq": "E330029E12Rik; Srp54c", "protein_names_uniprotkb": "Signal recognition particle 54 kDa protein; 3.6.5.-", "protein_names_refseq": "signal recognition particle 54C isoform 1", "tax_id": 10090, "disease": "Shwachman-Diamond syndrome (Disease Ontology:DOID:0060479); severe congenital neutropenia 8 (Disease Ontology:DOID:0112135); neutropenia (Disease Ontology:DOID:1227)", "pathway": " (mmu:100101806)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Component of the signal recognition particle (SRP) complex, a ribonucleoprotein complex that mediates the cotranslational targeting of secretory and membrane proteins to the endoplasmic reticulum (ER). As part of the SRP complex, associates with the SRP receptor (SR) component SRPRA to target secretory proteins to the endoplasmic reticulum membrane. Binds to the signal sequence of presecretory proteins when they emerge from the ribosomes. Displays basal GTPase activity, and stimulates reciprocal GTPase activation of the SR subunit SRPRA. Forms a guanosine 5'-triphosphate (GTP)-dependent complex with the SR subunit SRPRA. SR compaction and GTPase mediated rearrangement of SR drive SRP-mediated cotranslational protein translocation into the ER. Requires the presence of SRP9/SRP14 and/or SRP19 to stably interact with RNA. 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Gm5726; Gm8677; Vmn1r255", "gene_names_refseq": "EG435946; Gm5726; Vmn1r105; Vmn1r245", "protein_names_uniprotkb": "Vomeronasal type-1 receptor", "protein_names_refseq": "vomeronasal 1 receptor Vmn1r105", "tax_id": 10090, "disease": "", "pathway": " (mmu:435946); (mmu:667512)", "pathway_count": 2, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005550 pheromone binding;GO:0016503 pheromone receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0019236 response to pheromone;GO:0007606 sensory perception of chemical stimulus", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "K9J7G9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3ZAS0-1", "uniprot_id": "SL9A2_MOUSE", "mass": 91646.0, "length": 814, "protein_name": "Sodium/hydrogen exchanger 2", "gene_name": "Slc9a2", "organism": "Mouse", "refseq_name": "sodium/hydrogen exchanger 2 precursor", "refseq_ac": "NP_001028461", "gene_names_uniprotkb": "Slc9a2; Nhe2", "gene_names_refseq": "2210416H12Rik; 4932415O19Rik; NHE-2; NHE2; Slc9a2", "protein_names_uniprotkb": "Sodium/hydrogen exchanger 2; NHE-2; Na(+)/H(+) exchanger 2; Sodium/hydrogen exchanger; Solute carrier family 9 member 2", "protein_names_refseq": "Na(+)/H(+) exchanger 2; sodium/hydrogen exchanger 2 precursor; sodium/hydrogen exchanger 2; sodium/hydrogen exchanger; solute carrier family 9 member 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:226999); (R-MMU-425986)", "pathway_count": 2, "publication_count": 8, "publication_id_list": "11099134;11705743;14962844;16690903;21900251;30073618;34985202;9502765", "class_list": "", "function": "Expression of solute carrier family 40 (iron-regulated transporter) member 1 (Slc40a1) within the mammary gland can mediate the effect of milk mineral concentration quantitative trait loci 9 (Mmcq9) on milk iron concentration., [RefSeq, PubMed]; Plasma membrane Na(+)/H(+) antiporter (PubMed:14962844, PubMed:16690903). Mediates the electroneutral exchange of intracellular H(+) ions for extracellular Na(+) (PubMed:14962844). Major apical Na(+)/H(+) exchanger in the base of the colonic crypt (PubMed:14962844, PubMed:16690903). Controls in the colonic crypt intracellular pH (pHi) to direct colonic epithelial cell differentiation into the absorptive enterocyte lineage at the expense of the secretory lineage (PubMed:14962844, PubMed:34985202)., [UniProtKB, PubMed, PubMed, PubMed]; Sodium/hydrogen-exchanger-2 modulates colonocyte lineage differentiation., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0015385 sodium:proton antiporter activity;GO:0015386 potassium:proton antiporter activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0005903 brush border;GO:0030054 cell junction;GO:0016324 apical plasma membrane", "go_biological_process": "GO:0030855 epithelial cell differentiation;GO:0008104 intracellular protein localization;GO:0035725 sodium ion transmembrane transport;GO:0006814 sodium ion transport;GO:0051453 regulation of intracellular pH", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "Q3ZAS0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q5NCD6-1", "uniprot_id": "Q5NCD6_MOUSE", "mass": 36050.0, "length": 327, "protein_name": "Olfactory receptor", "gene_name": "Or2w3b", "organism": "Mouse", "refseq_name": "olfactory receptor 317", "refseq_ac": "NP_001011769", "gene_names_uniprotkb": "Or2w3b; Olfr179; Olfr317", "gene_names_refseq": "MOR256-47; Olfr317; Or2w3b", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x5J8B7W3KVV-2795544-2795410; GA_x6K02T2NKPP-680866-681849; olfactory receptor 317; olfactory receptor MOR256-47", "tax_id": 10090, "disease": "", "pathway": " (mmu:257931)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell;GO:0050911 detection of chemical stimulus involved in sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q5NCD6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q5NCD7-1", "uniprot_id": "Q5NCD7_MOUSE", "mass": 33911.0, "length": 306, "protein_name": "Olfactory receptor", "gene_name": "Or2ak5", "organism": "Mouse", "refseq_name": "olfactory receptor 318", "refseq_ac": "NP_666712", "gene_names_uniprotkb": "Or2ak5; Olfr316; Olfr318", "gene_names_refseq": "MOR285-1; Olfr318; Or2ak5", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2NKPP-692816-693736; olfactory receptor 318; olfactory receptor MOR285-1", "tax_id": 10090, "disease": "", "pathway": " (mmu:258494)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "A0A087WP04", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell;GO:0050911 detection of chemical stimulus involved in sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q5NCD7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TQU8-1", "uniprot_id": "Q7TQU8_MOUSE", "mass": 35475.0, "length": 320, "protein_name": "Olfactory receptor", "gene_name": "Or7c70", "organism": "Mouse", "refseq_name": "olfactory receptor family 7 subfamily C member 70", "refseq_ac": "NP_666420", "gene_names_uniprotkb": "Or7c70; Olfr1356", "gene_names_refseq": "MOR142-1; MOR142-2_p; Olfr1356; Or7c70", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2QGN0-2962025-2962987; olfactory receptor 1356; olfactory receptor MOR142-1; olfactory receptor family 7 subfamily C member 70", "tax_id": 10090, "disease": "", "pathway": " (mmu:258305); (R-MMU-381753)", "pathway_count": 2, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0005789 endoplasmic reticulum membrane", "go_biological_process": "GO:0007165 signal transduction;GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q7TQU8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TQW3-1", "uniprot_id": "Q7TQW3_MOUSE", "mass": 34809.0, "length": 310, "protein_name": "Olfactory receptor", "gene_name": "Or11n2", "organism": "Mouse", "refseq_name": "olfactory receptor family 11 subfamily N member 2", "refseq_ac": "NP_001011794", "gene_names_uniprotkb": "Or11n2; Olfr1322", "gene_names_refseq": "MOR264-16P; Olfr1322; Or11n2", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2Q64A-11927171-11926215; olfactory receptor 1322; olfactory receptor MOR264-16P; olfactory receptor family 11 subfamily N member 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:257978)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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[provided by RefSeq, Jul 2008]., [RefSeq]; This odorant receptor, Olfr190, responds to the odorant isoamyl acetate in vivo., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "K7N5T5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "L7MU51-1", "uniprot_id": "L7MU51_MOUSE", "mass": 35481.0, "length": 318, "protein_name": "Olfactory receptor", "gene_name": "Or4a76", "organism": "Mouse", "refseq_name": "olfactory receptor 1249", "refseq_ac": "NP_001011796", "gene_names_uniprotkb": "Or4a76; Olfr1249", "gene_names_refseq": "MOR231-16P; MOR231-17P; Olfr1249; Olfr1541-ps1; Or4a76", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2Q125-51072323-51071367; MOR231-25_p; olfactory receptor 1249; olfactory receptor 1541, pseudogene 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:257984)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "L7MU51-1", "record_type": "protein" }, { "uniprot_canonical_ac": "L7N1X5-1", "uniprot_id": "L7N1X5_MOUSE", "mass": 35045.0, "length": 310, "protein_name": "Olfactory receptor", "gene_name": "Or8b1c", "organism": "Mouse", "refseq_name": "olfactory receptor 905", "refseq_ac": "NP_667015", "gene_names_uniprotkb": "Or8b1c; Olfr905", "gene_names_refseq": "MOR167-1; Olfr905; Or8b1c", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2PVTD-32165709-32166641; olfactory receptor 905; olfactory receptor MOR167-1", "tax_id": 10090, "disease": "", "pathway": " (mmu:258800)", "pathway_count": 1, "publication_count": 3, "publication_id_list": "21750661;25428506;32061665", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]; This odorant receptor, Olfr905, responds to the odorant whiskey lactone in vivo, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.4, "record_id": "L7N1X5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "L7N1Z1-1", "uniprot_id": "L7N1Z1_MOUSE", "mass": 34704.0, "length": 317, "protein_name": "Olfactory receptor", "gene_name": "Or2g25", "organism": "Mouse", "refseq_name": "olfactory receptor 117", "refseq_ac": "NP_997038", "gene_names_uniprotkb": "Or2g25; Olfr117", "gene_names_refseq": "MOR256-33; Olfr117; Or2g25", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2PSCP-2119438-2118485; olfactory receptor 117; olfactory receptor MOR256-33", "tax_id": 10090, "disease": "", "pathway": " (mmu:258263)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21750661;25428506", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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Also binds Asprosin in the arcuate nucleus of the hypothalamus, thereby stimulating appetite by promoting orexigenic AgRP neuronal activity (PubMed:32337066). In testis, Asprosin-binding promotes sperm progressive motility and enhances male fertility (PubMed:31798959). The activity of this receptor is mediated by G proteins which activate adenylyl cyclase, resulting in an elevation of intracellular cAMP (PubMed:31230984)., [UniProtKB, PubMed, PubMed, PubMed]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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[provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell;GO:0071396 cellular response to lipid", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "Q8VH12-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VIB8-1", "uniprot_id": "Q8VIB8_MOUSE", "mass": 35573.0, "length": 308, "protein_name": "Vomeronasal type-1 receptor", "gene_name": "Vmn1r85", "organism": "Mouse", "refseq_name": "vomeronasal 1 receptor 85", "refseq_ac": "NP_665846", "gene_names_uniprotkb": "Vmn1r85", "gene_names_refseq": "V1rj3; Vmn1r85", "protein_names_uniprotkb": "Vomeronasal type-1 receptor", "protein_names_refseq": "vomernasal 1 receptor Vmn1r85; vomeronasal 1 receptor 85; vomeronasal 1 receptor, J3; vomeronasal type 1 receptor J3", "tax_id": 10090, "disease": "", "pathway": " (mmu:252909)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Putative pheromone receptor., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005550 pheromone binding;GO:0016503 pheromone receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0019236 response to pheromone;GO:0007606 sensory perception of chemical stimulus", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q8VIB8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q920Z0-1", "uniprot_id": "Q920Z0_MOUSE", "mass": 34952.0, "length": 308, "protein_name": "Olfactory receptor", "gene_name": "Or12d12", "organism": "Mouse", "refseq_name": "olfactory receptor 101", "refseq_ac": "NP_667045", "gene_names_uniprotkb": "Or12d12; Olfr101", "gene_names_refseq": "MOR250-2; Olfr101; Or12d12", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2PSCP-1761617-1760691; olfactory receptor 101; olfactory receptor MOR250-2", "tax_id": 10090, "disease": "", "pathway": " (mmu:258831)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell;GO:0050911 detection of chemical stimulus involved in sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q920Z0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q99NB3-1", "uniprot_id": "Q99NB3_MOUSE", "mass": 60729.0, "length": 548, "protein_name": "Intercellular adhesion molecule 1", "gene_name": "Tcam1", "organism": "Mouse", "refseq_name": "testicular cell adhesion molecule 1 precursor", "refseq_ac": "NP_083743", "gene_names_uniprotkb": "Tcam1", "gene_names_refseq": "4930570F09Rik; Tcam1", "protein_names_uniprotkb": "Intercellular adhesion molecule 1", "protein_names_refseq": "testicular cell adhesion molecule 1 precursor", "tax_id": 10090, "disease": "dilated cardiomyopathy (Disease Ontology:DOID:12930)", "pathway": " (mmu:75870)", "pathway_count": 1, "publication_count": 4, "publication_id_list": "19766163;21750661;25020229;26495903", "class_list": "", "function": "A conserved noncoding sequence (CNS1) located upstream of TCAM1 is a novel enhancer for Tcam1 gene expression. Erratum:[J Mol Biol. 2015 May 22;427(10):1993-4], [RefSeq, PubMed]; Cell adhesion molecule that functions as a receptor ligand of the signaling receptor ITGAL:ITGB2/LFA-1 (lymphocyte-function associated (LFA) molecule 1) ensuring leukocyte cell-cell adhesion, by providing a calibrated system to namely adjust T-cell killing to the antigen stimulation strength. Also functions as a ligand receptor of the signaling receptor ITGAM:ITGB2/MAC-1 ensuring adhesion between stimulated neutrophils and stimulated endothelial cells. During leukocyte trans-endothelial migration, ICAM1 engagement promotes the assembly of endothelial apical cups through ARHGEF26/SGEF and RHOG activation. Promotes cell aggregation in epithelial cells through interaction with MUC1., [UniProtKB, UniProtKB]; Data show that TCAM1 is not essential for male fertility or germ cell function in Mus musculus., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005178 integrin binding", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0006955 immune response;GO:0007155 cell adhesion;GO:0071333 cellular response to glucose stimulus;GO:0098609 cell-cell adhesion;GO:0007159 leukocyte cell-cell adhesion", "synthesized_glycan_count": 0, "hit_score": 0.5, "record_id": "Q99NB3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9QWV1-1", "uniprot_id": "Q9QWV1_MOUSE", "mass": 28167.0, "length": 250, "protein_name": "Histocompatibility 2, O region alpha locus", "gene_name": "H2-Oa", "organism": "Mouse", "refseq_name": "histocompatibility 2, O region alpha locus", "refseq_ac": "NP_032232", "gene_names_uniprotkb": "H2-Oa", "gene_names_refseq": "H-2Oa; H2-Oa", "protein_names_uniprotkb": "Histocompatibility 2, O region alpha locus", "protein_names_refseq": "MHC class II antigen O region alpha locus; histocompatibility 2, O region alpha locus", "tax_id": 10090, "disease": "occupational asthma (Disease Ontology:DOID:0080820)", "pathway": " (mmu:15001); (R-MMU-2132295)", "pathway_count": 2, "publication_count": 3, "publication_id_list": "21750661;32069316;37908352", "class_list": "", "function": "Mouse MHC class II chaperone H2-O antigen affects the repertoire of presented self-peptides by B cells and thymic epithelium. H2-O induces differential effects on epitope presentation and thymic selection, thereby altering CD4 T-cell precursor frequencies. Lack of H2-O increases autoreactivity and susceptibility to autoimmune disease development. Publication Status: Online-Only, [RefSeq, PubMed]; Proper development of long-lived memory CD4 T cells requires HLA-DO function. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0023026 MHC class II protein complex binding;GO:0042605 peptide antigen binding", "go_cellular_component": "GO:0005765 lysosomal membrane;GO:0009897 external side of plasma membrane;GO:0031902 late endosome membrane;GO:0042613 MHC class II protein complex", "go_biological_process": "GO:0019886 antigen processing and presentation of exogenous peptide antigen via MHC class II;GO:0002503 peptide antigen assembly with MHC class II protein complex;GO:0002250 adaptive immune response;GO:0045580 regulation of T cell differentiation;GO:0050870 positive regulation of T cell activation", "synthesized_glycan_count": 0, "hit_score": 0.4, "record_id": "Q9QWV1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A075B5V0-1", "uniprot_id": "A0A075B5V0_MOUSE", "mass": 12911.0, "length": 117, "protein_name": "Immunoglobulin heavy variable 1-26", "gene_name": "Ighv1-26", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Ighv1-26", "gene_names_refseq": "", "protein_names_uniprotkb": "Immunoglobulin heavy variable 1-26", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": " (R-MMU-173623); (R-MMU-198933); (R-MMU-202733); (R-MMU-2029481); (R-MMU-2029482); (R-MMU-2029485); (R-MMU-2168880); (R-MMU-2454202); (R-MMU-2730905); (R-MMU-2871796); (R-MMU-2871809); (R-MMU-2871837); (R-MMU-5690714); (R-MMU-977606); (R-MMU-983695)", "pathway_count": 15, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003823 antigen binding", "go_cellular_component": "GO:0005576 extracellular region;GO:0019814 immunoglobulin complex", "go_biological_process": "GO:0016064 immunoglobulin mediated immune response", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A075B5V0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A075B604-1", "uniprot_id": "A0A075B604_MOUSE", "mass": 12620.0, "length": 112, "protein_name": "T cell receptor alpha variable 7D-5; T cell receptor alpha variable 7N-5", "gene_name": "Trav7d-5", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Trav7d-5; Trav7n-5", "gene_names_refseq": "", "protein_names_uniprotkb": "T cell receptor alpha variable 7D-5; T cell receptor alpha variable 7N-5", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0042605 peptide antigen binding", "go_cellular_component": "GO:0042101 T cell receptor complex", "go_biological_process": "GO:0002250 adaptive immune response", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A075B604-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A075B619-1", "uniprot_id": "A0A075B619_MOUSE", "mass": 13453.0, "length": 120, "protein_name": "T cell receptor alpha variable 14D-3-DV8", "gene_name": "Trav14d-3-dv8", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Trav14d-3-dv8", "gene_names_refseq": "", "protein_names_uniprotkb": "T cell receptor alpha variable 14D-3-DV8", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0042605 peptide antigen binding", "go_cellular_component": "GO:0042101 T cell receptor complex", "go_biological_process": "GO:0002250 adaptive immune response", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A075B619-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A0R4J8U2-1", "uniprot_id": "A0A0R4J8U2_MOUSE", "mass": 34289.0, "length": 307, "protein_name": "Olfactory receptor", "gene_name": "Or2d3b", "organism": "Mouse", "refseq_name": "olfactory receptor 708", "refseq_ac": "NP_001011542", "gene_names_uniprotkb": "Or2d3b; Olfr1532-ps1; Olfr1532; Olfr709-ps1", "gene_names_refseq": "GA_x6K02T2PBJ9-9297671-9298594; MOR260-6P; MOR260-9P; Olfr1532-ps1; Olfr1532; Olfr708; Or2d3b", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "B5 olfactory receptor; olfactory receptor 1532, pseudogene 1; olfactory receptor 708; olfactory receptor MOR260-6P; olfactory receptor MOR260-9P", "tax_id": 10090, "disease": "", "pathway": " (mmu:258173)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0050911 detection of chemical stimulus involved in sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A0R4J8U2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A1B0GSB0-1", "uniprot_id": "A0A1B0GSB0_MOUSE", "mass": 106248.0, "length": 991, "protein_name": "Scavenger receptor family member expressed on T cells 1", "gene_name": "Scart1", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Scart1; 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V3R4; Vmn1r58", "protein_names_uniprotkb": "Vomeronasal type-1 receptor", "protein_names_refseq": "pheromone receptor V3R4; vomeronasal 1 receptor 58; vomeronasal 1 receptor Vmn1r58; vomeronasal 1 receptor, D4", "tax_id": 10090, "disease": "", "pathway": " (mmu:81014)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005550 pheromone binding;GO:0016503 pheromone receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0019236 response to pheromone;GO:0007606 sensory perception of chemical stimulus", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "G3X9U3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G3X9V8-1", "uniprot_id": "G3X9V8_MOUSE", "mass": 44453.0, "length": 387, "protein_name": "Serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 3A", "gene_name": "Serpinb3a", "organism": "Mouse", "refseq_name": "serine peptidase inhibitor, clade B, member 3A", "refseq_ac": "NP_033152", "gene_names_uniprotkb": "Serpinb3a", "gene_names_refseq": "1110001H02Rik; 1110013A16Rik; Scca2; Serpinb3a; Serpinb4; Sqn5", "protein_names_uniprotkb": "Serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 3A", "protein_names_refseq": "serine (or cysteine) proteinase inhibitor, clade B (ovalbumin), member 3A; serine peptidase inhibitor, clade B, member 3A; squamous cell carcinoma antigen 2", "tax_id": 10090, "disease": "familial encephalopathy with neuroserpin inclusion bodies (Disease Ontology:DOID:0050831); alpha 1-antitrypsin deficiency (Disease Ontology:DOID:13372)", "pathway": " (mmu:20248); (R-MMU-6798695)", "pathway_count": 2, "publication_count": 6, "publication_id_list": "11863458;12702576;15504361;21750661;25111616;35022507", "class_list": "", "function": "Characerization of the functional properties of Serpinb3c., [RefSeq, PubMed]; Lysoptosis is an evolutionarily conserved cell death pathway moderated by intracellular serpins. Publication Status: Online-Only, [RefSeq, PubMed]; SCCA2-like serpins mediate genetic predisposition to skin cancer in a mouse model and in humans., [RefSeq, PubMed]; SQN-5 employed different reactive centers to neutralize the serine and cysteine proteinases., [RefSeq, PubMed]; Serpinb3a deficiency attenuates barrier dysfunction and the early inflammatory response following cutaneous allergen exposure, supporting a role for Serpinb3a (mice) and SERPINB3/B4 (humans) early in atopic dermatitis., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0002020 protease binding;GO:0004867 serine-type endopeptidase inhibitor activity;GO:0019899 enzyme binding;GO:0004869 cysteine-type endopeptidase inhibitor activity", "go_cellular_component": "GO:0005615 extracellular space;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.7, "record_id": "G3X9V8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G5E8C2-1", "uniprot_id": "G5E8C2_MOUSE", "mass": 77618.0, "length": 690, "protein_name": "Kelch repeat and BTB (POZ) domain containing 7", "gene_name": "Kbtbd7", "organism": "Mouse", "refseq_name": "kelch repeat and BTB domain-containing protein 7", "refseq_ac": "NP_001019306", "gene_names_uniprotkb": "Kbtbd7", "gene_names_refseq": "1110008P08Rik; Gm295; Kbtbd7", "protein_names_uniprotkb": "Kelch repeat and BTB (POZ) domain containing 7", "protein_names_refseq": "kelch repeat and BTB domain-containing protein 7", "tax_id": 10090, "disease": "", "pathway": " (mmu:211255); (R-MMU-5658442); (R-MMU-8951664); (R-MMU-983168)", "pathway_count": 4, "publication_count": 4, "publication_id_list": "10.1101/2023.09.13.557529;19527686;21750661;38652964", "class_list": "", "function": "Kbtbd7 encodes an adapter protein with BTB/POZ, BACK, and Kelch motifs, previously shown to recruit substrates to the enzymatic complexes of the histone modifying or E3 ubiquitin ligase activities., [RefSeq, PubMed]; Knockdown of KBTBD7 attenuates septic lung injury by inhibiting ferroptosis and improving mitochondrial dysfunction., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 9343, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:1990756 ubiquitin-like ligase-substrate adaptor activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0031463 Cul3-RING ubiquitin ligase complex", "go_biological_process": "GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0070936 protein K48-linked ubiquitination;GO:0035020 regulation of Rac protein signal transduction", "synthesized_glycan_count": 0, "hit_score": 0.7, "record_id": "G5E8C2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "H3BJ46-1", "uniprot_id": "H3BJ46_MOUSE", "mass": 34987.0, "length": 303, "protein_name": "Vomeronasal type-1 receptor", "gene_name": "Vmn1r14", "organism": "Mouse", "refseq_name": "vomeronasal 1 receptor, C7", "refseq_ac": "NP_444467", "gene_names_uniprotkb": "Vmn1r14", "gene_names_refseq": "V1rc7; Vmn1r14", "protein_names_uniprotkb": "Vomeronasal type-1 receptor", "protein_names_refseq": "vomernasal 1 receptor Vmn1r14; vomeronasal 1 receptor, C7", "tax_id": 10090, "disease": "", "pathway": " (mmu:113864)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005550 pheromone binding;GO:0016503 pheromone receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0019236 response to pheromone;GO:0007606 sensory perception of chemical stimulus", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "H3BJ46-1", "record_type": "protein" }, { "uniprot_canonical_ac": "J3QNT6-1", "uniprot_id": "J3QNT6_MOUSE", "mass": 16499.0, "length": 144, "protein_name": "Eukaryotic translation initiation factor 4C", "gene_name": "Eif1ad15", "organism": "Mouse", "refseq_name": "eukaryotic translation initiation factor 1A domain containing 15", "refseq_ac": "NP_001423261", "gene_names_uniprotkb": "Eif1ad15", "gene_names_refseq": "EG266459; Eif1ad15; Gm5039", "protein_names_uniprotkb": "Eukaryotic translation initiation factor 4C", "protein_names_refseq": "eukaryotic translation initiation factor 1A domain containing 15; eukaryotic translation initiation factor 1A pseudogene", "tax_id": 10090, "disease": "uveal melanoma (Disease Ontology:DOID:6039)", "pathway": " (mmu:266459)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Component of the 43S pre-initiation complex (43S PIC), which binds to the mRNA cap-proximal region, scans mRNA 5'-untranslated region, and locates the initiation codon. This protein enhances formation of the cap-proximal complex. Together with EIF1, facilitates scanning, start codon recognition, promotion of the assembly of 48S complex at the initiation codon (43S PIC becomes 48S PIC after the start codon is reached), and dissociation of aberrant complexes. After start codon location, together with EIF5B orients the initiator methionine-tRNA in a conformation that allows 60S ribosomal subunit joining to form the 80S initiation complex. Is released after 80S initiation complex formation, just after GTP hydrolysis by EIF5B, and before release of EIF5B. Its globular part is located in the A site of the 40S ribosomal subunit. Its interaction with EIF5 during scanning contribute to the maintenance of EIF1 within the open 43S PIC. In contrast to yeast orthologs, does not bind EIF1., [UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "A0A1W2P883", "ec_number_list": "", "go_molecular_function": "GO:0000049 tRNA binding;GO:0003743 translation initiation factor activity", "go_cellular_component": "GO:0005737 cytoplasm", "go_biological_process": "GO:0006413 translational initiation", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "J3QNT6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "K7N609-1", "uniprot_id": "K7N609_MOUSE", "mass": 36334.0, "length": 323, "protein_name": "Olfactory receptor", "gene_name": "Or51aa5", "organism": "Mouse", "refseq_name": "olfactory receptor 611", "refseq_ac": "NP_666938", "gene_names_uniprotkb": "Or51aa5; Olfr611", "gene_names_refseq": "MOR15-1; MOR15-4; Olfr611; Or51aa5", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "GA_x6K02T2PBJ9-6236637-6235666; olfactory receptor 611; olfactory receptor MOR15-1", "tax_id": 10090, "disease": "", "pathway": " (mmu:258722)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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Kcnh4", "protein_names_uniprotkb": "Voltage-gated delayed rectifier potassium channel KCNH4; Brain-specific eag-like channel 2; Ether-a-go-go-like potassium channel 1; Potassium voltage-gated channel subfamily H member 4; Voltage-gated potassium channel subunit Kv12.3", "protein_names_refseq": "potassium voltage-gated channel subfamily H member 4", "tax_id": 10090, "disease": "", "pathway": " (mmu:380728); (R-MMU-1296072)", "pathway_count": 2, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Pore-forming (alpha) subunit of a voltage-gated delayed rectifier. Activates at more negative voltages, exhibits fast prepulse-independent activation kinetics and deactivates much more slowly, but shows no inactivation., [UniProtKB, UniProtKB]", "predicted_glycosites": 3, "predicted_n_glycosites": 0, "predicted_o_glycosites": 3, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "1.8.-.-", "go_molecular_function": "GO:0005249 voltage-gated potassium channel activity;GO:0005242 inward rectifier potassium channel activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0034702 monoatomic ion channel complex", "go_biological_process": "GO:0042391 regulation of membrane potential;GO:0071805 potassium ion transmembrane transport", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A2A5F7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "B1ARV3-1", "uniprot_id": "B1ARV3_MOUSE", "mass": 58052.0, "length": 523, "protein_name": "Amine oxidase", "gene_name": "Lao1", "organism": "Mouse", "refseq_name": "L-amino acid oxidase 1 precursor", "refseq_ac": "NP_598653", "gene_names_uniprotkb": "Lao1", "gene_names_refseq": "Lao1", "protein_names_uniprotkb": "Amine oxidase; 1.4.3.-", "protein_names_refseq": "L-amino acid oxidase 1 precursor", "tax_id": 10090, "disease": "", "pathway": " (mmu:100470)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "19276171;21750661;25820447;30038322;33590844", "class_list": "", "function": "L-amino acid oxidase 1 in sperm is associated with reproductive performance in male mice and bulls., [RefSeq, PubMed]; LAO-knockout mice were healthy and had normal mammary gland development; however, the antibacterial activity normally observed in milk from wild-type mice was absent from the milk of knockout mice., [RefSeq, PubMed]; LAO1 KO mice exhibited impaired fear learning and memory owing to low hippocampal acetylcholine levels. Publication Status: Online-Only, [RefSeq, PubMed]; This is the first demonstration showing that LAO expression is induced in cell culture, and stimulation of lactogenic hormone and change of histone modification are promising signals to show highly expression of LAO in lactating mammary glands., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 3, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "1.4.3.-;1.4.3.2;1.4.3.25", "go_molecular_function": "GO:0001716 L-amino-acid oxidase activity;GO:0090729 toxin activity", "go_cellular_component": "GO:0005576 extracellular region", "go_biological_process": "GO:0042742 defense response to bacterium;GO:0009063 amino acid catabolic process", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "B1ARV3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9Q9W7-1", "uniprot_id": "PDZD7_MOUSE", "mass": 110694.0, "length": 1021, "protein_name": "PDZ domain-containing protein 7", "gene_name": "Pdzd7", "organism": "Mouse", "refseq_name": "PDZ domain-containing protein 7", "refseq_ac": "NP_001182194", "gene_names_uniprotkb": "Pdzd7", "gene_names_refseq": "9130207N01; EG435601; Pdzd7; Pdzk7", "protein_names_uniprotkb": "PDZ domain-containing protein 7", "protein_names_refseq": "PDZ domain-containing protein 7", "tax_id": 10090, "disease": "Usher syndrome type 2A (Disease Ontology:DOID:0110838); Usher syndrome type 2C (Disease Ontology:DOID:0110839); autosomal recessive nonsyndromic deafness 57 (Disease Ontology:DOID:0111635)", "pathway": " (mmu:100503041)", "pathway_count": 1, "publication_count": 7, "publication_id_list": "23055499;24334608;24962568;25406310;29796015;31914662;40885482", "class_list": "", "function": "In cochlear developing hair cells, essential in organizing the USH2 complex at stereocilia ankle links (PubMed:24334608). Blocks inhibition of adenylate cyclase activity mediated by ADGRV1 (PubMed:24962568)., [UniProtKB, PubMed, PubMed]; It is clear that PDZD7 plays an essential role in organizing the USH2 complex at ankle links in developing cochlear hair cells., [RefSeq, PubMed]; PDZD7 long isoform has a role in the ankle-link complex and causes hearing loss in mice, [RefSeq, PubMed]; Several novel PDZD7-binding proteins were identified in a Cadm1-knockout model of deafness. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "E9Q9U9;X4YT42;X4YT46;X4YZM3;X4ZGA7", "ec_number_list": "", "go_molecular_function": "GO:0042802 identical protein binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005886 plasma membrane;GO:0005929 cilium;GO:0036064 ciliary basal body", "go_biological_process": "GO:0050910 detection of mechanical stimulus involved in sensory perception of sound;GO:0045184 establishment of protein localization;GO:0007605 sensory perception of sound;GO:0060088 auditory receptor cell stereocilium organization;GO:0060113 inner ear receptor cell differentiation", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "E9Q9W7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "F8VPY8-1", "uniprot_id": "OCAT2_MOUSE", "mass": 27812.0, "length": 253, "protein_name": "POU Class 2 homeobox-associating factor 3", "gene_name": "Pou2af3", "organism": "Mouse", "refseq_name": "POU Class 2 homeobox-associating factor 3", "refseq_ac": "NP_001182610", "gene_names_uniprotkb": "Pou2af3; Colca2; Gm684", "gene_names_refseq": "Colca2; Gm684; OCA-T2; Pou2af3", "protein_names_uniprotkb": "POU Class 2 homeobox-associating factor 3; Protein OCA-T2", "protein_names_refseq": "COLCA2 homolog; POU Class 2 homeobox-associating factor 3; colorectal cancer-associated protein 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:100502940)", "pathway_count": 1, "publication_count": 0, "publication_id_list": "", "class_list": "", "function": "Transcriptional coactivator that specifically associates with POU2F3. This complex drives the development of tuft cells, a rare a rare chemosensory cells that coordinate immune and neural functions within mucosal epithelial tissues., [UniProtKB, UniProtKB]", "predicted_glycosites": 2, "predicted_n_glycosites": 0, "predicted_o_glycosites": 2, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "A0A6I8MWX2", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0003713 transcription coactivator activity;GO:0070974 POU domain binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol", "go_biological_process": "GO:0006351 DNA-templated transcription", "synthesized_glycan_count": 0, "hit_score": 0.1, "record_id": "F8VPY8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G3UW56-1", "uniprot_id": "G3UW56_MOUSE", "mass": 96876.0, "length": 850, "protein_name": "Vomeronasal 2, receptor 85", "gene_name": "Vmn2r85", "organism": "Mouse", "refseq_name": "vomeronasal 2, receptor 85 precursor", "refseq_ac": "NP_001096072", "gene_names_uniprotkb": "Vmn2r85", "gene_names_refseq": "EG623734; Vmn2r85", "protein_names_uniprotkb": "Vomeronasal 2, receptor 85", "protein_names_refseq": "vomeronasal 2 receptor Vmn2r85; vomeronasal 2, receptor 85 precursor", "tax_id": 10090, "disease": "", "pathway": " (mmu:623734)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "G3UW56-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G3X992-1", "uniprot_id": "MS3L2_MOUSE", "mass": 41400.0, "length": 371, "protein_name": "MSL complex subunit 3B", "gene_name": "Msl3b", "organism": "Mouse", "refseq_name": "MSL complex subunit 3B", "refseq_ac": "NP_001157305", "gene_names_uniprotkb": "Msl3b; Msl3l2", "gene_names_refseq": "1700060H10Rik; Msl3b; Msl3l2", "protein_names_uniprotkb": "MSL complex subunit 3B; MSL3 like 2; MSL3-like 2; Male-specific lethal-3 homolog 2; Male-specific lethal-3 protein-like 2", "protein_names_refseq": "MSL complex subunit 3B; male-specific lethal 3-like 2; male-specific lethal-3 homolog 2; male-specific lethal-3 protein-like 2", "tax_id": 10090, "disease": "Basilicata-Akhtar syndrome (Disease Ontology:DOID:0111838)", "pathway": " (mmu:73390)", "pathway_count": 1, "publication_count": 0, "publication_id_list": "", "class_list": "", "function": "Probable non-catalytic component of the MSL histone acetyltransferase complex, a multiprotein complex that mediates the majority of histone H4 acetylation at 'Lys-16' (H4K16ac), an epigenetic mark that prevents chromatin compaction., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3U2B0", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005634 nucleus;GO:0035267 NuA4 histone acetyltransferase complex;GO:0072487 MSL complex", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0006325 chromatin organization", "synthesized_glycan_count": 0, "hit_score": 0.1, "record_id": "G3X992-1", "record_type": "protein" }, { "uniprot_canonical_ac": "J3QK38-1", "uniprot_id": "J3QK38_MOUSE", "mass": 25816.0, "length": 227, "protein_name": "Predicted gene, 20826; Predicted gene, 21244", "gene_name": "Gm20826", "organism": "Mouse", "refseq_name": "uncharacterized protein LOC100040160", "refseq_ac": "NP_001095093", "gene_names_uniprotkb": "Gm20826; Gm21244", "gene_names_refseq": "Gm20826", "protein_names_uniprotkb": "Predicted gene, 20826; Predicted gene, 21244", "protein_names_refseq": "spermiogenesis specific transcript on the Y family member; uncharacterized protein LOC100040160", "tax_id": 10090, "disease": "", "pathway": " (mmu:100040160); (mmu:108168669)", "pathway_count": 2, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005829 cytosol", "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0007276 gamete generation", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "J3QK38-1", "record_type": "protein" }, { "uniprot_canonical_ac": "K7N693-1", "uniprot_id": "K7N693_MOUSE", "mass": 25724.0, "length": 218, "protein_name": "Predicted gene 10408; 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The reference sequence was derived from AF282295.1. Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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3.4.22.-", "protein_names_refseq": "", "tax_id": 10090, "disease": "cancer (Disease Ontology:DOID:162)", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Cysteine protease that plays a key role in autophagy by mediating both proteolytic activation and delipidation of ATG8 family proteins., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "3.4.22.-", "go_molecular_function": "GO:0004197 cysteine-type endopeptidase activity;GO:0008234 cysteine-type peptidase activity;GO:0019786 protein-phosphatidylethanolamide deconjugating activity", "go_cellular_component": "GO:0005737 cytoplasm", "go_biological_process": "GO:0000045 autophagosome assembly;GO:0006508 proteolysis;GO:0006629 lipid metabolic process;GO:0015031 protein transport;GO:0016485 protein processing", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A0G2JFS9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A0G2JGM3-1", "uniprot_id": "A0A0G2JGM3_MOUSE", "mass": 2018.0, "length": 19, "protein_name": "T cell receptor alpha joining 34", "gene_name": "Traj34", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Traj34", "gene_names_refseq": "", "protein_names_uniprotkb": "T cell receptor alpha joining 34", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A0G2JGM3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A0G2JGW7-1", "uniprot_id": "A0A0G2JGW7_MOUSE", "mass": 2129.0, "length": 20, "protein_name": "T cell receptor gamma joining 1; T cell receptor gamma joining 2", "gene_name": "Trgj2", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Trgj2; Trgj1", "gene_names_refseq": "", "protein_names_uniprotkb": "T cell receptor gamma joining 1; T cell receptor gamma joining 2", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A0G2JGW7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A1W2P7N1-1", "uniprot_id": "A0A1W2P7N1_MOUSE", "mass": 28197.0, "length": 277, "protein_name": "Keratin associated protein 10-30", "gene_name": "Krtap10-30", "organism": "Mouse", "refseq_name": "uncharacterized protein LOC77763", "refseq_ac": "NP_001357737", "gene_names_uniprotkb": "Krtap10-30; Gm9736", "gene_names_refseq": "77763; Gm9736; Krtap10-30", "protein_names_uniprotkb": "Keratin associated protein 10-30", "protein_names_refseq": "uncharacterized protein LOC77763", "tax_id": 10090, "disease": "", "pathway": " (mmu:77763); (R-MMU-6805567)", "pathway_count": 2, "publication_count": 2, "publication_id_list": "21750661;25428506", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0042802 identical protein binding", "go_cellular_component": "GO:0005829 cytosol;GO:0045095 keratin filament", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "A0A1W2P7N1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A2AJW4-1", "uniprot_id": "A2AJW4_MOUSE", "mass": 30510.0, "length": 279, "protein_name": "Protein phosphatase 1 regulatory subunit", "gene_name": "Ppp1r3d", "organism": "Mouse", "refseq_name": "protein phosphatase 1 regulatory subunit 3D", "refseq_ac": "NP_001078970", "gene_names_uniprotkb": "Ppp1r3d", "gene_names_refseq": "2610024M03Rik; Gm359; Ppp1r3d", "protein_names_uniprotkb": "Protein phosphatase 1 regulatory subunit", "protein_names_refseq": "protein phosphatase 1 regulatory subunit 3D", "tax_id": 10090, "disease": "", "pathway": " (mmu:228966)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21750661;32892347", "class_list": "", "function": "Acts as a glycogen-targeting subunit for PP1. PP1 is involved in glycogen metabolism and contributes to the activation of glycogen synthase leading to an increase in glycogen synthesis., [UniProtKB, UniProtKB]; Ppp1r3d deficiency preferentially inhibits neuronal and cardiac Lafora body formation in a mouse model of the fatal epilepsy Lafora disease., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0019899 enzyme binding;GO:0008157 protein phosphatase 1 binding;GO:0004721 phosphoprotein phosphatase activity;GO:2001069 glycogen binding", "go_cellular_component": "GO:0000164 protein phosphatase type 1 complex;GO:0042587 glycogen granule", "go_biological_process": "GO:0005981 regulation of glycogen catabolic process;GO:0005977 glycogen metabolic process;GO:0005979 regulation of glycogen biosynthetic process", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "A2AJW4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q91WF0-1", "uniprot_id": "TAZ_MOUSE", "mass": 30334.0, "length": 262, "protein_name": "Tafazzin", "gene_name": "Tafazzin", "organism": "Mouse", "refseq_name": "tafazzin isoform 4", "refseq_ac": "NP_001229545", "gene_names_uniprotkb": "Tafazzin; TAZ; Taz", "gene_names_refseq": "5031411C02Rik; 9130012G04Rik; G4.5; Tafazzin; Taz", "protein_names_uniprotkb": "Tafazzin; 2.3.1.-; Taz", "protein_names_refseq": "tafazzin isoform 4", "tax_id": 10090, "disease": "Barth syndrome (Disease Ontology:DOID:0050476); visceral heterotaxy (Disease Ontology:DOID:0050545); cardiomyopathy (Disease Ontology:DOID:0050700); dilated cardiomyopathy (Disease Ontology:DOID:12930)", "pathway": " (mmu:66826); (R-MMU-1482798)", "pathway_count": 2, "publication_count": 14, "publication_id_list": "10.1101/2023.09.13.557529;15499385;19114128;21068380;21091282;21750661;23130124;23616771;25919711;26114544;30055293;30389594;37724047;38433278", "class_list": "", "function": "AMPK stimulation inhibits YAP/TAZ signaling to ameliorate hepatic fibrosis. Publication Status: Online-Only, [RefSeq, PubMed]; Acyltransferase required to remodel newly synthesized phospholipid cardiolipin (1',3'-bis-[1,2-diacyl-sn-glycero-3-phospho]-glycerol or CL), a key component of the mitochondrial inner membrane, with tissue specific acyl chains necessary for adequate mitochondrial function (PubMed:19114128, PubMed:21068380, PubMed:21091282, PubMed:23130124, PubMed:26114544, PubMed:30055293, PubMed:30389594). Its role in cellular physiology is to improve mitochondrial performance (By similarity). CL is critical for the coassembly of lipids and proteins in mitochondrial membranes, for instance, remodeling of the acyl groups of CL in the mitochondrial inner membrane affects the assembly and stability of respiratory chain complex IV and its supercomplex forms (By similarity). Catalyzes the transacylation between phospholipids and lysophospholipids, with the highest rate being between phosphatidylcholine (1,2-diacyl-sn-glycero-3-phosphocholine or PC) and CL. Catalyzes both 1-acyl-sn-glycero-3-phosphocholine (lysophosphatidylcholine or LPC) reacylation and PC-CL transacylation, that means, it exchanges acyl groups between CL and PC by a combination of forward and reverse transacylations. Also catalyzes transacylations between other phospholipids such as phosphatidylethanolamine (1,2-diacyl-sn-glycero-3-phosphoethanolamine or PE) and CL, between PC and PE, and between PC and phosphatidate (1,2-diacyl-sn-glycero-3-phosphate or PA), although at lower rate. Not regiospecific, it transfers acyl groups into any of the sn-1 and sn-2 positions of the monolysocardiolipin (MLCL), which is an important prerequisite for uniformity and symmetry in CL acyl distribution. Cannot transacylate dilysocardiolipin (DLCL), thus, the role of MLCL is limited to that of an acyl acceptor. CoA-independent, it can reshuffle molecular species within a single phospholipid class. Redistributes fatty acids between MLCL, CL, and other lipids, which prolongs the half-life of CL. Its action is completely reversible, which allows for cyclic changes, such as fission and fusion or bending and flattening of the membrane. Hence, by contributing to the flexibility of the lipid composition, it plays an important role in the dynamics of mitochondria membranes. Essential for the final stage of spermatogenesis, spermatid individualization (By similarity). Required for the initiation of mitophagy (PubMed:25919711). Required to ensure progression of spermatocytes through meiosis (PubMed:26114544)., [UniProtKB, UniProtKB, PubMed, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed, UniProtKB, PubMed, PubMed]; Acyltransferase which is required to remodel newly synthesized phospholipid cardiolipin, a key component of the mitochondrial inner membrane. Required for the initiation of mitophagy. Required to ensure progression of spermatocytes through meiosis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Tafazzin knockdown mice provide a mammalian model system for Barth syndrome in which the pathophysiological relationships between altered content of mitochondrial phospholipids, ultrastructural abnormalities, myocardial and mitochondrial dysfunction, [RefSeq, PubMed]; The data suggest that tafazzin deficiency affects cardiolipin in all mitochondria, but significant alterations of the ultrastructure, such as remodeling and aggregation of inner membranes, will only occur after specific differentiation., [RefSeq, PubMed]; This gene encodes a mitochondrial phospholipid-lysophospholipid transacylase necessary for normal composition and content of cardiolipin. In humans, mutations of this gene result in Barth syndrome, most often characterized by cardioskeletal myopathy, neutropenia and abnormal mitochondria. This gene is distinct from the gene encoding transcriptional coactivator with PDZ binding motif. Both genes share the gene symbol Taz. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010]., [RefSeq]; YAP and TAZ regulate remyelination in the central nervous system., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 4, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q810E8", "ec_number_list": "2.3.1.-", "go_molecular_function": "GO:0047184 1-acylglycerophosphocholine O-acyltransferase activity;GO:0016746 acyltransferase activity", "go_cellular_component": "GO:0005739 mitochondrion;GO:0005741 mitochondrial outer membrane;GO:0005743 mitochondrial inner membrane;GO:0005758 mitochondrial intermembrane space;GO:0031966 mitochondrial membrane", "go_biological_process": "GO:2001171 positive regulation of ATP biosynthetic process;GO:1900210 positive regulation of cardiolipin metabolic process;GO:0035965 cardiolipin acyl-chain remodeling;GO:0042407 cristae formation;GO:0046471 phosphatidylglycerol metabolic process", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "Q91WF0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A2I3BR64-1", "uniprot_id": "A0A2I3BR64_MOUSE", "mass": 36102.0, "length": 321, "protein_name": "Olfactory receptor", "gene_name": "Or10ag2", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Or10ag2; Olfr1123", "gene_names_refseq": "", "protein_names_uniprotkb": "Olfactory receptor", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": " (mmu:258347)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell;GO:0050911 detection of 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"hit_score": 0.2, "record_id": "A0A3B2WBA1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P0DPD9-1", "uniprot_id": "EFCE2_MOUSE", "mass": 99480.0, "length": 881, "protein_name": "EEF1AKMT4-ECE2 readthrough transcript protein", "gene_name": "Ece2; Eef1akmt4-Ece2", "organism": "Mouse", "refseq_name": "Eef1akmt4-Ece2 readthrough isoform b", "refseq_ac": "NP_808809", "gene_names_uniprotkb": "Ece2; Eef1akmt4-Ece2", "gene_names_refseq": "Eef1akmt4-ece2; Eef1akmt4; Eef1ece2; Gm49333", "protein_names_uniprotkb": "EEF1AKMT4-ECE2 readthrough transcript protein; 3.4.24.71", "protein_names_refseq": "EEF1A lysine methyltransferase 4; EEF1AKMT4-ECE2 readthrough transcript protein; Eef1akmt4-Ece2 readthrough isoform b", "tax_id": 10090, "disease": "", "pathway": " (mmu:107522); (mmu:110599584); (R-MMU-375276)", "pathway_count": 3, "publication_count": 6, "publication_id_list": "10.1101/2023.09.13.557529;10811845;12054617;12464614;21750661;34428180", "class_list": "", "function": "Converts big endothelin-1 to endothelin-1. Also involved in the processing of various neuroendocrine peptides, including neurotensin, angiotensin I, substance P, proenkephalin-derived peptides, and prodynorphin-derived peptides (By similarity). May play a role in amyloid-beta processing (PubMed:12464614)., [UniProtKB, PubMed, UniProtKB]; Converts big endothelin-1 to endothelin-1. May also have methyltransferase activity (By similarity). May play a role in amyloid-beta processing (PubMed:12464614)., [UniProtKB, PubMed, UniProtKB]; This locus represents naturally occurring readthrough transcription between the adjacent genes eukaryotic translation elongation factor 1 alpha lysine specific methyltransferase 4 (GeneID:110599566) and endothelin converting enzyme 2 (GeneID:107522). The readthrough transcript representing this gene encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Jul 2017]., [RefSeq]", "predicted_glycosites": 7, "predicted_n_glycosites": 7, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 2, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 9409, "biomarker_type": "", "glycan_count": 3, "disease_count": 0, "glyco_site_count": 9, "binding_glycan_count": 0, "secondary_ac_list": "E9QKA6;Q14BY3;Q80Z59;Q80Z60;Q9D8Q9;Q9D928", "ec_number_list": "2.1.1.-;3.4.24.71", "go_molecular_function": "GO:0004222 metalloendopeptidase activity;GO:0046872 metal ion binding;GO:0008168 methyltransferase activity", "go_cellular_component": "GO:0000139 Golgi membrane;GO:0030658 transport vesicle membrane;GO:0005886 plasma membrane;GO:0030659 cytoplasmic vesicle membrane", "go_biological_process": "GO:0007507 heart development;GO:0016486 peptide hormone processing;GO:0007420 brain development;GO:0010002 cardioblast differentiation;GO:0006508 proteolysis", "synthesized_glycan_count": 0, "hit_score": 1.2, "record_id": "P0DPD9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G3UWA8-1", "uniprot_id": "G3UWA8_MOUSE", "mass": 47460.0, "length": 416, "protein_name": "Pyroglutamylated RF-amide peptide receptor", "gene_name": "Qrfprl", "organism": "Mouse", "refseq_name": "uncharacterized protein LOC243407", "refseq_ac": "NP_780733", "gene_names_uniprotkb": "Qrfprl; C130060K24Rik", "gene_names_refseq": "C130060K24Rik; Gpr103b; Qrfprl", "protein_names_uniprotkb": "Pyroglutamylated RF-amide peptide receptor; AQ27; G-protein coupled receptor 103; Orexigenic neuropeptide QRFP receptor; SP9155", "protein_names_refseq": "uncharacterized protein LOC243407", "tax_id": 10090, "disease": "", "pathway": " (mmu:243407); (R-MMU-389397); (R-MMU-416476)", "pathway_count": 3, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Receptor for the orexigenic neuropeptide QRFP. The activity of this receptor is mediated by G proteins that modulate adenylate cyclase activity and intracellular calcium levels., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004983 neuropeptide Y receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0032870 cellular response to hormone stimulus", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "G3UWA8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A571BGC3-1", "uniprot_id": "A0A571BGC3_MOUSE", "mass": 529500.0, "length": 4596, "protein_name": "Dynein, axonemal, heavy chain 14", "gene_name": "Dnah14", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Dnah14", "gene_names_refseq": "", "protein_names_uniprotkb": "Dynein, axonemal, heavy chain 14", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 2, "predicted_n_glycosites": 0, "predicted_o_glycosites": 2, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008569 minus-end-directed microtubule motor activity;GO:0051959 dynein light intermediate chain binding;GO:0045505 dynein intermediate chain binding;GO:0000166 nucleotide binding", "go_cellular_component": "GO:0005874 microtubule;GO:0005930 axoneme;GO:0030286 dynein complex;GO:0005929 cilium;GO:0005813 centrosome", "go_biological_process": "GO:0007018 microtubule-based movement;GO:0060294 cilium movement involved in cell motility", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A571BGC3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "F6UK53-1", "uniprot_id": "F6UK53_MOUSE", "mass": 42305.0, "length": 379, "protein_name": "Testis expressed gene 16", "gene_name": "Tex16", "organism": "Mouse", "refseq_name": "testis expressed gene 16 isoform 3", "refseq_ac": "NP_001170860", "gene_names_uniprotkb": "Tex16", "gene_names_refseq": "4933403O08Rik; Tex16", "protein_names_uniprotkb": "Testis expressed gene 16", "protein_names_refseq": "testis expressed gene 16 isoform 3", "tax_id": 10090, "disease": "", "pathway": " (mmu:83556)", "pathway_count": 1, "publication_count": 4, "publication_id_list": "11279525;16118233;17660561;21750661", "class_list": "", "function": "Germ-cell-specific sex-linked genes, like Tex16, are subject to meiotic sex-chromosome inactivation (MSCI) during spermatogenesis., [RefSeq, PubMed]; Tex16 is a gene that is expressed in testis that was identified in a genome-wide cDNA subtraction screen., [RefSeq, PubMed]; Transcripts highly enriched in ovary; gene identified as candidate female fertility factor., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "F6RC93", "ec_number_list": "", "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity", "go_cellular_component": "", "go_biological_process": "GO:0007167 enzyme-linked receptor protein signaling pathway", "synthesized_glycan_count": 0, "hit_score": 0.5, "record_id": "F6UK53-1", "record_type": "protein" }, { "uniprot_canonical_ac": "F8VPN4-1", "uniprot_id": "F8VPN4_MOUSE", "mass": 174287.0, "length": 1532, "protein_name": "Glycogen debranching enzyme", "gene_name": "Agl", "organism": "Mouse", "refseq_name": "glycogen debranching enzyme isoform 1", "refseq_ac": "NP_001074795", "gene_names_uniprotkb": "Agl", "gene_names_refseq": "1110061O17Rik; 9430004C13Rik; 9630046L06Rik; Agl", "protein_names_uniprotkb": "Glycogen debranching enzyme; 2.4.1.25; 3.2.1.33; Glycogen debrancher", "protein_names_refseq": "glycogen debranching enzyme isoform 1", "tax_id": 10090, "disease": "glycogen storage disease III (Disease Ontology:DOID:2748); uremia (Disease Ontology:DOID:4676); congenital disorder of glycosylation (Disease Ontology:DOID:5212)", "pathway": " (mmu:77559); (R-MMU-6798695); (R-MMU-70221)", "pathway_count": 3, "publication_count": 3, "publication_id_list": "21750661;37507081;39927985", "class_list": "glycogene;glycosylhydrolase", "function": "Multifunctional enzyme acting as 1,4-alpha-D-glucan:1,4-alpha-D-glucan 4-alpha-D-glycosyltransferase and amylo-1,6-glucosidase in glycogen degradation., [UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 64, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "2.4.1.25;3.2.1.33;3.5.4.6;1.11.1.24;3.4.22.52;3.4.19.12;3.4.22.27;1.1.1.42;3.4.21.46;4.1.2.13;5.3.1.9;5.1.3.-;3.6.4.10;2.4.2.7;1.16.3.1;3.6.5.-;4.2.1.24;3.4.22.1;3.2.1.31;2.7.1.11;2.7.10.2;5.2.1.8;3.4.23.5;2.5.1.18;4.2.99.18;5.6.2.4;2.4.2.1;3.2.1.23;1.11.1.6;3.3.2.6;3.4.11.4;1.1.1.205;5.3.2.1;5.3.3.12;3.4.24.35;3.6.1.-;2.7.11.24;1.13.11.-;1.13.11.34;1.11.1.7;3.1.6.12;2.7.11.1;2.7.1.40;3.5.4.5;3.4.25.1;2.7.11.39;2.7.4.6;2.7.13.3;3.6.4.6;2.7.1.1;2.7.1.-;3.1.1.47;3.6.4.13;2.7.11.22;2.7.11.23;2.3.2.26;5.4.2.2;5.4.2.7;2.3.2.27;3.1.6.14;2.7.1.35;3.4.19.1;3.6.1.6;2.3.3.8;4.1.2.4;2.3.2.5;5.4.2.11;5.4.2.4;2.4.1.1;2.4.1.186;3.4.18.1;3.5.1.23;3.5.1.-", "go_molecular_function": "GO:0004134 4-alpha-glucanotransferase activity;GO:0004135 amylo-alpha-1,6-glucosidase activity;GO:0030247 polysaccharide binding;GO:0031593 polyubiquitin modification-dependent protein binding;GO:0030246 carbohydrate binding", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0016604 nuclear body", "go_biological_process": "GO:0005978 glycogen biosynthetic process;GO:0005980 glycogen catabolic process;GO:0007584 response to nutrient;GO:0005977 glycogen metabolic process;GO:0051384 response to glucocorticoid", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "F8VPN4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A3B2WBC8-1", "uniprot_id": "A0A3B2WBC8_MOUSE", "mass": 97132.0, "length": 853, "protein_name": "Vomeronasal 2, receptor 60", "gene_name": "Vmn2r60", "organism": "Mouse", "refseq_name": "vomeronasal 2, receptor 60 precursor", "refseq_ac": "NP_001098527", "gene_names_uniprotkb": "Vmn2r60", "gene_names_refseq": "Casr-rs3; EG637898; Gprc2a-rs3; Vmn2r60", "protein_names_uniprotkb": "Vomeronasal 2, receptor 60", "protein_names_refseq": "G protein coupled receptor, family C, group 2, member A, related sequence 3; calcium sensing receptor, related sequence 3; vomeronasal 2, receptor 60 precursor; vomeronasal receptor Vmn2r60", "tax_id": 10090, "disease": "", "pathway": " (mmu:637898)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A3B2WBC8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9QUK9-1", "uniprot_id": "TRY5_MOUSE", "mass": 26277.0, "length": 246, "protein_name": "Trypsin-5", "gene_name": "Try5", "organism": "Mouse", "refseq_name": "trypsin-5 precursor", "refseq_ac": "NP_001003405", "gene_names_uniprotkb": "Try5; Tc; Tesp4", "gene_names_refseq": "1810049H19Rik; T9; Tc; Tesp4; Try5", "protein_names_uniprotkb": "Trypsin-5; 3.4.21.4; T9; Testicular-specific serine protease 4; Trypsinogen 9", "protein_names_refseq": "testicular-specific serine protease 4; trypsin-5 precursor; trypsinogen 9", "tax_id": 10090, "disease": "cholangiocarcinoma (Disease Ontology:DOID:4947); pancreatitis (Disease Ontology:DOID:4989)", "pathway": " (mmu:103964); (R-MMU-1462054); (R-MMU-1592389); (R-MMU-6798695); (R-MMU-6803157)", "pathway_count": 5, "publication_count": 5, "publication_id_list": "10506205;11160223;21750661;23814066;34887587", "class_list": "", "function": "Serine protease capable of autoactivation., [UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "3.4.24.22;3.4.24.34;3.4.22.27;1.1.1.42;4.1.2.13;3.4.21.4;3.4.21.-;3.2.1.17;1.16.3.1;3.4.23.5;3.4.21.39;3.4.21.59;3.3.2.6;3.4.11.4;3.4.21.34;3.4.21.20;3.4.24.17;3.1.3.48;3.4.24.-;3.4.24.35;3.5.4.5;3.4.24.23;3.4.21.37;1.8.3.2;3.6.1.6;3.4.21.1;2.3.2.5;5.4.2.2;3.2.1.14;3.4.24.7;3.5.1.3;3.5.1.23;3.5.1.-;3.4.19.9", "go_molecular_function": "GO:0004252 serine-type endopeptidase activity;GO:0005509 calcium ion binding;GO:0008236 serine-type peptidase activity", "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0001669 acrosomal vesicle", "go_biological_process": "GO:0006508 proteolysis", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q9QUK9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A338P6G2-1", "uniprot_id": "A0A338P6G2_MOUSE", "mass": 47674.0, "length": 436, "protein_name": "Coiled-coil domain containing 188", "gene_name": "Ccdc188", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Ccdc188; Gm7873", "gene_names_refseq": "", "protein_names_uniprotkb": "Coiled-coil domain containing 188", "protein_names_refseq": "", "tax_id": 10090, "disease": "male infertility due to acephalic spermatozoa (Disease Ontology:DOID:0112311)", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0016020 membrane", "go_biological_process": "GO:0030382 sperm mitochondrion organization;GO:0007283 spermatogenesis;GO:0007286 spermatid development;GO:0007338 single fertilization;GO:0007289 spermatid nucleus differentiation", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A338P6G2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BGL3-1", "uniprot_id": "ST2A8_MOUSE", "mass": 33295.0, "length": 282, "protein_name": "Sulfotransferase 2A8", "gene_name": "Sult2a8", "organism": "Mouse", "refseq_name": "sulfotransferase 2A8", "refseq_ac": "NP_001186235", "gene_names_uniprotkb": "Sult2a8; 2810007J24Rik", "gene_names_refseq": "2810007J24Rik; L-STL; Sult2a8; mL-STL", "protein_names_uniprotkb": "Sulfotransferase 2A8; 2.8.2.34; Glycochenodeoxycholate sulfotransferase 2A8; L-STL; Liver sulfotransferase-like protein; SULT2A8", "protein_names_refseq": "glycochenodeoxycholate sulfotransferase 2A8; liver sulfotransferase-like protein; sulfotransferase 2A8; sulfotransferase-like protein 1", "tax_id": 10090, "disease": "prostate cancer (Disease Ontology:DOID:10283)", "pathway": " (mmu:76971)", "pathway_count": 1, "publication_count": 7, "publication_id_list": "21750661;25428506;28442498;29685090;33029720;33872606;34030040", "class_list": "", "function": "A novel PPARalpha-dependent gene, [RefSeq, PubMed]; Findings suggested that substitutions of two amino acids, which might have occurred during the evolution of the mouse SULT2A8 gene, endowed mouse SULT2A8 the capacity to catalyze the 7-O-sulfation of bile acids, [RefSeq, PubMed]; Hepatic sulfotransferase involved in the maintenance of bile acid homeostasis and energy balance. Catalyzes the transfer of sulfonate group from 3'-phosphoadenylyl sulfate (PAPS) to the 7-alpha hydroxy group of primary bile acids to form 7-monosulfate derivatives in the pathway of bile acid elimination. Displays high catalytic efficiency toward cholate, chenodeoxycholate and their glycine and taurine conjugates., [UniProtKB, PubMed, PubMed, PubMed]; Male-biased fasting-induced changes in hepatic tauro-cholic acid and plasma cholesterol in Sult2a8-haplodeficient mice., [RefSeq, PubMed]; Structure of mouse cytosolic sulfotransferase SULT2A8 provides insight into sulfonation of 7alpha-hydroxyl bile acids., [RefSeq, PubMed]; The crystal structure of mouse SULT2A8 reveals the mechanism of 7alpha-hydroxyl, bile acid sulfation., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 11, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "B1PQU4", "ec_number_list": "2.8.2.-;2.8.2.34", "go_molecular_function": "GO:0008146 sulfotransferase activity;GO:0050656 3'-phosphoadenosine 5'-phosphosulfate binding;GO:0004027 alcohol sulfotransferase activity;GO:0047704 bile-salt sulfotransferase activity;GO:0050294 steroid sulfotransferase activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol", "go_biological_process": "GO:0051923 sulfation;GO:0008203 cholesterol metabolic process;GO:0016042 lipid catabolic process;GO:0006068 ethanol catabolic process;GO:0006805 xenobiotic metabolic process", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q8BGL3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G3X9B1-1", "uniprot_id": "G3X9B1_MOUSE", "mass": 242072.0, "length": 2143, "protein_name": "HEAT repeat-containing protein 1", "gene_name": "Heatr1", "organism": "Mouse", "refseq_name": "HEAT repeat-containing protein 1", "refseq_ac": "NP_659084", "gene_names_uniprotkb": "Heatr1", "gene_names_refseq": "B130016L12Rik; Heatr1", "protein_names_uniprotkb": "HEAT repeat-containing protein 1", "protein_names_refseq": "HEAT repeat-containing protein 1", "tax_id": 10090, "disease": "glioblastoma (Disease Ontology:DOID:3068); pancreatic ductal carcinoma (Disease Ontology:DOID:3587)", "pathway": " (mmu:217995); (R-MMU-6791226)", "pathway_count": 2, "publication_count": 3, "publication_id_list": "21750661;25428506;31599954", "class_list": "", "function": "Involved in nucleolar processing of pre-18S ribosomal RNA., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0030515 snoRNA binding", "go_cellular_component": "GO:0005730 nucleolus;GO:1990904 ribonucleoprotein complex;GO:0005739 mitochondrion;GO:0001650 fibrillar center;GO:0034455 t-UTP complex", "go_biological_process": "GO:0006364 rRNA processing;GO:2000234 positive regulation of rRNA processing;GO:1902570 protein localization to nucleolus;GO:0045943 positive regulation of transcription by RNA polymerase I;GO:0061351 neural precursor cell proliferation", "synthesized_glycan_count": 0, "hit_score": 0.4, "record_id": "G3X9B1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9Q0B6-1", "uniprot_id": "E9Q0B6_MOUSE", "mass": 474815.0, "length": 4144, "protein_name": "Dynein, axonemal, heavy chain 6", "gene_name": "Dnah6", "organism": "Mouse", "refseq_name": "dynein axonemal heavy chain 6", "refseq_ac": "NP_001158141", "gene_names_uniprotkb": "Dnah6; Dnahc6", "gene_names_refseq": "9830168K20; A730004I20Rik; Dnah6; Dnahc6; mKIAA1697; mdhc6", "protein_names_uniprotkb": "Dynein, axonemal, heavy chain 6", "protein_names_refseq": "axonemal dynein heavy chain; dynein axonemal heavy chain 6; dynein, axon, heavy chain 6", "tax_id": 10090, "disease": "", "pathway": " (mmu:330355)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21750661;26918822", "class_list": "", "function": "Dnah6 genetically interacts with Dnai1 and Dnah5 to cause heterotaxy and primary ciliary dyskinesia. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 3, "predicted_n_glycosites": 0, "predicted_o_glycosites": 3, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0003777 microtubule motor activity;GO:0008569 minus-end-directed microtubule motor activity;GO:0051959 dynein light intermediate chain binding;GO:0045505 dynein intermediate chain binding", "go_cellular_component": "GO:0005874 microtubule;GO:0036126 sperm flagellum;GO:0030286 dynein complex;GO:0036156 inner dynein arm;GO:0097729 9+2 motile cilium", "go_biological_process": "GO:0060294 cilium movement involved in cell motility;GO:0003341 cilium movement;GO:0007018 microtubule-based movement", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "E9Q0B6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A338P6T0-1", "uniprot_id": "A0A338P6T0_MOUSE", "mass": 97082.0, "length": 845, "protein_name": "Vomeronasal 2, receptor 95", "gene_name": "Vmn2r95", "organism": "Mouse", "refseq_name": "vomeronasal 2, receptor 95", "refseq_ac": "NP_001096051", "gene_names_uniprotkb": "Vmn2r95", "gene_names_refseq": "Vmn2r95", "protein_names_uniprotkb": "Vomeronasal 2, receptor 95", "protein_names_refseq": "vomeronasal 2, receptor 95; vomeronasal receptor Vmn2r95", "tax_id": 10090, "disease": "", "pathway": " (mmu:328759)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "10.1101/2023.09.13.557529;21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 9671, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.7, "record_id": "A0A338P6T0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "W4VSP4-1", "uniprot_id": "W4VSP4_MOUSE", "mass": 42914.0, "length": 379, "protein_name": "Serine (or cysteine) peptidase inhibitor, clade B, member 6c", "gene_name": "Serpinb6c", "organism": "Mouse", "refseq_name": "serine proteinase inhibitor member 6C", "refseq_ac": "NP_683744", "gene_names_uniprotkb": "Serpinb6c", "gene_names_refseq": "SPI3C; SPIC; Serpinb6c; ovalbumin", "protein_names_uniprotkb": "Serine (or cysteine) peptidase inhibitor, clade B, member 6c", "protein_names_refseq": "serine (or cysteine) proteinase inhibitor, clade B, member 6c; serine proteinase inhibitor member 6C", "tax_id": 10090, "disease": "autosomal recessive nonsyndromic deafness 91 (Disease Ontology:DOID:0110536)", "pathway": " (mmu:97848)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004867 serine-type endopeptidase inhibitor activity;GO:0002020 protease binding", "go_cellular_component": "GO:0005615 extracellular space;GO:0005737 cytoplasm;GO:0097180 serine protease inhibitor complex", "go_biological_process": "GO:0007605 sensory perception of sound;GO:0071470 cellular response to osmotic stress", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "W4VSP4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3U1C4-1", "uniprot_id": "SEBP2_MOUSE", "mass": 94814.0, "length": 858, "protein_name": "Selenocysteine insertion sequence-binding protein 2", "gene_name": "Secisbp2", "organism": "Mouse", "refseq_name": "selenocysteine insertion sequence-binding protein 2 isoform 1", "refseq_ac": "NP_083555", "gene_names_uniprotkb": "Secisbp2; Sbp2", "gene_names_refseq": "2210413N07Rik; 2810012K13Rik; SBP2; Secisbp2", "protein_names_uniprotkb": "Selenocysteine insertion sequence-binding protein 2; SECIS-binding protein 2", "protein_names_refseq": "selenocysteine insertion sequence-binding protein 2 isoform 1; selenocysteine insertion sequence-binding protein 2", "tax_id": 10090, "disease": "thyroid gland disease (Disease Ontology:DOID:50)", "pathway": " (mmu:75420)", "pathway_count": 1, "publication_count": 7, "publication_id_list": "10.1101/2023.09.13.557529;22308032;22992746;24274065;24844465;31826256;33122797", "class_list": "", "function": "Role of the Thyroid Gland in Expression of the Thyroid Phenotype of Sbp2-Deficient Mice., [RefSeq, PubMed]; SBP2/SECIS complex activates eEFSec by directing functional interactions between Domain IV and the ribosome to promote Sec-tRNA(Sec) binding and accommodation into the ribosomal A-site, [RefSeq, PubMed]; Secisbp2 is essential for embryonic development and enhances selenoprotein expression., [RefSeq, PubMed]; Selenocysteine insertion sequence (SECIS)-binding protein 2 alters conformational dynamics of residues involved in tRNA accommodation in 80 S ribosomes., [RefSeq, PubMed]; Selenocysteine insertion sequence binding protein 2 (Sbp2) in the sex-specific regulation of selenoprotein gene expression in mouse pancreatic islets. Publication Status: Online-Only, [RefSeq, PubMed]; The incorporation of selenocysteine into a protein requires the concerted action of an mRNA element called a sec insertion sequence (SECIS), a selenocysteine-specific translation elongation factor and a SECIS binding protein. With these elements in place, a UGA codon can be decoded as selenocysteine. The gene described in this record encodes a nuclear protein that functions as a SECIS binding protein. Mutations in a similar gene in human have been associated with a reduction in activity of a specific thyroxine deiodinase, a selenocysteine-containing enzyme, and abnormal thyroid hormone metabolism. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2015]., [RefSeq]; mRNA-binding protein that binds to the SECIS (selenocysteine insertion sequence) element present in the 3'-UTR of mRNAs encoding selenoproteins and facilitates the incorporation of the rare amino acid selenocysteine (PubMed:22992746, PubMed:24274065, PubMed:24844465). Insertion of selenocysteine at UGA codons is mediated by SECISBP2 and EEFSEC: SECISBP2 (1) specifically binds the SECIS sequence once the 80S ribosome encounters an in-frame UGA codon and (2) contacts the RPS27A/eS31 of the 40S ribosome before ribosome stalling (By similarity). (3) GTP-bound EEFSEC then delivers selenocysteinyl-tRNA(Sec) to the 80S ribosome and adopts a preaccommodated state conformation (By similarity). (4) After GTP hydrolysis, EEFSEC dissociates from the assembly, selenocysteinyl-tRNA(Sec) accommodates, and peptide bond synthesis and selenoprotein elongation occur (By similarity)., [UniProtKB, PubMed, PubMed, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 9577, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q3TGQ4", "ec_number_list": "", "go_molecular_function": "GO:0035368 selenocysteine insertion sequence binding;GO:0003677 DNA binding;GO:0003723 RNA binding;GO:0043021 ribonucleoprotein complex binding;GO:0003730 mRNA 3'-UTR binding", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005739 mitochondrion;GO:1990904 ribonucleoprotein complex", "go_biological_process": "GO:0001514 selenocysteine incorporation;GO:0048255 mRNA stabilization;GO:0006412 translation;GO:0048666 neuron development;GO:0021756 striatum development", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "Q3U1C4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VF63-1", "uniprot_id": "Q8VF63_MOUSE", "mass": 35508.0, "length": 314, "protein_name": "Olfactory receptor family 8 subfamily B member 35", "gene_name": "Or8b35", "organism": "Mouse", "refseq_name": "olfactory receptor 881", "refseq_ac": "NP_666530", "gene_names_uniprotkb": "Or8b35; Olfr881", "gene_names_refseq": "MOR162-7; Olfr881; Or8b35", "protein_names_uniprotkb": "Olfactory receptor family 8 subfamily B member 35", "protein_names_refseq": "GA_x6K02T2PVTD-31676771-31677700; olfactory receptor 881; olfactory receptor MOR162-7", "tax_id": 10090, "disease": "", "pathway": " (mmu:258413)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q8VF63-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A2R8VKG2-1", "uniprot_id": "A0A2R8VKG2_MOUSE", "mass": 225983.0, "length": 2099, "protein_name": "RIKEN cDNA D430041D05 gene", "gene_name": "D430041D05Rik", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "D430041D05Rik", "gene_names_refseq": "", "protein_names_uniprotkb": "RIKEN cDNA D430041D05 gene", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": " (mmu:241589)", "pathway_count": 1, "publication_count": 6, "publication_id_list": "10.1101/2023.09.13.557529;15345747;16452087;21750661;24129315;34678516", "class_list": "", "function": "", "predicted_glycosites": 5, "predicted_n_glycosites": 0, "predicted_o_glycosites": 5, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 5, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 5, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 5, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 6, "disease_count": 0, "glyco_site_count": 10, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 1.9, "record_id": "A0A2R8VKG2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q5RIS0-1", "uniprot_id": "Q5RIS0_MOUSE", "mass": 40845.0, "length": 354, "protein_name": "Myb/SANT DNA binding domain containing 5 family member 6", "gene_name": "Msantd5f6", "organism": "Mouse", "refseq_name": "uncharacterized protein LOC433719", "refseq_ac": "NP_001013411", "gene_names_uniprotkb": "Msantd5f6", "gene_names_refseq": "Gm11487; Msantd5f6", "protein_names_uniprotkb": "Myb/SANT DNA binding domain containing 5 family member 6", "protein_names_refseq": "uncharacterized protein LOC433719", "tax_id": 10090, "disease": "", "pathway": " (mmu:433719)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "This gene belongs to a family of related genes tandemly arranged in two clusters on chromosome 4. This family, which appears to be mouse-specific and composed of multiple highly similar members, is supported by limited transcript data. Members of the family maintain an intact open reading frame although the encoded protein has no known function. This gene is inferred from alignment of paralogous transcripts. [provided by RefSeq, Apr 2013]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q5RIS0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A2BFE8-1", "uniprot_id": "A2BFE8_MOUSE", "mass": 25060.0, "length": 218, "protein_name": "Proline rich Gla (G-carboxyglutamic acid) 1", "gene_name": "Prrg1", "organism": "Mouse", "refseq_name": "transmembrane gamma-carboxyglutamic acid protein 1", "refseq_ac": "NP_001157747", "gene_names_uniprotkb": "Prrg1", "gene_names_refseq": "2010007L08Rik; Prrg1", "protein_names_uniprotkb": "Proline rich Gla (G-carboxyglutamic acid) 1", "protein_names_refseq": "ortholog of proline rich Gla (G-carboxyglutamic acid) 1 PRRG1; transmembrane gamma-carboxyglutamic acid protein 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:546336)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004252 serine-type endopeptidase activity;GO:0005509 calcium ion binding", "go_cellular_component": "GO:0005615 extracellular space;GO:0005576 extracellular region", "go_biological_process": "GO:0006508 proteolysis;GO:0007596 blood coagulation", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A2BFE8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A2R8VHP3-1", "uniprot_id": "A0A2R8VHP3_MOUSE", "mass": 57920.0, "length": 535, "protein_name": "Predicted pseudogene 5478", "gene_name": "Gm5478", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Gm5478; Krt6a", "gene_names_refseq": "", "protein_names_uniprotkb": "Predicted pseudogene 5478", "protein_names_refseq": "", "tax_id": 10090, "disease": "pachyonychia congenita (Disease Ontology:DOID:0050449); focal or diffuse nonepidermolytic palmoplantar keratoderma (Disease Ontology:DOID:0111710)", "pathway": " (R-MMU-6805567); (R-MMU-6809371)", "pathway_count": 2, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0030280 structural constituent of skin epidermis", "go_cellular_component": "GO:0045095 keratin filament;GO:0045111 intermediate filament cytoskeleton", "go_biological_process": "GO:0031424 keratinization;GO:0045109 intermediate filament organization", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A2R8VHP3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9Q492-1", "uniprot_id": "E9Q492_MOUSE", "mass": 47372.0, "length": 415, "protein_name": "PiggyBac transposable element derived 1", "gene_name": "Pgbd1", "organism": "Mouse", "refseq_name": "piggyBac transposable element-derived protein 1 isoform a", "refseq_ac": "NP_001156391", "gene_names_uniprotkb": "Pgbd1", "gene_names_refseq": "4921509E05Rik; Pgbd1", "protein_names_uniprotkb": "PiggyBac transposable element derived 1", "protein_names_refseq": "piggyBac transposable element-derived protein 1 isoform a", "tax_id": 10090, "disease": "", "pathway": " (mmu:319207)", "pathway_count": 1, "publication_count": 3, "publication_id_list": "10.1101/2023.09.13.557529;21750661;24928388", "class_list": "", "function": "Thus SB and PB transposons represent a promising non-viral approach for iPS cell derivation., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0042802 identical protein binding;GO:0043565 sequence-specific DNA binding", "go_cellular_component": "GO:0005634 nucleus", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "E9Q492-1", "record_type": "protein" }, { "uniprot_canonical_ac": "G3X8X0-1", "uniprot_id": "G3X8X0_MOUSE", "mass": 119072.0, "length": 1044, "protein_name": "Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16", "gene_name": "Dhx16", "organism": "Mouse", "refseq_name": "pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16", "refseq_ac": "NP_081263", "gene_names_uniprotkb": "Dhx16", "gene_names_refseq": "2410006N22Rik; DBP2; Ddx16; Dhx16; mKIAA0577", "protein_names_uniprotkb": "Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16; 3.6.4.13; DEAH-box protein 16", "protein_names_refseq": "DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 16; DEAH (Asp-Glu-Ala-His) box polypeptide 16; pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16", "tax_id": 10090, "disease": "", "pathway": " (mmu:69192); (R-MMU-72163)", "pathway_count": 2, "publication_count": 3, "publication_id_list": "15345747;17242355;21750661", "class_list": "", "function": "Required for pre-mRNA splicing as a component of the spliceosome. Contributes to pre-mRNA splicing after spliceosome formation and prior to the first transesterification reaction. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs. Also plays a role in innate antiviral response by acting as a pattern recognition receptor sensing splicing signals in viral RNA. Mechanistically, TRIM6 promotes the interaction between unanchored 'Lys-48'-polyubiquitin chains and DHX16, leading to DHX16 interaction with RIGI and ssRNA to amplify RIGI-dependent innate antiviral immune responses., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "3.6.4.13;3.6.4.10;3.6.4.-;5.6.2.3;5.2.1.8;5.6.2.4;2.3.2.-;2.3.2.27;3.1.13.1;5.6.2.6;3.1.-.-;7.6.2.1;3.6.1.5;3.4.24.-;3.6.-.-;3.1.13.-;2.7.7.48;2.7.7.6;3.1.3.1;3.9.1.1;3.6.1.-;5.6.2.5;4.2.99.18;3.6.4.12;5.6.1.6;3.6.4.6;3.6.5.-;3.6.1.15;3.1.4.-;5.6.2.-;7.2.2.-;7.6.2.16;3.4.21.53;2.7.7.7;2.7.7.49;2.7.11.1;2.7.4.3", "go_molecular_function": "GO:0003724 RNA helicase activity;GO:0060090 molecular adaptor activity;GO:0003723 RNA binding;GO:0005524 ATP binding;GO:0016787 hydrolase activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005681 spliceosomal complex;GO:0071006 U2-type catalytic step 1 spliceosome", "go_biological_process": "GO:0000398 mRNA splicing, via spliceosome;GO:0140374 antiviral innate immune response", "synthesized_glycan_count": 0, "hit_score": 0.4, "record_id": "G3X8X0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A2I3BPG7-1", "uniprot_id": "A0A2I3BPG7_MOUSE", "mass": 39218.0, "length": 339, "protein_name": "Vomeronasal type-1 receptor", "gene_name": "Vmn1r81", "organism": "Mouse", "refseq_name": "vomeronasal 1 receptor 81 isoform 1", "refseq_ac": "NP_001423072", "gene_names_uniprotkb": "Vmn1r81", "gene_names_refseq": "V1rg9; Vmn1r81", "protein_names_uniprotkb": "Vomeronasal type-1 receptor", "protein_names_refseq": "vomernasal 1 receptor Vmn1r81; vomeronasal 1 receptor 81 isoform 1; vomeronasal 1 receptor, G9; vomeronasal type 1 receptor G9", "tax_id": 10090, "disease": "", "pathway": " (mmu:171244)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0016503 pheromone receptor activity;GO:0005550 pheromone binding", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0019236 response to pheromone;GO:0007606 sensory perception of chemical stimulus", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A2I3BPG7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "B1ATY8-1", "uniprot_id": "ARL16_MOUSE", "mass": 18788.0, "length": 173, "protein_name": "ADP-ribosylation factor-like protein 16", "gene_name": "Arl16", "organism": "Mouse", "refseq_name": "ADP-ribosylation factor-like protein 16", "refseq_ac": "NP_932112", "gene_names_uniprotkb": "Arl16", "gene_names_refseq": "2600005N12Rik; Arl16", "protein_names_uniprotkb": "ADP-ribosylation factor-like protein 16", "protein_names_refseq": "ADP-ribosylation factor-like protein 16", "tax_id": 10090, "disease": "", "pathway": " (mmu:70317)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21233210;35196065", "class_list": "", "function": "ARF-like protein 16 (ARL16) inhibits RIG-I by binding with its C-terminal domain in a GTP-dependent manner, [RefSeq, PubMed]; Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E., [RefSeq, PubMed]; Required for trafficking of ciliary proteins IFT140 and INPP5E from the Golgi to the cilia, thus playing a role in ciliogenesis (PubMed:35196065). Suppresses the RNA sensing activity of RIGI in a GTP-dependent manner (By similarity)., [UniProtKB, PubMed, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3V3L8", "ec_number_list": "", "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0001917 photoreceptor inner segment;GO:0005930 axoneme", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "B1ATY8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "B1AUF7-1", "uniprot_id": "P3URF_MOUSE", "mass": 9886.0, "length": 90, "protein_name": "PIK3R3 upstream open reading frame protein", "gene_name": "P3r3urf", "organism": "Mouse", "refseq_name": "P3R3URF protein", "refseq_ac": "NP_001092765", "gene_names_uniprotkb": "P3r3urf", "gene_names_refseq": "1700042G07Rik; P3r3urf", "protein_names_uniprotkb": "PIK3R3 upstream open reading frame protein", "protein_names_refseq": "P3R3URF protein", "tax_id": 10090, "disease": "", "pathway": " (mmu:67323)", "pathway_count": 1, "publication_count": 0, "publication_id_list": "", "class_list": "", "function": "", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "GO:0019221 cytokine-mediated signaling pathway", "synthesized_glycan_count": 0, "hit_score": 0.1, "record_id": "B1AUF7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "B9EJ80-1", "uniprot_id": "PDZD8_MOUSE", "mass": 127739.0, "length": 1147, "protein_name": "PDZ domain-containing protein 8", "gene_name": "Pdzd8", "organism": "Mouse", "refseq_name": "PDZ domain-containing protein 8", "refseq_ac": "NP_001028394", "gene_names_uniprotkb": "Pdzd8", "gene_names_refseq": "A630041P07Rik; Pdzd8; Pdzk8", "protein_names_uniprotkb": "PDZ domain-containing protein 8", "protein_names_refseq": "PDZ domain-containing protein 8", "tax_id": 10090, "disease": "syndromic intellectual disability (Disease Ontology:DOID:0050888)", "pathway": " (mmu:107368)", "pathway_count": 1, "publication_count": 15, "publication_id_list": "10.1101/2023.09.13.557529;17242355;18250455;21183079;25428506;29097544;32917905;33649389;34428180;35227461;36465123;36658656;39069376;40016860;40246839", "class_list": "", "function": "Lipid transfer and molecular tethering protein, which plays a key role in the formation of membrane contact sites between the endoplasmic reticulum and other organelles, such as late endosomes/lysosomes and mitochondria (PubMed:29097544, PubMed:32917905, PubMed:36465123, PubMed:39069376). Faciliates the exchange of lipids at membrane contact sites between the endoplasmic reticulum and organelles by mediating the transport of lipids, such as ceramide, cholesterol and phosphatidylserine (PubMed:32917905, PubMed:36465123). Also acts as a molecular glue by undergoing liquid-liquid phase separation, forming condensates that mediate stable adhesion between endoplasmic reticulum and surrounding organelles, connecting two distinct membrane-bound vesicles coupled together (By similarity). Connects the endoplasmic reticulum to late endosomes/lysosomes, facilitating the exchange of lipids, which is crucial for membrane remodeling and processes, such as neurite outgrowth (PubMed:32917905, PubMed:36465123). PDZD8-dependent endoplasmic reticulum-mitochondria membrane tethering is essential for endoplasmic reticulum-mitochondria Ca(2+) transfer (PubMed:29097544, PubMed:39069376, PubMed:40246839). In neurons, involved in the regulation of dendritic Ca(2+) dynamics by regulating mitochondrial Ca(2+) uptake in neurons (PubMed:29097544). Mediates lysosomal vacuolation, a process during which lysosomes abnormally enlarge into large membrane-bound sacs in response to stress such as osmotic stress: acts by mediating bulk lipid transfer from the endoplasmic reticulum to lysosomes, leading to vacuole formation (By similarity). Plays an indirect role in the regulation of cell morphology and cytoskeletal organization (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed]; PDZD8 represents a critical an endoplasmic reticulum -mitochondria tethering protein in metazoans., [RefSeq, PubMed]; PDZD8-deficient mice manifest behavioral abnormalities related to emotion, cognition, and adaptation due to dyslipidemia in the brain. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 5, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q3UMB1", "ec_number_list": "1.6.5.5;3.1.-.-", "go_molecular_function": "GO:0008270 zinc ion binding;GO:0008289 lipid binding", "go_cellular_component": "GO:0005739 mitochondrion;GO:0005789 endoplasmic reticulum membrane;GO:0044233 mitochondria-associated endoplasmic reticulum membrane contact site", "go_biological_process": "GO:0006869 lipid transport;GO:0007010 cytoskeleton organization;GO:0022604 regulation of cell morphogenesis;GO:0051560 mitochondrial calcium ion homeostasis;GO:1990456 mitochondrion-endoplasmic reticulum membrane tethering", "synthesized_glycan_count": 0, "hit_score": 1.8, "record_id": "B9EJ80-1", "record_type": "protein" }, { "uniprot_canonical_ac": "B9UIU9-1", "uniprot_id": "SCPPQ_MOUSE", "mass": 9783.0, "length": 90, "protein_name": "Secretory calcium-binding phosphoprotein proline- and glutamine-rich 1", "gene_name": "Scpppq1", "organism": "Mouse", "refseq_name": "secretory calcium-binding phosphoprotein proline- and glutamine-rich 1 precursor", "refseq_ac": "NP_001157244", "gene_names_uniprotkb": "Scpppq1; Gm17660", "gene_names_refseq": "Gm17660; Scpppq1", "protein_names_uniprotkb": "Secretory calcium-binding phosphoprotein proline- and glutamine-rich 1", "protein_names_refseq": "secretory calcium-binding phosphoprotein proline- and glutamine-rich 1 precursor; secretory calcium-binding phosphoprotein proline- and glutamine-rich 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:100271704)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "16674676;19255778;25193156;25428506;28436474", "class_list": "", "function": "Data suggest that amelotin (AMTN), odontogenic ameloblast-associated protein (ODAM) and secretory calcium-binding phosphoprotein proline-glutamine rich 1 (SCPPPQ1) participate in structuring an extracellular matrix with the distinctive capacity of attaching epithelial cells to mineralized surfaces. Publication Status: Online-Only, [RefSeq, PubMed]; The gene, protein and pattern of expression of a related protein called secretory calcium-binding phosphoprotein-proline-glutamine-rich 1 (SCPPPQ1), is reported., [RefSeq, PubMed]; Tooth-associated epithelia protein that may participate in structuring the basal lamina at cell-tooth interface., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005576 extracellular region", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "B9UIU9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "D3Z0W3-1", "uniprot_id": "D3Z0W3_MOUSE", "mass": 58624.0, "length": 525, "protein_name": "Zinc finger protein 648", "gene_name": "Zfp648", "organism": "Mouse", "refseq_name": "zinc finger protein 648", "refseq_ac": "NP_001191837", "gene_names_uniprotkb": "Zfp648", "gene_names_refseq": "Gm10178; Gm203; Zfp648", "protein_names_uniprotkb": "Zinc finger protein 648", "protein_names_refseq": "zinc finger protein 648", "tax_id": 10090, "disease": "", "pathway": " (mmu:100503355)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21750661;25428506", "class_list": "", "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific", "go_cellular_component": "GO:0005634 nucleus", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "D3Z0W3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9PWV2-1", "uniprot_id": "E9PWV2_MOUSE", "mass": 34867.0, "length": 313, "protein_name": "Olfactory receptor family 10 subfamily J member 3B", "gene_name": "Or10j3", "organism": "Mouse", "refseq_name": "olfactory receptor 218", "refseq_ac": "NP_001001809", "gene_names_uniprotkb": "Or10j3; Olfr218", "gene_names_refseq": "MOR267-3; Olfr1405-ps1; Olfr218-ps1; Olfr218; Or10j3", "protein_names_uniprotkb": "Olfactory receptor family 10 subfamily J member 3B", "protein_names_refseq": "GA_x6K02SYWG4P-534-1100; GA_x6K02T2R7CC-643715-642847; olfactory receptor 1405, pseudogene 1; olfactory receptor 218, pseudogene 1; olfactory receptor 218; olfactory receptor MOR267-3; olfactory receptor family 10 subfamily J member 3B", "tax_id": 10090, "disease": "", "pathway": " (mmu:258880)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. 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Gm5771; Prss1l", "protein_names_uniprotkb": "trypsin; 3.4.21.4", "protein_names_refseq": "trypsinogen 12 precursor; trypsinogen 12", "tax_id": 10090, "disease": "cholangiocarcinoma (Disease Ontology:DOID:4947); pancreatitis (Disease Ontology:DOID:4989)", "pathway": " (mmu:436523); (R-MMU-1462054); (R-MMU-1592389); (R-MMU-6798695); (R-MMU-6803157)", "pathway_count": 5, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "3.4.24.22;3.4.24.34;3.4.22.27;1.1.1.42;4.1.2.13;3.4.21.4;3.4.21.-;3.2.1.17;1.16.3.1;3.4.23.5;3.4.21.39;3.4.21.59;3.3.2.6;3.4.11.4;3.4.21.34;3.4.21.20;3.4.24.17;3.1.3.48;3.4.24.-;3.4.24.35;3.5.4.5;3.4.24.23;3.4.21.37;1.8.3.2;3.6.1.6;3.4.21.1;2.3.2.5;5.4.2.2;3.2.1.14;3.4.24.7;3.5.1.3;3.5.1.23;3.5.1.-;3.4.19.9", "go_molecular_function": "GO:0004252 serine-type endopeptidase activity;GO:0005509 calcium ion binding;GO:0008236 serine-type peptidase activity", "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0031012 extracellular matrix", "go_biological_process": "GO:0006508 proteolysis", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q792Y9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TS04-1", "uniprot_id": "Q7TS04_MOUSE", "mass": 35025.0, "length": 311, "protein_name": "Olfactory receptor family 14 subfamily C member 44", "gene_name": "Or14c44", "organism": "Mouse", "refseq_name": "olfactory receptor 301", "refseq_ac": "NP_997601", "gene_names_uniprotkb": "Or14c44; Olfr301", "gene_names_refseq": "MOR211-8P; MOR221-1P; MOR221-4; Olfr1531-ps1; Olfr301; Or14c44", "protein_names_uniprotkb": "Olfactory receptor family 14 subfamily C member 44", "protein_names_refseq": "GA_x6K02T2NHDJ-9693313-9692378; olfactory receptor 1531, pseudogene 1; olfactory receptor 301; olfactory receptor MOR211-8P; olfactory receptor MOR221-1P", "tax_id": 10090, "disease": "", "pathway": " (mmu:257958)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21750661;32061665", "class_list": "", "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]; This odorant receptor, Olfr301, responds to the odorant isoamyl acetate in vivo., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "Q7TS04-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VGU6-1", "uniprot_id": "Q8VGU6_MOUSE", "mass": 35663.0, "length": 319, "protein_name": "Olfactory receptor family 7 subfamily A member 35", "gene_name": "Or7a35", "organism": "Mouse", "refseq_name": "olfactory receptor 1351", "refseq_ac": "NP_667251", "gene_names_uniprotkb": "Or7a35; Olfr1351", "gene_names_refseq": "MOR139-4; Olfr1351; Or7a35", "protein_names_uniprotkb": "Olfactory receptor family 7 subfamily A member 35", "protein_names_refseq": "GA_x6K02T2QGN0-2794907-2793948; olfactory receptor 1351; olfactory receptor MOR139-4", "tax_id": 10090, "disease": "", "pathway": " (mmu:259042)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0007165 signal transduction;GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q8VGU6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "W4VSP7-1", "uniprot_id": "W4VSP7_MOUSE", "mass": 23317.0, "length": 230, "protein_name": "Keratin associated protein 10-22", "gene_name": "Krtap10-22", "organism": "Mouse", "refseq_name": "keratin associated protein 10-like", "refseq_ac": "NP_001095100", "gene_names_uniprotkb": "Krtap10-22; Gm3238", "gene_names_refseq": "100041261; Gm3238; Krtap10-22", "protein_names_uniprotkb": "Keratin associated protein 10-22", "protein_names_refseq": "keratin associated protein 10-like", "tax_id": 10090, "disease": "", "pathway": " (mmu:100041261); (R-MMU-6805567)", "pathway_count": 2, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "In the hair cortex, hair keratin intermediate filaments are embedded in an interfilamentous matrix, consisting of hair keratin-associated proteins (KRTAP), which are essential for the formation of a rigid and resistant hair shaft through their extensive disulfide bond cross-linking with abundant cysteine residues of hair keratins. The matrix proteins include the high-sulfur and high-glycine-tyrosine keratins., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0042802 identical protein binding", "go_cellular_component": "GO:0005829 cytosol;GO:0045095 keratin filament", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "W4VSP7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A2R8VH94-1", "uniprot_id": "A0A2R8VH94_MOUSE", "mass": 17655.0, "length": 162, "protein_name": "Transmembrame protein 274", "gene_name": "Tmem274", "organism": "Mouse", "refseq_name": "uncharacterized protein LOC102636051", "refseq_ac": "NP_001353331", "gene_names_uniprotkb": "Tmem274; 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0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0043021 ribonucleoprotein complex binding;GO:0030295 protein kinase activator activity;GO:0003735 structural constituent of ribosome", "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005829 cytosol;GO:0022626 cytosolic ribosome;GO:0022625 cytosolic large ribosomal subunit", "go_biological_process": "GO:0006417 regulation of translation;GO:0006414 translational elongation;GO:0002181 cytoplasmic translation", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A494BA26-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A571BEN2-1", "uniprot_id": "A0A571BEN2_MOUSE", "mass": 47812.0, "length": 409, "protein_name": "Zinc finger protein 1001", "gene_name": "Zfp1001", "organism": "Mouse", "refseq_name": "uncharacterized protein LOC102633750", 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"record_id": "A0A2I3BPT7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A2R8VJU7-1", "uniprot_id": "SEP12_MOUSE", "mass": 40875.0, "length": 357, "protein_name": "Septin 12", "gene_name": "Septin12", "organism": "Mouse", "refseq_name": "septin-12 isoform 3", "refseq_ac": "NP_001360874", "gene_names_uniprotkb": "Septin12; Sept12", "gene_names_refseq": "1700028G04Rik; 4933413B09Rik; Sept12; Septin12", "protein_names_uniprotkb": "Septin 12", "protein_names_refseq": "septin-12 isoform 3", "tax_id": 10090, "disease": "spermatogenic failure 10 (Disease Ontology:DOID:0070178)", "pathway": " (mmu:71089)", "pathway_count": 1, "publication_count": 7, "publication_id_list": "20801438;25588830;27854341;28346465;35547809;36715674;38870534", "class_list": "", "function": "Filament-forming cytoskeletal GTPase (By similarity). Involved in the morphogenesis of sperm heads and the elongation of sperm tails probably implicating the association with alpha- and beta-tubulins (By similarity). Facilitates the formation of Septin filament structures with SEPTIN7, SEPTIN6, SEPTIN2 and SEPTIN4 at the sperm annulus (PubMed:25588830, PubMed:28346465). Correct formation of the annulus is required for development of normal structural morphology and motility of the sperm during steps 13 to 16 of spermiogenesis (PubMed:25588830, PubMed:28346465). Essential component of the LMNB1/SUN5/SEPT12 bridge that connects the sperm proximal centriole to the implantation fossa, the bridge functions to prevent detachment of the proximal centriole from the posterior nucleus during steps 13 to 16 of spermiogenesis (PubMed:38870534). Required for PLCZ1 localization at the sperm acrosome during spermiogenesis (PubMed:35547809). May also play a role in the initiation of calcium oscillations in embryos (PubMed:35547809)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed, PubMed, UniProtKB]; In mice sperm with mutated SEPT12, NDC1 dispersed around the manchette region of the sperm head and annulus, compared with concentrating at the sperm neck of wild-type sperm. Publication Status: Online-Only, [RefSeq, PubMed]; Oocytes fertilized with spermatozoa obtained from Septin 12+/- chimeric mice failed to develop beyond the morula stage after IVF and intracytoplasmic sperm injection because of significant DNA defects in the spermatozoa, [RefSeq, PubMed]; Proper phosphorylation of septin 12 regulates septin 4 and soluble adenylyl cyclase expression to induce sperm capacitation., [RefSeq, PubMed]; Results demonstrate the molecular architecture of SEPT12 filaments at the sperm annulus, their mechanical support of sperm motility, and their correlation with male infertility., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, 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Also mediates Cl(-)/HCO3(-) exchange activity in the presence of K(+) as well as Cs(+), Li(+), and Rb(+) (PubMed:27114614). Does not contribute to Cl(-)/HCO3(-) exchanger in the apical membrane of the upper villous epithelium (PubMed:17170027)., [UniProtKB, PubMed, PubMed, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Novel functions of the anion exchanger AE4 (SLC4A9). Review article, [RefSeq, PubMed]; The AE4 promoter is identified as a direct target of Foxi1., [RefSeq, PubMed]; The AE4 transporter mediates kidney acid-base sensing. 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Isomaltase activity is specific for both alpha-1,4- and alpha-1,6-oligosaccharides., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; The alpha-glucogenic activities of the jejunal mucosa with and without added recombinant pancreatic alpha-amylase, using a range of food starch substrates are reported., [RefSeq, PubMed]", "predicted_glycosites": 4, "predicted_n_glycosites": 0, "predicted_o_glycosites": 4, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 8, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 8, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 8, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 113, "reported_interactions": 0, "missing_score": 9373, "biomarker_type": "", "glycan_count": 8, "disease_count": 0, "glyco_site_count": 12, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0030246 carbohydrate binding;GO:0004574 oligo-1,6-glucosidase activity;GO:0004575 sucrose alpha-glucosidase activity;GO:0004558 alpha-1,4-glucosidase activity;GO:0016160 amylase activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0045177 apical part of cell;GO:0012505 endomembrane system;GO:0016324 apical plasma membrane", "go_biological_process": "GO:0005975 carbohydrate metabolic process;GO:0000025 maltose catabolic process;GO:1901027 dextrin catabolic process", "synthesized_glycan_count": 0, "hit_score": 2.2, "record_id": "A0A571BF69-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A5F8MPH2-1", "uniprot_id": "A0A5F8MPH2_MOUSE", "mass": 48266.0, "length": 446, "protein_name": "CUGBP, Elav-like family member 5", "gene_name": "Celf5", "organism": "Mouse", "refseq_name": "CUGBP Elav-like family member 5 isoform 5", "refseq_ac": "NP_001361632", "gene_names_uniprotkb": "Celf5", "gene_names_refseq": "4930565A21Rik; Brunol5; Celf5", "protein_names_uniprotkb": "CUGBP, Elav-like family member 5", "protein_names_refseq": "CUGBP Elav-like family member 5 isoform 5; bruno-like 5, RNA binding protein", "tax_id": 10090, "disease": "myotonic dystrophy type 1 (Disease Ontology:DOID:11722); dilated cardiomyopathy (Disease Ontology:DOID:12930)", "pathway": " (mmu:319586)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003723 RNA binding;GO:0003729 mRNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:1990904 ribonucleoprotein complex", "go_biological_process": "GO:0006397 mRNA processing;GO:0006376 mRNA splice site recognition;GO:0000381 regulation of alternative mRNA splicing, via spliceosome", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A5F8MPH2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P0DW87-1", "uniprot_id": "ZTRF1_MOUSE", "mass": 43439.0, "length": 399, "protein_name": "Zinc finger TRAF-type-containing protein 1", "gene_name": "Zftraf1", "organism": "Mouse", "refseq_name": "zinc finger TRAF-type-containing protein 1 isoform 1", "refseq_ac": "NP_001263250", "gene_names_uniprotkb": "Zftraf1; Chrp; Cyhr1; Kiaa0496", "gene_names_refseq": "1110031M01Rik; Chrp; Cyhr1; Zftraf1", "protein_names_uniprotkb": "Zinc finger TRAF-type-containing protein 1; Cysteine and histidine-rich protein 1", "protein_names_refseq": "Zinc finger TRAF-type-containing protein 1; cysteine and histidine rich 1; cysteine and histidine-rich cytoplasmic protein; cysteine and histidine-rich protein 1; zinc finger TRAF-type-containing protein 1 isoform 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:125488414); (mmu:54151)", "pathway_count": 2, "publication_count": 4, "publication_id_list": "10745073;12765788;21750661;31219806", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "H3BIV6;Q6P6J7;Q6ZQA2;Q9D134;Q9QXA1", "ec_number_list": "", "go_molecular_function": "GO:0008270 zinc ion binding", "go_cellular_component": "GO:0005635 nuclear envelope;GO:0005737 cytoplasm;GO:0048471 perinuclear region of cytoplasm", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.5, "record_id": "P0DW87-1", "record_type": "protein" }, { "uniprot_canonical_ac": "F6UGR1-1", "uniprot_id": "F6UGR1_MOUSE", "mass": 137893.0, "length": 1233, "protein_name": "PDZ and pleckstrin homology domains 1", "gene_name": "Pdzph1", "organism": "Mouse", "refseq_name": "PDZ and pleckstrin homology domains 1", "refseq_ac": "NP_081277", "gene_names_uniprotkb": "Pdzph1", "gene_names_refseq": "2610034M16Rik; Pdzph1", "protein_names_uniprotkb": "PDZ and pleckstrin homology domains 1", "protein_names_refseq": "PDZ and pleckstrin homology domains 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:69239)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "F6UGR1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7M753-1", "uniprot_id": "PANK2_MOUSE", "mass": 50212.0, "length": 456, "protein_name": "Pantothenate kinase 2, mitochondrial", "gene_name": "Pank2", "organism": "Mouse", "refseq_name": "pantothenate kinase 2, mitochondrial isoform a", "refseq_ac": "NP_705721", "gene_names_uniprotkb": "Pank2", "gene_names_refseq": "4933409I19Rik; Pank2; hPanK2", "protein_names_uniprotkb": "Pantothenate kinase 2, mitochondrial; 2.7.1.33; Pantothenic acid kinase 2; hPanK2", "protein_names_refseq": "pantothenate kinase 2 (Hallervorden-Spatz syndrome); pantothenate kinase 2, mitochondrial isoform a; pantothenate kinase 2, mitochondrial; pantothenic acid kinase 2", "tax_id": 10090, "disease": "pantothenate kinase-associated neurodegeneration (Disease Ontology:DOID:3981)", "pathway": " (mmu:74450); (R-MMU-196783)", "pathway_count": 2, "publication_count": 7, "publication_id_list": "17379144;17825826;21750661;22815849;23152917;29325618;34428180", "class_list": "", "function": "Catalyzes the phosphorylation of pantothenate to generate 4'-phosphopantothenate in the first and rate-determining step of coenzyme A (CoA) synthesis., [UniProtKB, PubMed, PubMed, PubMed]; This study showed that PANK2 genes account for disease of patients diagnosed with an Neurodegeneration with brain iron accumulation disorder. Review article, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3U4S0", "ec_number_list": "2.7.1.33", "go_molecular_function": "GO:0005524 ATP binding;GO:0004594 pantothenate kinase activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005739 mitochondrion;GO:0005758 mitochondrial intermembrane space;GO:0005829 cytosol;GO:0005737 cytoplasm", "go_biological_process": "GO:0001525 angiogenesis;GO:0015939 pantothenate metabolic process;GO:0019217 regulation of fatty acid metabolic process;GO:0051881 regulation of mitochondrial membrane potential;GO:0007286 spermatid development", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q7M753-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A5F8MPV9-1", "uniprot_id": "A0A5F8MPV9_MOUSE", "mass": 35990.0, "length": 327, "protein_name": "RIKEN cDNA 4930579F01 gene", "gene_name": "4930579F01Rik", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "4930579F01Rik", "gene_names_refseq": "", "protein_names_uniprotkb": "RIKEN cDNA 4930579F01 gene", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": " (mmu:67741)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A5F8MPV9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A571BF63-1", "uniprot_id": "ANKF1_MOUSE", "mass": 145202.0, "length": 1286, "protein_name": "Ankyrin-repeat and fibronectin type III domain-containing 1", "gene_name": "Ankfn1", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Ankfn1; 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Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005615 extracellular space", "go_biological_process": "GO:0042127 regulation of cell population proliferation", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "A0A5F8MPL8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A5F8MPM5-1", "uniprot_id": "A0A5F8MPM5_MOUSE", "mass": 30624.0, "length": 278, "protein_name": "E4 promoter-binding protein 4", "gene_name": "Nfilz", "organism": "Mouse", "refseq_name": "NFIL3 like protein", "refseq_ac": "NP_001388168", "gene_names_uniprotkb": "Nfilz; Gm4125", "gene_names_refseq": "100042953; Gm4125; Nfilz", "protein_names_uniprotkb": "E4 promoter-binding protein 4", "protein_names_refseq": "NFIL3 like protein; nuclear factor, interleukin 3, regulated pseudogene", "tax_id": 10090, "disease": "", "pathway": " (mmu:100042953)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Acts as a transcriptional regulator that recognizes and binds to the sequence 5'-[GA]TTA[CT]GTAA[CT]-3', a sequence present in many cellular and viral promoters. Represses transcription from promoters with activating transcription factor (ATF) sites. Represses promoter activity in osteoblasts. Represses transcriptional activity of PER1. Represses transcriptional activity of PER2 via the B-site on the promoter. Activates transcription from the interleukin-3 promoter in T-cells. Competes for the same consensus-binding site with PAR DNA-binding factors (DBP, HLF and TEF). Component of the circadian clock that acts as a negative regulator for the circadian expression of PER2 oscillation in the cell-autonomous core clock. Protects pro-B cells from programmed cell death. Represses the transcription of CYP2A5. Positively regulates the expression and activity of CES2 by antagonizing the repressive action of NR1D1 on CES2. Required for the development of natural killer cell precursors., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity", "go_cellular_component": "GO:0005634 nucleus", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0007623 circadian rhythm", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A5F8MPM5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A5F8MPN6-1", "uniprot_id": "A0A5F8MPN6_MOUSE", "mass": 5305.0, "length": 42, "protein_name": "Predicted gene, 56675", "gene_name": "Gm56675", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Gm56675", "gene_names_refseq": "", "protein_names_uniprotkb": "Predicted gene, 56675", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A5F8MPN6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A5F8MPE6-1", "uniprot_id": "CX058_MOUSE", "mass": 43040.0, "length": 368, "protein_name": "Uncharacterized protein CXorf58 homolog", "gene_name": "", "organism": "Mouse", "refseq_name": "uncharacterized protein CXorf58 homolog", "refseq_ac": "NP_001349810", "gene_names_uniprotkb": "", "gene_names_refseq": "4932442L08Rik; CXorf58; Fam90a1b", "protein_names_uniprotkb": "Uncharacterized protein CXorf58 homolog", "protein_names_refseq": "uncharacterized protein CXorf58 homolog", "tax_id": 10090, "disease": "", "pathway": " (mmu:631145)", "pathway_count": 1, "publication_count": 0, "publication_id_list": "", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.1, "record_id": "A0A5F8MPE6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A5F8MPH1-1", "uniprot_id": "A0A5F8MPH1_MOUSE", "mass": 37477.0, "length": 344, "protein_name": "Low density lipoprotein receptor class A domain containing 2", "gene_name": "Ldlrad2", "organism": "Mouse", "refseq_name": "low-density lipoprotein receptor class A domain-containing protein 2 isoform 2 precursor", "refseq_ac": "NP_001392348", "gene_names_uniprotkb": "Ldlrad2", "gene_names_refseq": "Ldlrad2", "protein_names_uniprotkb": "Low density lipoprotein receptor class A domain containing 2", "protein_names_refseq": "low density lipoprotein receptor A domain containing 2; low-density lipoprotein receptor class A domain-containing protein 2 isoform 2 precursor", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A5F8MPH1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A5F8MPV3-1", "uniprot_id": "A0A5F8MPV3_MOUSE", "mass": 6382.0, "length": 61, "protein_name": "Predicted gene 13398", "gene_name": "Gm13398", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Gm13398", "gene_names_refseq": "", "protein_names_uniprotkb": "Predicted gene 13398", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A5F8MPV3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3UUD2-1", "uniprot_id": "SPRY3_MOUSE", "mass": 31363.0, "length": 288, "protein_name": "Protein sprouty homolog 3", "gene_name": "Spry3", "organism": "Mouse", "refseq_name": "protein sprouty homolog 3", "refseq_ac": "NP_001025464", "gene_names_uniprotkb": "Spry3", "gene_names_refseq": "Gm1409; Gm391; Spry3; sprouty3", "protein_names_uniprotkb": "Protein sprouty homolog 3; Sprouty RTK signaling antagonist 3; Sprouty3; Spry-3", "protein_names_refseq": "protein sprouty homolog 3; sprouty homolog 3", "tax_id": 10090, "disease": "", "pathway": " (mmu:236576)", "pathway_count": 1, "publication_count": 4, "publication_id_list": "16877379;22645316;26089202;30878395", "class_list": "", "function": "Inhibits neurite branching, arbor length and neurite complexity (PubMed:26089202). Inhibits EGF-mediated p42/44 ERK signaling (PubMed:16877379). Negatively regulates the MAPK cascade, resulting in a reduction of extracellular matrix protein accumulation (By similarity). May function as an antagonist of fibroblast growth factor (FGF) pathways and may negatively modulate respiratory organogenesis (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed]; MiR-143-3p promoted fibrosis along with SPRY3 degradation and the activation of its downstream P38, ERK, and JNK pathways., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004860 protein kinase inhibitor activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane", "go_biological_process": "GO:0046580 negative regulation of Ras protein signal transduction;GO:0007399 nervous system development;GO:0070373 negative regulation of ERK1 and ERK2 cascade;GO:0042059 negative regulation of epidermal growth factor receptor signaling pathway;GO:0043409 negative regulation of MAPK cascade", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q3UUD2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A7N9VR94-1", "uniprot_id": "A0A7N9VR94_MOUSE", "mass": 368474.0, "length": 3501, "protein_name": "AHNAK nucleoprotein 2", "gene_name": "Ahnak2", "organism": "Mouse", "refseq_name": "protein AHNAK2 isoform 1", "refseq_ac": "NP_001365427", "gene_names_uniprotkb": "Ahnak2", "gene_names_refseq": "Ahnak2; Gm1185; Gm72", "protein_names_uniprotkb": "AHNAK nucleoprotein 2", "protein_names_refseq": "protein AHNAK2 isoform 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:100041194)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "20833135;21750661;25560297;35882062;39927985", "class_list": "", "function": "Inhibition of AHNAK nucleoprotein 2 alleviates pulmonary fibrosis by downregulating the TGF-beta1/Smad3 signaling pathway., [RefSeq, PubMed]; Results show that stress functionally associates FGF1 with AHNAK2 and both proteins with the cytoskeleton and their co-localization in the vicinity of the cell membrane. AHNAK2 seems to be an important element of the FGF1 export pathway., [RefSeq, PubMed]; These results demonstrate the exclusive expression of AHNAK1 and AHNAK2 in the costameres of adult skeletal muscles., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0030659 cytoplasmic vesicle membrane", "go_biological_process": "GO:0043484 regulation of RNA splicing", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "A0A7N9VR94-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A7N9VSG0-1", "uniprot_id": "AFG2B_MOUSE", "mass": 80742.0, "length": 747, "protein_name": "ATPase family gene 2 protein homolog B", "gene_name": "Afg2b", "organism": "Mouse", "refseq_name": "ATPase family gene 2 protein homolog B", "refseq_ac": "NP_001028428", "gene_names_uniprotkb": "Afg2b; Spata5l1", "gene_names_refseq": "Afg2b; C130039A10Rik; Spata5l1", "protein_names_uniprotkb": "ATPase family gene 2 protein homolog B; 3.6.4.10; AFG2 AAA ATPase homolog B; Ribosome biogenesis protein SPATA5L1; Spermatogenesis-associated protein 5-like protein 1", "protein_names_refseq": "ATPase family gene 2 protein homolog B; ribosome biogenesis protein SPATA5L1; spermatogenesis associated 5-like 1; spermatogenesis-associated protein 5-like protein 1", "tax_id": 10090, "disease": "autosomal recessive nonsyndromic deafness (Disease Ontology:DOID:0050565)", "pathway": " (mmu:214616)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "34626583", "class_list": "", "function": "ATP-dependent chaperone part of the 55LCC heterohexameric ATPase complex which is chromatin-associated and promotes replisome proteostasis to maintain replication fork progression and genome stability. Required for replication fork progression, sister chromatid cohesion, and chromosome stability. The ATPase activity is specifically enhanced by replication fork DNA and is coupled to cysteine protease-dependent cleavage of replisome substrates in response to replication fork damage. Uses ATPase activity to process replisome substrates in S-phase, facilitating their proteolytic turnover from chromatin to ensure DNA replication and mitotic fidelity. Plays an essential role in the cytoplasmic maturation steps of pre-60S ribosomal particles by promoting the release of shuttling protein RSL24D1/RLP24 from the pre-ribosomal particles., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "3.6.4.13;3.6.4.10;3.6.4.-;5.6.2.3;5.6.2.4;2.3.2.-;2.3.2.27;3.1.13.1;5.6.2.6;3.1.-.-;7.6.2.1;3.6.1.5;3.4.24.-;3.6.-.-;3.1.3.1;3.9.1.1;3.6.1.-;5.6.2.5;4.2.99.18;3.6.4.12;5.6.1.6;3.6.4.6;3.6.5.-;3.6.1.15;3.1.4.-;5.6.2.-;7.2.2.-;7.6.2.16;3.4.21.53;2.7.7.7;2.7.7.49;2.7.11.1;2.7.4.3", "go_molecular_function": "GO:1990275 preribosome binding;GO:0005524 ATP binding;GO:0031593 polyubiquitin modification-dependent protein binding;GO:0042802 identical protein binding;GO:0016887 ATP hydrolysis activity", "go_cellular_component": "GO:0034098 VCP-NPL4-UFD1 AAA ATPase complex;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005819 spindle;GO:0005829 cytosol", "go_biological_process": "GO:0097352 autophagosome maturation;GO:0042273 ribosomal large subunit biogenesis;GO:0006260 DNA replication;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0051228 mitotic spindle disassembly", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A7N9VSG0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A668KL92-1", "uniprot_id": "A0A668KL92_MOUSE", "mass": 32620.0, "length": 296, "protein_name": "Predicted pseudogene 7609", "gene_name": "Gm7609", "organism": "Mouse", "refseq_name": "component of Sp100-rs-like", "refseq_ac": "NP_001075215", "gene_names_uniprotkb": "Gm7609", "gene_names_refseq": "EG665378; Gm7609", "protein_names_uniprotkb": "Predicted pseudogene 7609", "protein_names_refseq": "component of Sp100-rs-like", "tax_id": 10090, "disease": "", "pathway": " (mmu:665378)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "This gene is one of several duplicated genes in a repeat cluster in the homogeneously staining region (HSR) of chromosome 1. It is an Sp100-rs gene copy, which arose by duplication following the fusion of the Csprs (component of Sp100-rs) gene and the 5' part of the Sp100 (nuclear antigen Sp100) gene. The coding sequence of this gene is intact compared to that of the Csprs gene, and therefore NCBI represents this as a protein-coding gene. However, it is also possible to interpret this fusion gene as a pseudogene of the Sp100 gene. It is unknown if this gene produces a protein in vivo. [provided by RefSeq, Mar 2011]., [RefSeq]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0050911 detection of chemical stimulus involved in sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A668KL92-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A668KLC8-1", "uniprot_id": "A0A668KLC8_MOUSE", "mass": 58828.0, "length": 542, "protein_name": "Predicted gene 3858", "gene_name": "Gm3858", "organism": "Mouse", "refseq_name": "uncharacterized protein CXorf49 homolog", "refseq_ac": "XP_054875640", "gene_names_uniprotkb": "Gm3858", "gene_names_refseq": "Gm3858", "protein_names_uniprotkb": "Predicted gene 3858", "protein_names_refseq": "uncharacterized protein CXorf49 homolog", "tax_id": 10090, "disease": "", "pathway": " (mmu:100042465)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A668KLC8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A668KM50-1", "uniprot_id": "A0A668KM50_MOUSE", "mass": 69177.0, "length": 636, "protein_name": "RIKEN cDNA A930007A09 gene", "gene_name": "A930007A09Rik", "organism": "Mouse", "refseq_name": "uncharacterized protein LOC432999", "refseq_ac": "NP_001344883", "gene_names_uniprotkb": "A930007A09Rik", "gene_names_refseq": "A930007A09Rik", "protein_names_uniprotkb": "RIKEN cDNA A930007A09 gene", "protein_names_refseq": "uncharacterized protein LOC432999", "tax_id": 10090, "disease": "", "pathway": " (mmu:432999)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, 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"tax_id": 10090, "disease": "Huntington's disease (Disease Ontology:DOID:12858)", "pathway": " (mmu:544752)", "pathway_count": 1, "publication_count": 7, "publication_id_list": "15797018;21750661;32894169;37642238;37721623;38318762;38490634", "class_list": "", "function": "Aerobic exercise suppresses cognitive injury in patients with Alzheimer's disease by regulating long non-coding RNA TUG1., [RefSeq, PubMed]; LncRNA Tug1 relieves the steatosis of SelenoF-knockout hepatocytes via sponging miR-1934-3p., [RefSeq, PubMed]; Long non-coding RNA LncTUG1 regulates favourable compression force-induced cementocytes mineralization via PU.1/TLR4/SphK1 signalling., [RefSeq, PubMed]; Long noncoding RNA TUG1 regulates smooth muscle cell differentiation via KLF4-myocardin axis., [RefSeq, PubMed]; Taurine upregulated gene 1 is necessary for the proper formation of photoreceptors in the developing rodent retina, [RefSeq, PubMed]; The Tug1 lncRNA locus is essential for male fertility. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0000987 cis-regulatory region sequence-specific DNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0031965 nuclear membrane;GO:0031966 mitochondrial membrane", "go_biological_process": "GO:0007283 spermatogenesis;GO:0010628 positive regulation of gene expression;GO:0007005 mitochondrion organization;GO:0010468 regulation of gene expression;GO:0042461 photoreceptor cell development", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "A0A6I8MX38-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A668KLU9-1", "uniprot_id": "A0A668KLU9_MOUSE", "mass": 37978.0, "length": 332, "protein_name": "Complement factor H-related 2", "gene_name": "Cfhr2", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": 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"uniprot_canonical_ac": "A0A668KLB6-1", "uniprot_id": "A0A668KLB6_MOUSE", "mass": 3827.0, "length": 32, "protein_name": "Predicted gene, 56303", "gene_name": "Gm56303", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Gm56303", "gene_names_refseq": "", "protein_names_uniprotkb": "Predicted gene, 56303", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, 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"publication_count": 0, "publication_id_list": "", "class_list": "", "function": "Olfactory receptor., [UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 1, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell", "synthesized_glycan_count": 0, "hit_score": 0.1, "record_id": "Q8VFR8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A1D9BZF0-1", "uniprot_id": "GCNA_MOUSE", "mass": 53394.0, "length": 507, "protein_name": "Germ cell nuclear acidic protein", "gene_name": "Gcna", "organism": "Mouse", "refseq_name": "germ cell nuclear acidic protein", "refseq_ac": "NP_001369163", "gene_names_uniprotkb": "Gcna", "gene_names_refseq": "Gcna1; Gcna; Gm52429", "protein_names_uniprotkb": "Germ cell nuclear acidic protein; Acidic repeat-containing protein; Germ cell nuclear antigen", "protein_names_refseq": "acidic repeat-containing protein; germ cell nuclear acidic protein; germ cell nuclear antigen 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:115489118)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "31839538;36919611", "class_list": "", "function": "GCNA is a histone binding protein required for spermatogonial stem cell maintenance., [RefSeq, PubMed]; May play a role in DNA-protein cross-links (DPCs) clearance through a SUMO-dependent recruitment to sites of DPCs, ensuring the genomic stability by protecting germ cells and early embryos from various sources of damage (PubMed:31839538). Can resolve the topoisomerase II (TOP2A) DPCs (PubMed:31839538)., [UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0000793 condensed chromosome;GO:0016605 PML body", "go_biological_process": "GO:0006974 DNA damage response;GO:0007129 homologous chromosome pairing at meiosis;GO:0010032 meiotic chromosome condensation;GO:0035825 homologous recombination;GO:0106300 protein-DNA covalent cross-linking repair", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "A0A1D9BZF0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q2QKR2-1", "uniprot_id": "DESPR_MOUSE", "mass": 14117.0, "length": 127, "protein_name": "Dual endothelin-1/VEGF signal peptide receptor", "gene_name": "Fbxw7-as1", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Fbxw7-as1; Dear1; Dear; Fbxw7as1", "gene_names_refseq": "", "protein_names_uniprotkb": "Dual endothelin-1/VEGF signal peptide receptor; DEspR protein; Dual endothelin-1/VEGFsp receptor; FBXW7 antisense RNA 1 homolog", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "16293765", "class_list": "", "function": "Dual receptor for both endothelin-1 and the signal sequence of vascular endothelial growth factor A (PubMed:16293765). Does not act as a receptor for angiotensin-2 (By similarity). Does not bind the VEGFA mature protein (PubMed:16293765). May play a role in angiogenesis with a significant role in cardiovascular and neural development (PubMed:16293765)., [UniProtKB, PubMed, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "Q2QKR2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0A8I4SYN6-1", "uniprot_id": "A0A8I4SYN6_MOUSE", "mass": 15429.0, "length": 136, "protein_name": "Histone H3", "gene_name": "H3f4", "organism": "Mouse", "refseq_name": "uncharacterized protein LOC382523", "refseq_ac": "NP_001304932", "gene_names_uniprotkb": "H3f4", "gene_names_refseq": "Gm12260; H304; H3f4; H3mmT; H3t", "protein_names_uniprotkb": "Histone H3", "protein_names_refseq": "H3.4 histone; histone cluster 1, H3 pseudogene; uncharacterized protein LOC382523", "tax_id": 10090, "disease": "", "pathway": " (mmu:382523); (R-MMU-110330); (R-MMU-110331); (R-MMU-2299718); (R-MMU-2559586); (R-MMU-5693565); (R-MMU-5693571); (R-MMU-5693607); (R-MMU-69473); (R-MMU-9670095)", "pathway_count": 10, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. [provided by RefSeq, Dec 2015]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0046982 protein heterodimerization activity;GO:0031492 nucleosomal DNA binding;GO:0030527 structural constituent of chromatin", "go_cellular_component": "GO:0000794 condensed nuclear chromosome;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0000792 heterochromatin;GO:0000786 nucleosome", "go_biological_process": "GO:0006334 nucleosome assembly;GO:0006335 DNA replication-dependent chromatin assembly;GO:0007284 spermatogonial cell division;GO:0031507 heterochromatin formation", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0A8I4SYN6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0AAQ4VMW3-1", "uniprot_id": "A0AAQ4VMW3_MOUSE", "mass": 194187.0, "length": 1713, "protein_name": "LIM domain only 7", "gene_name": "Lmo7", "organism": "Mouse", "refseq_name": "LIM domain only protein 7 isoform X19", "refseq_ac": "XP_006519245", "gene_names_uniprotkb": "Lmo7", "gene_names_refseq": "FBXO20; Gm914; Lmo7; mKIAA0858", "protein_names_uniprotkb": "LIM domain only 7", "protein_names_refseq": "LIM domain only protein 7 isoform X19", "tax_id": 10090, "disease": "", "pathway": " (mmu:380928); (R-MMU-8951664); (R-MMU-983168)", "pathway_count": 3, "publication_count": 5, "publication_id_list": "10.1101/2023.09.13.557529;16452087;21750661;25428506;34887587", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 4, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0046872 metal ion binding;GO:0042805 actinin binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005635 nuclear envelope;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005886 plasma membrane", "go_biological_process": "GO:0030155 regulation of cell adhesion;GO:0023051 regulation of signaling;GO:0045944 positive regulation of transcription by RNA polymerase II", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "A0AAQ4VMW3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q91VE2-1", "uniprot_id": "P2RX5_MOUSE", "mass": 51362.0, "length": 455, "protein_name": "P2X purinoceptor 5", "gene_name": "P2rx5", "organism": "Mouse", "refseq_name": "P2X purinoceptor 5 isoform 1", "refseq_ac": "NP_201578", "gene_names_uniprotkb": "P2rx5", "gene_names_refseq": "P2X5; P2rx5", "protein_names_uniprotkb": "P2X purinoceptor 5; P2X5", "protein_names_refseq": "P2X purinoceptor 5 isoform 1; P2X purinoceptor 5; purinergic receptor P2X5-2", "tax_id": 10090, "disease": "", "pathway": " (mmu:94045)", "pathway_count": 1, "publication_count": 8, "publication_id_list": "10.1101/2023.09.13.557529;11404011;15231720;17605080;18773945;21750661;28298636;36940138", "class_list": "", "function": "ATP-gated nonselective transmembrane cation channel permeable to potassium, sodium and calcium (PubMed:11404011, PubMed:36940138). Unlike other P2RX receptors, the P2X5 receptor is also permeable to chloride (By similarity). Acts as an important regulator of inflammatory-related bone loss and osteoclast multinucleation (PubMed:28298636)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed]; Immunoreactivity for P2X3-, P2X5-, and P2X6-purinoceptors was observed in mouse retina., [RefSeq, PubMed]; Receptor for ATP that acts as a ligand-gated ion channel., [UniProtKB, UniProtKB]; Sequential expression of the P2X5, P2Y1, and P2X2 receptors during the process of muscle regeneration, [RefSeq, PubMed]; The identification of extensive P2X5 receptor immunoreactivity and mRNA distribution within the CNS of the mouse demonstrated here is consistent with a role for extracellular ATP acting as a fast neurotransmitter., [RefSeq, PubMed]", "predicted_glycosites": 2, "predicted_n_glycosites": 2, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 1, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 2, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "B9EHM6;Q3UYI1", "ec_number_list": "5.6.1.6;1.8.-.-;2.7.11.1;1.8.5.1", "go_molecular_function": "GO:0005524 ATP binding;GO:0042802 identical protein binding;GO:0005244 voltage-gated monoatomic ion channel activity;GO:0001614 purinergic nucleotide receptor activity;GO:0004931 extracellularly ATP-gated monoatomic cation channel activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0098794 postsynapse", "go_biological_process": "GO:0036179 osteoclast maturation;GO:0007166 cell surface receptor signaling pathway;GO:0010043 response to zinc ion;GO:0051592 response to calcium ion;GO:0098655 monoatomic cation transmembrane transport", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q91VE2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "J9SQF3-1", "uniprot_id": "TRPM3_MOUSE", "mass": 197458.0, "length": 1732, "protein_name": "Transient receptor potential cation channel subfamily M member 3", "gene_name": "Trpm3", "organism": "Mouse", "refseq_name": "transient receptor potential cation channel subfamily M member 3 isoform b", "refseq_ac": "NP_001030317", "gene_names_uniprotkb": "Trpm3", "gene_names_refseq": "6330504P12Rik; 9330180E14; B930001P07Rik; LTRPC3; MLSN2; Trpm3", "protein_names_uniprotkb": "Transient receptor potential cation channel subfamily M member 3", "protein_names_refseq": "melastatin 2; transient receptor potential cation channel subfamily M member 3 isoform b; transient receptor potential melastatin 3 beta 1", "tax_id": 10090, "disease": "MASA syndrome (Disease Ontology:DOID:0060246); chromosome 15q13.3 microdeletion syndrome (Disease Ontology:DOID:0060394); microphthalmia (Disease Ontology:DOID:10629); cataract (Disease Ontology:DOID:83)", "pathway": " (mmu:226025)", "pathway_count": 1, "publication_count": 16, "publication_id_list": "15824111;18978782;20401728;20485683;21555074;21750661;22961981;24251620;29880196;30853321;32780479;33122432;33478988;36283409;38084411;38334649", "class_list": "", "function": "A Cataract-Causing Mutation in the TRPM3 Cation Channel Disrupts Calcium Dynamics in the Lens. Publication Status: Online-Only, [RefSeq, PubMed]; Constitutively active, non-selective divalent cation-conducting channel that is permeable to Ca(2+), Mn(2+), and Mg(2+), with a high permeability for Ca(2+) (PubMed:15824111, PubMed:20401728, PubMed:32780479). However, can be enhanced by increasing temperature and by ligands, including the endogenous neurosteroid pregnenolone sulfate and sphingosine-1 and suppressed by intracellular Mg(2+) (PubMed:20401728, PubMed:21555074). Implicated in a variety of cellular processes, including insulin/peptide secretion, vascular constriction and dilation, noxious heat sensing, inflammatory and spontaneous pain sensitivity (PubMed:21555074, PubMed:30853321, PubMed:33478988). In neurons of the dorsal root ganglia, functions as thermosensitive channel for the detection of noxious heat and spontaneous pain (PubMed:21555074, PubMed:33478988). Suggested to function as an ionotropic steroid receptor in beta-cell, indeed pregnenolone sulfate leads to Ca(2+) influx and enhanced insulin secretion (PubMed:18978782). Mediates Zn(2+) uptake into the lumen of pancreatic beta cell secretory granules, thereby regulating insulin secretion (PubMed:20401728). Forms heteromultimeric ion channels with TRPM1 which are permeable for Ca(2+) and Zn(2+) ions (By similarity). Exists as multiple splice variants which differ significantly in their biophysical properties (PubMed:15824111, PubMed:22961981)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]; Displays strongly reduced permeability for divalent cations and high selectivity toward monovalent cations., [UniProtKB, PubMed]; Expression and function of transient receptor potential melastatin 3 in the spinal afferent innervation of the mouse colon., [RefSeq, PubMed]; No channel activity., [UniProtKB, PubMed]; The divalent cation selectivity of TRPM3 channels is regulated by altenrative splicing, [RefSeq, PubMed]", "predicted_glycosites": 2, "predicted_n_glycosites": 0, "predicted_o_glycosites": 2, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 12, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 4, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "B2RUS0;F6M2J8;J9S2Z5;J9S305;J9SQE7;J9SQF8;J9SUA7;J9T153;Q5F4S6;Q5F4S7;Q5F4S8;Q5F4S9;Q5F4T0", "ec_number_list": "1.8.-.-;2.7.11.1", "go_molecular_function": "GO:0005385 zinc ion transmembrane transporter activity;GO:0005262 calcium channel activity;GO:0005516 calmodulin binding;GO:0005546 phosphatidylinositol-4,5-bisphosphate binding;GO:0031683 G-protein beta/gamma-subunit complex binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane", "go_biological_process": "GO:0071577 zinc ion transmembrane transport;GO:0051289 protein homotetramerization;GO:0006812 monoatomic cation transport;GO:0070588 calcium ion transmembrane transport;GO:0006814 sodium ion transport", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "J9SQF3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0AAQ4VMT0-1", "uniprot_id": "A0AAQ4VMT0_MOUSE", "mass": 77777.0, "length": 695, "protein_name": "Predicted gene 5134", "gene_name": "Gm5134", "organism": "Mouse", "refseq_name": "solute carrier family 5 (sodium/glucose cotransporter)-like isoform X1", "refseq_ac": "XP_006513854", "gene_names_uniprotkb": "Gm5134", "gene_names_refseq": "EG333669; Gm5134", "protein_names_uniprotkb": "Predicted gene 5134", 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Publication Status: Online-Only, [RefSeq, PubMed]; Non-enzymatic component of C3 and C5 convertases (By similarity). Generated following cleavage by complement proteases (C1S, MASP2 or GZMK, depending on the complement pathway), it covalently attaches to the surface of pathogens, where it acts as an opsonin that marks the surface of antigens for removal (By similarity). It then recruits the serine protease complement C2b to form the C3 and C5 convertases, which cleave and activate C3 and C5, respectively, the next components of the complement pathways (By similarity). Complement C4b-A isotype is responsible for effective binding to form amide bonds with immune aggregates or protein antigens, while complement C4b-B isotype catalyzes the transacylation of the thioester carbonyl group to form ester bonds with carbohydrate antigens (By similarity)., [UniProtKB, UniProtKB]; Overexpression of schizophrenia susceptibility factor human complement C4A promotes excessive synaptic loss and behavioral changes in mice., [RefSeq, PubMed]; Precursor of non-enzymatic components of the classical, lectin and GZMK complement pathways, which consist in a cascade of proteins that leads to phagocytosis and breakdown of pathogens and signaling that strengthens the adaptive immune system., [UniProtKB, PubMed, PubMed]; Putative humoral mediator released following cleavage by complement proteases (C1S, MASP2 or GZMK, depending on the complement pathway). While it is strongly similar to anaphylatoxins, its role is unclear. 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"predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0ABJ3HP72-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0ABJ3HP78-1", "uniprot_id": "A0ABJ3HP78_MOUSE", "mass": 3715.0, "length": 32, "protein_name": "Uncharacterized protein", "gene_name": "", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "", "gene_names_refseq": "", "protein_names_uniprotkb": "Uncharacterized protein", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0ABJ3HP78-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0ABJ3HPA8-1", "uniprot_id": "A0ABJ3HPA8_MOUSE", "mass": 142058.0, "length": 1250, "protein_name": "Vigilin", "gene_name": "Gm382", "organism": "Mouse", "refseq_name": "uncharacterized protein LOC211208", "refseq_ac": "NP_001028413", "gene_names_uniprotkb": "Gm382", "gene_names_refseq": "Gm382", "protein_names_uniprotkb": "Vigilin", "protein_names_refseq": "uncharacterized protein LOC211208", "tax_id": 10090, "disease": "", "pathway": " (mmu:211208)", "pathway_count": 1, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003723 RNA binding", "go_cellular_component": "GO:0005737 cytoplasm", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0ABJ3HPA8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A0ABJ3HPD8-1", "uniprot_id": "A0ABJ3HPD8_MOUSE", "mass": 3301.0, "length": 29, "protein_name": "Uncharacterized protein", "gene_name": "", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "", "gene_names_refseq": "", "protein_names_uniprotkb": "Uncharacterized protein", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 1, "publication_id_list": "21750661", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.2, "record_id": "A0ABJ3HPD8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6NSQ3-1", "uniprot_id": "SIM48_MOUSE", "mass": 13409.0, "length": 121, "protein_name": "Small integral membrane protein 48", "gene_name": "Smim48", "organism": "Mouse", "refseq_name": "small integral membrane protein 48", "refseq_ac": "NP_598783", "gene_names_uniprotkb": "Smim48; 6330403K07Rik; Ugs148", "gene_names_refseq": "6330403K07Rik; Smim48; UGS148", "protein_names_uniprotkb": "Small integral membrane protein 48", "protein_names_refseq": "small integral membrane protein 48", "tax_id": 10090, "disease": "", "pathway": " (mmu:103712)", "pathway_count": 1, "publication_count": 4, "publication_id_list": "15711547;16720340;25662290;34897904", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q8VBZ2", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.5, "record_id": "Q6NSQ3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9CRY7-1", "uniprot_id": "GDPD1_MOUSE", "mass": 35867.0, "length": 314, "protein_name": "Lysophospholipase D GDPD1", "gene_name": "Gdpd1", "organism": "Mouse", "refseq_name": "lysophospholipase D GDPD1", "refseq_ac": "NP_079914", "gene_names_uniprotkb": "Gdpd1; Gde4", "gene_names_refseq": "2610020H15Rik; Gdpd1", "protein_names_uniprotkb": "Lysophospholipase D GDPD1; 3.1.4.-; Glycerophosphodiester phosphodiesterase 4; Glycerophosphodiester phosphodiesterase domain-containing protein 1", "protein_names_refseq": "glycerophosphodiester phosphodiesterase 4; glycerophosphodiester phosphodiesterase domain-containing protein 1; lysophospholipase D GDPD1", "tax_id": 10090, "disease": "", "pathway": " (mmu:66569)", "pathway_count": 1, "publication_count": 6, "publication_id_list": "10.1101/2023.09.13.557529;25428506;25528375;25596343;27637550;34523685", "class_list": "", "function": "Characterization of recombinant murine GDE4 and GDE7, enzymes producing lysophosphatidic acid and/or cyclic phosphatidic acid. Erratum:[J Biochem. 2022 Mar 31;171(4):467. doi: 10.1093/jb/mvab152. PMID: 35137094], [RefSeq, PubMed]; GDE4 may act as lysophospholipase D, which is involved in the generation of N-acylethanolamines and lysophhosphatidic acid., [RefSeq, PubMed]; Hydrolyzes lysoglycerophospholipids to produce lysophosphatidic acid (LPA) and the corresponding amines (PubMed:25528375, PubMed:25596343, PubMed:27637550). Shows a preference for 1-O-alkyl-sn-glycero-3-phosphocholine (lyso-PAF), lysophosphatidylethanolamine (lyso-PE) and lysophosphatidylcholine (lyso-PC) (PubMed:25528375, PubMed:25596343, PubMed:27637550). May be involved in bioactive N-acylethanolamine biosynthesis from both N-acyl-lysoplasmenylethanolamin (N-acyl-lysoPlsEt) and N-acyl-lysophosphatidylethanolamin (N-acyl-lysoPE) (PubMed:25596343, PubMed:27637550). In addition, hydrolyzes glycerophospho-N-acylethanolamine to N-acylethanolamine (PubMed:25596343, PubMed:27637550). Does not display glycerophosphodiester phosphodiesterase activity, since it cannot hydrolyze either glycerophosphoinositol or glycerophosphocholine (PubMed:25528375)., [UniProtKB, PubMed, PubMed, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q9CT14;Q9D4X7", "ec_number_list": "3.1.4.54;3.1.4.-;3.1.4.44;3.1.4.39;3.1.4.4", "go_molecular_function": "GO:0046872 metal ion binding;GO:0004622 phosphatidylcholine lysophospholipase activity;GO:0008081 phosphoric diester hydrolase activity", "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0016020 membrane;GO:0048471 perinuclear region of cytoplasm;GO:0005789 endoplasmic reticulum membrane", "go_biological_process": "GO:0070291 N-acylethanolamine metabolic process;GO:0046475 glycerophospholipid catabolic process;GO:0006644 phospholipid metabolic process", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "Q9CRY7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O70172-1", "uniprot_id": "PI42A_MOUSE", "mass": 46152.0, "length": 405, "protein_name": "Phosphatidylinositol 5-phosphate 4-kinase type-2 alpha", "gene_name": "Pip4k2a", "organism": "Mouse", "refseq_name": "phosphatidylinositol 5-phosphate 4-kinase type-2 alpha isoform 1", "refseq_ac": "NP_032871", "gene_names_uniprotkb": "Pip4k2a; Pi5p4ka; Pip5k2a", "gene_names_refseq": "Pip4k2a; Pip5k2a", "protein_names_uniprotkb": "Phosphatidylinositol 5-phosphate 4-kinase type-2 alpha; 1-phosphatidylinositol 5-phosphate 4-kinase 2-alpha; 2.7.1.149; Diphosphoinositide kinase 2-alpha; PI(5)P 4-kinase type II alpha; PI5P4Kalpha; PIP4KII-alpha; Phosphatidylinositol 5-Phosphate 4-Kinase; Phosphatidylinositol 5-phosphate 4-kinase type II alpha; PtdIns(5)P-4-kinase isoform 2-alpha", "protein_names_refseq": "1-phosphatidylinositol 5-phosphate 4-kinase 2-alpha; PI(5)P 4-kinase type II alpha; PI5P4Kalpha; PIP4KII-alpha; diphosphoinositide kinase 2-alpha; phosphatidylinositol 5-phosphate 4-kinase type-2 alpha isoform 1; phosphatidylinositol 5-phosphate 4-kinase type-2 alpha; phosphatidylinositol-4-phosphate 5-kinase, type II, alpha", "tax_id": 10090, "disease": "cancer (Disease Ontology:DOID:162)", "pathway": " (mmu:18718); (R-MMU-1660499); (R-MMU-6811555); (R-MMU-6811558); (R-MMU-8847453)", "pathway_count": 5, "publication_count": 6, "publication_id_list": "16434494;20204506;21750661;29727621;33300544;9535851", "class_list": "", "function": "Catalyzes the phosphorylation of phosphatidylinositol 5-phosphate (PtdIns5P) on the fourth hydroxyl of the myo-inositol ring, to form phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2). Has both ATP- and GTP-dependent kinase activities. May exert its function by regulating the levels of PtdIns5P, which functions in the cytosol by increasing AKT activity and in the nucleus signals through ING2 (By similarity). May regulate the pool of cytosolic PtdIns5P in response to the activation of tyrosine phosphorylation (By similarity). Required for lysosome-peroxisome membrane contacts and intracellular cholesterol transport through modulating peroxisomal PtdIns(4,5)P2 level (By similarity). In collaboration with PIP4K2B, has a role in mediating autophagy in times of nutrient stress (PubMed:29727621). Required for autophagosome-lysosome fusion and the regulation of cellular lipid metabolism (PubMed:29727621). Negatively regulates insulin signaling through a catalytic-independent mechanism. PIP4Ks interact with PIP5Ks and suppress PIP5K-mediated PtdIns(4,5)P2 synthesis and insulin-dependent conversion to PtdIns(3,4,5)P3 (By similarity). May be involved in thrombopoiesis, and the terminal maturation of megakaryocytes and regulation of their size (PubMed:16434494)., [UniProtKB, UniProtKB, PubMed, PubMed, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "2.7.1.68;2.7.1.149;2.7.12.2;5.2.1.8", "go_molecular_function": "GO:0016309 1-phosphatidylinositol-5-phosphate 4-kinase activity;GO:0005524 ATP binding;GO:0042803 protein homodimerization activity;GO:0016308 1-phosphatidylinositol-4-phosphate 5-kinase activity;GO:0052742 phosphatidylinositol kinase activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0005764 lysosome;GO:0001917 photoreceptor inner segment", "go_biological_process": "GO:0046627 negative regulation of insulin receptor signaling pathway;GO:0010506 regulation of autophagy;GO:0035855 megakaryocyte development;GO:2000786 positive regulation of autophagosome assembly;GO:0046854 phosphatidylinositol phosphate biosynthetic process", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "O70172-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6ZWS8-1", "uniprot_id": "SPOP_MOUSE", "mass": 42132.0, "length": 374, "protein_name": "Speckle-type POZ protein", "gene_name": "Spop", "organism": "Mouse", "refseq_name": "speckle-type POZ protein", "refseq_ac": "NP_079563", "gene_names_uniprotkb": "Spop; Pcif1", "gene_names_refseq": "Pcif1; Spop; TEF2", "protein_names_uniprotkb": "Speckle-type POZ protein; HIB homolog 1; PDX-1 C-terminal-interacting factor 1", "protein_names_refseq": "HIB homolog 1; PDX-1 C-terminal-interacting factor 1; speckle-type POZ protein", "tax_id": 10090, "disease": "stomach cancer (Disease Ontology:DOID:10534); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung adenocarcinoma (Disease Ontology:DOID:3910); hepatocellular carcinoma (Disease Ontology:DOID:684); hepatoblastoma (Disease Ontology:DOID:687); colorectal cancer (Disease Ontology:DOID:9256)", "pathway": " (mmu:20747); (R-MMU-5632684); (R-MMU-9929491)", "pathway_count": 3, "publication_count": 13, "publication_id_list": "12183056;15121856;16740475;20463034;20811152;21750661;21952136;25428506;30084848;30779550;31219806;32726616;34428180", "class_list": "", "function": "Component of a cullin-RING-based BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complex that mediates the ubiquitination of target proteins, leading most often to their proteasomal degradation. The cullin-RING-based BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complex containing homodimeric SPOP has higher ubiquitin ligase activity than the complex that contains the heterodimer formed by SPOP and SPOPL (By similarity). In complex with CUL3, involved in ubiquitination and proteasomal degradation of BRMS1, DAXX, PDX1/IPF1, GLI2 and GLI3. In complex with CUL3, involved in ubiquitination of MACROH2A1 and BMI1; this does not lead to their proteasomal degradation. Inhibits transcriptional activation of PDX1/IPF1 targets, such as insulin, by promoting PDX1/IPF1 degradation. Involved in the regulation of bromodomain and extra-terminal motif (BET) proteins BRD2, BRD3, BRD4 stability (By similarity). Plays an essential role for proper translation, but not for their degradation, of critical DNA replication licensing factors CDT1 and CDC6, thereby participating in DNA synthesis and cell proliferation. Regulates interferon regulatory factor 1/IRF1 proteasomal turnover by targeting S/T-rich degrons in IRF1 (By similarity). Involved in ubiquitination of BRDT and promotes its degradation, thereby regulates histone removal in early condensing spermatids prior to histone-to-protamine exchange (PubMed:32726616)., [UniProtKB, PubMed, PubMed, PubMed, UniProtKB, PubMed, PubMed]; MacroH2A1.2 binds the nuclear protein Spop., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 6, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3TLC2;Q5ST07;Q76LV9", "ec_number_list": "", "go_molecular_function": "GO:0042802 identical protein binding;GO:0031625 ubiquitin protein ligase binding;GO:0061629 RNA polymerase II-specific DNA-binding transcription factor binding;GO:0140678 molecular function inhibitor activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0016607 nuclear speck;GO:0031463 Cul3-RING ubiquitin ligase complex", "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0042593 glucose homeostasis;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0030162 regulation of proteolysis;GO:1902237 positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway", "synthesized_glycan_count": 0, "hit_score": 1.4, "record_id": "Q6ZWS8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P62880-1", "uniprot_id": "GBB2_MOUSE", "mass": 37331.0, "length": 340, "protein_name": "Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2", "gene_name": "Gnb2", "organism": "Mouse", "refseq_name": "guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2", "refseq_ac": "NP_034442", "gene_names_uniprotkb": "Gnb2", "gene_names_refseq": "Gnb-2; Gnb2; Hg2c1", "protein_names_uniprotkb": "Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2; G protein subunit beta-2; Transducin beta chain 2", "protein_names_refseq": "g protein subunit beta-2; guanine nucleotide binding protein, beta 2; guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2; guanine nucleotide-binding protein, beta-2 subunit; heterotrimeric guanine nucleotide-binding protein 2c1; transducin beta chain 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:14693); (R-MMU-1296041); (R-MMU-202040); (R-MMU-381676); (R-MMU-392170); (R-MMU-392451); (R-MMU-392851); (R-MMU-400042); (R-MMU-4086398); (R-MMU-416476); (R-MMU-416482); (R-MMU-418217); (R-MMU-418555); (R-MMU-418592); (R-MMU-418594); (R-MMU-418597); (R-MMU-420092); (R-MMU-428930); (R-MMU-432040); (R-MMU-456926); (R-MMU-500657); (R-MMU-6814122); (R-MMU-8964315); (R-MMU-8964616); (R-MMU-9009391); (R-MMU-9634597); (R-MMU-9856530); (R-MMU-997272)", "pathway_count": 28, "publication_count": 13, "publication_id_list": "11239002;11913780;18034455;21750661;22872234;25428506;31219806;33300544;34203471;34428180;37453647;37828378;8858601", "class_list": "", "function": "Guanine nucleotide-binding proteins (G proteins) are involved as a modulator or transducer in various transmembrane signaling systems. The beta and gamma chains are required for the GTPase activity, for replacement of GDP by GTP, and for G protein-effector interaction., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "P11016;P54312", "ec_number_list": "", "go_molecular_function": "GO:0003924 GTPase activity;GO:0005246 calcium channel regulator activity;GO:0044877 protein-containing complex binding;GO:0051020 GTPase binding;GO:0030159 signaling receptor complex adaptor activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0043209 myelin sheath;GO:0045202 synapse;GO:0048471 perinuclear region of cytoplasm", "go_biological_process": "GO:1901379 regulation of potassium ion transmembrane transport;GO:0007186 G protein-coupled receptor signaling pathway;GO:0007165 signal transduction", "synthesized_glycan_count": 0, "hit_score": 1.6, "record_id": "P62880-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P55258-1", "uniprot_id": "RAB8A_MOUSE", "mass": 23668.0, "length": 207, "protein_name": "Ras-related protein Rab-8A", "gene_name": "Rab8a", "organism": "Mouse", "refseq_name": "ras-related protein Rab-8A", "refseq_ac": "NP_075615", "gene_names_uniprotkb": "Rab8a; Mel; Rab8", "gene_names_refseq": "Mel; Rab8a", "protein_names_uniprotkb": "Ras-related protein Rab-8A; 3.6.5.2; Oncogene c-mel", "protein_names_refseq": "cell line NK14 derived transforming oncogene; oncogene c-mel; ras-related protein Rab-8A", "tax_id": 10090, "disease": "Smith-McCort dysplasia (Disease Ontology:DOID:0060247); Dyggve-Melchior-Clausen disease (Disease Ontology:DOID:0111167)", "pathway": " (mmu:17274); (R-MMU-2565942); (R-MMU-5620912); (R-MMU-5620916); (R-MMU-8854214); (R-MMU-8873719); (R-MMU-8876198)", "pathway_count": 7, "publication_count": 23, "publication_id_list": "12578829;12590134;16541104;17509819;18094055;1886711;19144319;19625297;20643351;21183079;23807208;25860027;26824392;29125462;29743203;30209220;32017888;32643832;33300544;33976349;34428180;37453647;8643544", "class_list": "", "function": "The small GTPases Rab are key regulators of intracellular membrane trafficking, from the formation of transport vesicles to their fusion with membranes. Rabs cycle between an inactive GDP-bound form and an active GTP-bound form that is able to recruit to membranes different sets of downstream effectors directly responsible for vesicle formation, movement, tethering and fusion. RAB8A is involved in polarized vesicular trafficking and neurotransmitter release. Together with RAB11A, RAB3IP, the exocyst complex, PARD3, PRKCI, ANXA2, CDC42 and DNMBP promotes transcytosis of PODXL to the apical membrane initiation sites (AMIS), apical surface formation and lumenogenesis (By similarity). Regulates the compacted morphology of the Golgi (By similarity). Together with MYO5B and RAB11A participates in epithelial cell polarization (By similarity). Also involved in membrane trafficking to the cilium and ciliogenesis (PubMed:25860027). Together with MICALL2, may also regulate adherens junction assembly (PubMed:18094055). May play a role in insulin-induced transport to the plasma membrane of the glucose transporter GLUT4 and therefore play a role in glucose homeostasis (By similarity). Involved in autophagy (By similarity). Participates in the export of a subset of neosynthesized proteins through a Rab8-Rab10-Rab11-dependent endososomal export route (By similarity). Targeted to and stabilized on stressed lysosomes through LRRK2 phosphorylation (PubMed:30209220). Suppresses stress-induced lysosomal enlargement through EHBP1 and EHNP1L1 effector proteins (By similarity)., [UniProtKB, UniProtKB, UniProtKB, PubMed, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q8VCF6", "ec_number_list": "3.6.5.-;3.6.5.2;3.6.5.3;2.7.11.1;3.6.1.5;2.7.11.11;3.6.4.10;2.7.11.22;2.7.11.23;3.6.5.4;3.6.5.5;2.5.1.60;3.6.4.-;3.6.1.-;2.7.11.21;3.6.1.15;3.6.-.-;2.7.11.26", "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0019901 protein kinase binding;GO:0046872 metal ion binding;GO:0031267 small GTPase binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005768 endosome;GO:0005794 Golgi apparatus", "go_biological_process": "GO:0048210 Golgi vesicle fusion to target membrane;GO:0051223 regulation of protein transport;GO:0098887 neurotransmitter receptor transport, endosome to postsynaptic membrane;GO:0098969 neurotransmitter receptor transport to postsynaptic membrane;GO:0007409 axonogenesis", "synthesized_glycan_count": 0, "hit_score": 2.6, "record_id": "P55258-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P61027-1", "uniprot_id": "RAB10_MOUSE", "mass": 22541.0, "length": 200, "protein_name": "Ras-related protein Rab-10", "gene_name": "Rab10", "organism": "Mouse", "refseq_name": "ras-related protein Rab-10", "refseq_ac": "NP_057885", "gene_names_uniprotkb": "Rab10", "gene_names_refseq": "Rab10", "protein_names_uniprotkb": "Ras-related protein Rab-10; 3.6.5.2", "protein_names_refseq": "ras-related protein Rab-10", "tax_id": 10090, "disease": "Smith-McCort dysplasia (Disease Ontology:DOID:0060247); Dyggve-Melchior-Clausen disease (Disease Ontology:DOID:0111167)", "pathway": " (mmu:19325); (R-MMU-6798695); (R-MMU-8873719); (R-MMU-8876198)", "pathway_count": 4, "publication_count": 25, "publication_id_list": "17403373;19570034;20576682;20643919;21454697;22645316;22762500;22908308;26740625;26824392;27354378;27474410;29125462;29743203;30209220;33105882;33135724;33300544;33459343;34428180;36210013;36897066;37156612;38110990;39927985", "class_list": "", "function": "Behavioral and Transcriptome Profiling of Heterozygous Rab10 Knock-Out Mice. Publication Status: Online-Only, [RefSeq, PubMed]; Cellular and subcellular localization of Rab10 and phospho-T73 Rab10 in the mouse and human brain. Publication Status: Online-Only, [RefSeq, PubMed]; Rab10 regulates the sorting of internalised TrkB for retrograde axonal transport. Publication Status: Online-Only, [RefSeq, PubMed]; The small GTPases Rab are key regulators of intracellular membrane trafficking, from the formation of transport vesicles to their fusion with membranes. Rabs cycle between an inactive GDP-bound form and an active GTP-bound form that is able to recruit to membranes different set of downstream effectors directly responsible for vesicle formation, movement, tethering and fusion (By similarity). RAB10 is mainly involved in the biosynthetic transport of proteins from the Golgi to the plasma membrane (PubMed:17403373, PubMed:20643919, PubMed:22908308, PubMed:27354378). Regulates, for instance, SLC2A4/GLUT4 glucose transporter-enriched vesicles delivery to the plasma membrane (PubMed:17403373, PubMed:22908308, PubMed:27354378). In parallel, RAB10 regulates the transport of TLR4, a toll-like receptor to the plasma membrane and therefore may be important for innate immune response (PubMed:20643919). Also plays a specific role in asymmetric protein transport to the plasma membrane (By similarity). In neurons, involved in axonogenesis through regulation of vesicular membrane trafficking toward the axonal plasma membrane (By similarity). In epithelial cells, regulates transport from the Golgi to the basolateral membrane (By similarity). May play a role in the basolateral recycling pathway and in phagosome maturation (By similarity). May play a role in endoplasmic reticulum dynamics and morphology controlling tubulation along microtubules and tubules fusion. Together with LRRK2, RAB8A, and RILPL1, regulates ciliogenesis. When phosphorylated by LRRK2 on Thr-73, binds RILPL1 and inhibits ciliogenesis. Participates in the export of a subset of neosynthesized proteins through a Rab8-Rab10-Rab11-dependent endososomal export route. Targeted to and stabilized on stressed lysosomes through LRRK2 phosphorylation where it promotes the extracellular release of lysosomal content through EHBP1 and EHNP1L1 effector proteins (PubMed:30209220)., [UniProtKB, PubMed, UniProtKB, UniProtKB, PubMed, UniProtKB, PubMed, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "O88386;Q9D7X6", "ec_number_list": "3.6.5.-;3.6.5.2;3.6.5.3;3.6.1.5;3.1.3.48;3.6.5.4;2.4.1.-;2.4.1.275;2.4.1.22;2.4.1.38;2.4.1.90;3.6.5.5;2.5.1.60;3.6.4.-;3.4.11.2;3.6.1.-;3.6.1.15;2.7.11.1;7.6.2.-;3.4.24.11;1.2.1.5;1.2.1.28;1.2.1.7;1.2.1.48;3.6.-.-", "go_molecular_function": "GO:0051021 GDP-dissociation inhibitor binding;GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0046872 metal ion binding;GO:0019003 GDP binding", "go_cellular_component": "GO:0099503 secretory vesicle;GO:0005768 endosome;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0005929 cilium", "go_biological_process": "GO:0071786 endoplasmic reticulum tubular network organization;GO:0097051 establishment of protein localization to endoplasmic reticulum membrane;GO:0006886 intracellular protein transport;GO:0007409 axonogenesis;GO:0032869 cellular response to insulin stimulus", "synthesized_glycan_count": 0, "hit_score": 2.8, "record_id": "P61027-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q62520-1", "uniprot_id": "ZIC2_MOUSE", "mass": 54954.0, "length": 530, "protein_name": "Zinc finger protein ZIC 2", "gene_name": "Zic2", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Zic2", "gene_names_refseq": "", "protein_names_uniprotkb": "Zinc finger protein ZIC 2; Zinc finger protein of the cerebellum 2", "protein_names_refseq": "", "tax_id": 10090, "disease": "holoprosencephaly 5 (Disease Ontology:DOID:0110878); holoprosencephaly (Disease Ontology:DOID:4621); schizophrenia (Disease Ontology:DOID:5419)", "pathway": " (mmu:22772)", "pathway_count": 1, "publication_count": 14, "publication_id_list": "10677508;11053430;11238441;11756505;13678579;15207726;15465018;18068128;18363970;18417618;18524895;20676059;21750661;8557628", "class_list": "", "function": "Acts as a transcriptional activator or repressor. Plays important roles in the early stage of organogenesis of the CNS. Activates the transcription of the serotonin transporter SERT in uncrossed ipsilateral retinal ganglion cells (iRGCs) to refine eye-specific projections in primary visual targets. Its transcriptional activity is repressed by MDFIC. Involved in the formation of the ipsilateral retinal projection at the optic chiasm midline. Drives the expression of EPHB1 on ipsilaterally projecting growth cones. Binds to the minimal GLI-consensus sequence 5'-TGGGTGGTC-3'. Associates to the basal SERT promoter region from ventrotemporal retinal segments of retinal embryos., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 2, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 3, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0016604 nuclear body", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007399 nervous system development;GO:0030154 cell differentiation;GO:0045944 positive regulation of transcription by RNA polymerase II", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "Q62520-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P46684-1", "uniprot_id": "ZIC1_MOUSE", "mass": 48331.0, "length": 447, "protein_name": "Zinc finger protein ZIC 1", "gene_name": "Zic1", "organism": "Mouse", "refseq_name": "zinc finger protein ZIC 1", "refseq_ac": "NP_033599", "gene_names_uniprotkb": "Zic1; Zic", "gene_names_refseq": "ZIC; ZNF201; Zic1", "protein_names_uniprotkb": "Zinc finger protein ZIC 1; Zinc finger protein of the cerebellum 1", "protein_names_refseq": "Zic family member 1 (odd-paired homolog, Drosophila); zinc finger protein ZIC 1", "tax_id": 10090, "disease": "Joubert syndrome (Disease Ontology:DOID:0050777); craniosynostosis 6 (Disease Ontology:DOID:0061008); Dandy-Walker syndrome (Disease Ontology:DOID:2785); holoprosencephaly (Disease Ontology:DOID:4621)", "pathway": " (mmu:22771)", "pathway_count": 1, "publication_count": 8, "publication_id_list": "11053430;11238441;11944941;15207726;19303920;20354137;25428506;7931345", "class_list": "glycogene", "function": "Acts as a transcriptional activator. Involved in neurogenesis. Plays important roles in the early stage of organogenesis of the CNS, as well as during dorsal spinal cord development and maturation of the cerebellum. Involved in the spatial distribution of mossy fiber (MF) neurons within the pontine gray nucleus (PGN). Plays a role in the regulation of MF axon pathway choice. Promotes MF migration towards ipsilaterally-located cerebellar territories. May have a role in shear flow mechanotransduction in osteocytes. Retains nuclear GLI1 and GLI3 in the cytoplasm. Binds to the minimal GLI-consensus sequence 5'-TGGGTGGTC-3'., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 23, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 4, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q6PAK5;Q80Y18", "ec_number_list": "", "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm", "go_biological_process": "GO:0042307 positive regulation of protein import into nucleus;GO:0098727 maintenance of cell number;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0021510 spinal cord development", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "P46684-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9DBC3-1", "uniprot_id": "CMTR1_MOUSE", "mass": 95676.0, "length": 837, "protein_name": "Cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 1", "gene_name": "Cmtr1", "organism": "Mouse", "refseq_name": "cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 1", "refseq_ac": "NP_083067", "gene_names_uniprotkb": "Cmtr1; Ftsjd2; Kiaa0082", "gene_names_refseq": "1300018I05Rik; Cmtr1; Ftsjd2; MTr1", "protein_names_uniprotkb": "Cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 1; 2.1.1.57; Cap methyltransferase 1; Cap1 2'O-ribose methyltransferase 1; FtsJ methyltransferase domain-containing protein 2; MTr1", "protein_names_refseq": "FtsJ methyltransferase domain-containing protein 2; S-adenosyl-L-methionine-dependent methyltransferase FTSJD2; cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 1; cap1 2'O-ribose methyltransferase 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:74157)", "pathway_count": 1, "publication_count": 13, "publication_id_list": "10.1101/2023.09.13.557529;17242355;21183079;21750661;25428506;29187734;30084848;30779550;31219806;33086056;34428180;35820727;36210013", "class_list": "", "function": "CMTR1-Catalyzed 2'-O-Ribose Methylation Controls Neuronal Development by Regulating Camk2alpha Expression Independent of RIG-I Signaling., [RefSeq, PubMed]; S-adenosyl-L-methionine-dependent methyltransferase that mediates RNA cap1 2'-O-ribose methylation to the 5'-cap structure of RNAs. Methylates the ribose of the first nucleotide of a m(7)GpppG-capped mRNA to produce m(7)GpppNmp (cap1)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; S-adenosyl-L-methionine-dependent methyltransferase that mediates mRNA cap1 2'-O-ribose methylation to the 5'-cap structure of mRNAs. Methylates the ribose of the first nucleotide of a m(7)GpppG-capped mRNA and small nuclear RNA (snRNA) to produce m(7)GpppRm (cap1). Displays a preference for cap0 transcripts. Cap1 modification is linked to higher levels of translation. May be involved in the interferon response pathway., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q3U3G5;Q3U7Y9;Q6A0D5;Q8C7V0", "ec_number_list": "2.1.1.57", "go_molecular_function": "GO:0004483 methyltransferase cap1 activity;GO:0003676 nucleic acid binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm", "go_biological_process": "GO:0006397 mRNA processing;GO:0032259 methylation;GO:0006370 7-methylguanosine mRNA capping;GO:0016556 mRNA modification", "synthesized_glycan_count": 0, "hit_score": 1.8, "record_id": "Q9DBC3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O35054-1", "uniprot_id": "CLD4_MOUSE", "mass": 22339.0, "length": 210, "protein_name": "Claudin-4", "gene_name": "Cldn4", "organism": "Mouse", "refseq_name": "claudin-4", "refseq_ac": "NP_034033", "gene_names_uniprotkb": "Cldn4; Cper; Cpetr1", "gene_names_refseq": "Cep-r; Cldn4; Cpetr1; Cpetr", "protein_names_uniprotkb": "Claudin-4; CPE-R; CPE-receptor; Clostridium perfringens enterotoxin receptor", "protein_names_refseq": "CPE-R; CPE-receptor; claudin-4; clostridium perfringens enterotoxin receptor", "tax_id": 10090, "disease": "peptic esophagitis (Disease Ontology:DOID:13976); pancreatic cancer (Disease Ontology:DOID:1793); ovarian cancer (Disease Ontology:DOID:2394); pancreatic ductal carcinoma (Disease Ontology:DOID:3587)", "pathway": " (mmu:12740)", "pathway_count": 1, "publication_count": 11, "publication_id_list": "10601346;16236711;20921420;25831548;28011936;30734065;35773259;36803098;37806357;9334247;9892664", "class_list": "", "function": "Can associate with other claudins to regulate tight junction structural and functional strand dynamics (By similarity) (PubMed:20921420, PubMed:35773259). May coassemble with CLDN8 into tight junction strands containing anion-selective channels that convey paracellular chloride permeability in renal collecting ducts (PubMed:20921420, PubMed:25831548). May integrate into CLDN3 strands to modulate localized tight junction barrier properties (By similarity). May disrupt strand assembly of channel-forming CLDN2 and CLDN15 and inhibit cation conductance. Cannot form tight junction strands on its own (By similarity)., [UniProtKB, PubMed, PubMed, UniProtKB, PubMed]; Increase in Paracellular Leakage of Amino Acids Mediated by Aging-Induced Reduction of Claudin-4 Expression., [RefSeq, PubMed]; RBM15 suppresses hepatic insulin sensitivity of offspring of gestational diabetes mellitus mice via m6A-mediated regulation of CLDN4. Publication Status: Online-Only, [RefSeq, PubMed]; This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is a high-affinity receptor for clostridium perfringens enterotoxin (CPE) produced by the bacterium Clostridium perfringens, and the interaction with CPE results in increased membrane permeability by forming small pores in plasma membrane. This protein augments alveolar epithelial barrier function and is induced in acute lung injury. It is highly expressed in pancreatic and ovarian cancers. [provided by RefSeq, Aug 2010]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 5, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 4, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "5.6.1.6;1.8.-.-;1.8.5.1", "go_molecular_function": "GO:0042802 identical protein binding;GO:0005198 structural molecule activity;GO:0005254 chloride channel activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0005911 cell-cell junction;GO:0005923 bicellular tight junction;GO:0016020 membrane;GO:0016324 apical plasma membrane", "go_biological_process": "GO:0030335 positive regulation of cell migration;GO:0061436 establishment of skin barrier;GO:0007565 female pregnancy;GO:0032570 response to progesterone;GO:0090303 positive regulation of wound healing", "synthesized_glycan_count": 0, "hit_score": 1.2, "record_id": "O35054-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P16330-1", "uniprot_id": "CN37_MOUSE", "mass": 47123.0, "length": 420, "protein_name": "2',3'-cyclic-nucleotide 3'-phosphodiesterase", "gene_name": "Cnp", "organism": "Mouse", "refseq_name": "2',3'-cyclic-nucleotide 3'-phosphodiesterase isoform 1", "refseq_ac": "NP_001139790", "gene_names_uniprotkb": "Cnp; Cnp1", "gene_names_refseq": "CNPase; Cnp-1; Cnp1; Cnp", "protein_names_uniprotkb": "2',3'-cyclic-nucleotide 3'-phosphodiesterase; 3.1.4.37; CNPase; CNP", "protein_names_refseq": "2',3'-cyclic-nucleotide 3'-phosphodiesterase isoform 1; cyclic nucleotide phosphodiesterase 1", "tax_id": 10090, "disease": "restless legs syndrome (Disease Ontology:DOID:0050425); hypomyelinating leukodystrophy 20 (Disease Ontology:DOID:0112153); carotid stenosis (Disease Ontology:DOID:13001); alcoholic liver cirrhosis (Disease Ontology:DOID:14018); multiple sclerosis (Disease Ontology:DOID:2377); schizophrenia (Disease Ontology:DOID:5419)", "pathway": " (mmu:12799)", "pathway_count": 1, "publication_count": 14, "publication_id_list": "10.1101/2023.09.13.557529;11471062;18034455;18076147;21183079;2167669;22393399;2558653;26495903;28011936;29187734;33300544;37507081;39627609", "class_list": "", "function": "Myelin-associated enzyme that catalyzes the phosphodiester hydrolysis of 2',3'-cyclic nucleotides to 2'-nucleotides (PubMed:22393399). In the mitochondria, regulates the functioning of the mitochondrial permeability transition pore (mPTP), and thus is involved in the mechanisms of cell death, both apoptosis and necrosis. Acts as an antiviral factor by suppressing the assembly of SARS-CoV-2 virions., [UniProtKB, UniProtKB, PubMed, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 6, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 6, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q61424;Q8C7C9;Q91V42;Q923F3", "ec_number_list": "3.1.4.37", "go_molecular_function": "GO:0004113 2',3'-cyclic-nucleotide 3'-phosphodiesterase activity;GO:0030551 cyclic nucleotide binding;GO:0003723 RNA binding", "go_cellular_component": "GO:0035748 myelin sheath abaxonal region;GO:0005615 extracellular space;GO:0005737 cytoplasm;GO:0005741 mitochondrial outer membrane;GO:0005743 mitochondrial inner membrane", "go_biological_process": "GO:0009214 cyclic nucleotide catabolic process;GO:0007409 axonogenesis;GO:0008344 adult locomotory behavior;GO:0009636 response to toxic substance;GO:0046902 regulation of mitochondrial membrane permeability", "synthesized_glycan_count": 0, "hit_score": 1.9, "record_id": "P16330-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q01147-2", "uniprot_id": "CREB1_MOUSE", "mass": 35122.0, "length": 327, "protein_name": "Cyclic AMP-responsive element-binding protein 1", "gene_name": "Creb1", "organism": "Mouse", "refseq_name": "cyclic AMP-responsive element-binding protein 1 isoform B", "refseq_ac": "NP_034082", "gene_names_uniprotkb": "Creb1; Creb-1", "gene_names_refseq": "2310001E10Rik; 3526402H21Rik; Creb-1; Creb1; Creb", "protein_names_uniprotkb": "Cyclic AMP-responsive element-binding protein 1; CREB-1; cAMP-responsive element-binding protein 1", "protein_names_refseq": "cyclic AMP-responsive element-binding protein 1 isoform B; cyclic AMP-responsive element-binding protein 1", "tax_id": 10090, "disease": "alcohol dependence (Disease Ontology:DOID:0050741); nicotine dependence (Disease Ontology:DOID:0050742); withdrawal disorder (Disease Ontology:DOID:0060001); autism spectrum disorder (Disease Ontology:DOID:0060041); hypertension (Disease Ontology:DOID:10763); amnestic disorder (Disease Ontology:DOID:10914); obsessive-compulsive disorder (Disease Ontology:DOID:10933); opioid abuse (Disease Ontology:DOID:11206); sciatic neuropathy (Disease Ontology:DOID:11446); Pick's disease (Disease Ontology:DOID:11870); Huntington's disease (Disease Ontology:DOID:12858); Parkinson's disease (Disease Ontology:DOID:14330); alcohol use disorder (Disease Ontology:DOID:1574); depressive disorder (Disease Ontology:DOID:1596); anxiety disorder (Disease Ontology:DOID:2030); transient cerebral ischemia (Disease Ontology:DOID:224); brain ischemia (Disease Ontology:DOID:2316); morphine dependence (Disease Ontology:DOID:2560); middle cerebral artery infarction (Disease Ontology:DOID:3525); schizophrenia (Disease Ontology:DOID:5419); congestive heart failure (Disease Ontology:DOID:6000); amphetamine abuse (Disease Ontology:DOID:670); cocaine abuse (Disease Ontology:DOID:809); vascular dementia (Disease Ontology:DOID:8725); substance dependence (Disease Ontology:DOID:9973); drug dependence (Disease Ontology:DOID:9974); cocaine dependence (Disease Ontology:DOID:9975); heroin dependence (Disease Ontology:DOID:9976)", "pathway": " (mmu:12912)", "pathway_count": 1, "publication_count": 20, "publication_id_list": "10952992;11970866;1387109;1532935;17692820;18690222;20122921;20852621;21728997;22267118;22554507;26866564;29187734;30566056;31219806;34428180;34914893;36210013;40997131;8552098", "class_list": "", "function": "Phosphorylation-dependent transcription factor that stimulates transcription upon binding to the DNA cAMP response element (CRE), a sequence present in many viral and cellular promoters (By similarity). Transcription activation is enhanced by the TORC coactivators which act independently of Ser-119 phosphorylation (By similarity). Involved in different cellular processes including the synchronization of circadian rhythmicity and the differentiation of adipose cells (PubMed:11970866, PubMed:21728997). Regulates the expression of apoptotic and inflammatory response factors in cardiomyocytes in response to ERFE-mediated activation of AKT signaling (PubMed:30566056)., [UniProtKB, UniProtKB, PubMed, PubMed, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 4, "reported_mutagensis": 3, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 28, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0019899 enzyme binding;GO:0042802 identical protein binding;GO:1990763 arrestin family protein binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005759 mitochondrial matrix;GO:0005813 centrosome;GO:0005829 cytosol", "go_biological_process": "GO:1990910 response to hypobaric hypoxia;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006468 protein phosphorylation;GO:0007409 axonogenesis;GO:0007613 memory", "synthesized_glycan_count": 0, "hit_score": 2.3, "record_id": "Q01147-2", "record_type": "protein" }, { "uniprot_canonical_ac": "Q05AA6-1", "uniprot_id": "DRP2_MOUSE", "mass": 108050.0, "length": 957, "protein_name": "Dystrophin-related protein 2", "gene_name": "Drp2", "organism": "Mouse", "refseq_name": "dystrophin-related protein 2 isoform 3", "refseq_ac": "NP_034208", "gene_names_uniprotkb": "Drp2", "gene_names_refseq": "DRP-2; Drp2", "protein_names_uniprotkb": "Dystrophin-related protein 2; DRP-2", "protein_names_refseq": "dystrophin-related protein 2 isoform 3", "tax_id": 10090, "disease": "Duchenne muscular dystrophy (Disease Ontology:DOID:11723)", "pathway": " (mmu:13497); (R-MMU-9913351)", "pathway_count": 2, "publication_count": 6, "publication_id_list": "11430802;17114649;21750661;22764250;23152929;8640231", "class_list": "", "function": "Cajal band appositions contain a dystroglycan complex that includes periaxin and dystrophin-related protein (Drp)2., [RefSeq, PubMed]; Required for normal myelination and for normal organization of the cytoplasm and the formation of Cajal bands in myelinating Schwann cells (PubMed:22764250). Required for normal PRX location at appositions between the abaxonal surface of the myelin sheath and the Schwann cell plasma membrane (PubMed:22764250). Possibly involved in membrane-cytoskeleton interactions of the central nervous system., [UniProtKB, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q61095;Q8C4R1", "ec_number_list": "", "go_molecular_function": "GO:0008270 zinc ion binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0014069 postsynaptic density;GO:0030425 dendrite", "go_biological_process": "GO:0050808 synapse organization;GO:0007417 central nervous system development;GO:0099536 synaptic signaling", "synthesized_glycan_count": 0, "hit_score": 0.7, "record_id": "Q05AA6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O54839-1", "uniprot_id": "EOMES_MOUSE", "mass": 74801.0, "length": 707, "protein_name": "Eomesodermin homolog", "gene_name": "Eomes", "organism": "Mouse", "refseq_name": "eomesodermin homolog isoform 2", "refseq_ac": "NP_001158261", "gene_names_uniprotkb": "Eomes; Tbr2", "gene_names_refseq": "Eomes; TBR-2; Tbr2", "protein_names_uniprotkb": "Eomesodermin homolog; T-box brain protein 2; T-brain-2; TBR-2", "protein_names_refseq": "T-box brain protein 2; T-brain-2; eomesodermin homolog isoform 2; eomesodermin homolog", "tax_id": 10090, "disease": "", "pathway": " (mmu:13813)", "pathway_count": 1, "publication_count": 12, "publication_id_list": "10407135;10716450;10974533;14605368;18171685;18940588;21183079;21750661;25428506;33488348;34428180;9503012", "class_list": "", "function": "Functions as a transcriptional activator playing a crucial role during development. Functions in trophoblast differentiation and later in gastrulation, regulating both mesoderm delamination and endoderm specification (PubMed:10716450). Plays a role in brain development being required for the specification and the proliferation of the intermediate progenitor cells and their progeny in the cerebral cortex (PubMed:18171685, PubMed:18940588). Required for differentiation and migration of unipolar dendritic brush cells (PubMed:33488348). Also involved in the differentiation of CD8+ T-cells during immune response regulating the expression of lytic effector genes (PubMed:14605368)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 3, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q3UPL1;Q52KJ1;Q8BN22;Q9JJL1;Q9QYG7", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0003700 DNA-binding transcription factor activity;GO:0003714 transcription corepressor activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0000785 chromatin", "go_biological_process": "GO:0048708 astrocyte differentiation;GO:0001714 endodermal cell fate specification;GO:0002302 CD8-positive, alpha-beta T cell differentiation involved in immune response;GO:0060706 cell differentiation involved in embryonic placenta development;GO:0060809 mesodermal to mesenchymal transition involved in gastrulation", "synthesized_glycan_count": 0, "hit_score": 1.3, "record_id": "O54839-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P58252-1", "uniprot_id": "EF2_MOUSE", "mass": 95314.0, "length": 858, "protein_name": "Elongation factor 2", "gene_name": "Eef2", "organism": "Mouse", "refseq_name": "elongation factor 2", "refseq_ac": "NP_031933", "gene_names_uniprotkb": "Eef2", "gene_names_refseq": "Eef2; Ef-2", "protein_names_uniprotkb": "Elongation factor 2; 3.6.5.-; EF-2", "protein_names_refseq": "elongation factor 2", "tax_id": 10090, "disease": "spinocerebellar ataxia 26 (Disease Ontology:DOID:0050975); prostate cancer (Disease Ontology:DOID:10283); stomach cancer (Disease Ontology:DOID:10534); Alzheimer's disease (Disease Ontology:DOID:10652); glaucoma (Disease Ontology:DOID:1686); rectum adenocarcinoma (Disease Ontology:DOID:1996); colon adenocarcinoma (Disease Ontology:DOID:234); brain glioblastoma multiforme (Disease Ontology:DOID:3073); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung adenocarcinoma (Disease Ontology:DOID:3910); lung small cell carcinoma (Disease Ontology:DOID:5409); colorectal cancer (Disease Ontology:DOID:9256)", "pathway": " (mmu:13629); (R-MMU-156902); (R-MMU-5358493); (R-MMU-6798695); (R-MMU-8876725)", "pathway_count": 5, "publication_count": 31, "publication_id_list": "10.1101/2023.09.13.557529;16075062;16139798;20173027;23806337;24788674;25153642;25428506;25605945;28011936;29187734;30084848;30779550;31219806;32152506;33300544;33725478;34428180;34815424;34887587;35820727;35984892;36210013;36288343;37453647;37507081;37828378;39113018;39627609;39927985;40684658", "class_list": "", "function": "Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post-translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome., [UniProtKB, UniProtKB]; TNKS1BP1 mediates AECII senescence and radiation induced lung injury through suppressing EEF2 degradation. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 9, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 3, "disease_count": 12, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q544E4", "ec_number_list": "3.6.5.-;3.6.5.2;2.4.1.25;3.2.1.33;3.6.5.3;3.5.4.6;1.11.1.24;3.4.22.52;3.4.19.12;3.6.1.5;3.4.22.27;1.1.1.42;3.4.21.46;4.1.2.13;5.3.1.9;5.1.3.-;3.6.4.10;2.4.2.7;1.16.3.1;4.2.1.24;3.4.22.1;3.2.1.31;2.7.1.11;2.7.10.2;3.6.5.4;5.2.1.8;3.4.23.5;2.5.1.18;4.2.99.18;5.6.2.4;2.4.2.1;3.2.1.23;1.11.1.6;3.3.2.6;3.4.11.4;1.1.1.205;5.3.2.1;5.3.3.12;3.6.5.5;3.4.24.35;3.6.1.-;2.7.11.24;1.13.11.-;1.13.11.34;1.11.1.7;3.1.6.12;2.7.11.1;2.7.1.40;3.5.4.5;3.4.25.1;2.7.11.39;2.7.4.6;2.7.13.3;3.6.4.6;3.6.1.15;2.7.1.1;2.7.1.-;2.1.1.-;2.5.1.108;3.1.1.47;3.6.4.13;2.7.11.22;2.7.11.23;2.3.2.26;5.4.2.2;5.4.2.7;2.3.2.27;3.1.6.14;3.6.-.-;2.7.1.35;3.4.19.1;3.6.1.6;2.3.3.8;4.1.2.4;6.3.1.14;2.1.1.314;2.3.2.5;5.4.2.11;5.4.2.4;2.4.1.1;2.4.1.186;3.4.18.1;3.5.1.23;3.5.1.-", "go_molecular_function": "GO:0003723 RNA binding;GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0019901 protein kinase binding;GO:0051015 actin filament binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0045202 synapse", "go_biological_process": "GO:2000767 positive regulation of cytoplasmic translation;GO:1990416 cellular response to brain-derived neurotrophic factor stimulus;GO:0002931 response to ischemia;GO:0003009 skeletal muscle contraction;GO:0045471 response to ethanol", "synthesized_glycan_count": 0, "hit_score": 3.8, "record_id": "P58252-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P62631-1", "uniprot_id": "EF1A2_MOUSE", "mass": 50454.0, "length": 463, "protein_name": "Elongation factor 1-alpha 2", "gene_name": "Eef1a2", "organism": "Mouse", "refseq_name": "elongation factor 1-alpha 2", "refseq_ac": "NP_031932", "gene_names_uniprotkb": "Eef1a2; Eef1al; Stn", "gene_names_refseq": "EEF1AL; EF-1-alpha-2; Eef1a2; Eef1a; S1; STN; wasted; wst", "protein_names_uniprotkb": "Elongation factor 1-alpha 2; 3.6.5.-; EF-1-alpha-2; Eukaryotic elongation factor 1 A-2; Statin-S1; eEF1A-2", "protein_names_refseq": "elongation factor 1-alpha 2; eukaryotic elongation factor 1 A-2; statin-S1", "tax_id": 10090, "disease": "autosomal dominant intellectual developmental disorder 38 (Disease Ontology:DOID:0070068); developmental and epileptic encephalopathy 33 (Disease Ontology:DOID:0080463); Alzheimer's disease (Disease Ontology:DOID:10652); dilated cardiomyopathy (Disease Ontology:DOID:12930); epilepsy (Disease Ontology:DOID:1826); ovarian cancer (Disease Ontology:DOID:2394)", "pathway": " (mmu:13628)", "pathway_count": 1, "publication_count": 22, "publication_id_list": "10.1101/2023.09.13.557529;20923971;21750661;22645316;25428506;25605945;30084848;32069316;33300544;34203471;34428180;35820727;35984892;36288343;37429391;37507081;37695913;38179821;38442201;39927985;7595213;7945283", "class_list": "", "function": "Autism- and epilepsy-associated EEF1A2 mutations lead to translational dysfunction and altered actin bundling., [RefSeq, PubMed]; EEF1A2 promotes PTEN-GSK3beta-SCF complex-dependent degradation of Aurora kinase A and is inactivated in breast cancer., [RefSeq, PubMed]; Endogenous epitope tagging of eEF1A2 in mice reveals early embryonic expression of eEF1A2 and subcellular compartmentalisation of neuronal eEF1A1 and eEF1A2., [RefSeq, PubMed]; Face-valid phenotypes in a mouse model of the most common mutation in EEF1A2-related neurodevelopmental disorder., [RefSeq, PubMed]; This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis., [UniProtKB, UniProtKB]; Translation elongation factor that catalyzes the GTP-dependent binding of aminoacyl-tRNA (aa-tRNA) to the A-site of ribosomes during the elongation phase of protein synthesis. Base pairing between the mRNA codon and the aa-tRNA anticodon promotes GTP hydrolysis, releasing the aa-tRNA from EEF1A1 and allowing its accommodation into the ribosome (By similarity). The growing protein chain is subsequently transferred from the P-site peptidyl tRNA to the A-site aa-tRNA, extending it by one amino acid through ribosome-catalyzed peptide bond formation (By similarity)., [UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 3, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 3, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 3, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 4, "disease_count": 6, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "P27706", "ec_number_list": "3.6.5.-;3.6.5.2;3.6.5.3;3.6.1.5;3.6.5.4;3.6.5.5;3.6.1.-;3.6.1.15;2.7.11.1;3.6.-.-", "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0019901 protein kinase binding;GO:0046872 metal ion binding;GO:0003746 translation elongation factor activity", "go_cellular_component": "GO:0098982 GABA-ergic synapse;GO:0005737 cytoplasm;GO:0043025 neuronal cell body;GO:0043209 myelin sheath;GO:0045202 synapse", "go_biological_process": "GO:0043065 positive regulation of apoptotic process;GO:0006412 translation;GO:0006414 translational elongation;GO:0090218 positive regulation of lipid kinase activity;GO:0099150 regulation of postsynaptic specialization assembly", "synthesized_glycan_count": 0, "hit_score": 3.1, "record_id": "P62631-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9D8Y0-1", "uniprot_id": "EFHD2_MOUSE", "mass": 26791.0, "length": 240, "protein_name": "EF-hand domain-containing protein D2", "gene_name": "Efhd2", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Efhd2; Sws1", "gene_names_refseq": "", "protein_names_uniprotkb": "EF-hand domain-containing protein D2; Swiprosin-1", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 8, "publication_id_list": "15749887;17242355;17673920;18034455;21183079;32152506;34428180;36288343", "class_list": "", "function": "May regulate B-cell receptor (BCR)-induced immature and primary B-cell apoptosis. Plays a role as negative regulator of the canonical NF-kappa-B-activating branch. Controls spontaneous apoptosis through the regulation of BCL2L1 abundance., [UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q9D0P4", "ec_number_list": "", "go_molecular_function": "GO:0005509 calcium ion binding", "go_cellular_component": "GO:0045121 membrane raft", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q9D8Y0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9DD18-1", "uniprot_id": "DTD1_MOUSE", "mass": 23384.0, "length": 209, "protein_name": "D-aminoacyl-tRNA deacylase 1", "gene_name": "Dtd1", "organism": "Mouse", "refseq_name": "D-aminoacyl-tRNA deacylase 1", "refseq_ac": "NP_079590", "gene_names_uniprotkb": "Dtd1; Hars2", "gene_names_refseq": "0610006H08Rik; DTD; DUE-B; Dtd1; Hars2", "protein_names_uniprotkb": "D-aminoacyl-tRNA deacylase 1; 3.1.1.96; DNA-unwinding element-binding protein B; DTD; DUE-B; Gly-tRNA(Ala) deacylase", "protein_names_refseq": "D-aminoacyl-tRNA deacylase 1; D-tyrosyl-tRNA deacylase 1 homolog; D-tyrosyl-tRNA(Tyr) deacylase 1; DNA-unwinding element-binding protein B; gly-tRNA(Ala) deacylase", "tax_id": 10090, "disease": "", "pathway": " (mmu:66044)", "pathway_count": 1, "publication_count": 3, "publication_id_list": "17242355;21183079;26495903", "class_list": "", "function": "ATPase involved in DNA replication, may facilitate loading of CDC45 onto pre-replication complexes., [UniProtKB, UniProtKB]; An aminoacyl-tRNA editing enzyme that deacylates mischarged D-aminoacyl-tRNAs. Also deacylates mischarged glycyl-tRNA(Ala), protecting cells against glycine mischarging by AlaRS. Acts via tRNA-based rather than protein-based catalysis; rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "A2ANA2;Q3TY44;Q9CRE8;Q9CYL0;Q9D013;Q9D1G4", "ec_number_list": "3.1.1.96", "go_molecular_function": "GO:0051500 D-tyrosyl-tRNA(Tyr) deacylase activity;GO:0003677 DNA binding;GO:0046872 metal ion binding;GO:0000049 tRNA binding;GO:0106026 Gly-tRNA(Ala) deacylase activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm", "go_biological_process": "GO:0006399 tRNA metabolic process;GO:0006260 DNA replication", "synthesized_glycan_count": 0, "hit_score": 0.4, "record_id": "Q9DD18-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P27601-1", "uniprot_id": "GNA13_MOUSE", "mass": 44055.0, "length": 377, "protein_name": "Guanine nucleotide-binding protein subunit alpha-13", "gene_name": "Gna13", "organism": "Mouse", "refseq_name": "guanine nucleotide-binding protein subunit alpha-13 isoform 1", "refseq_ac": "NP_034433", "gene_names_uniprotkb": "Gna13; Gna-13", "gene_names_refseq": "Galpha13; Gna13", "protein_names_uniprotkb": "Guanine nucleotide-binding protein subunit alpha-13; G alpha-13; G protein subunit alpha-13", "protein_names_refseq": "G-protein subunit alpha-13; g alpha-13; guanine nucleotide-binding protein subunit alpha-13 isoform 1; guanine nucleotide-binding protein subunit alpha-13", "tax_id": 10090, "disease": "McCune Albright syndrome (Disease Ontology:DOID:1858)", "pathway": " (mmu:14674); (R-MMU-193648); (R-MMU-416482); (R-MMU-428930); (R-MMU-456926); (R-MMU-9013148); (R-MMU-9013149)", "pathway_count": 7, "publication_count": 20, "publication_id_list": "15240885;16388592;18703424;18940608;1905812;19151758;21212405;22645316;23994616;2508088;25274307;26495903;29187734;31219806;31875850;32152506;34428180;35413491;36210013;37828378", "class_list": "", "function": "GNA13 promotes the proliferation and migration of lung squamous cell carcinoma cells through regulating the PI3K/AKT signaling pathway., [RefSeq, PubMed]; Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems (PubMed:16388592, PubMed:19151758, PubMed:21212405). Activates effector molecule RhoA by binding and activating RhoGEFs (ARHGEF1/p115RhoGEF, ARHGEF11/PDZ-RhoGEF and ARHGEF12/LARG) (PubMed:16388592). GNA13-dependent Rho signaling subsequently regulates transcription factor AP-1 (activating protein-1) (PubMed:19151758, PubMed:21212405). Promotes tumor cell invasion and metastasis by activating Rho/ROCK signaling pathway (By similarity). Inhibits CDH1-mediated cell adhesion in a process independent from Rho activation (By similarity). In lymphoid follicles, transmits P2RY8- and S1PR2-dependent signals that lead to inhibition of germinal center (GC) B cell growth and migration outside the GC niche., [UniProtKB, PubMed, PubMed, UniProtKB, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q6PF99", "ec_number_list": "", "go_molecular_function": "GO:0031752 D5 dopamine receptor binding;GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0046872 metal ion binding;GO:0031683 G-protein beta/gamma-subunit complex binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0042470 melanosome", "go_biological_process": "GO:0010762 regulation of fibroblast migration;GO:0001525 angiogenesis;GO:0001701 in utero embryonic development;GO:0007186 G protein-coupled receptor signaling pathway;GO:0007189 adenylate cyclase-activating G protein-coupled receptor signaling pathway", "synthesized_glycan_count": 0, "hit_score": 2.4, "record_id": "P27601-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P55937-2", "uniprot_id": "GOGA3_MOUSE", "mass": 167220.0, "length": 1487, "protein_name": "Golgin subfamily A member 3", "gene_name": "Golga3", "organism": "Mouse", "refseq_name": "golgin subfamily A member 3 isoform 2", "refseq_ac": "NP_032172", "gene_names_uniprotkb": "Golga3; Mea2", "gene_names_refseq": "5330413L04; 5430416E01Rik; G1-499-14; Golga3; Mea-2; Mea2/Golga3; Mea2; repro27", "protein_names_uniprotkb": "Golgin subfamily A member 3; Golgin-160; MEA-2; Male-enhanced antigen 2", "protein_names_refseq": "golgi autoantigen, golgin subfamily a, 3; golgin subfamily A member 3 isoform 2; golgin subfamily A member 3; golgin-160; male-enhanced antigen 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:269682); (R-MMU-9696270)", "pathway_count": 2, "publication_count": 17, "publication_id_list": "11835574;17242355;19144319;21183079;22517741;22645316;23495255;26495903;28528544;31219806;31599954;32848054;34428180;35820727;35822049;37090114;9063644", "class_list": "", "function": "Golga3(repro27) mice lack GOLGA3 protein and thus provide an in vivo tool to aid in deciphering the role of GOLGA3 in Golgi complex positioning, cargo trafficking and apoptosis signalling in male germ cells, [RefSeq, PubMed]; Mutation of S461, in the GOLGA3 phosphorylation site, does not affect mouse spermatogenesis. Publication Status: Online-Only, [RefSeq, PubMed]; Plays an important role in spermatogenesis and/or testis development. Probably identical with the serologically detectable male antigen (SDM). Probably involved in maintaining Golgi structure., [UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 9, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q80VF5;Q8CCK4;Q9QYT2;Q9QYT3", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005794 Golgi apparatus;GO:0005829 cytosol", "go_biological_process": "GO:0007283 spermatogenesis;GO:0030154 cell differentiation", "synthesized_glycan_count": 0, "hit_score": 2.0, "record_id": "P55937-2", "record_type": "protein" }, { "uniprot_canonical_ac": "P63216-1", "uniprot_id": "GBG3_MOUSE", "mass": 8305.0, "length": 75, "protein_name": "Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-3", "gene_name": "Gng3", "organism": "Mouse", "refseq_name": "guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-3", "refseq_ac": "NP_034446", "gene_names_uniprotkb": "Gng3; Gngt3", "gene_names_refseq": "Gng3; Hg3d", "protein_names_uniprotkb": "Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-3", "protein_names_refseq": "guanine nucleotide binding protein (G protein), gamma 3 subunit; guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-3; heterotrimeric guanine nucleotide-binding protein 3d", "tax_id": 10090, "disease": "obesity (Disease Ontology:DOID:9970)", "pathway": " (mmu:14704); (R-MMU-1296041); (R-MMU-202040); (R-MMU-381676); (R-MMU-392170); (R-MMU-392451); (R-MMU-392851); (R-MMU-400042); (R-MMU-4086398); (R-MMU-416476); (R-MMU-416482); (R-MMU-418217); (R-MMU-418555); (R-MMU-418592); (R-MMU-418594); (R-MMU-418597); (R-MMU-420092); (R-MMU-428930); (R-MMU-432040); (R-MMU-456926); (R-MMU-500657); (R-MMU-6814122); (R-MMU-8964315); (R-MMU-8964616); (R-MMU-9009391); (R-MMU-9634597); (R-MMU-9856530); (R-MMU-997272)", "pathway_count": 28, "publication_count": 6, "publication_id_list": "17114649;21183079;22207761;7488078;8858601;9790771", "class_list": "", "function": "Guanine nucleotide-binding proteins (G proteins) are involved as a modulator or transducer in various transmembrane signaling systems. The beta and gamma chains are required for the GTPase activity, for replacement of GDP by GTP, and for G protein-effector interaction., [UniProtKB]; Synergistic roles for G-protein gamma3 and gamma7 subtypes in seizure susceptibility as revealed in double knock-out mice., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "P29798;Q61014", "ec_number_list": "", "go_molecular_function": "GO:0031681 G-protein beta-subunit binding;GO:0003924 GTPase activity", "go_cellular_component": "GO:0014069 postsynaptic density;GO:0030425 dendrite;GO:0045202 synapse;GO:0044297 cell body;GO:0005834 heterotrimeric G-protein complex", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007204 positive regulation of cytosolic calcium ion concentration", "synthesized_glycan_count": 0, "hit_score": 0.7, "record_id": "P63216-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BUV3-1", "uniprot_id": "GEPH_MOUSE", "mass": 83282.0, "length": 769, "protein_name": "Gephyrin", "gene_name": "Gphn", "organism": "Mouse", "refseq_name": "gephyrin isoform 2", "refseq_ac": "NP_766540", "gene_names_uniprotkb": "Gphn", "gene_names_refseq": "5730552E08Rik; C230040D23; GPHRYN; GPH; Gphn; geph", "protein_names_uniprotkb": "Gephyrin; Domain E; Domain G; Mo insertase", "protein_names_refseq": "gephyrin isoform 2", "tax_id": 10090, "disease": "alcohol dependence (Disease Ontology:DOID:0050741); molybdenum cofactor deficiency type C (Disease Ontology:DOID:0111166); inherited metabolic disorder (Disease Ontology:DOID:655)", "pathway": " (mmu:268566); (R-MMU-947581)", "pathway_count": 2, "publication_count": 22, "publication_id_list": "16452087;17242355;18630941;21183079;22126966;22645316;25025157;27373832;27609886;27819299;29237092;31080408;31599954;32782141;32848054;33300544;34428180;35245123;35822049;36852467;40021952;40885482", "class_list": "", "function": "Also has a catalytic activity and catalyzes two steps in the biosynthesis of the molybdenum cofactor. In the first step, molybdopterin is adenylated. Subsequently, molybdate is inserted into adenylated molybdopterin and AMP is released., [UniProtKB, UniProtKB]; Microtubule-associated protein involved in membrane protein-cytoskeleton interactions. It is thought to anchor the inhibitory glycine receptor (GLYR) to subsynaptic microtubules (By similarity). Acts as a major instructive molecule at inhibitory synapses, where it also clusters GABA type A receptors (PubMed:25025157)., [UniProtKB, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 8, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 8, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 8, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 10, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 8, "binding_glycan_count": 0, "secondary_ac_list": "E9QKJ1", "ec_number_list": "2.10.1.1;2.7.7.75", "go_molecular_function": "GO:0008940 nitrate reductase activity;GO:0061598 molybdopterin adenylyltransferase activity;GO:0061599 molybdopterin molybdotransferase activity;GO:0060090 molecular adaptor activity;GO:0005102 signaling receptor binding", "go_cellular_component": "GO:0098982 GABA-ergic synapse;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005856 cytoskeleton;GO:0014069 postsynaptic density", "go_biological_process": "GO:0072579 glycine receptor clustering;GO:0097112 gamma-aminobutyric acid receptor clustering;GO:0007529 establishment of synaptic specificity at neuromuscular junction;GO:0045184 establishment of protein localization;GO:0010038 response to metal ion", "synthesized_glycan_count": 0, "hit_score": 3.2, "record_id": "Q8BUV3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q920G9-1", "uniprot_id": "GMCL1_MOUSE", "mass": 59654.0, "length": 524, "protein_name": "Germ cell-less protein-like 1", "gene_name": "Gmcl1", "organism": "Mouse", "refseq_name": "germ cell-less protein-like 1", "refseq_ac": "NP_035948", "gene_names_uniprotkb": "Gmcl1; Gcl1; Gcl", "gene_names_refseq": "2810049L19Rik; Btbd13; DIP; Gcl-1; Gcl; Gmcl1; glc-1; mglc-1", "protein_names_uniprotkb": "Germ cell-less protein-like 1; DIP; DP-interacting protein; mGcl-1", "protein_names_refseq": "DP-interacting protein; germ cell-less homolog 1; germ cell-less protein-like 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:23885)", "pathway_count": 1, "publication_count": 8, "publication_id_list": "10448096;10727854;11591818;12556490;12927808;21183079;34428180;9878064", "class_list": "", "function": "Gmcl1 interacts with the DP component of the E2F transcription factor., [RefSeq, PubMed]; MGCL-1 is a factor modulating MDM2-p53 axis by enhanced degradation of MDM2, [RefSeq, PubMed]; Possible function in spermatogenesis. Enhances the degradation of MDM2 and increases the amount of p53 probably by modulating the nucleocytoplasmic transport., [UniProtKB]; The mgcl-1 gene product appears to be essential for appropriate nuclear-lamina organization, which in turn is essential for normal sperm morphogenesis and chromatin remodeling., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q9DBW5;Q9QUP6", "ec_number_list": "", "go_molecular_function": "GO:0042802 identical protein binding;GO:0097602 cullin family protein binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005635 nuclear envelope;GO:0016363 nuclear matrix", "go_biological_process": "GO:0007283 spermatogenesis;GO:0006355 regulation of DNA-templated transcription;GO:0007281 germ cell development", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "Q920G9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9DAG6-1", "uniprot_id": "GPRL1_MOUSE", "mass": 27074.0, "length": 236, "protein_name": "GLIPR1-like protein 1", "gene_name": "Glipr1l1", "organism": "Mouse", "refseq_name": "GLIPR1-like protein 1 precursor", "refseq_ac": "NP_081294", "gene_names_uniprotkb": "Glipr1l1", "gene_names_refseq": "1700011E04Rik; Glipr1l1", "protein_names_uniprotkb": "GLIPR1-like protein 1", "protein_names_refseq": "GLIPR1-like protein 1 precursor; GLIPR1-like protein 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:69286)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "20219979;31672133", "class_list": "", "function": "Required for optimal fertilization at the stage of sperm-oocyte fusion, plays a role in optimizing acrosome function, the translocation of IZUMO1 during the acrosome reaction and the fertilization process (PubMed:20219979, PubMed:31672133). Component of epididymosomes, one type of membranous microvesicules which mediate the transfer of lipids and proteins to spermatozoa plasma membrane during epididymal maturation. Also component of the CD9-positive microvesicules found in the cauda region., [UniProtKB, UniProtKB, PubMed, PubMed]; Zona pellucida binding assays indicate that GLIPR1L1 has a role in the binding of sperm to the zona pellucida surrounding the oocyte., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 1, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0060090 molecular adaptor activity", "go_cellular_component": "GO:0005615 extracellular space;GO:0005886 plasma membrane;GO:0045121 membrane raft;GO:0001669 acrosomal vesicle;GO:0002081 outer acrosomal membrane", "go_biological_process": "GO:0007339 binding of sperm to zona pellucida;GO:0007342 fusion of sperm to egg plasma membrane involved in single fertilization;GO:0060476 protein localization involved in acrosome reaction", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "Q9DAG6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P30115-1", "uniprot_id": "GSTA3_MOUSE", "mass": 25361.0, "length": 221, "protein_name": "Glutathione S-transferase A3", "gene_name": "Gsta3", "organism": "Mouse", "refseq_name": "glutathione S-transferase A3 isoform a", "refseq_ac": "NP_001070821", "gene_names_uniprotkb": "Gsta3; Gstyc", "gene_names_refseq": "Gst2-3; Gsta3", "protein_names_uniprotkb": "Glutathione S-transferase A3; 2.5.1.18; GST class-alpha member 3; Glutathione S-transferase Ya3; Glutathione S-transferase Yc", "protein_names_refseq": "GST class-alpha member 3; glutathione S-transferase A3 isoform a; glutathione S-transferase A3; glutathione S-transferase Ya3; glutathione S-transferase Yc", "tax_id": 10090, "disease": "ovarian cancer (Disease Ontology:DOID:2394); asthma (Disease Ontology:DOID:2841)", "pathway": " (mmu:14859); (R-MMU-156590); (R-MMU-189483); (R-MMU-9748787)", "pathway_count": 4, "publication_count": 12, "publication_id_list": "1637297;1728405;2049074;21750661;23806337;28535182;29804515;30084848;34428180;35820727;37453647;8605288", "class_list": "", "function": "Aflatoxin B1 induces cholangiocarcinomas in GSTA3-/- mice, [RefSeq, PubMed]; Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. Catalyzes isomerization reactions that contribute to the biosynthesis of steroid hormones. Efficiently catalyze obligatory double-bond isomerizations of delta(5)-androstene-3,17-dione and delta(5)-pregnene-3,20-dione, precursors to testosterone and progesterone, respectively (By similarity). Has a high catalytic activity for aflatoxin B1-8,9 epoxide (PubMed:1637297)., [UniProtKB, PubMed, UniProtKB]; There were no significant compensatory changes in KO mice GST subunits, GST enzymatic activity, epoxide hydrolase, or CYP1A2 and CYP3A11 levels. Finally, there was a modest increase in F2-isoprostane and isofuran in KO mice that confirmed putative GSTA3 hydroperoxidase activity in vivo for the first time., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q544Y6", "ec_number_list": "1.11.1.-;4.4.1.20;2.5.1.18;1.20.4.2;1.8.5.1;5.3.3.-;1.1.1.270;1.1.1.145;5.3.3.1;1.1.1.210;5.3.99.2;5.2.1.2", "go_molecular_function": "GO:0004364 glutathione transferase activity;GO:0043295 glutathione binding;GO:0005504 fatty acid binding;GO:0004769 steroid Delta-isomerase activity;GO:0035731 dinitrosyl-iron complex binding", "go_cellular_component": "GO:0005739 mitochondrion;GO:0005829 cytosol", "go_biological_process": "GO:0046223 aflatoxin catabolic process;GO:0006629 lipid metabolic process;GO:0006805 xenobiotic metabolic process;GO:0001657 ureteric bud development;GO:0006749 glutathione metabolic process", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "P30115-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P13707-1", "uniprot_id": "GPDA_MOUSE", "mass": 37573.0, "length": 349, "protein_name": "Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic", "gene_name": "Gpd1", "organism": "Mouse", "refseq_name": "glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic", "refseq_ac": "NP_034401", "gene_names_uniprotkb": "Gpd1; Gdc-1; Gdc1; Kiaa4010", "gene_names_refseq": "GPD-C; GPDH-C; Gdc-1; Gdc1; Gpd1", "protein_names_uniprotkb": "Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic; 1.1.1.8; GPD-C; GPDH-C", "protein_names_refseq": "glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic; glycerolphosphate dehydrogenase 1, cytoplasmic adult", "tax_id": 10090, "disease": "", "pathway": " (mmu:14555); (R-MMU-1483166)", "pathway_count": 2, "publication_count": 16, "publication_id_list": "21750661;22645316;23806337;25428506;30084848;3015943;3027100;30779550;31599954;32662756;34428180;36632231;37453647;37507081;3755721;39927985", "class_list": "", "function": "Has glycerol-3-phosphate dehydrogenase activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Non-bioenergetic roles of mitochondrial GPD2 promote tumor progression. Publication Status: Online-Only, [RefSeq, PubMed]; The enhancement of fat oxidation during the active phase and suppression of body weight gain in glycerol-3-phosphate dehydrogenase 1 deficient mice., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3UVM3;Q5DTS5", "ec_number_list": "1.1.1.8", "go_molecular_function": "GO:0004368 glycerol-3-phosphate dehydrogenase (quinone) activity;GO:0042803 protein homodimerization activity;GO:0051287 NAD binding;GO:0047952 glycerol-3-phosphate dehydrogenase [NAD(P)+] activity;GO:0141152 glycerol-3-phosphate dehydrogenase (NAD+) activity", "go_cellular_component": "GO:0005739 mitochondrion;GO:0005829 cytosol;GO:0005737 cytoplasm", "go_biological_process": "GO:0006127 glycerol-3-phosphate shuttle;GO:0071320 cellular response to cAMP;GO:0006094 gluconeogenesis;GO:0045821 positive regulation of glycolytic process;GO:0071356 cellular response to tumor necrosis factor", "synthesized_glycan_count": 0, "hit_score": 1.9, "record_id": "P13707-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P35802-1", "uniprot_id": "GPM6A_MOUSE", "mass": 31149.0, "length": 278, "protein_name": "Neuronal membrane glycoprotein M6-a", "gene_name": "Gpm6a", "organism": "Mouse", "refseq_name": "neuronal membrane glycoprotein M6-a isoform 2", "refseq_ac": "NP_001240683", "gene_names_uniprotkb": "Gpm6a; M6a", "gene_names_refseq": "Gpm6a; Gpm6; M6A", "protein_names_uniprotkb": "Neuronal membrane glycoprotein M6-a; M6a", "protein_names_refseq": "neuronal membrane glycoprotein M6-a isoform 2; neuronal membrane glycoprotein M6-a", "tax_id": 10090, "disease": "intellectual disability (Disease Ontology:DOID:1059); depressive disorder (Disease Ontology:DOID:1596)", "pathway": " (mmu:234267)", "pathway_count": 1, "publication_count": 12, "publication_id_list": "10.1101/2023.09.13.557529;18522499;18776950;21183079;21714103;22162747;25242528;33300544;36877222;37269288;37354721;8398137", "class_list": "", "function": "Involved in neuronal differentiation, including differentiation and migration of neuronal stem cells. Plays a role in neuronal plasticity and is involved in neurite and filopodia outgrowth, filopodia motility and probably synapse formation. Gpm6a-induced filopodia formation involves mitogen-activated protein kinase (MAPK) and Src signaling pathways. Conflictingly, PubMed:22162747 reports that induced cellular protrusions are simple membrane-wrapped tubules without actin or tubulin-based cytoskeletons and with Gpm6a gliding along membrane edges indicative for a function in actin-independent membrane deformation. May be involved in neuronal NGF-dependent Ca(2+) influx. May be involved in regulation of endocytosis and intracellular trafficking of G protein-coupled receptors (GPCRs); enhances internalization and recycling of mu-type opioid receptor., [UniProtKB, PubMed, PubMed, PubMed]; Mettl14-mediated m[6]A modification ensures the cell-cycle progression of late-born retinal progenitor cells., [RefSeq, PubMed]; SILENCING M 6 A READER YTHDC1 REDUCES INFLAMMATORY RESPONSE IN SEPSIS-INDUCED CARDIOMYOPATHY BY INHIBITING SERPINA3N EXPRESSION., [RefSeq, PubMed]; Sperm Rhoa m6A modification mediates intergenerational transmission of paternally acquired hippocampal neuronal senescence and cognitive deficits after combined exposure to environmental cadmium and high-fat diet in mice., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 1, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 1, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 2, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005262 calcium channel activity", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0048787 presynaptic active zone membrane;GO:0005886 plasma membrane;GO:0043025 neuronal cell body;GO:0043197 dendritic spine", "go_biological_process": "GO:0003407 neural retina development;GO:0031175 neuron projection development;GO:0048863 stem cell differentiation;GO:0001764 neuron migration;GO:0048812 neuron projection morphogenesis", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "P35802-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3UN16-1", "uniprot_id": "GP162_MOUSE", "mass": 64148.0, "length": 588, "protein_name": "Probable G protein-coupled receptor 162", "gene_name": "Gpr162", "organism": "Mouse", "refseq_name": "probable G-protein coupled receptor 162 isoform a", "refseq_ac": "NP_038561", "gene_names_uniprotkb": "Gpr162", "gene_names_refseq": "A-2; Gpr162; Grca", "protein_names_uniprotkb": "Probable G protein-coupled receptor 162", "protein_names_refseq": "gene rich cluster, A; probable G-protein coupled receptor 162 isoform a; probable G-protein coupled receptor 162", "tax_id": 10090, "disease": "", "pathway": " (mmu:14788)", "pathway_count": 1, "publication_count": 4, "publication_id_list": "10.1101/2023.09.13.557529;21183079;25275856;9445485", "class_list": "", "function": "GPR162 is widely expressed in GABAergic as well as other neurons within the mouse hippocampus, whereas extensive expression is observed in areas related to energy homeostasis and hedonic feeding such as hypothalamus, amygdala and ventral tegmental area, [RefSeq, PubMed]; Orphan receptor., [UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 1, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "O88835", "ec_number_list": "", "go_molecular_function": "GO:0004930 G protein-coupled receptor activity", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.7, "record_id": "Q3UN16-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9DC51-1", "uniprot_id": "GNAI3_MOUSE", "mass": 40538.0, "length": 354, "protein_name": "Guanine nucleotide-binding protein G(i) subunit alpha-3", "gene_name": "Gnai3", "organism": "Mouse", "refseq_name": "guanine nucleotide-binding protein G(i) subunit alpha-3", "refseq_ac": "NP_034436", "gene_names_uniprotkb": "Gnai3", "gene_names_refseq": "Galphai3; Gnai-3; Gnai3; Hg1a", "protein_names_uniprotkb": "Guanine nucleotide-binding protein G(i) subunit alpha-3; G(i) alpha-3", "protein_names_refseq": "g(i) alpha-3; guanine nucleotide binding protein (G protein), alpha inhibiting 3; guanine nucleotide binding protein, alpha inhibiting 3; guanine nucleotide-binding protein G(i) subunit alpha-3; guanine nucleotide-binding protein G(i) subunit alpha; guanine nucleotide-binding protein G(k) subunit alpha; heterotrimeric guanine nucleotide-binding protein 1a", "tax_id": 10090, "disease": "hypertension (Disease Ontology:DOID:10763); McCune Albright syndrome (Disease Ontology:DOID:1858)", "pathway": " (mmu:14679); (R-MMU-170670); (R-MMU-392170); (R-MMU-418594); (R-MMU-9009391)", "pathway_count": 5, "publication_count": 7, "publication_id_list": "16009138;22645316;28528544;34428180;35820727;36210013;8858601", "class_list": "", "function": "Heterotrimeric guanine nucleotide-binding proteins (G proteins) function as transducers downstream of G protein-coupled receptors (GPCRs) in numerous signaling cascades. The alpha chain contains the guanine nucleotide binding site and alternates between an active, GTP-bound state and an inactive, GDP-bound state. Signaling by an activated GPCR promotes GDP release and GTP binding. The alpha subunit has a low GTPase activity that converts bound GTP to GDP, thereby terminating the signal (By similarity). Both GDP release and GTP hydrolysis are modulated by numerous regulatory proteins (By similarity). Signaling is mediated via effector proteins, such as adenylate cyclase. Inhibits adenylate cyclase activity, leading to decreased intracellular cAMP levels (By similarity). Stimulates the activity of receptor-regulated K(+) channels (By similarity). The active GTP-bound form prevents the association of RGS14 with centrosomes and is required for the translocation of RGS14 from the cytoplasm to the plasma membrane. May play a role in cell division (By similarity). The active GTP-bound form activates the calcium permeant TRPC5 ion channels (By similarity)., [UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "A2AE36;Q3TGV1;Q61019", "ec_number_list": "", "go_molecular_function": "GO:0031821 G protein-coupled serotonin receptor binding;GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0019904 protein domain specific binding;GO:0046872 metal ion binding", "go_cellular_component": "GO:0042588 zymogen granule;GO:0000139 Golgi membrane;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm", "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007193 adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway;GO:0032930 positive regulation of superoxide anion generation;GO:0051301 cell division;GO:0007188 adenylate cyclase-modulating G protein-coupled receptor signaling pathway", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q9DC51-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P40936-1", "uniprot_id": "INMT_MOUSE", "mass": 29460.0, "length": 264, "protein_name": "Indolethylamine N-methyltransferase", "gene_name": "Inmt", "organism": "Mouse", "refseq_name": "indolethylamine N-methyltransferase", "refseq_ac": "NP_033375", "gene_names_uniprotkb": "Inmt; Temt", "gene_names_refseq": "Inmt; Temt", "protein_names_uniprotkb": "Indolethylamine N-methyltransferase; 2.1.1.49; 2.1.1.96; Amine N-methyltransferase; Aromatic alkylamine N-methyltransferase; Arylamine N-methyltransferase; Indolamine N-methyltransferase; TEMT; Thioether S-methyltransferase", "protein_names_refseq": "amine N-methyltransferase; aromatic alkylamine N-methyltransferase; arylamine N-methyltransferase; indolamine N-methyltransferase; indolethylamine N-methyltransferase; nicotine N-methyltransferase; thioether S-methyltransferase", "tax_id": 10090, "disease": "", "pathway": " (mmu:21743)", "pathway_count": 1, "publication_count": 7, "publication_id_list": "23806337;30084848;3350800;34428180;37453647;37507081;7819283", "class_list": "", "function": "Catalyzes the N-methylation of tryptamine and structurally related compounds (By similarity). Functions as a thioether S-methyltransferase and is active with a variety of thioethers and the corresponding selenium and tellurium compounds, including 3-methylthiopropionaldehyde, dimethyl selenide, dimethyl telluride, 2-methylthioethylamine, 2-methylthioethanol, methyl-n-propyl sulfide and diethyl sulfide. Plays an important role in the detoxification of selenium compounds., [UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q9CZ50", "ec_number_list": "2.1.1.49;2.1.1.96", "go_molecular_function": "GO:0004790 thioether S-methyltransferase activity;GO:0030748 amine N-methyltransferase activity;GO:0008170 N-methyltransferase activity;GO:0098615 dimethyl selenide methyltransferase activity", "go_cellular_component": "GO:0005829 cytosol", "go_biological_process": "GO:0009636 response to toxic substance;GO:0009308 amine metabolic process;GO:0032259 methylation", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "P40936-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9EQ14-1", "uniprot_id": "IL23A_MOUSE", "mass": 22071.0, "length": 196, "protein_name": "Interleukin-23 subunit alpha", "gene_name": "Il23a", "organism": "Mouse", "refseq_name": "interleukin-23 subunit alpha precursor", "refseq_ac": "NP_112542", "gene_names_uniprotkb": "Il23a", "gene_names_refseq": "IL-23; Il23a; p19", "protein_names_uniprotkb": "Interleukin-23 subunit alpha; IL-23 subunit alpha; IL-23-A; IL-23p19; Interleukin-23 subunit p19", "protein_names_refseq": "IL-23 subunit alpha; IL-23-A; IL-23p19; interleukin-23 subunit alpha precursor; interleukin-23 subunit alpha; interleukin-23 subunit p19", "tax_id": 10090, "disease": "asthma (Disease Ontology:DOID:2841)", "pathway": " (mmu:83430); (R-MMU-9020933)", "pathway_count": 2, "publication_count": 18, "publication_id_list": "11114383;11390512;11801672;12162874;12417590;12610626;12847224;14568135;14662908;14978083;16157683;16339539;16648837;16670770;16688182;19900478;39072698;39107827", "class_list": "", "function": "Associates with IL12B to form the pro-inflammatory cytokine IL-23 that plays different roles in innate and adaptive immunity (PubMed:11114383, PubMed:11390512, PubMed:16670770). Released by antigen-presenting cells such as dendritic cells or macrophages, binds to a heterodimeric receptor complex composed of IL12RB1 and IL23R to activate JAK2 and TYK2 which then phosphorylate the receptor to form a docking site leading to the phosphorylation of STAT3 and STAT4 (By similarity). This process leads to activation of several pathways including p38 MAPK or NF-kappa-B and promotes the production of pro-inflammatory cytokines such as interleukin-17A/IL17A (PubMed:19900478). In turn, participates in the early and effective intracellular bacterial clearance (PubMed:16157683). Promotes the expansion and survival of T-helper 17 cells, a CD4-positive helper T-cell subset that produces IL-17, as well as other IL-17-producing cells (PubMed:16648837)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, UniProtKB, PubMed, PubMed, PubMed]; Renal IL-23-Dependent Type 3 Innate Lymphoid Cells Link Crystal-induced Intrarenal Inflammasome Activation with Kidney Fibrosis., [RefSeq, PubMed]; The mode of action of IL-23 in experimental inflammatory arthritic pain and disease. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0045519 interleukin-23 receptor binding;GO:0005125 cytokine activity", "go_cellular_component": "GO:0070743 interleukin-23 complex;GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0005886 plasma membrane;GO:0072536 interleukin-23 receptor complex", "go_biological_process": "GO:0051142 positive regulation of NK T cell proliferation;GO:0032693 negative regulation of interleukin-10 production;GO:0032740 positive regulation of interleukin-17 production;GO:0051135 positive regulation of NK T cell activation;GO:0006954 inflammatory response", "synthesized_glycan_count": 0, "hit_score": 1.9, "record_id": "Q9EQ14-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9WU62-1", "uniprot_id": "INCE_MOUSE", "mass": 101209.0, "length": 880, "protein_name": "Inner centromere protein", "gene_name": "Incenp", "organism": "Mouse", "refseq_name": "inner centromere protein isoform 2", "refseq_ac": "NP_057901", "gene_names_uniprotkb": "Incenp", "gene_names_refseq": "2700067E22Rik; C130081E20; Incenp", "protein_names_uniprotkb": "Inner centromere protein", "protein_names_refseq": "inner centromere protein isoform 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:16319); (R-MMU-141430); (R-MMU-141444); (R-MMU-2467813); (R-MMU-2500257); (R-MMU-4615885); (R-MMU-5663220); (R-MMU-68877); (R-MMU-9648025)", "pathway_count": 9, "publication_count": 14, "publication_id_list": "10087305;12584241;12660166;14722118;17242355;19144319;20571061;21183079;21750661;25428506;30084848;30779550;31219806;34428180", "class_list": "", "function": "Component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. Acts as a scaffold regulating CPC localization and activity. The C-terminus associates with AURKB or AURKC, the N-terminus associated with BIRC5/survivin and CDCA8/borealin tethers the CPC to the inner centromere, and the microtubule binding activity within the central SAH domain directs AURKB/C toward substrates near microtubules. The flexibility of the SAH domain is proposed to allow AURKB/C to follow substrates on dynamic microtubules while ensuring CPC docking to static chromatin (By similarity). Activates AURKB and AURKC. Controls the kinetochore localization of BUB1., [UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 1, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 30, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 8752, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q7TN28;Q8BGN4;Q8CGI4", "ec_number_list": "", "go_molecular_function": "GO:0140677 molecular function activator activity", "go_cellular_component": "GO:0000801 central element;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005819 spindle;GO:0005829 cytosol", "go_biological_process": "GO:0051310 metaphase chromosome alignment;GO:0000278 mitotic cell cycle;GO:0001934 positive regulation of protein phosphorylation;GO:0007059 chromosome segregation;GO:0000281 mitotic cytokinesis", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "Q9WU62-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P33173-1", "uniprot_id": "KIF1A_MOUSE", "mass": 191725.0, "length": 1695, "protein_name": "Kinesin-like protein KIF1A", "gene_name": "Kif1a", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Kif1a; Atsv; Kif1", "gene_names_refseq": "", "protein_names_uniprotkb": "Kinesin-like protein KIF1A; 5.6.1.3; Axonal transporter of synaptic vesicles", "protein_names_refseq": "", "tax_id": 10090, "disease": "hereditary sensory and autonomic neuropathy (Disease Ontology:DOID:0050548); synucleinopathy (Disease Ontology:DOID:0050890); NESCAV syndrome (Disease Ontology:DOID:0070039); hereditary sensory neuropathy type 2C (Disease Ontology:DOID:0070147); hereditary spastic paraplegia 30B (Disease Ontology:DOID:0070646); hereditary spastic paraplegia 30A (Disease Ontology:DOID:0070647); Graves ophthalmopathy (Disease Ontology:DOID:0081120); hereditary spastic paraplegia 30 (Disease Ontology:DOID:0110781); hereditary spastic paraplegia (Disease Ontology:DOID:2476); nervous system disease (Disease Ontology:DOID:863)", "pathway": " (mmu:16560); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 3, "publication_count": 17, "publication_id_list": "10.1101/2023.09.13.557529;11373668;12891363;1447303;15286375;18322192;18806800;18849981;21183079;21750661;30084848;30808661;30899004;31219806;33300544;35132656;7539720", "class_list": "", "function": "Kinesin motor with a plus-end-directed microtubule motor activity, required for anterograde axonal transport of synaptic vesicle precursors (PubMed:12891363, PubMed:7539720). Also required for neuronal dense core vesicles (DCVs) transport to the dendritic spines and axons. The interaction calcium-dependent with CALM1 increases vesicle motility and interaction with the scaffolding proteins PPFIA2 and TANC2 recruits DCVs to synaptic sites (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 3, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 3, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 3, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 14, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 4, "disease_count": 10, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "Q61770", "ec_number_list": "3.6.5.-;3.6.4.-;5.6.1.3;3.6.5.2", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0042802 identical protein binding;GO:0046872 metal ion binding;GO:0016887 ATP hydrolysis activity", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0098992 neuronal dense core vesicle;GO:0005737 cytoplasm;GO:0005874 microtubule;GO:0030424 axon", "go_biological_process": "GO:0098840 protein transport along microtubule;GO:0016192 vesicle-mediated transport;GO:0008089 anterograde axonal transport;GO:0048490 anterograde synaptic vesicle transport;GO:0060998 regulation of dendritic spine development", "synthesized_glycan_count": 0, "hit_score": 2.6, "record_id": "P33173-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3UM83-1", "uniprot_id": "KLRG2_MOUSE", "mass": 41831.0, "length": 387, "protein_name": "Killer cell lectin-like receptor subfamily G member 2", "gene_name": "Klrg2", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Klrg2", "gene_names_refseq": "", "protein_names_uniprotkb": "Killer cell lectin-like receptor subfamily G member 2", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": " (mmu:74253)", "pathway_count": 1, "publication_count": 3, "publication_id_list": "21183079;21750661;35820727", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3TE30", "ec_number_list": "", "go_molecular_function": "GO:0030246 carbohydrate binding", "go_cellular_component": "GO:0016020 membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.4, "record_id": "Q3UM83-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6IE82-1", "uniprot_id": "JADE3_MOUSE", "mass": 93455.0, "length": 823, "protein_name": "Protein Jade-3", "gene_name": "Jade3", "organism": "Mouse", "refseq_name": "protein Jade-3 isoform 1", "refseq_ac": "NP_001393170", "gene_names_uniprotkb": "Jade3; Kiaa0215; Phf16", "gene_names_refseq": "5730598B06; Jade3; Phf16; mKIAA0215", "protein_names_uniprotkb": "Protein Jade-3; Jade family PHD finger protein 3; PHD finger protein 16", "protein_names_refseq": "PHD finger protein 16; jade family PHD finger protein 3; protein Jade-3 isoform 1; protein Jade-3", "tax_id": 10090, "disease": "", "pathway": " (mmu:382207); (R-MMU-3214847)", "pathway_count": 2, "publication_count": 7, "publication_id_list": "14612400;21183079;21750661;23806337;30272815;34428180;39627609", "class_list": "", "function": "Scaffold subunit of some HBO1 complexes, which have a histone H4 acetyltransferase activity., [UniProtKB, UniProtKB]; These data showed previously uncovered roles of Phf16 and Pnpla3 in adipogenesis, highlighting the potential of using phytochemicals for further investigation of adipocyte biology., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 5, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "A1L3T5;Q6ZQG2", "ec_number_list": "", "go_molecular_function": "GO:0008270 zinc ion binding;GO:0140566 histone reader activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0000123 histone acetyltransferase complex", "go_biological_process": "GO:2000278 regulation of DNA biosynthetic process;GO:0006338 chromatin remodeling;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription;GO:0001558 regulation of cell growth", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "Q6IE82-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9D2Z8-1", "uniprot_id": "KIF12_MOUSE", "mass": 70706.0, "length": 642, "protein_name": "Kinesin-like protein KIF12", "gene_name": "Kif12", "organism": "Mouse", "refseq_name": "kinesin-like protein KIF12 isoform 2", "refseq_ac": "NP_034746", "gene_names_uniprotkb": "Kif12", "gene_names_refseq": "Kif12", "protein_names_uniprotkb": "Kinesin-like protein KIF12", "protein_names_refseq": "N-9 kinesin; kinesin 12; kinesin superfamily protein 12; kinesin-like protein KIF12 isoform 2; kinesin-like protein KIF12", "tax_id": 10090, "disease": "progressive familial intrahepatic cholestasis (Disease Ontology:DOID:0070221); metabolic dysfunction-associated steatohepatitis (Disease Ontology:DOID:0080547)", "pathway": " (mmu:16552); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 3, "publication_count": 9, "publication_id_list": "15728779;21183079;21750661;26295839;30084848;30250217;37828378;39920308;9275178", "class_list": "", "function": "Involved in the negative regulation of fatty acid biosynthesis, probably acting as an adapter that allows ubiquitination of acetyl-CoA carboxylase 1 (ACACA) by E3 ubiquitin-protein ligase COP1, and promotes ACACA degradation. The adapter function requires the C-terminal proline-rich domain and may be apart from the kinesin motor activity., [UniProtKB, UniProtKB, UniProtKB, PubMed]; Kif12 is a candidate gene within the major polycystic kidney disease modifier 2 locus that modulates renal cystic disease severity in the Cys1cpk mouse. Publication Status: Online-Only, [RefSeq, PubMed]; Positional candidate gene, Kif12, fulfills the major criteria for quantitative trait loci gene discovery established by the Complex Trait Consortium, and, thus, it is proposed that Kif12 is a cpk modifier gene., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 3, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "O35061", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0003777 microtubule motor activity;GO:1990756 ubiquitin-like ligase-substrate adaptor activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005874 microtubule;GO:0005929 cilium;GO:0070062 extracellular exosome;GO:0005871 kinesin complex", "go_biological_process": "GO:0045717 negative regulation of fatty acid biosynthetic process;GO:0007018 microtubule-based movement;GO:0006511 ubiquitin-dependent protein catabolic process", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "Q9D2Z8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9EQW7-1", "uniprot_id": "KI13A_MOUSE", "mass": 195813.0, "length": 1749, "protein_name": "Kinesin-like protein KIF13A", "gene_name": "Kif13a", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Kif13a", "gene_names_refseq": "", "protein_names_uniprotkb": "Kinesin-like protein KIF13A", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": " (mmu:16553)", "pathway_count": 1, "publication_count": 10, "publication_id_list": "11106728;11374900;17242355;21183079;21750661;26680000;30084848;32152506;34428180;9275178", "class_list": "", "function": "Plus end-directed microtubule-dependent motor protein involved in intracellular transport and regulating various processes such as mannose-6-phosphate receptor (M6PR) transport to the plasma membrane, endosomal sorting during melanosome biogenesis and cytokinesis. During melanosome maturation, required for delivering melanogenic enzymes from recycling endosomes to nascent melanosomes by creating peripheral recycling endosomal subdomains in melanocytes. Also required for the abscission step in cytokinesis: mediates translocation of ZFYVE26, and possibly TTC19, to the midbody during cytokinesis (By similarity). Mediates the transport of M6PR-containing vesicles from trans-Golgi network to the plasma membrane via direct interaction with the AP-1 complex., [UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 8, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "O35062", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0003777 microtubule motor activity", "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005874 microtubule;GO:0032588 trans-Golgi network membrane", "go_biological_process": "GO:0006886 intracellular protein transport;GO:0051301 cell division;GO:0008333 endosome to lysosome transport;GO:0007018 microtubule-based movement;GO:0032438 melanosome organization", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q9EQW7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A2A9F4-1", "uniprot_id": "KDF1_MOUSE", "mass": 43496.0, "length": 397, "protein_name": "Keratinocyte differentiation factor 1", "gene_name": "Kdf1", "organism": "Mouse", "refseq_name": "keratinocyte differentiation factor 1", "refseq_ac": "NP_001077385", "gene_names_uniprotkb": "Kdf1; 1810019J16Rik", "gene_names_refseq": "1810019J16Rik; Kdf1", "protein_names_uniprotkb": "Keratinocyte differentiation factor 1", "protein_names_refseq": "keratinocyte differentiation factor 1", "tax_id": 10090, "disease": "ectodermal dysplasia 12 (Disease Ontology:DOID:0111652)", "pathway": " (mmu:69073)", "pathway_count": 1, "publication_count": 4, "publication_id_list": "21183079;21750661;24075906;32239614", "class_list": "", "function": "Plays a role in the regulation of the epidermis formation during early development. Required both as an inhibitor of basal cell proliferation and a promoter of differentiation of basal progenitor cell progeny., [UniProtKB, PubMed]; Regulation of epidermal differentiation through KDF1-mediated deubiquitination of IKKalpha., [RefSeq, PubMed]; The Keratinocyte differentiation factor 1 is an essential regulator of the proliferation-differentiation balance in epidermal progenitor cells., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q8C1Q5", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005938 cell cortex;GO:0030054 cell junction;GO:0031252 cell leading edge;GO:0070161 anchoring junction", "go_biological_process": "GO:0009913 epidermal cell differentiation;GO:0060887 limb epidermis development;GO:2000647 negative regulation of stem cell proliferation;GO:0016579 protein deubiquitination;GO:0061436 establishment of skin barrier", "synthesized_glycan_count": 0, "hit_score": 0.5, "record_id": "A2A9F4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A2CG49-1", "uniprot_id": "KALRN_MOUSE", "mass": 337000.0, "length": 2964, "protein_name": "Kalirin", "gene_name": "Kalrn", "organism": "Mouse", "refseq_name": "kalirin isoform 2", "refseq_ac": "NP_001157740", "gene_names_uniprotkb": "Kalrn", "gene_names_refseq": "2210407G14Rik; DUET; E530005C20Rik; Gm539; Hapip; Kalrn; TRAD", "protein_names_uniprotkb": "Kalirin; 2.7.11.1; Protein Duo; Serine/threonine-protein kinase with Dbl- and pleckstrin homology domain", "protein_names_refseq": "huntingtin-associated protein interacting protein (duo); kalirin isoform 2; protein Duo; serine/threonine kinase with Dbl- and pleckstrin homology domains; serine/threonine-protein kinase with Dbl- and pleckstrin homology domain", "tax_id": 10090, "disease": "cerebral atherosclerosis (Disease Ontology:DOID:12720); epilepsy (Disease Ontology:DOID:1826); coronary artery disease (Disease Ontology:DOID:3393); cerebral infarction (Disease Ontology:DOID:3526)", "pathway": " (mmu:545156); (R-MMU-193648); (R-MMU-3928662); (R-MMU-416476); (R-MMU-416482); (R-MMU-5687128); (R-MMU-8980692); (R-MMU-9013149); (R-MMU-9013408)", "pathway_count": 9, "publication_count": 10, "publication_id_list": "10.1101/2023.09.13.557529;17242355;19625617;19800004;21183079;21750661;33300544;34428180;35716086;35820727", "class_list": "", "function": "Kalirin mediates Rac1 activation downstream of calcium/calmodulin-dependent protein kinase II to stimulate glucose uptake during muscle contraction., [RefSeq, PubMed]; Kalirin regulates cortical spine morphogenesis and disease-related behavioral phenotypes. Erratum:[Proc Natl Acad Sci U S A. 2009 Sep 29;106(39):16890. Photowala, Huzefa [added]], [RefSeq, PubMed]; Promotes the exchange of GDP by GTP. Activates specific Rho GTPase family members, thereby inducing various signaling mechanisms that regulate neuronal shape, growth, and plasticity, through their effects on the actin cytoskeleton. Induces lamellipodia independent of its GEF activity (By similarity)., [UniProtKB, UniProtKB]; These data demonstrate important roles for kalirin in the regulation of cortical structure, ultrastructure, and spine structural plasticity., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 8, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 3, "disease_count": 4, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "A2CG50;A2CG51;A2CG52;A2CG53;B2RXR5;D3Z559;Q3TXY8;Q3TYL1;Q3UTA5;Q8BTT9;Q8C4Q2;Q9CVA9", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;3.6.5.-;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;2.7.10.1;3.6.5.2;2.7.11.39;2.3.1.-;2.7.11.31;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0019899 enzyme binding;GO:0046872 metal ion binding;GO:0005085 guanyl-nucleotide exchange factor activity", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005856 cytoskeleton", "go_biological_process": "GO:0046959 habituation;GO:0060125 negative regulation of growth hormone secretion;GO:0007399 nervous system development;GO:0007409 axonogenesis;GO:0007528 neuromuscular junction development", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "A2CG49-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O88448-1", "uniprot_id": "KLC2_MOUSE", "mass": 66662.0, "length": 599, "protein_name": "Kinesin light chain 2", "gene_name": "Klc2", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Klc2", "gene_names_refseq": "", "protein_names_uniprotkb": "Kinesin light chain 2; KLC 2", "protein_names_refseq": "", "tax_id": 10090, "disease": "nonsyndromic deafness (Disease Ontology:DOID:0050563); SPOAN syndrome (Disease Ontology:DOID:0060491); Alzheimer's disease 1 (Disease Ontology:DOID:0080348)", "pathway": " (R-MMU-2132295); (R-MMU-5625970); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 4, "publication_count": 7, "publication_id_list": "19131326;21183079;21750661;30973865;31219806;34428180;9624122", "class_list": "", "function": "Kinesin is a microtubule-associated force-producing protein that play a role in organelle transport., [UniProtKB, UniProtKB]; Kinesin is a microtubule-associated force-producing protein that plays a role in organelle transport. The light chain functions in coupling of cargo to the heavy chain or in the modulation of its ATPase activity. Through binding with PLEKHM2 and ARL8B, recruits kinesin-1 to lysosomes and hence direct lysosomes movement toward microtubule plus ends., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 8, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 3, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0019894 kinesin binding", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005829 cytosol;GO:0005874 microtubule", "go_biological_process": "GO:0008088 axo-dendritic transport;GO:0007018 microtubule-based movement;GO:0032418 lysosome localization", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "O88448-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3TES0-1", "uniprot_id": "IQEC3_MOUSE", "mass": 129119.0, "length": 1195, "protein_name": "IQ motif and SEC7 domain-containing protein 3", "gene_name": "Iqsec3", "organism": "Mouse", "refseq_name": "IQ motif and SEC7 domain-containing protein 3 isoform 1", "refseq_ac": "NP_001028526", "gene_names_uniprotkb": "Iqsec3; Kiaa1110", "gene_names_refseq": "BRAG3; Iqsec3; mKIAA1110; synarfGEF", "protein_names_uniprotkb": "IQ motif and SEC7 domain-containing protein 3", "protein_names_refseq": "IQ motif and SEC7 domain-containing protein 3 isoform 1; IQ motif and SEC7 domain-containing protein 3", "tax_id": 10090, "disease": "", "pathway": " (mmu:243621)", "pathway_count": 1, "publication_count": 8, "publication_id_list": "17981261;21183079;21750661;22886754;27609886;32049026;34289353;35820727", "class_list": "", "function": "Acts as a guanine nucleotide exchange factor (GEF) for ARF1., [UniProtKB, UniProtKB]; BRAG2 localized to postsynaptic processes at bipolar dyads, while BRAG3 localized to postsynaptic components at conventional synapses in mouse retina, [RefSeq, PubMed]; Loss of IQSEC3 Disrupts GABAergic Synapse Maintenance and Decreases Somatostatin Expression in the Hippocampus. Erratum:[Cell Rep. 2024 May 28;43(5):114254. doi: 10.1016/j.celrep.2024.114254. PMID: 38748876], [RefSeq, PubMed]; Npas4 regulates IQSEC3 expression in hippocampal somatostatin interneurons to mediate anxiety-like behavior., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q3UHP8;Q80TJ8", "ec_number_list": "", "go_molecular_function": "GO:0005085 guanyl-nucleotide exchange factor activity", "go_cellular_component": "GO:0098982 GABA-ergic synapse;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0014069 postsynaptic density;GO:0045211 postsynaptic membrane", "go_biological_process": "GO:0051056 regulation of small GTPase mediated signal transduction;GO:0016192 vesicle-mediated transport;GO:0090630 activation of GTPase activity;GO:0032012 regulation of ARF protein signal transduction;GO:0099173 postsynapse organization", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "Q3TES0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9WTP7-1", "uniprot_id": "KAD3_MOUSE", "mass": 25426.0, "length": 227, "protein_name": "GTP:AMP phosphotransferase AK3, mitochondrial", "gene_name": "Ak3", "organism": "Mouse", "refseq_name": "GTP:AMP phosphotransferase AK3, mitochondrial isoform 1", "refseq_ac": "NP_067274", "gene_names_uniprotkb": "Ak3", "gene_names_refseq": "AK-3; Ak3l1; Ak3l; Ak3; Akl3l", "protein_names_uniprotkb": "GTP:AMP phosphotransferase AK3, mitochondrial; 2.7.4.10; Adenylate kinase 3", "protein_names_refseq": "GTP:AMP phosphotransferase AK3, mitochondrial isoform 1; GTP:AMP phosphotransferase AK3, mitochondrial; adenylate kinase 3 alpha-like 1", "tax_id": 10090, "disease": "chronic lymphocytic leukemia (Disease Ontology:DOID:1040); hepatocellular carcinoma (Disease Ontology:DOID:684)", "pathway": " (mmu:56248); (R-MMU-983231)", "pathway_count": 2, "publication_count": 8, "publication_id_list": "21183079;21750661;23576753;23806337;34428180;36288343;37453647;37507081", "class_list": "", "function": "Mitochondrial adenylate kinase with a specific GTP:AMP phosphotransferase activity. Could also use ITP as phosphate donor. Its physiological function is to recycle GTP into GDP which is necessary for the TCA cycle in the mitochondrial matrix., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3UDN7;Q8BGX5;Q9D7Z1;Q9DB57;Q9DBM5", "ec_number_list": "2.7.4.6;2.7.4.4;2.7.4.10", "go_molecular_function": "GO:0004017 AMP kinase activity;GO:0046899 nucleoside triphosphate adenylate kinase activity;GO:0005524 ATP binding;GO:0005525 GTP binding;GO:0042802 identical protein binding", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix", "go_biological_process": "GO:0006172 ADP biosynthetic process;GO:0046033 AMP metabolic process;GO:0046041 ITP metabolic process;GO:0046051 UTP metabolic process;GO:0046060 dATP metabolic process", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q9WTP7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9JHD1-1", "uniprot_id": "KAT2B_MOUSE", "mass": 91769.0, "length": 813, "protein_name": "Histone acetyltransferase KAT2B", "gene_name": "Kat2b", "organism": "Mouse", "refseq_name": "histone acetyltransferase KAT2B isoform 1", "refseq_ac": "NP_064389", "gene_names_uniprotkb": "Kat2b; Pcaf", "gene_names_refseq": "A930006P13Rik; Kat2b; Pcaf; p/CAF", "protein_names_uniprotkb": "Histone acetyltransferase KAT2B; 2.3.1.48; 2.3.1.57; Histone acetylase PCAF; Histone acetyltransferase PCAF; Lysine acetyltransferase 2B; P/CAF; P300/CBP-associated factor; Spermidine acetyltransferase KAT2B", "protein_names_refseq": "histone acetylase PCAF; histone acetyltransferase KAT2B isoform 1; histone acetyltransferase KAT2B; histone acetyltransferase PCAF; lysine acetyltransferase 2B; p300/CBP-associated factor; spermidine acetyltransferase KAT2B", "tax_id": 10090, "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); breast cancer (Disease Ontology:DOID:1612); familial nephrotic syndrome (Disease Ontology:DOID:2590); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); hepatocellular carcinoma (Disease Ontology:DOID:684); rheumatoid arthritis (Disease Ontology:DOID:7148)", "pathway": " (mmu:18519); (R-MMU-2032785); (R-MMU-2122947); (R-MMU-350054); (R-MMU-5250924); (R-MMU-5689901); (R-MMU-8936459); (R-MMU-8941856); (R-MMU-9018519); (R-MMU-9617629); (R-MMU-9772755)", "pathway_count": 11, "publication_count": 12, "publication_id_list": "11017084;12709428;17187077;18299400;18682553;20940255;21750661;25428506;25605945;29187734;34428180;9742083", "class_list": "", "function": "Functions as a histone acetyltransferase (HAT) to promote transcriptional activation. Has significant histone acetyltransferase activity with core histones (H3 and H4), and also with nucleosome core particles. Has a a strong preference for acetylation of H3 at 'Lys-9' (H3K9ac). Also acetylates non-histone proteins, such as ACLY, MAPRE1/EB1, PLK4, RRP9/U3-55K and TBX5. Acts as a circadian transcriptional coactivator which enhances the activity of the circadian transcriptional activators: NPAS2-BMAL1 and CLOCK-BMAL1 heterodimers. Involved in heart and limb development by mediating acetylation of TBX5, acetylation regulating nucleocytoplasmic shuttling of TBX5. Acts as a negative regulator of centrosome amplification by mediating acetylation of PLK4. Acetylates RRP9/U3-55K, a core subunit of the U3 snoRNP complex, impairing pre-rRNA processing. Acetylates MAPRE1/EB1, promoting dynamic kinetochore-microtubule interactions in early mitosis. Also acetylates spermidine., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 6, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q3U142;Q640M9", "ec_number_list": "2.3.1.48;2.3.1.-;2.1.1.364;3.6.4.-;3.5.1.-;3.5.1.98;2.7.7.6;2.3.2.27;2.3.2.-;2.1.1.-;3.6.4.13;3.4.19.-;2.7.11.1;2.3.1.259;2.3.1.57;2.1.1.319;2.3.1.80;4.2.1.-;2.7.10.2", "go_molecular_function": "GO:0061733 protein-lysine-acetyltransferase activity;GO:0003682 chromatin binding;GO:0003713 transcription coactivator activity;GO:0008047 enzyme activator activity;GO:0019901 protein kinase binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol", "go_biological_process": "GO:0051315 attachment of mitotic spindle microtubules to kinetochore;GO:0090043 regulation of tubulin deacetylation;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006338 chromatin remodeling;GO:0006351 DNA-templated transcription", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "Q9JHD1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9QXL1-1", "uniprot_id": "KI21B_MOUSE", "mass": 186180.0, "length": 1668, "protein_name": "Kinesin-like protein KIF21B", "gene_name": "Kif21b", "organism": "Mouse", "refseq_name": "kinesin-like protein KIF21B", "refseq_ac": "NP_001034561", "gene_names_uniprotkb": "Kif21b; Kif6", "gene_names_refseq": "2610511N21Rik; Kif21b; mKIAA0449", "protein_names_uniprotkb": "Kinesin-like protein KIF21B; Kinesin-like protein KIF6", "protein_names_refseq": "N-5 kinesin; kinesin-like protein KIF21B; kinesin-like protein KIF6", "tax_id": 10090, "disease": "", "pathway": " (mmu:16565); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 3, "publication_count": 14, "publication_id_list": "10.1101/2023.09.13.557529;10225949;15345747;21183079;21750661;24086586;25172774;25428506;27117409;30059200;30084848;34105348;36210013;37418324", "class_list": "", "function": "Plus-end directed microtubule-dependent motor protein which displays processive activity (PubMed:10225949, PubMed:27117409). Is involved in regulation of microtubule dynamics, synapse function and neuronal morphology, including dendritic tree branching and spine formation (PubMed:27117409). Plays a role in lerning and memory (PubMed:27117409). Involved in delivery of gamma-aminobutyric acid (GABA(A)) receptor to cell surface (PubMed:25172774)., [UniProtKB, PubMed, PubMed, PubMed]; Plus-end directed microtubule-dependent motor protein which displays processive activity. Is involved in regulation of microtubule dynamics, synapse function and neuronal morphology, including dendritic tree branching and spine formation. Plays a role in lerning and memory. Involved in delivery of gamma-aminobutyric acid (GABA(A)) receptor to cell surface., [UniProtKB, UniProtKB]; TRIM3, also known as BERP, interacts with KIF21B via its RBCC domain. Publication Status: Online-Only, [RefSeq, PubMed]; The kinesin Kif21b regulates radial migration of cortical projection neurons through a non-canonical function on actin cytoskeleton., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 7, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 3, "disease_count": 0, "glyco_site_count": 5, "binding_glycan_count": 0, "secondary_ac_list": "E9PUY6;P97424", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0003777 microtubule motor activity", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005874 microtubule;GO:0030426 growth cone;GO:0005871 kinesin complex", "go_biological_process": "GO:0007420 brain development;GO:0007018 microtubule-based movement;GO:0022038 corpus callosum development;GO:0099072 regulation of postsynaptic membrane neurotransmitter receptor levels;GO:0098934 retrograde dendritic transport", "synthesized_glycan_count": 0, "hit_score": 2.2, "record_id": "Q9QXL1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "L0N7N1-1", "uniprot_id": "KIF14_MOUSE", "mass": 186445.0, "length": 1674, "protein_name": "Kinesin-like protein KIF14", "gene_name": "Kif14", "organism": "Mouse", "refseq_name": "kinesin-like protein KIF14", "refseq_ac": "NP_001274108", "gene_names_uniprotkb": "Kif14", "gene_names_refseq": "D1Ertd367e; E130203M01; Kif14", "protein_names_uniprotkb": "Kinesin-like protein KIF14", "protein_names_refseq": "N-3 kinesin; kinesin-like protein KIF14", "tax_id": 10090, "disease": "Meckel syndrome (Disease Ontology:DOID:0050778); primary autosomal recessive microcephaly 20 (Disease Ontology:DOID:0051031)", "pathway": " (mmu:381293); (R-MMU-5625900); (R-MMU-9696270); (R-MMU-9696273)", "pathway_count": 4, "publication_count": 8, "publication_id_list": "21750661;23308235;24931760;24949858;27270502;30385851;34131133;34428180", "class_list": "", "function": "Data provide the first evidence that Kif14 can promote tumor formation in susceptible cells in vivo, [RefSeq, PubMed]; Microtubule motor protein that binds to microtubules with high affinity through each tubulin heterodimer and has an ATPase activity (PubMed:24949858). Plays a role in many processes like cell division, cytokinesis and also in cell proliferation and apoptosis (By similarity). During cytokinesis, targets to central spindle and midbody through its interaction with PRC1 and CIT respectively (By similarity). Regulates cell growth through regulation of cell cycle progression and cytokinesis. During cell cycle progression acts through SCF-dependent proteasomal ubiquitin-dependent protein catabolic process which controls CDKN1B degradation, resulting in positive regulation of cyclins, including CCNE1, CCND1 and CCNB1 (By similarity). During late neurogenesis, regulates the cerebellar and cerebral cortex development and olfactory bulb development through regulation of apoptosis, cell proliferation and cell division (PubMed:23308235, PubMed:24931760). Also is required for chromosome congression and alignment during mitotic cell cycle process (By similarity). Regulates cell spreading, focal adhesion dynamics, and cell migration through its interaction with RADIL resulting in regulation of RAP1A-mediated inside-out integrin activation by tethering RADIL on microtubules (By similarity)., [UniProtKB, PubMed, PubMed, PubMed, UniProtKB]; Structural basis of mechano-chemical coupling by the mitotic kinesin KIF14. Publication Status: Online-Only, [RefSeq, PubMed]; This work reveals a novel association of Kif14 overexpression with lymphoma but suggests that Kif14 does not have as prominent a role in initiating cancer in other cell types as it does in accelerating tumour development in response to other oncogenic insults. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0019901 protein kinase binding;GO:0016887 ATP hydrolysis activity;GO:0030165 PDZ domain binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005874 microtubule;GO:0005886 plasma membrane", "go_biological_process": "GO:0021693 cerebellar Purkinje cell layer structural organization;GO:0021685 cerebellar granular layer structural organization;GO:0032487 regulation of Rap protein signal transduction;GO:0033624 negative regulation of integrin activation;GO:1903429 regulation of cell maturation", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "L0N7N1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P28652-1", "uniprot_id": "KCC2B_MOUSE", "mass": 60461.0, "length": 542, "protein_name": "Calcium/calmodulin-dependent protein kinase type II subunit beta", "gene_name": "Camk2b", "organism": "Mouse", "refseq_name": "calcium/calmodulin-dependent protein kinase type II subunit beta isoform 2", "refseq_ac": "NP_031621", "gene_names_uniprotkb": "Camk2b; Camk2d", "gene_names_refseq": "CaMKII; Camk2b", "protein_names_uniprotkb": "Calcium/calmodulin-dependent protein kinase type II subunit beta; 2.7.11.17; CaM kinase II subunit beta; CaMK-II subunit beta", "protein_names_refseq": "CaMK II; caM kinase II subunit beta; caMK-II subunit beta; calcium/calmodulin-dependent protein kinase type II subunit beta isoform 2; calcium/calmodulin-dependent protein kinase type II subunit beta", "tax_id": 10090, "disease": "autosomal dominant intellectual developmental disorder 54 (Disease Ontology:DOID:0080230); heart conduction disease (Disease Ontology:DOID:10273)", "pathway": " (mmu:12323); (R-MMU-3371571); (R-MMU-399719); (R-MMU-438066); (R-MMU-5578775); (R-MMU-5673000); (R-MMU-5673001); (R-MMU-877300); (R-MMU-936837)", "pathway_count": 9, "publication_count": 24, "publication_id_list": "10.1101/2023.09.13.557529;1321343;16452087;17114649;18034455;21183079;21750661;21752990;22517741;22645316;23805378;25990311;27244486;28657654;29100089;32848054;33300544;34678516;37977072;38769542;39927985;40021952;40885482;7730306", "class_list": "", "function": "CaMKIIbeta deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I. Publication Status: Online-Only, [RefSeq, PubMed]; Calcium/calmodulin-dependent protein kinase that functions autonomously after Ca(2+)/calmodulin-binding and autophosphorylation, and is involved in dendritic spine and synapse formation, neuronal plasticity and regulation of sarcoplasmic reticulum Ca(2+) transport in skeletal muscle. In neurons, plays an essential structural role in the reorganization of the actin cytoskeleton during plasticity by binding and bundling actin filaments in a kinase-independent manner. This structural function is required for correct targeting of CaMK2A, which acts downstream of NMDAR to promote dendritic spine and synapse formation and maintain synaptic plasticity which enables long-term potentiation (LTP) and hippocampus-dependent learning. In developing hippocampal neurons, promotes arborization of the dendritic tree and in mature neurons, promotes dendritic remodeling. Also regulates the migration of developing neurons (PubMed:29100089). Participates in the modulation of skeletal muscle function in response to exercise. In slow-twitch muscles, is involved in regulation of sarcoplasmic reticulum (SR) Ca(2+) transport and in fast-twitch muscle participates in the control of Ca(2+) release from the SR through phosphorylation of triadin, a ryanodine receptor-coupling factor, and phospholamban (PLN/PLB), an endogenous inhibitor of SERCA2A/ATP2A2 (PubMed:21752990). In response to interferon-gamma (IFN-gamma) stimulation, catalyzes phosphorylation of STAT1, stimulating the JAK-STAT signaling pathway (By similarity). Phosphorylates reticulophagy regulator RETREG1 at 'Thr-134' under endoplasmic reticulum stress conditions which enhances RETREG1 oligomerization and its membrane scission and reticulophagy activity (By similarity)., [UniProtKB, UniProtKB, UniProtKB, PubMed, PubMed]; MFG-E8 facilitates heart repair through M1/M2 polarization after myocardial infarction by inhibiting CaMKII., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 11, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 11, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 11, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 11, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 3, "disease_count": 2, "glyco_site_count": 13, "binding_glycan_count": 0, "secondary_ac_list": "Q5SVH9", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;3.2.1.31;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;7.2.2.10;2.7.11.10;2.7.11.11;2.7.10.1;2.7.11.26;2.7.11.19;2.7.11.17;3.6.5.2;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;3.1.3.48;2.3.2.27;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;2.7.11.39;2.3.1.-;2.7.11.31;3.6.5.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005516 calmodulin binding;GO:0005524 ATP binding;GO:0019901 protein kinase binding;GO:0042802 identical protein binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0014069 postsynaptic density", "go_biological_process": "GO:0002030 inhibitory G protein-coupled receptor phosphorylation;GO:0060466 activation of meiosis involved in egg activation;GO:0007399 nervous system development;GO:0010976 positive regulation of neuron projection development;GO:0030154 cell differentiation", "synthesized_glycan_count": 0, "hit_score": 4.1, "record_id": "P28652-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q60575-1", "uniprot_id": "KIF1B_MOUSE", "mass": 204081.0, "length": 1816, "protein_name": "Kinesin-like protein KIF1B", "gene_name": "Kif1b", "organism": "Mouse", "refseq_name": "kinesin-like protein KIF1B isoform c", "refseq_ac": "NP_001277924", "gene_names_uniprotkb": "Kif1b", "gene_names_refseq": "A530096N05Rik; D4Mil1e; KIF1Bp130; KIF1Bp204; Kif1b", "protein_names_uniprotkb": "Kinesin-like protein KIF1B; 5.6.1.3", "protein_names_refseq": "N-3 kinesin; kinesin heavy chain member 1B; kinesin-like protein KIF1B isoform c; kinesin-like protein KIF1B", "tax_id": 10090, "disease": "synucleinopathy (Disease Ontology:DOID:0050890); Charcot-Marie-Tooth disease type 2A1 (Disease Ontology:DOID:0110154); ovary epithelial cancer (Disease Ontology:DOID:2152); multiple sclerosis (Disease Ontology:DOID:2377); amyotrophic lateral sclerosis (Disease Ontology:DOID:332); hepatocellular carcinoma (Disease Ontology:DOID:684); neuroblastoma (Disease Ontology:DOID:769); nervous system disease (Disease Ontology:DOID:863)", "pathway": " (mmu:16561); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 3, "publication_count": 15, "publication_id_list": "10341097;10571041;11389829;17242355;18630941;18849981;21183079;21750661;25428506;28528544;30084848;30126838;34428180;35820727;7528108", "class_list": "", "function": "Has a plus-end-directed microtubule motor activity and functions as a motor for anterograde synaptic vesicle transport along axonal microtubules from the cell body to the presynapse in neuronal cells (PubMed:11389829, PubMed:18849981). Functions as a downstream effector in a developmental apoptotic pathway that is activated when nerve growth factor (NGF) becomes limiting for neuronal progenitor cells (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed]; Has a plus-end-directed microtubule motor activity and functions as a motor for anterograde transport of mitochondria., [UniProtKB, PubMed]; Has a plus-end-directed microtubule motor activity and functions as a motor for transport of vesicles and organelles along microtubules., [UniProtKB, PubMed, PubMed]; These data have supported the relevance of KIF1Bbeta in IGF1R transport, which may give new clue to the neuropathic pathogenesis., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 11, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 8, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q9R0B4;Q9WVE5;Q9Z119", "ec_number_list": "3.6.5.-;3.6.4.-;5.6.1.3;3.6.5.2", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0019900 kinase binding;GO:0097110 scaffold protein binding", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005874 microtubule;GO:0030424 axon;GO:0030425 dendrite", "go_biological_process": "GO:0009792 embryo development ending in birth or egg hatching;GO:0047497 mitochondrion transport along microtubule;GO:1990778 protein localization to cell periphery;GO:0007274 neuromuscular synaptic transmission;GO:0010628 positive regulation of gene expression", "synthesized_glycan_count": 0, "hit_score": 1.8, "record_id": "Q60575-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6NWW5-1", "uniprot_id": "KIF24_MOUSE", "mass": 150207.0, "length": 1356, "protein_name": "Kinesin-like protein KIF24", "gene_name": "Kif24", "organism": "Mouse", "refseq_name": "kinesin-like protein KIF24", "refseq_ac": "NP_077203", "gene_names_uniprotkb": "Kif24", "gene_names_refseq": "4933425J19Rik; 9430029L23Rik; Kif24", "protein_names_uniprotkb": "Kinesin-like protein KIF24", "protein_names_refseq": "kinesin-like protein KIF24", "tax_id": 10090, "disease": "", "pathway": " (mmu:109242); (R-MMU-5620912)", "pathway_count": 2, "publication_count": 5, "publication_id_list": "11416179;21183079;21750661;31219806;40021952", "class_list": "", "function": "Microtubule-dependent motor protein that acts as a negative regulator of ciliogenesis by mediating recruitment of CCP110 to mother centriole in cycling cells, leading to restrict nucleation of cilia at centrioles. Mediates depolymerization of microtubules of centriolar origin, possibly to suppress aberrant cilia formation. Following activation by NEK2 involved in disassembly of primary cilium during G2/M phase but does not disassemble fully formed ciliary axonemes. As cilium assembly and disassembly is proposed to coexist in a dynamic equilibrium may suppress nascent cilium assembly and, potentially, ciliar re-assembly in cells that have already disassembled their cilia ensuring the completion of cilium removal in the later stages of the cell cycle (By similarity). Plays an important role in recruiting MPHOSPH9, a negative regulator of cilia formation to the distal end of mother centriole (By similarity)., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 9, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "A2BGK6;Q8BUI2;Q99PT7", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0042802 identical protein binding;GO:0003777 microtubule motor activity", "go_cellular_component": "GO:0005813 centrosome;GO:0005874 microtubule;GO:0005814 centriole;GO:0032991 protein-containing complex", "go_biological_process": "GO:1902018 negative regulation of cilium assembly;GO:0060271 cilium assembly;GO:0007018 microtubule-based movement;GO:0007019 microtubule depolymerization", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "Q6NWW5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6PCQ0-1", "uniprot_id": "IQCE_MOUSE", "mass": 86356.0, "length": 778, "protein_name": "IQ domain-containing protein E", "gene_name": "Iqce", "organism": "Mouse", "refseq_name": "IQ domain-containing protein E isoform 2", "refseq_ac": "NP_001334446", "gene_names_uniprotkb": "Iqce", "gene_names_refseq": "1700028P05Rik; Iqce; mKIAA1023", "protein_names_uniprotkb": "IQ domain-containing protein E", "protein_names_refseq": "IQ domain-containing protein E isoform 2; IQ domain-containing protein E", "tax_id": 10090, "disease": "", "pathway": " (mmu:74239)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "10.1101/2023.09.13.557529;21183079;21750661;24582806;40021952", "class_list": "", "function": "Component of the EvC complex that positively regulates ciliary Hedgehog (Hh) signaling (PubMed:24582806). Required for proper limb morphogenesis (By similarity)., [UniProtKB, PubMed, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "Q8CDZ1;Q9D9U3", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0031514 motile cilium;GO:0009898 cytoplasmic side of plasma membrane;GO:0060170 ciliary membrane", "go_biological_process": "GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0008589 regulation of smoothened signaling pathway;GO:0035108 limb morphogenesis;GO:0120229 protein localization to motile cilium", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q6PCQ0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q71RI9-1", "uniprot_id": "KAT3_MOUSE", "mass": 51126.0, "length": 455, "protein_name": "Kynurenine--oxoglutarate transaminase 3", "gene_name": "Kyat3", "organism": "Mouse", "refseq_name": "kynurenine--oxoglutarate transaminase 3 isoform 1", "refseq_ac": "NP_001280489", "gene_names_uniprotkb": "Kyat3; Ccbl2; Kat3", "gene_names_refseq": "Ccbl2; KATIII; Kat3; Kyat3", "protein_names_uniprotkb": "Kynurenine--oxoglutarate transaminase 3; 2.6.1.63; 2.6.1.7; 4.4.1.13; Cysteine-S-conjugate beta-lyase 2; KATIII; Kynurenine aminotransferase 3; Kynurenine aminotransferase III; Kynurenine--glyoxylate transaminase; Kynurenine--oxoglutarate transaminase III", "protein_names_refseq": "cysteine conjugate-beta lyase 2; cysteine-S-conjugate beta-lyase 2; kynurenine aminotransferase III; kynurenine--glyoxylate transaminase; kynurenine--oxoglutarate transaminase 3 isoform 1; kynurenine--oxoglutarate transaminase 3; kynurenine--oxoglutarate transaminase III", "tax_id": 10090, "disease": "", "pathway": " (mmu:229905)", "pathway_count": 1, "publication_count": 14, "publication_id_list": "16376499;19029248;20482848;21750661;23576753;23806337;29113027;30084848;31219806;32444594;34428180;37453647;37507081;37594155", "class_list": "", "function": "Catalyzes the irreversible transamination of the L-tryptophan metabolite L-kynurenine to form kynurenic acid (KA), an intermediate in the tryptophan catabolic pathway which is also a broad spectrum antagonist of the three ionotropic excitatory amino acid receptors among others (PubMed:19029248). May catalyze the beta-elimination of S-conjugates and Se-conjugates of L-(seleno)cysteine, resulting in the cleavage of the C-S or C-Se bond (PubMed:19029248). Has transaminase activity towards L-kynurenine, tryptophan, phenylalanine, serine, cysteine, methionine, histidine, glutamine and asparagine with glyoxylate as an amino group acceptor (in vitro). Has lower activity with 2-oxoglutarate as amino group acceptor (in vitro) (PubMed:19029248)., [UniProtKB, PubMed]; Differential Kat3 Coactivator Usage Regulates Brain Metabolism and Neuronal Differentiation., [RefSeq, PubMed]; KAT III inhibited by equimolar methionine and half-life is 3.9 minutes at 65 degree C. Publication Status: Online-Only, [RefSeq, PubMed]; KAT3-dependent acetylation of cell type-specific genes maintains neuronal identity in the adult mouse brain. Publication Status: Online-Only, [RefSeq, PubMed]; The biochemical and structural properties of mouse KAT III (mKAT III) were determined. Erratum:[Mol Cell Biol. 2018 Apr 30;38(10):e00099-18. doi: 10.1128/MCB.00099-18. PMID: 29712768], [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q8BJ84", "ec_number_list": "2.6.1.7;2.6.1.1;4.4.1.13;2.6.1.63;2.6.1.64;2.6.1.39;2.6.1.4;2.6.1.73", "go_molecular_function": "GO:0047315 kynurenine-glyoxylate transaminase activity;GO:0016212 kynurenine-oxoglutarate transaminase activity;GO:0030170 pyridoxal phosphate binding;GO:0042803 protein homodimerization activity;GO:0047804 cysteine-S-conjugate beta-lyase activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion", "go_biological_process": "GO:0097053 L-kynurenine catabolic process;GO:0006103 2-oxoglutarate metabolic process;GO:0070189 kynurenine metabolic process;GO:0006520 amino acid metabolic process", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "Q71RI9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BFX3-1", "uniprot_id": "KCTD3_MOUSE", "mass": 88862.0, "length": 815, "protein_name": "BTB/POZ domain-containing protein KCTD3", "gene_name": "Kctd3", "organism": "Mouse", "refseq_name": "BTB/POZ domain-containing protein KCTD3 isoform 1", "refseq_ac": "NP_766238", "gene_names_uniprotkb": "Kctd3", "gene_names_refseq": "4930438A20Rik; 9330185B06; E330032J19Rik; Kctd3; NY-REN-45", "protein_names_uniprotkb": "BTB/POZ domain-containing protein KCTD3", "protein_names_refseq": "BTB/POZ domain-containing protein KCTD3 isoform 1; BTB/POZ domain-containing protein KCTD3", "tax_id": 10090, "disease": "", "pathway": " (mmu:226823)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "21750661;23382386;31219806;34428180;35820727", "class_list": "", "function": "Accessory subunit of potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3 (HCN3) up-regulating its cell-surface expression and current density without affecting its voltage dependence and kinetics., [UniProtKB, PubMed, UniProtKB, UniProtKB]; KCTD3 is an accessory subunit of native HCN3 complexes, [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q6P7X4", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005886 plasma membrane", "go_biological_process": "GO:0051260 protein homooligomerization", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "Q8BFX3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BK63-1", "uniprot_id": "KC1A_MOUSE", "mass": 38915.0, "length": 337, "protein_name": "Casein kinase I isoform alpha", "gene_name": "Csnk1a1", "organism": "Mouse", "refseq_name": "casein kinase I isoform alpha isoform 4", "refseq_ac": "NP_001344429", "gene_names_uniprotkb": "Csnk1a1", "gene_names_refseq": "2610208K14Rik; 4632404G05Rik; 5430427P18Rik; CK1a; Csnk1a1; Csnk1a", "protein_names_uniprotkb": "Casein kinase I isoform alpha; 2.7.11.1; CK1; CKI-alpha", "protein_names_refseq": "CK1; CKI-alpha; casein kinase I isoform alpha isoform 4; casein kinase I-alpha", "tax_id": 10090, "disease": "syndromic X-linked intellectual disability Najm type (Disease Ontology:DOID:0060807); Alzheimer's disease (Disease Ontology:DOID:10652); inclusion body myositis (Disease Ontology:DOID:3429)", "pathway": " (mmu:93687); (R-MMU-195253); (R-MMU-196299); (R-MMU-4641262); (R-MMU-5610785); (R-MMU-5635838); (R-MMU-69601)", "pathway_count": 7, "publication_count": 15, "publication_id_list": "11465105;11884395;21750661;21930935;23806337;25644602;26495903;31219806;31338967;34428180;34615873;35931121;36210013;39183304;9522121", "class_list": "", "function": "Casein kinase 1alpha mediates estradiol secretion via CYP19A1 expression in mouse ovarian granulosa cells. Publication Status: Online-Only, [RefSeq, PubMed]; Casein kinase I and casein kinase II differentially regulate axin function, [RefSeq, PubMed]; Casein kinases are operationally defined by their preferential utilization of acidic proteins such as caseins as substrates (By similarity). Can phosphorylate a large number of proteins (By similarity). Participates in Wnt signaling (By similarity). Phosphorylates CTNNB1 at 'Ser-45' (By similarity). May phosphorylate PER1 and PER2 (PubMed:21930935). May play a role in segregating chromosomes during mitosis (By similarity). May play a role in keratin cytoskeleton disassembly and thereby, it may regulate epithelial cell migration (By similarity). Acts as a positive regulator of mTORC1 and mTORC2 signaling in response to nutrients by mediating phosphorylation of DEPTOR inhibitor (By similarity). Acts as an inhibitor of NLRP3 inflammasome assembly by mediating phosphorylation of NLRP3 (PubMed:34615873)., [UniProtKB, PubMed, UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 3, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3UIL0;Q64506;Q80XI2;Q99LY3", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;3.4.19.12;2.7.10.2;2.7.11.-;2.7.11.4;3.4.25.1;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.1.153;2.7.1.137;3.1.3.48;2.7.1.40;2.7.11.21;3.1.3.16;2.3.2.27;2.3.2.32;2.7.11.39;2.3.1.-;2.7.11.31;3.6.5.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;2.7.11.15;2.7.11.16;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0004672 protein kinase activity;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0051219 phosphoprotein binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005819 spindle;GO:0005829 cytosol", "go_biological_process": "GO:1904263 positive regulation of TORC1 signaling;GO:0031670 cellular response to nutrient;GO:0044546 NLRP3 inflammasome complex assembly;GO:0000045 autophagosome assembly;GO:0006468 protein phosphorylation", "synthesized_glycan_count": 0, "hit_score": 1.6, "record_id": "Q8BK63-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BX02-1", "uniprot_id": "KANK2_MOUSE", "mass": 90245.0, "length": 843, "protein_name": "KN motif and ankyrin repeat domain-containing protein 2", "gene_name": "Kank2", "organism": "Mouse", "refseq_name": "KN motif and ankyrin repeat domain-containing protein 2", "refseq_ac": "NP_663586", "gene_names_uniprotkb": "Kank2; Ankrd25", "gene_names_refseq": "Ankrd25; Kank2", "protein_names_uniprotkb": "KN motif and ankyrin repeat domain-containing protein 2; Ankyrin repeat domain-containing protein 25", "protein_names_refseq": "KN motif and ankyrin repeat domain-containing protein 2; ankyrin repeat domain 25; ankyrin repeat domain-containing protein 25", "tax_id": 10090, "disease": "palmoplantar keratoderma and woolly hair (Disease Ontology:DOID:0070554); nephrotic syndrome type 16 (Disease Ontology:DOID:0080272); cancer (Disease Ontology:DOID:162)", "pathway": " (mmu:235041)", "pathway_count": 1, "publication_count": 19, "publication_id_list": "16024821;17242355;20720434;21183079;21750661;22645316;22872234;24129315;25961457;27548916;28528544;30016717;31219806;33253712;34274317;34428180;36210013;36852467;37507081", "class_list": "", "function": "Identify Kank proteins as talin activators that decrease the grip between the integrin-talin complex and actomyosin to regulate cell migration velocity, [RefSeq, PubMed]; Involved in transcription regulation by sequestering in the cytoplasm nuclear receptor coactivators such as NCOA1, NCOA2 and NCOA3 (By similarity). Involved in regulation of caspase-independent apoptosis by sequestering the proapoptotic factor AIFM1 in mitochondria (By similarity). Pro-apoptotic stimuli can induce its proteasomal degradation allowing the translocation of AIFM1 to the nucleus to induce apoptosis (By similarity). Involved in the negative control of vitamin D receptor signaling pathway (By similarity). Involved in actin stress fibers formation through its interaction with ARHGDIA and the regulation of the Rho signaling pathway (PubMed:25961457). May thereby play a role in cell adhesion and migration, regulating for instance podocytes migration during development of the kidney (PubMed:25961457). Through the Rho signaling pathway may also regulate cell proliferation (PubMed:16024821)., [UniProtKB, PubMed, UniProtKB, PubMed]; Nephrotic-syndrome-associated mutation of KANK2 induces pathologic binding competition with physiological interactor KIF21A., [RefSeq, PubMed]; Sult1b1 may be involved in the sulfonylation of podocyte protein podocalyxin, whereas ankrd25 may contribute to controlling actin dynamics in podocyte foot processes., [RefSeq, PubMed]; Tissue distribution and subcellular localization of the family of Kidney Ankyrin Repeat Domain (KANK) proteins., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 9, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q8BLD5;Q91Z35", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005829 cytosol", "go_biological_process": "GO:0070563 negative regulation of vitamin D receptor signaling pathway;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0008285 negative regulation of cell population proliferation;GO:0006915 apoptotic process", "synthesized_glycan_count": 0, "hit_score": 2.2, "record_id": "Q8BX02-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9D9K8-1", "uniprot_id": "IQCF1_MOUSE", "mass": 21456.0, "length": 182, "protein_name": "IQ domain-containing protein F1", "gene_name": "Iqcf1", "organism": "Mouse", "refseq_name": "IQ domain-containing protein F1 isoform 2", "refseq_ac": "NP_001140173", "gene_names_uniprotkb": "Iqcf1", "gene_names_refseq": "1700055J15Rik; Iqcf1", "protein_names_uniprotkb": "IQ domain-containing protein F1", "protein_names_refseq": "IQ domain-containing protein F1 isoform 2; IQ domain-containing protein F1", "tax_id": 10090, "disease": "", "pathway": " (mmu:74267)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "21750661;25380116", "class_list": "", "function": "A newly identified acrosomal protein, IQCF1, is closely related to sperm capacitation and AR; in particular, it is involved in tyrosine phosphorylation of sperm proteins through interaction with CaM, [RefSeq, PubMed]; Involved in sperm capacitation and acrosome reaction., [UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q810M2", "ec_number_list": "", "go_molecular_function": "GO:0005516 calmodulin binding", "go_cellular_component": "GO:0001669 acrosomal vesicle", "go_biological_process": "GO:2000344 positive regulation of acrosome reaction;GO:0060474 positive regulation of flagellated sperm motility involved in capacitation", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "Q9D9K8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9Z1P7-1", "uniprot_id": "KANK3_MOUSE", "mass": 84186.0, "length": 791, "protein_name": "KN motif and ankyrin repeat domain-containing protein 3", "gene_name": "Kank3", "organism": "Mouse", "refseq_name": "KN motif and ankyrin repeat domain-containing protein 3 isoform 1", "refseq_ac": "NP_109622", "gene_names_uniprotkb": "Kank3; Ankrd47; D17Ertd288e; Ng28", "gene_names_refseq": "0610013D04Rik; Ankrd47; D17Ertd288e; Kank3; NG28", "protein_names_uniprotkb": "KN motif and ankyrin repeat domain-containing protein 3; Ankyrin repeat domain-containing protein 47", "protein_names_refseq": "KN motif and ankyrin repeat domain-containing protein 3 isoform 1; KN motif and ankyrin repeat domain-containing protein 3; ankyrin repeat domain 47; ankyrin repeat domain-containing protein 47; putative KN motif and ankyrin repeat domains 3", "tax_id": 10090, "disease": "cancer (Disease Ontology:DOID:162)", "pathway": " (mmu:80880)", "pathway_count": 1, "publication_count": 8, "publication_id_list": "14656967;15112104;21183079;21750661;30084848;31219806;33253712;34428180", "class_list": "", "function": "May be involved in the control of cytoskeleton formation by regulating actin polymerization., [UniProtKB]; Tissue distribution and subcellular localization of the family of Kidney Ankyrin Repeat Domain (KANK) proteins., [RefSeq, PubMed]", "predicted_glycosites": 4, "predicted_n_glycosites": 0, "predicted_o_glycosites": 4, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 7, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 4, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005856 cytoskeleton", "go_biological_process": "GO:0035023 regulation of Rho protein signal transduction;GO:0090521 podocyte cell migration;GO:0051497 negative regulation of stress fiber assembly;GO:0030837 negative regulation of actin filament polymerization", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "Q9Z1P7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P28660-1", "uniprot_id": "NCKP1_MOUSE", "mass": 128784.0, "length": 1128, "protein_name": "Nck-associated protein 1", "gene_name": "Nckap1", "organism": "Mouse", "refseq_name": "nck-associated protein 1 isoform b", "refseq_ac": "NP_058661", "gene_names_uniprotkb": "Nckap1; Hem2; Kiaa0587; Nap1", "gene_names_refseq": "H19; Hem-2; Hem2; Nap1; Nckap1; mKIAA0587; mh19; p125Nap1", "protein_names_uniprotkb": "Nck-associated protein 1; Brain protein H19; MH19; Membrane-associated protein HEM-2; NAP 1; p125Nap1", "protein_names_refseq": "brain protein H19; membrane-associated protein HEM-2; nck-associated protein 1 isoform b", "tax_id": 10090, "disease": "developmental disorder of mental health (Disease Ontology:DOID:0060037)", "pathway": " (mmu:50884); (R-MMU-2029482); (R-MMU-4420097); (R-MMU-5663213); (R-MMU-9013149); (R-MMU-9013404); (R-MMU-9013423)", "pathway_count": 7, "publication_count": 25, "publication_id_list": "12106288;14765121;20173027;21750661;21946561;22645316;22872234;25428506;25428507;25605945;27605705;30084848;30779550;31219806;31599954;32777214;32848054;33300544;34203471;34428180;35820727;36210013;37507081;37828378;39627609", "class_list": "", "function": "Nap1 is a constitutive and essential component of a WAVE2- and Abi-1-containing complex linking Rac to site-directed actin assembly., [RefSeq, PubMed]; Part of the WAVE complex that regulates lamellipodia formation. The WAVE complex regulates actin filament reorganization via its interaction with the Arp2/3 complex. Actin remodeling activity is regulated by RAC1. As component of the WAVE1 complex, required for BDNF-NTRK2 endocytic trafficking and signaling from early endosomes (PubMed:27605705)., [UniProtKB, PubMed, PubMed]; The RAC1 Target NCKAP1 Plays a Crucial Role in the Progression of Braf;Pten-Driven Melanoma in Mice., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 4, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 4, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 4, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "Q3UPY6;Q80TX0;Q8CG49;Q99KY0", "ec_number_list": "", "go_molecular_function": "GO:0031267 small GTPase binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0014069 postsynaptic density;GO:0030027 lamellipodium;GO:0098794 postsynapse;GO:0031209 SCAR complex", "go_biological_process": "GO:0007354 zygotic determination of anterior/posterior axis, embryo;GO:0010172 embryonic body morphogenesis;GO:0048570 notochord morphogenesis;GO:0048340 paraxial mesoderm morphogenesis;GO:0001701 in utero embryonic development", "synthesized_glycan_count": 0, "hit_score": 3.1, "record_id": "P28660-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6PDK2-1", "uniprot_id": "KMT2D_MOUSE", "mass": 600245.0, "length": 5588, "protein_name": "Histone-lysine N-methyltransferase 2D", "gene_name": "Kmt2d", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Kmt2d; Mll2; Mll4", "gene_names_refseq": "", "protein_names_uniprotkb": "Histone-lysine N-methyltransferase 2D; 2.1.1.364; ALL1-related protein; Lysine N-methyltransferase 2D; Myeloid/lymphoid or mixed-lineage leukemia protein 2", "protein_names_refseq": "", "tax_id": 10090, "disease": "oral squamous cell carcinoma (Disease Ontology:DOID:0050866); Kabuki syndrome (Disease Ontology:DOID:0060473); Kleefstra syndrome 2 (Disease Ontology:DOID:0080598); prostate cancer (Disease Ontology:DOID:10283); stomach cancer (Disease Ontology:DOID:10534); intracranial aneurysm (Disease Ontology:DOID:10941); colon carcinoma (Disease Ontology:DOID:1520); breast cancer (Disease Ontology:DOID:1612); congenital heart disease (Disease Ontology:DOID:1682); breast carcinoma (Disease Ontology:DOID:3459); meningioma (Disease Ontology:DOID:3565); gastric adenocarcinoma (Disease Ontology:DOID:3717); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); lung squamous cell carcinoma (Disease Ontology:DOID:3907); lung non-small cell carcinoma (Disease Ontology:DOID:3908); papillary thyroid carcinoma (Disease Ontology:DOID:3969); lung small cell carcinoma (Disease Ontology:DOID:5409); primary ovarian insufficiency (Disease Ontology:DOID:5426); gastrointestinal lymphoma (Disease Ontology:DOID:903)", "pathway": " (mmu:381022); (R-MMU-3214841); (R-MMU-8936459); (R-MMU-9772755); (R-MMU-9818564)", "pathway_count": 5, "publication_count": 18, "publication_id_list": "16452087;17242355;21183079;21335234;21750661;23806337;24129315;25428506;30084848;30779550;31219806;31361958;32782141;34428180;35822049;36852467;39927985;40885482", "class_list": "", "function": "Histone methyltransferase that catalyzes methyl group transfer from S-adenosyl-L-methionine to the epsilon-amino group of 'Lys-4' of histone H3 (H3K4). Part of chromatin remodeling machinery predominantly forms H3K4me1 methylation marks at active chromatin sites where transcription and DNA repair take place. Acts as a coactivator for estrogen receptor by being recruited by ESR1, thereby activating transcription., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 13, "predicted_n_glycosites": 0, "predicted_o_glycosites": 13, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 4, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 4, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 4, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 22, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 5, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 19, "glyco_site_count": 17, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "2.3.1.48;2.3.1.-;2.1.1.364;3.1.1.23;1.14.11.68;2.7.11.2;2.7.11.-;3.5.1.-;3.5.1.98;2.3.2.-;3.1.13.-;2.7.7.48;2.7.7.6;3.1.1.32;3.1.1.34;1.14.19.1;6.2.1.3;6.2.1.24;6.2.1.15;3.1.1.79;2.1.1.-;6.2.1.1;6.2.1.17;2.1.1.356;2.3.1.15;2.1.1.370;2.1.1.371;2.3.1.199;3.1.1.4;3.1.1.3;2.3.1.51;2.7.11.22;2.7.11.23;2.1.1.85;3.1.3.4;2.1.1.359;2.1.1.355;2.1.1.354;2.1.1.362;2.1.1.361;2.3.1.20;2.3.1.76;2.3.1.57;2.1.1.319", "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0008270 zinc ion binding;GO:0000976 transcription cis-regulatory region binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific;GO:0042800 histone H3K4 methyltransferase activity", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0035097 histone methyltransferase complex;GO:0044666 MLL3/4 complex;GO:0005634 nucleus", "go_biological_process": "GO:0001701 in utero embryonic development;GO:0006351 DNA-templated transcription;GO:0008284 positive regulation of cell population proliferation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0043627 response to estrogen", "synthesized_glycan_count": 0, "hit_score": 2.4, "record_id": "Q6PDK2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O54781-1", "uniprot_id": "SRPK2_MOUSE", "mass": 76757.0, "length": 681, "protein_name": "SRSF protein kinase 2", "gene_name": "Srpk2", "organism": "Mouse", "refseq_name": "SRSF protein kinase 2 isoform c", "refseq_ac": "NP_033300", "gene_names_uniprotkb": "Srpk2", "gene_names_refseq": "Srpk2; Wbp6; mSRPK2", "protein_names_uniprotkb": "SRSF protein kinase 2; 2.7.11.1; SFRS protein kinase 2; SR-protein-specific kinase 2; Serine/arginine-rich protein-specific kinase 2", "protein_names_refseq": "SFRS protein kinase 2; SR-protein-specific kinase 2; SRSF protein kinase 2 isoform c; SRSF protein kinase 2; WW domain binding protein 6; serine/threonine-protein kinase SRPK2", "tax_id": 10090, "disease": "", "pathway": " (mmu:20817)", "pathway_count": 1, "publication_count": 10, "publication_id_list": "18559500;19592491;21183079;21750661;23197718;30059200;30745339;34428180;37507081;9446799", "class_list": "", "function": "SRPK2 may contribute to the formation of hyperphosphorylated tau and the pathogenesis of Alzheimer disease., [RefSeq, PubMed]; Serine/arginine-rich protein-specific kinase which specifically phosphorylates its substrates at serine residues located in regions rich in arginine/serine dipeptides, known as RS domains and is involved in the phosphorylation of SR splicing factors and the regulation of splicing (PubMed:9446799). Promotes neuronal apoptosis by up-regulating cyclin-D1 (CCND1) expression (PubMed:19592491). This is done by the phosphorylation of SRSF2, leading to the suppression of p53/TP53 phosphorylation thereby relieving the repressive effect of p53/TP53 on cyclin-D1 (CCND1) expression (By similarity). Phosphorylates ACIN1, and redistributes it from the nuclear speckles to the nucleoplasm, resulting in cyclin A1 but not cyclin A2 up-regulation (By similarity). Plays an essential role in spliceosomal B complex formation via the phosphorylation of DDX23/PRP28 (By similarity). Probably by phosphorylating DDX23, leads to the suppression of incorrect R-loops formed during transcription; R-loops are composed of a DNA:RNA hybrid and the associated non-template single-stranded DNA (By similarity). Phosphorylates the N-terminus of ERC1 (PubMed:30745339)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 13, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q8VCD9", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;2.7.11.39;2.3.1.-;2.7.11.31;3.6.5.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0071889 14-3-3 protein binding;GO:0106310 protein serine kinase activity", "go_cellular_component": "GO:0097229 sperm end piece;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm", "go_biological_process": "GO:0001525 angiogenesis;GO:0006468 protein phosphorylation;GO:0008284 positive regulation of cell population proliferation;GO:0010628 positive regulation of gene expression;GO:0030154 cell differentiation", "synthesized_glycan_count": 0, "hit_score": 1.4, "record_id": "O54781-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9Z1B3-1", "uniprot_id": "PLCB1_MOUSE", "mass": 138396.0, "length": 1216, "protein_name": "1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-1", "gene_name": "Plcb1", "organism": "Mouse", "refseq_name": "1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-1 isoform 1", "refseq_ac": "NP_001139302", "gene_names_uniprotkb": "Plcb1; Plcb", "gene_names_refseq": "3110043I21Rik; Plcb1; Plcb; mKIAA0581", "protein_names_uniprotkb": "1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-1; 3.1.4.11; PLC-154; PLC-beta-1; Phosphoinositide phospholipase C-beta-1; Phospholipase C-beta-1", "protein_names_refseq": "1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-1 isoform 1; 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-1; PLC-154; PLC-beta-1; phosphoinositide phospholipase C-beta-1; phosphoinositide phospholipase C; phospholipase C-beta-1a", "tax_id": 10090, "disease": "myelodysplastic syndrome (Disease Ontology:DOID:0050908); developmental and epileptic encephalopathy 12 (Disease Ontology:DOID:0080459); Alzheimer's disease (Disease Ontology:DOID:10652); schizophrenia (Disease Ontology:DOID:5419); myocardial infarction (Disease Ontology:DOID:5844); acute myeloid leukemia (Disease Ontology:DOID:9119); obesity (Disease Ontology:DOID:9970)", "pathway": " (mmu:18795); (R-MMU-112043); (R-MMU-1855204); (R-MMU-399997); (R-MMU-4086398); (R-MMU-416476); (R-MMU-418217); (R-MMU-434316); (R-MMU-500657)", "pathway_count": 9, "publication_count": 12, "publication_id_list": "11278470;11287604;11471062;16538662;18802028;21183079;21750661;27653213;31219806;38959322;8687404;9753089", "class_list": "", "function": "Catalyzes the hydrolysis of 1-phosphatidylinositol 4,5-bisphosphate into diacylglycerol (DAG) and inositol 1,4,5-trisphosphate (IP3) and mediates intracellular signaling downstream of G protein-coupled receptors (PubMed:27653213). Regulates the function of the endothelial barrier (PubMed:27653213)., [UniProtKB, PubMed]; Phospholipase C beta 1 in the dentate gyrus gates fear memory formation through regulation of neuronal excitability., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 13, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 7, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q62075;Q6PDH1;Q8K5A5;Q8K5A6;Q9Z0E5;Q9Z2T5", "ec_number_list": "3.1.4.11;3.6.5.-", "go_molecular_function": "GO:0004435 phosphatidylinositol-4,5-bisphosphate phospholipase C activity;GO:0005096 GTPase activator activity;GO:0005516 calmodulin binding;GO:0005546 phosphatidylinositol-4,5-bisphosphate binding;GO:0019899 enzyme binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0098982 GABA-ergic synapse;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005886 plasma membrane", "go_biological_process": "GO:2000344 positive regulation of acrosome reaction;GO:0070498 interleukin-1-mediated signaling pathway;GO:0060466 activation of meiosis involved in egg activation;GO:2000438 negative regulation of monocyte extravasation;GO:1903140 regulation of establishment of endothelial barrier", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "Q9Z1B3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P37238-1", "uniprot_id": "PPARG_MOUSE", "mass": 57598.0, "length": 505, "protein_name": "Peroxisome proliferator-activated receptor gamma", "gene_name": "Pparg", "organism": "Mouse", "refseq_name": "peroxisome proliferator-activated receptor gamma isoform 1", "refseq_ac": "NP_001120802", "gene_names_uniprotkb": "Pparg; Nr1c3; PPARG", "gene_names_refseq": "Nr1c3; PPAR-gamma2; PPAR-gamma; PPARgamma2; PPARgamma; Pparg", "protein_names_uniprotkb": "Peroxisome proliferator-activated receptor gamma; Nuclear receptor subfamily 1 group C member 3; PPAR-gamma", "protein_names_refseq": "nuclear receptor subfamily 1 group C member 3; peroxisome proliferator activated receptor gamma 2; peroxisome proliferator activated receptor gamma 4; peroxisome proliferator-activated receptor gamma isoform 1", "tax_id": 10090, "disease": "familial partial lipodystrophy (Disease Ontology:DOID:0050440); diabetic encephalopathy (Disease Ontology:DOID:0050850); glomerulosclerosis (Disease Ontology:DOID:0050851); abdominal obesity-metabolic syndrome (Disease Ontology:DOID:0060611); familial partial lipodystrophy type 3 (Disease Ontology:DOID:0070204); polycystic kidney disease (Disease Ontology:DOID:0080322); Graves ophthalmopathy (Disease Ontology:DOID:0081120); congenital generalized lipodystrophy type 2 (Disease Ontology:DOID:0111136); pre-eclampsia (Disease Ontology:DOID:10591); Alzheimer's disease (Disease Ontology:DOID:10652); hypertension (Disease Ontology:DOID:10763); urinary bladder cancer (Disease Ontology:DOID:11054); hyperandrogenism (Disease Ontology:DOID:11613); cardiovascular system disease (Disease Ontology:DOID:1287); alcoholic cardiomyopathy (Disease Ontology:DOID:12935); proliferative diabetic retinopathy (Disease Ontology:DOID:13207); primary pulmonary hypertension (Disease Ontology:DOID:14557); cognitive disorder (Disease Ontology:DOID:1561); pancreatic cancer (Disease Ontology:DOID:1793); colon cancer (Disease Ontology:DOID:219); transient cerebral ischemia (Disease Ontology:DOID:224); arteriosclerosis (Disease Ontology:DOID:2349); acute kidney failure (Disease Ontology:DOID:3021); coronary artery disease (Disease Ontology:DOID:3393); carotid artery disease (Disease Ontology:DOID:3407); pancreatic ductal carcinoma (Disease Ontology:DOID:3587); pancreatitis (Disease Ontology:DOID:4989); hepatocellular carcinoma (Disease Ontology:DOID:684); end stage renal disease (Disease Ontology:DOID:783); lipodystrophy (Disease Ontology:DOID:811); systemic lupus erythematosus (Disease Ontology:DOID:9074); type 2 diabetes mellitus (Disease Ontology:DOID:9352); steatotic liver disease (Disease Ontology:DOID:9452); obesity (Disease Ontology:DOID:9970)", "pathway": " (mmu:19016); (R-MMU-381340); (R-MMU-383280); (R-MMU-9841922)", "pathway_count": 4, "publication_count": 68, "publication_id_list": "10549290;10549291;10549292;10788465;15507114;15687259;16971566;17595322;18204460;18719582;18981214;19037106;19041764;20078863;20498072;21035761;21459326;21521693;21750661;21994940;22140527;22226965;22405074;22584573;23178929;23473036;23525231;24703692;24933248;25100724;25316675;25409143;25519902;25827822;26385316;26670611;27197753;27498863;27747357;28180926;28683290;29107124;29160030;30008738;30034693;30320193;31611602;32683515;32941798;32966473;33539723;34339734;34428180;35450368;35491170;35710596;36329235;40355558;7838715;7926726;8001151;8041794;8240342;8262913;8521497;8521498;8647948;9325263", "class_list": "", "function": "Ligand-activated transcription factor that forms obligate heterodimers with the retinoic acid receptor and acts as a key regulator of biological processes, such as adipocyte differentiation, lipid metabolism, glucose homeostasis and beta-oxidation of fatty acids (PubMed:21035761, PubMed:23525231, PubMed:7838715, PubMed:7926726, PubMed:8041794, PubMed:8262913). Activated by lipid ligands: binds peroxisome proliferators, such as hypolipidemic drugs, and fatty acids, such as prostaglandin J2 metabolites (PubMed:21994940, PubMed:27197753, PubMed:8041794, PubMed:8262913). Ligand-binding results in a conformational change in the receptor, promoting dissociation of repressors and recruitment of coactivators, and subsequent activation of target gene expression (PubMed:21994940, PubMed:27197753, PubMed:8041794, PubMed:8262913). Specifically binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase (PubMed:8041794, PubMed:8262913). Acts as a critical regulator of gut homeostasis by suppressing NF-kappa-B-mediated pro-inflammatory responses (By similarity). Plays a role in the regulation of cardiovascular circadian rhythms by regulating the transcription of BMAL1 in the blood vessels (PubMed:19041764)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]; Nuclear receptor that acts as the key factor controlling the development of adipocytes (PubMed:10549290, PubMed:10549291, PubMed:10549292, PubMed:18719582, PubMed:21459326, PubMed:23473036, PubMed:7838715, PubMed:7926726, PubMed:8001151, PubMed:8521497, PubMed:8521498). Specifically activated by 15-deoxy-delta12,14-prostaglandin J2 ligand during early adipogenesis, driving differentiation of all types of adipocytes (white, beige and brown) (PubMed:7838715, PubMed:7926726, PubMed:8521497, PubMed:8521498). Acts together with retinoic acid receptor RXRA, forming the ARF6 complex, which acts as a key regulator of the tissue-specific adipocyte P2 (aP2) enhancer (PubMed:7838715). Following recruitment of TLE3, promotes differentiation of white adipocytes (PubMed:21459326, PubMed:23473036). Following recruitment of PRDM16, promotes differentiation of myoblastic precursors into brown adipose cells (BAT), which are specialized in dissipating energy in the form of heat in response to cold or excess feeding (PubMed:18719582, PubMed:24703692, PubMed:40355558). Also mediates diffentiation of white adipocytes into beige adipocytes by mediating recruitment of PRDM16 (PubMed:22405074)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]; Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm., [UniProtKB, UniProtKB, UniProtKB]; This gene encodes a nuclear receptor protein belonging to the peroxisome proliferator-activated receptor (Ppar) family. The encoded protein is a ligand-activated transcription factor that is involved in the regulation of adipocyte differentiation and glucose homeostasis. The encoded protein forms a heterodimer with retinoid X receptors and binds to DNA motifs termed 'peroxisome proliferator response elements' to either activate or inhibit gene expression. Mice lacking the encoded protein die at an embryonic stage due to severe defects in placental vascularization. When the embryos lacking this gene are supplemented with healthy placentas, the mutants survive to term, but succumb to lipodystrophy and multiple hemorrhages. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 1, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 4, "reported_mutagensis": 4, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 34, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0050693 LBD domain binding;GO:0097677 STAT family protein binding;GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0003700 DNA-binding transcription factor activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0043235 receptor complex", "go_biological_process": "GO:1903845 negative regulation of cellular response to transforming growth factor beta stimulus;GO:1904179 positive regulation of adipose tissue development;GO:2000230 negative regulation of pancreatic stellate cell proliferation;GO:0010888 negative regulation of lipid storage;GO:0002246 wound healing involved in inflammatory response", "synthesized_glycan_count": 0, "hit_score": 7.0, "record_id": "P37238-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3UIL6-1", "uniprot_id": "PKHA7_MOUSE", "mass": 126742.0, "length": 1118, "protein_name": "Pleckstrin homology domain-containing family A member 7", "gene_name": "Plekha7", "organism": "Mouse", "refseq_name": "pleckstrin homology domain-containing family A member 7 isoform 1", "refseq_ac": "NP_001292114", "gene_names_uniprotkb": "Plekha7; Hadp1", "gene_names_refseq": "A430081P20Rik; Plekha7", "protein_names_uniprotkb": "Pleckstrin homology domain-containing family A member 7; Heart adapter protein 1; PH domain-containing family A member 7", "protein_names_refseq": "PH domain-containing family A member 7; heart adapter protein 1; pleckstrin homology domain-containing family A member 7 isoform 1", "tax_id": 10090, "disease": "glomerulosclerosis (Disease Ontology:DOID:0050851); hypertension (Disease Ontology:DOID:10763)", "pathway": " (mmu:233765)", "pathway_count": 1, "publication_count": 12, "publication_id_list": "16452087;17242355;20808826;21183079;21750661;22517741;23990464;30463011;31219806;31599954;36852467;40885482", "class_list": "", "function": "PLEKHA7 is a cytoplasmic component of the epithelial adherens junction belt, distinct from ZO-1 and E-cadherin Publication Status: Online-Only, [RefSeq, PubMed]; Required for zonula adherens biogenesis and maintenance. Acts via its interaction with CAMSAP3, which anchors microtubules at their minus-ends to zonula adherens, leading to the recruitment of KIFC3 kinesin to the junctional site (By similarity). Mediates docking of ADAM10 to zonula adherens through a PDZD11-dependent interaction with the ADAM10-binding protein TSPAN33 (PubMed:30463011)., [UniProtKB, UniProtKB, PubMed, UniProtKB, UniProtKB]; Results indicate that PLEKHA7 plays a cooperative role with nectin and afadin in the proper formation of Adherens junction (AJ) in epithelial cell., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 13, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "B6RSP2;B6RSP3;Q3TUE4;Q5XG70;Q8BYE3", "ec_number_list": "", "go_molecular_function": "GO:0070097 delta-catenin binding", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0005911 cell-cell junction;GO:0030054 cell junction", "go_biological_process": "GO:0042311 vasodilation;GO:0046931 pore complex assembly;GO:0044331 cell-cell adhesion mediated by cadherin;GO:0045218 zonula adherens maintenance;GO:0090136 epithelial cell-cell adhesion", "synthesized_glycan_count": 0, "hit_score": 1.6, "record_id": "Q3UIL6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q80WE4-1", "uniprot_id": "KI20B_MOUSE", "mass": 203514.0, "length": 1774, "protein_name": "Kinesin-like protein KIF20B", "gene_name": "Kif20b", "organism": "Mouse", "refseq_name": "kinesin-like protein KIF20B isoform 1", "refseq_ac": "NP_898867", "gene_names_uniprotkb": "Kif20b; Mphosph1", "gene_names_refseq": "33cex; C330014J10Rik; Kif20b; MPP1; Mphosph1; magoo", "protein_names_uniprotkb": "Kinesin-like protein KIF20B; Kinesin family member 20B; Kinesin-related motor interacting with PIN1; M-phase phosphoprotein 1; MPP1", "protein_names_refseq": "M-phase phosphoprotein 1; N-6 kinesin; kinesin-like protein KIF20B isoform 1; kinesin-like protein KIF20B; kinesin-related motor interacting with PIN1", "tax_id": 10090, "disease": "microcephaly (Disease Ontology:DOID:10907)", "pathway": " (mmu:240641); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 3, "publication_count": 14, "publication_id_list": "11416179;17525332;19144319;21183079;21750661;22872234;23864681;24173802;30084848;31219806;32273386;34203471;34428180;35820727", "class_list": "", "function": "Plus-end-directed motor enzyme that is required for completion of cytokinesis (By similarity). Required for proper midbody organization and abscission in polarized cortical stem cells (PubMed:24173802). Plays a role in the regulation of neuronal polarization by mediating the transport of specific cargos. Participates in the mobilization of SHTN1 and in the accumulation of PIP3 in the growth cone of primary hippocampal neurons in a tubulin and actin-dependent manner (PubMed:23864681). In the developing telencephalon, cooperates with SHTN1 to promote both the transition from the multipolar to the bipolar stage and the radial migration of cortical neurons from the ventricular zone toward the superficial layer of the neocortex (PubMed:23864681). Involved in cerebral cortex growth (PubMed:24173802). Acts as an oncogene for promoting bladder cancer cells proliferation, apoptosis inhibition and carcinogenic progression (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed]; This study investigated whether polarized furrowing and abscission in mouse neural stem cells are regulated differently at earlier and later stages and in a cytokinesis mutant, Kif20b., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 8, "reported_mutagensis": 2, "reported_glycation": 0, "reported_snv": 3, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "E9QPW5;Q3V347;Q80VC0;Q8BLI2;Q99PT5", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0042803 protein homodimerization activity;GO:0016887 ATP hydrolysis activity;GO:0050699 WW domain binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005813 centrosome", "go_biological_process": "GO:1903438 positive regulation of mitotic cytokinetic process;GO:0008284 positive regulation of cell population proliferation;GO:0051301 cell division;GO:0090316 positive regulation of intracellular protein transport;GO:0048812 neuron projection morphogenesis", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "Q80WE4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q60665-1", "uniprot_id": "SKIL_MOUSE", "mass": 76359.0, "length": 675, "protein_name": "Ski-like protein", "gene_name": "Skil", "organism": "Mouse", "refseq_name": "ski-like protein isoform b", "refseq_ac": "NP_001034179", "gene_names_uniprotkb": "Skil; Skir; Sno", "gene_names_refseq": "Skil; Skir; SnoN; sno", "protein_names_uniprotkb": "Ski-like protein; Ski-related oncogene; Ski-related protein", "protein_names_refseq": "SKI-like; ski-like protein isoform b; ski-like protein; ski-related oncogene; ski/sno related", "tax_id": 10090, "disease": "ureteral obstruction (Disease Ontology:DOID:5199)", "pathway": " (mmu:20482); (R-MMU-2173795)", "pathway_count": 2, "publication_count": 11, "publication_id_list": "12522145;21750661;23610558;32782141;34428180;34473197;35822049;36852467;38468490;8834472;9207045", "class_list": "", "function": "Arkadia-SKI/SnoN signaling differentially regulates TGF-beta-induced iTreg and Th17 cell differentiation., [RefSeq, PubMed]; May have regulatory role in cell division or differentiation in response to extracellular signals., [UniProtKB]; NSUN2 promotes colorectal cancer progression by enhancing SKIL mRNA stabilization., [RefSeq, PubMed]; This gene encodes a member of a small family of proteins that play a key role in the response of cells to extracellular growth signals. The encoded protein regulates members of the transforming growth factor beta signaling pathway. It is highly expressed in certain cancer cells, where it may have both tumor-suppressing and tumor-promoting roles. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2012]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q60702;Q78E90;Q80VK5", "ec_number_list": "", "go_molecular_function": "GO:0003682 chromatin binding;GO:0019904 protein domain specific binding;GO:0042802 identical protein binding;GO:0044877 protein-containing complex binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0001669 acrosomal vesicle;GO:0005667 transcription regulator complex", "go_biological_process": "GO:0002260 lymphocyte homeostasis;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0007283 spermatogenesis;GO:0007179 transforming growth factor beta receptor signaling pathway;GO:0030514 negative regulation of BMP signaling pathway", "synthesized_glycan_count": 0, "hit_score": 1.4, "record_id": "Q60665-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BKC8-1", "uniprot_id": "PI4KB_MOUSE", "mass": 91515.0, "length": 816, "protein_name": "Phosphatidylinositol 4-kinase beta", "gene_name": "Pi4kb", "organism": "Mouse", "refseq_name": "phosphatidylinositol 4-kinase beta isoform 1", "refseq_ac": "NP_001280644", "gene_names_uniprotkb": "Pi4kb; Pik4cb", "gene_names_refseq": "ESTM41; PI4K-beta; PI4Kbeta; Pi4kb; Pik4cb", "protein_names_uniprotkb": "Phosphatidylinositol 4-kinase beta; 2.7.1.67; PI4K-beta; PI4Kbeta; PtdIns 4-kinase beta", "protein_names_refseq": "phosphatidylinositol 4-kinase beta isoform 1; phosphatidylinositol 4-kinase, catalytic, beta polypeptide; ptdIns 4-kinase beta", "tax_id": 10090, "disease": "autosomal dominant nonsyndromic deafness 87 (Disease Ontology:DOID:0070606)", "pathway": " (mmu:107650); (R-MMU-1660514)", "pathway_count": 2, "publication_count": 7, "publication_id_list": "17242355;21183079;21750661;23541637;33106410;34428180;38230579", "class_list": "", "function": "Locational and functional characterization of PI4KB in the mouse embryo., [RefSeq, PubMed]; Myelination of peripheral nerves is controlled by PI4KB through regulation of Schwann cell Golgi function., [RefSeq, PubMed]; Oijbih iuhg iugh uh jkgh uib, [RefSeq, PubMed]; Phosphorylates phosphatidylinositol (PI) in the first committed step in the production of the second messenger inositol-1,4,5,-trisphosphate (PIP). May regulate Golgi disintegration/reorganization during mitosis, possibly via its phosphorylation (By similarity). Involved in Golgi-to-plasma membrane trafficking (By similarity). May play an important role in the inner ear development., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 12, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q14CH6;Q14DJ4;Q3TA58;Q68FH2;Q8C146", "ec_number_list": "2.7.1.67;3.6.5.2", "go_molecular_function": "GO:0005524 ATP binding;GO:0071889 14-3-3 protein binding;GO:0004430 1-phosphatidylinositol 4-kinase activity;GO:0016301 kinase activity", "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005737 cytoplasm;GO:0005741 mitochondrial outer membrane;GO:0005794 Golgi apparatus;GO:0016020 membrane", "go_biological_process": "GO:0007040 lysosome organization;GO:0048015 phosphatidylinositol-mediated signaling;GO:0048839 inner ear development;GO:0046854 phosphatidylinositol phosphate biosynthetic process", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q8BKC8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VD65-1", "uniprot_id": "PI3R4_MOUSE", "mass": 152599.0, "length": 1358, "protein_name": "Phosphoinositide 3-kinase regulatory subunit 4", "gene_name": "Pik3r4", "organism": "Mouse", "refseq_name": "phosphoinositide 3-kinase regulatory subunit 4", "refseq_ac": "NP_001074778", "gene_names_uniprotkb": "Pik3r4; Vps15", "gene_names_refseq": "2210010O15Rik; C730038E05Rik; D9Ertd418e; Pik3r4; Vps15; p150", "protein_names_uniprotkb": "Phosphoinositide 3-kinase regulatory subunit 4; 2.7.11.1; PI3-kinase regulatory subunit 4", "protein_names_refseq": "PI3-kinase regulatory subunit 4; phosphatidylinositol 3 kinase, regulatory subunit, polypeptide 4, p150; phosphoinositide 3-kinase regulatory subunit 4", "tax_id": 10090, "disease": "", "pathway": " (mmu:75669); (R-MMU-109704); (R-MMU-1632852); (R-MMU-1660514); (R-MMU-1660516); (R-MMU-1660517); (R-MMU-168138); (R-MMU-5668599)", "pathway_count": 8, "publication_count": 14, "publication_id_list": "10.1101/2023.09.13.557529;21059846;21750661;23332761;23630012;24089209;25605945;29311744;30059200;32782141;32848054;34428180;34428398;40885482", "class_list": "", "function": "Regulatory subunit of the PI3K complex that mediates formation of phosphatidylinositol 3-phosphate; different complex forms are believed to play a role in multiple membrane trafficking pathways: PI3KC3-C1 is involved in initiation of autophagosomes and PI3KC3-C2 in maturation of autophagosomes and endocytosis. Involved in regulation of degradative endocytic trafficking and cytokinesis, probably in the context of PI3KC3-C2 (By similarity)., [UniProtKB, UniProtKB]; This study demonstrated that Mutations in Vps15 perturb neuronal migration in mice. Erratum:[Nat Neurosci. 2018 Aug;21(8):1139. doi: 10.1038/s41593-018-0170-9. PMID: 29875394], [RefSeq, PubMed]; Vps15-deficient mouse tissues are competent for LC3-positive autophagosome formation and maintain mTOR activation., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 5, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 5, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 5, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 5, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 6, "binding_glycan_count": 0, "secondary_ac_list": "Q56A65;Q8C948;Q8C9D7;Q9CVC5", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;3.2.1.31;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.10.1;3.1.3.48;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;2.7.11.39;2.3.1.-;2.7.11.31;3.6.5.-;2.7.1.154;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0106310 protein serine kinase activity", "go_cellular_component": "GO:0071561 nucleus-vacuole junction;GO:0005929 cilium;GO:0015630 microtubule cytoskeleton;GO:0045171 intercellular bridge;GO:0005770 late endosome", "go_biological_process": "GO:0097352 autophagosome maturation;GO:0036092 phosphatidylinositol-3-phosphate biosynthetic process;GO:0010506 regulation of autophagy;GO:0016241 regulation of macroautophagy;GO:0045022 early endosome to late endosome transport", "synthesized_glycan_count": 0, "hit_score": 2.3, "record_id": "Q8VD65-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BLV3-1", "uniprot_id": "SL9A7_MOUSE", "mass": 80289.0, "length": 726, "protein_name": "Sodium/hydrogen exchanger 7", "gene_name": "Slc9a7", "organism": "Mouse", "refseq_name": "sodium/hydrogen exchanger 7", "refseq_ac": "NP_796327", "gene_names_uniprotkb": "Slc9a7; Nhe7", "gene_names_refseq": "6330509M05Rik; A530087D17Rik; NHE7; Slc9a7", "protein_names_uniprotkb": "Sodium/hydrogen exchanger 7; NHE-7; Na(+)/H(+) exchanger 7; Solute carrier family 9 member 7", "protein_names_refseq": "Na(+)/H(+) exchanger 7; sodium/hydrogen exchanger 7", "tax_id": 10090, "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); X-linked intellectual developmental disorder 108 (Disease Ontology:DOID:0111844)", "pathway": " (mmu:236727); (R-MMU-425986)", "pathway_count": 2, "publication_count": 11, "publication_id_list": "10.1101/2023.09.13.557529;21183079;21750661;25428506;25605945;26495903;28011936;30084848;30779550;34428180;38152992", "class_list": "", "function": "Golgi Na(+), K(+)/(H+) antiporter. Mediates the electoneutral influx of Na(+) or K(+) in exchange for H(+). May contribute to the regulation of Golgi apparatus volume and pH., [UniProtKB, UniProtKB]; NHE7 upregulation potentiates the uptake of small extracellular vesicles by enhancing maturation of macropinosomes in hepatocellular carcinoma., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 1, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "A2ACD5;A2ACD6", "ec_number_list": "", "go_molecular_function": "GO:0015385 sodium:proton antiporter activity;GO:0015386 potassium:proton antiporter activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0055037 recycling endosome;GO:0055038 recycling endosome membrane;GO:0005802 trans-Golgi network", "go_biological_process": "GO:0051453 regulation of intracellular pH;GO:0006885 regulation of pH;GO:0071805 potassium ion transmembrane transport;GO:0098719 sodium ion import across plasma membrane;GO:1905526 regulation of Golgi lumen acidification", "synthesized_glycan_count": 0, "hit_score": 1.4, "record_id": "Q8BLV3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3UHX0-1", "uniprot_id": "NOL8_MOUSE", "mass": 128635.0, "length": 1147, "protein_name": "Nucleolar protein 8", "gene_name": "Nol8", "organism": "Mouse", "refseq_name": "nucleolar protein 8", "refseq_ac": "NP_001258326", "gene_names_uniprotkb": "Nol8", "gene_names_refseq": "4921532D18Rik; 5730412B09Rik; Nol8", "protein_names_uniprotkb": "Nucleolar protein 8", "protein_names_refseq": "nucleolar protein 8", "tax_id": 10090, "disease": "", "pathway": " (mmu:70930)", "pathway_count": 1, "publication_count": 8, "publication_id_list": "17242355;19144319;21183079;21750661;25153642;28528544;34428180;35820727", "class_list": "", "function": "Plays an essential role in the survival of diffuse-type gastric cancer cells. Acts as a nucleolar anchoring protein for DDX47. May be involved in regulation of gene expression at the post-transcriptional level or in ribosome biogenesis in cancer cells (By similarity)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 20, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q059P5;Q504M4;Q8CDJ7;Q9CUR0", "ec_number_list": "", "go_molecular_function": "GO:0003723 RNA binding", "go_cellular_component": "GO:0005730 nucleolus;GO:0005694 chromosome", "go_biological_process": "GO:1902570 protein localization to nucleolus;GO:1990830 cellular response to leukemia inhibitory factor;GO:0006364 rRNA processing", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q3UHX0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q62417-1", "uniprot_id": "SRBS1_MOUSE", "mass": 143070.0, "length": 1290, "protein_name": "Sorbin and SH3 domain-containing protein 1", "gene_name": "Sorbs1", "organism": "Mouse", "refseq_name": "sorbin and SH3 domain-containing protein 1 isoform 3", "refseq_ac": "NP_001030134", "gene_names_uniprotkb": "Sorbs1; Kiaa1296; Sh3d5", "gene_names_refseq": "2310065E01Rik; 9530001P15Rik; CAP; SH3P12; Sh3d5; Sorbs1; mKIAA1296", "protein_names_uniprotkb": "Sorbin and SH3 domain-containing protein 1; CAP; Ponsin; SH3 domain protein 5; SH3P12; c-Cbl-associated protein", "protein_names_refseq": "SH3 domain protein 5; c-Cbl-associated protein; ponsin; sorbin and SH3 domain-containing protein 1 isoform 3; sorbin and SH3 domain-containing protein 1", "tax_id": 10090, "disease": "type 2 diabetes mellitus (Disease Ontology:DOID:9352); obesity (Disease Ontology:DOID:9970)", "pathway": " (mmu:20411); (R-MMU-445355)", "pathway_count": 2, "publication_count": 36, "publication_id_list": "10.1101/2023.09.13.557529;10.3389/fragi.2021.757801;10085297;11001060;12079283;12842890;15047181;15777793;16452087;16452088;17114649;17242355;19891780;21183079;21750661;22517741;22645316;25428506;25605945;26192747;30016717;30084848;30779550;32848054;34428180;35820727;35822049;36288343;36834818;37507081;40021952;40885482;40997131;9447983;9461600;9630982", "class_list": "", "function": "CBL/CAP Is Essential for Mitochondria Respiration Complex I Assembly and Bioenergetics Efficiency in Muscle Cells. Publication Status: Online-Only, [RefSeq, PubMed]; Plays a role in tyrosine phosphorylation of CBL by linking CBL to the insulin receptor. Required for insulin-stimulated glucose transport. Involved in formation of actin stress fibers and focal adhesions., [UniProtKB, PubMed, PubMed, PubMed]", "predicted_glycosites": 3, "predicted_n_glycosites": 0, "predicted_o_glycosites": 3, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 12, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 12, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 12, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 27, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 4, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 2, "glyco_site_count": 15, "binding_glycan_count": 0, "secondary_ac_list": "Q80TF8;Q8BZI3;Q8K3Y2;Q921F8;Q9Z0Z8;Q9Z0Z9", "ec_number_list": "", "go_molecular_function": "GO:0005158 insulin receptor binding;GO:0019901 protein kinase binding;GO:0031625 ubiquitin protein ligase binding;GO:0030159 signaling receptor complex adaptor activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0005856 cytoskeleton", "go_biological_process": "GO:0032869 cellular response to insulin stimulus;GO:0095500 acetylcholine receptor signaling pathway;GO:0046889 positive regulation of lipid biosynthetic process;GO:0007010 cytoskeleton organization;GO:1903078 positive regulation of protein localization to plasma membrane", "synthesized_glycan_count": 0, "hit_score": 5.2, "record_id": "Q62417-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9QXN0-1", "uniprot_id": "SHRM3_MOUSE", "mass": 214888.0, "length": 1986, "protein_name": "Protein Shroom3", "gene_name": "Shroom3", "organism": "Mouse", "refseq_name": "protein Shroom3 isoform 2", "refseq_ac": "NP_001071063", "gene_names_uniprotkb": "Shroom3; Kiaa1481; Shrm", "gene_names_refseq": "D5Ertd287e; Shrm3; Shrm; Shroom3", "protein_names_uniprotkb": "Protein Shroom3", "protein_names_refseq": "protein Shroom3 isoform 2; protein Shroom3", "tax_id": 10090, "disease": "chronic kidney disease (Disease Ontology:DOID:784)", "pathway": " (mmu:27428)", "pathway_count": 1, "publication_count": 13, "publication_id_list": "10589677;14680628;16249236;16615870;16684770;17242355;21183079;21750661;22493320;25428506;33300544;34418053;34428180", "class_list": "", "function": "Controls cell shape changes in the neuroepithelium during neural tube closure (PubMed:10589677, PubMed:14680628). Induces apical constriction in epithelial cells by promoting the apical accumulation of F-actin and myosin II, and probably by bundling stress fibers (PubMed:14680628, PubMed:16249236, PubMed:16684770, PubMed:22493320). Induces apicobasal cell elongation by redistributing gamma-tubulin and directing the assembly of robust apicobasal microtubule arrays (By similarity)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, UniProtKB]", "predicted_glycosites": 3, "predicted_n_glycosites": 0, "predicted_o_glycosites": 3, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 12, "reported_mutagensis": 5, "reported_glycation": 0, "reported_snv": 3, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 4, "binding_glycan_count": 0, "secondary_ac_list": "Q3TNX1;Q6ZPP9;Q99L16;Q9QXM9", "ec_number_list": "", "go_molecular_function": "GO:0003779 actin binding;GO:0051015 actin filament binding", "go_cellular_component": "GO:0005856 cytoskeleton;GO:0005874 microtubule;GO:0005912 adherens junction;GO:0045177 apical part of cell;GO:0016324 apical plasma membrane", "go_biological_process": "GO:0043482 cellular pigment accumulation;GO:0007015 actin filament organization;GO:0000902 cell morphogenesis;GO:0030036 actin cytoskeleton organization;GO:0001843 neural tube closure", "synthesized_glycan_count": 0, "hit_score": 1.6, "record_id": "Q9QXN0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8R550-1", "uniprot_id": "SH3K1_MOUSE", "mass": 78170.0, "length": 709, "protein_name": "SH3 domain-containing kinase-binding protein 1", "gene_name": "Sh3kbp1", "organism": "Mouse", "refseq_name": "SH3 domain-containing kinase-binding protein 1 isoform 1", "refseq_ac": "NP_001129199", "gene_names_uniprotkb": "Sh3kbp1; Ruk; Seta", "gene_names_refseq": "1200007H22Rik; 1700125L08Rik; 5830464D22Rik; Cin85; IN85; Ruk; Seta; Sh3kbp1", "protein_names_uniprotkb": "SH3 domain-containing kinase-binding protein 1; Regulator of ubiquitous kinase; Ruk; SH3-containing, expressed in tumorigenic astrocytes", "protein_names_refseq": "Ruk(deltaA) protein; Ruk(h) protein; Ruk(l) protein; Ruk(m1) protein; Ruk(m3) protein; Ruk(t) protein; Ruk(xl) protein; SH3 domain-containing kinase-binding protein 1 isoform 1; SH3 domain-containing kinase-binding protein 1; SH3-containing, expressed in tumorigenic astrocytes; regulator of ubiquitous kinase", "tax_id": 10090, "disease": "immunodeficiency 61 (Disease Ontology:DOID:0111999); nephrotic syndrome (Disease Ontology:DOID:1184); tauopathy (Disease Ontology:DOID:680)", "pathway": " (mmu:58194); (R-MMU-182971); (R-MMU-6807004); (R-MMU-8856825); (R-MMU-8856828); (R-MMU-8866376); (R-MMU-983695)", "pathway_count": 7, "publication_count": 15, "publication_id_list": "10.1101/2023.09.13.557529;10965144;11152963;12242006;17242355;18602463;19144319;21183079;21750661;21830225;23178720;26495903;29589748;30723173;35548969", "class_list": "", "function": "ADAPTOR PROTEIN Ruk/CIN85REGULATES REDOX BALANCE IN 4T1MOUSE BREAST CANCER CELLS EXPOSED TO PLASMIN(OGEN)., [RefSeq, PubMed]; Adapter protein involved in regulating diverse signal transduction pathways. Involved in the regulation of endocytosis and lysosomal degradation of ligand-induced receptor tyrosine kinases, including EGFR and MET/hepatocyte growth factor receptor, through an association with CBL and endophilins. The association with CBL, and thus the receptor internalization, may be inhibited by an interaction with PDCD6IP and/or SPRY2. Involved in regulation of ligand-dependent endocytosis of the IgE receptor. Attenuates phosphatidylinositol 3-kinase activity by interaction with its regulatory subunit (By similarity). May be involved in regulation of cell adhesion; promotes the interaction between TTK2B and PDCD6IP. May be involved in the regulation of cellular stress response via the MAPK pathways through its interaction with MAP3K4. Is involved in modulation of tumor necrosis factor mediated apoptosis. Plays a role in the regulation of cell morphology and cytoskeletal organization. Required in the control of cell shape and migration (By similarity). Has an essential role in the stimulation of B cell activation (By similarity)., [UniProtKB, UniProtKB]; Analysis of cDNA clones, ESTs and products of RT-PCR amplifications with different combinations of primers revealed how alternative splicing and promoter usage generate a variety of Ruk transcripts and encoded protein isoforms in different mouse tissues., [RefSeq, PubMed]; Data show that Cbl-interacting protein of 85 kDa (CIN85) limited T cell responses to T cell receptor (TCR) stimulation. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 11, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 2, "disease_count": 3, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "B1AZ86;B1AZ87;Q8CAL8;Q8CEF6;Q8R545;Q8R546;Q8R547;Q8R548;Q8R549;Q8R551;Q9CTQ9;Q9DC14;Q9JKC3", "ec_number_list": "", "go_molecular_function": "GO:0060090 molecular adaptor activity;GO:0017124 SH3 domain binding;GO:0030674 protein-macromolecule adaptor activity;GO:0031625 ubiquitin protein ligase binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0098982 GABA-ergic synapse;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005856 cytoskeleton", "go_biological_process": "GO:0007015 actin filament organization;GO:0016477 cell migration;GO:0006915 apoptotic process;GO:0007010 cytoskeleton organization;GO:0008360 regulation of cell shape", "synthesized_glycan_count": 0, "hit_score": 2.0, "record_id": "Q8R550-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q5DU57-1", "uniprot_id": "SPT13_MOUSE", "mass": 75257.0, "length": 656, "protein_name": "Spermatogenesis-associated protein 13", "gene_name": "Spata13", "organism": "Mouse", "refseq_name": "spermatogenesis-associated protein 13 isoform 1", "refseq_ac": "NP_001028444", "gene_names_uniprotkb": "Spata13", "gene_names_refseq": "ESTM11; Spata13; asef2; mFLJ00298", "protein_names_uniprotkb": "Spermatogenesis-associated protein 13; APC-stimulated guanine nucleotide exchange factor 2; Asef2", "protein_names_refseq": "APC-stimulated guanine nucleotide exchange factor 2; spermatogenesis-associated protein 13 isoform 1; spermatogenesis-associated protein 13", "tax_id": 10090, "disease": "", "pathway": " (mmu:219140); (R-MMU-9013148); (R-MMU-9013149)", "pathway_count": 3, "publication_count": 7, "publication_id_list": "10.1101/2023.09.13.557529;17242355;19893577;21183079;21750661;23525008;31020388", "class_list": "", "function": "Acts as a guanine nucleotide exchange factor (GEF) for RHOA, RAC1 and CDC42 GTPases. Regulates cell migration and adhesion assembly and disassembly through a RAC1, PI3K, RHOA and AKT1-dependent mechanism. Increases both RAC1 and CDC42 activity, but decreases the amount of active RHOA (By similarity). Required for MMP9 up-regulation via the JNK signaling pathway in colorectal tumor cells. Involved in tumor angiogenesis and may play a role in intestinal adenoma formation and tumor progression., [UniProtKB, PubMed]; Asef and Asef2 are required for adenoma formation in Apc(Min/+)mice. [Asef2, mouse], [RefSeq, PubMed]; Spata13 modulates social hierarchy in both male and female mice in addition to affecting voluntary activity in females., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q3TZ09", "ec_number_list": "", "go_molecular_function": "GO:0042802 identical protein binding;GO:0005085 guanyl-nucleotide exchange factor activity", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0030027 lamellipodium;GO:0002102 podosome", "go_biological_process": "GO:0016477 cell migration;GO:0035556 intracellular signal transduction;GO:0046847 filopodium assembly;GO:0030032 lamellipodium assembly;GO:0030334 regulation of cell migration", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "Q5DU57-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3UG20-1", "uniprot_id": "KMT2E_MOUSE", "mass": 204543.0, "length": 1868, "protein_name": "Histone reader KMT2E", "gene_name": "Kmt2e", "organism": "Mouse", "refseq_name": "inactive histone-lysine N-methyltransferase 2E", "refseq_ac": "NP_081260", "gene_names_uniprotkb": "Kmt2e; Mll5", "gene_names_refseq": "1810033J14Rik; 9530077A04Rik; D230038D11Rik; Kmt2e; Mll5; NKp44L", "protein_names_uniprotkb": "Histone reader KMT2E; Inactive histone-lysine N-methyltransferase 2E; Inactive lysine N-methyltransferase 2E; Myeloid/lymphoid or mixed-lineage leukemia protein 5 homolog", "protein_names_refseq": "histone-lysine N-methyltransferase MLL5; inactive histone-lysine N-methyltransferase 2E; myeloid/lymphoid or mixed-lineage leukemia protein 5 homolog", "tax_id": 10090, "disease": "acute promyelocytic leukemia (Disease Ontology:DOID:0060318); prostate cancer (Disease Ontology:DOID:10283); autistic disorder (Disease Ontology:DOID:12849); breast cancer (Disease Ontology:DOID:1612); cervical cancer (Disease Ontology:DOID:4362); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526)", "pathway": " (mmu:69188)", "pathway_count": 1, "publication_count": 14, "publication_id_list": "10.1101/2023.09.13.557529;18376068;18818388;18854576;18952892;19264965;21183079;21750661;27641306;29593341;31219806;34428180;35820727;36534336", "class_list": "", "function": "Associates with chromatin regions downstream of transcriptional start sites of active genes and thus regulates gene transcription (By similarity). Chromatin interaction is mediated via the binding to tri-methylated histone H3 at 'Lys-4' (H3K4me3) (By similarity). Key regulator of hematopoiesis involved in terminal myeloid differentiation and in the regulation of hematopoietic stem cell (HSCs) self-renewal by a mechanism that involves DNA methylation (PubMed:18818388, PubMed:18854576, PubMed:18952892). Also acts as an important cell cycle regulator, participating in cell cycle regulatory network machinery at multiple cell cycle stages including G1/S transition, S phase progression and mitotic entry (PubMed:19264965). Recruited to E2F1 responsive promoters by HCFC1 where it stimulates tri-methylation of histone H3 at 'Lys-4' and transcriptional activation and thereby facilitates G1 to S phase transition (By similarity). During myoblast differentiation, required to suppress inappropriate expression of S-phase-promoting genes and maintain expression of determination genes in quiescent cells (PubMed:19264965)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed, PubMed]; Findings establish several nonredundant functions for Mll5, including an essential role in regulating proliferation and functional integrity of hematopoietic stem/progenitor cells, [RefSeq, PubMed]; Inactivation of the Mll5 gene in mice results in a 30% reduction in the average representation of hematopoietic stem cells and in functional impairment of long-term hematopoietic repopulation potential under competitive conditions, [RefSeq, PubMed]; KMT2E Haploinsufficiency Manifests Autism-Like Behaviors and Amygdala Neuronal Development Dysfunction in Mice., [RefSeq, PubMed]; MLL5 has a role in suppressing antiviral innate immune response by facilitating STUB1-mediated RIG-I degradation Publication Status: Online-Only, [RefSeq, PubMed]; MLL5 is a key regulator of normal hematopoiesis, [RefSeq, PubMed]; MLL5 plays an integral role in novel chromatin regulatory mechanisms that suppress inappropriate expression of S-phase-promoting genes and maintain expression of determination genes in quiescent cells., [RefSeq, PubMed]; Toxic reactive oxygen species levels in Mll5(-/-) mice are critically dependent on type 1 interferon (IFN-1) signaling, which triggers mitochondrial accumulation of full-length Bid.[IFN-1] Erratum:[Cell Stem Cell. 2017 Mar 2;20(3):415. doi: 10.1016/j.stem.2017.02.002. PMID: 28257711], [RefSeq, PubMed]", "predicted_glycosites": 13, "predicted_n_glycosites": 0, "predicted_o_glycosites": 13, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 5, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 9753, "biomarker_type": "", "glycan_count": 1, "disease_count": 6, "glyco_site_count": 14, "binding_glycan_count": 0, "secondary_ac_list": "Q3SYI5;Q3TUY2;Q3V410;Q5FWI1;Q6P3B3;Q8BS65;Q8CFX7;Q9CVK6", "ec_number_list": "", "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0008270 zinc ion binding;GO:0019899 enzyme binding;GO:0042800 histone H3K4 methyltransferase activity;GO:0140002 histone H3K4me3 reader activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0016607 nuclear speck", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0002446 neutrophil mediated immunity;GO:0006355 regulation of DNA-templated transcription;GO:0030218 erythrocyte differentiation;GO:0045893 positive regulation of DNA-templated transcription", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "Q3UG20-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8K3V7-1", "uniprot_id": "MNAR1_MOUSE", "mass": 102792.0, "length": 917, "protein_name": "Major intrinsically disordered Notch2-binding receptor 1", "gene_name": "Minar1", "organism": "Mouse", "refseq_name": "major intrinsically disordered Notch2-binding receptor 1", "refseq_ac": "NP_705729", "gene_names_uniprotkb": "Minar1; AF529169; Ubtor", "gene_names_refseq": "DD1; Kiaa1024; Minar1", "protein_names_uniprotkb": "Major intrinsically disordered Notch2-binding receptor 1; Membrane integral NOTCH2-associated receptor 1; Protein DD1; Ubiquitination and mTOR signaling protein", "protein_names_refseq": "major intrinsically disordered Notch2-binding receptor 1; ubiquitination and mTOR signaling protein", "tax_id": 10090, "disease": "", "pathway": " (mmu:209743)", "pathway_count": 1, "publication_count": 3, "publication_id_list": "21183079;21750661;34887587", "class_list": "", "function": "Intrinsically disordered protein which may negatively regulate mTOR signaling pathway by stabilizing the mTOR complex component DEPTOR. Negatively regulates angiogenesis. Negatively regulates cell growth (By similarity). Negatively regulates neurite outgrowth in hippocampal neurons (By similarity)., [UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q14CG5;Q69ZS9", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005886 plasma membrane;GO:0012505 endomembrane system", "go_biological_process": "GO:0001525 angiogenesis;GO:0008285 negative regulation of cell population proliferation;GO:0010977 negative regulation of neuron projection development;GO:0030308 negative regulation of cell growth;GO:0016525 negative regulation of angiogenesis", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "Q8K3V7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q99K10-1", "uniprot_id": "NLGN1_MOUSE", "mass": 94149.0, "length": 843, "protein_name": "Neuroligin-1", "gene_name": "Nlgn1", "organism": "Mouse", "refseq_name": "neuroligin-1 isoform 1 precursor", "refseq_ac": "NP_619607", "gene_names_uniprotkb": "Nlgn1; Kiaa1070", "gene_names_refseq": "6330415N05Rik; NL1; Nlg1; Nlgn1; mKIAA1070", "protein_names_uniprotkb": "Neuroligin-1", "protein_names_refseq": "neuroligin-1 isoform 1 precursor", "tax_id": 10090, "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); autistic disorder (Disease Ontology:DOID:12849); status epilepticus (Disease Ontology:DOID:1824)", "pathway": " (mmu:192167); (R-MMU-6794361)", "pathway_count": 2, "publication_count": 18, "publication_id_list": "10.1101/2023.09.13.557529;10892652;11329178;15620359;16982420;17897391;18084303;18434543;19926856;20147539;21750661;23716671;28841651;28972980;30100184;32324534;33300544;37865312", "class_list": "", "function": "Cell surface protein involved in cell-cell-interactions via its interactions with neurexin family members. Plays a role in synapse function and synaptic signal transmission, and probably mediates its effects by recruiting and clustering other synaptic proteins. May promote the initial formation of synapses, but is not essential for this. In vitro, triggers the de novo formation of presynaptic structures. May be involved in specification of excitatory synapses. Required to maintain wakefulness quality and normal synchrony of cerebral cortex activity during wakefulness and sleep (PubMed:23716671). The protein is involved in nervous system development., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 3, "predicted_n_glycosites": 1, "predicted_o_glycosites": 2, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 3, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 3, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 4, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 4, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 7, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 3, "disease_count": 3, "glyco_site_count": 7, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0042802 identical protein binding;GO:0050839 cell adhesion molecule binding;GO:0044877 protein-containing complex binding;GO:0030165 PDZ domain binding;GO:0097110 scaffold protein binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0014069 postsynaptic density", "go_biological_process": "GO:0072553 terminal button organization;GO:0016080 synaptic vesicle targeting;GO:0048789 cytoskeletal matrix organization at active zone;GO:0097091 synaptic vesicle clustering;GO:0097115 neurexin clustering involved in presynaptic membrane assembly", "synthesized_glycan_count": 0, "hit_score": 2.7, "record_id": "Q99K10-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8C5D8-1", "uniprot_id": "PIAS2_MOUSE", "mass": 68426.0, "length": 621, "protein_name": "E3 SUMO-protein ligase PIAS2", "gene_name": "Pias2", "organism": "Mouse", "refseq_name": "E3 SUMO-protein ligase PIAS2 isoform 2", "refseq_ac": "NP_001157639", "gene_names_uniprotkb": "Pias2; Miz1; Piasx", "gene_names_refseq": "ARIP3; DIP; Dib; Miz1; PIASxalpha6; PIASxalpha; PIASxbeta; PIASxb; Pias2; SIZ2", "protein_names_uniprotkb": "E3 SUMO-protein ligase PIAS2; 2.3.2.27; ARIP3; Androgen receptor-interacting protein 3; DAB2-interacting protein; DIP; Msx-interacting zinc finger protein; Protein inhibitor of activated STAT x; Protein inhibitor of activated STAT2; RING-type E3 ubiquitin transferase PIAS2", "protein_names_refseq": "DAB2-interacting protein; E3 SUMO-protein ligase PIAS2 isoform 2; E3 SUMO-protein ligase PIAS2; Msx-interacting-zinc finger; RING-type E3 ubiquitin transferase PIAS2; androgen receptor-interacting protein 3; msx-interacting zinc finger protein; protein inhibitor of activated STAT x", "tax_id": 10090, "disease": "hematologic cancer (Disease Ontology:DOID:2531)", "pathway": " (mmu:17344)", "pathway_count": 1, "publication_count": 17, "publication_id_list": "11104669;12077349;12193603;15767674;21183079;21750661;25428506;30084848;30779550;31219806;34203471;34428180;35833903;38579014;38593156;40997131;9256341", "class_list": "", "function": "Functions as an E3-type small ubiquitin-like modifier (SUMO) ligase, stabilizing the interaction between UBE2I and the substrate, and as a SUMO-tethering factor. Plays a crucial role as a transcriptional coregulation in various cellular pathways, including the STAT pathway, the p53 pathway and the steroid hormone signaling pathway. The effects of this transcriptional coregulation, transactivation or silencing may vary depending upon the biological context and PIAS2 isoform studied. However, it seems to be mostly involved in gene silencing. Binds to sumoylated ELK1 and enhances its transcriptional activity by preventing recruitment of HDAC2 by ELK1, thus reversing SUMO-mediated repression of ELK1 transactivation activity. Isoform PIASx-beta, but not isoform PIASx-alpha, promotes MDM2 sumoylation. Isoform PIASx-alpha promotes PARK7 sumoylation. Isoform PIASx-beta promotes NCOA2 sumoylation more efficiently than isoform PIASx-alpha (By similarity). Sumoylates PML at'Lys-65' and 'Lys-160' (By similarity)., [UniProtKB]; Miz1 represses type I interferon production and limits viral clearance during influenza A virus infection., [RefSeq, PubMed]; Regulation of BCR-mediated Ca[2+] mobilization by MIZ1-TMBIM4 safeguards IgG1[+] GC B cell-positive selection., [RefSeq, PubMed]; Suppression of Allergic Asthma by Loss of Function of Miz1-mediated Th1 Skewing., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "O54987;Q8C384;Q8CDQ8;Q8K208;Q99JX5;Q9D5W7;Q9QZ63", "ec_number_list": "", "go_molecular_function": "GO:0061665 SUMO ligase activity;GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0019904 protein domain specific binding;GO:0003714 transcription corepressor activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016607 nuclear speck;GO:0016604 nuclear body;GO:0016605 PML body", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0016925 protein sumoylation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription", "synthesized_glycan_count": 0, "hit_score": 2.0, "record_id": "Q8C5D8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9EPA7-1", "uniprot_id": "NMNA1_MOUSE", "mass": 32355.0, "length": 285, "protein_name": "Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1", "gene_name": "Nmnat1", "organism": "Mouse", "refseq_name": "nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1", "refseq_ac": "NP_597679", "gene_names_uniprotkb": "Nmnat1; D4Cole1e; Nmnat", "gene_names_refseq": "2610529L11Rik; 5730441G13Rik; D4Cole1e; Nmnat1; nmnat", "protein_names_uniprotkb": "Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1; 2.7.7.18; 2.7.7.1; NMN adenylyltransferase 1; NMN/NaMN adenylyltransferase 1; NaMN adenylyltransferase 1; Nicotinamide mononucleotide adenylyltransferase 1; Nicotinate-nucleotide adenylyltransferase 1", "protein_names_refseq": "NMN adenylyltransferase 1; NMN/NaMN adenylyltransferase 1; naMN adenylyltransferase 1; nicotinamide mononucleotide adenylyl transferase; nicotinamide mononucleotide adenylyltransferase 1; nicotinamide/nicotinate mononucleotide adenylyltransferase 1; nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1; nicotinate-nucleotide adenylyltransferase 1", "tax_id": 10090, "disease": "Leber congenital amaurosis 9 (Disease Ontology:DOID:0110005); spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis (Disease Ontology:DOID:0112290); sciatic neuropathy (Disease Ontology:DOID:11446); neurodegenerative disease (Disease Ontology:DOID:1289); retinal degeneration (Disease Ontology:DOID:8466)", "pathway": " (mmu:66454); (R-MMU-196807)", "pathway_count": 2, "publication_count": 13, "publication_id_list": "11027338;15310905;15381699;16914673;19403820;21750661;22425156;27735788;32822587;34428180;37421924;38237740;38928090", "class_list": "", "function": "Adipocyte NMNAT1 expression is essential for nuclear NAD[+] biosynthesis but dispensable for regulating thermogenesis and whole-body energy metabolism., [RefSeq, PubMed]; Catalyzes the formation of NAD(+) from nicotinamide mononucleotide (NMN) and ATP (PubMed:15381699, PubMed:19403820, PubMed:27735788). Can also use the deamidated form; nicotinic acid mononucleotide (NaMN) as substrate with the same efficiency (By similarity). Can use triazofurin monophosphate (TrMP) as substrate (By similarity). Also catalyzes the reverse reaction, i.e. the pyrophosphorolytic cleavage of NAD(+) (By similarity). For the pyrophosphorolytic activity, prefers NAD(+) and NaAD as substrates and degrades NADH, nicotinic acid adenine dinucleotide phosphate (NHD) and nicotinamide guanine dinucleotide (NGD) less effectively (By similarity). Involved in the synthesis of ATP in the nucleus, together with PARP1, PARG and NUDT5 (By similarity). Nuclear ATP generation is required for extensive chromatin remodeling events that are energy-consuming (By similarity). Fails to cleave phosphorylated dinucleotides NADP(+), NADPH and NaADP(+) (By similarity). Also acts as a cofactor for glutamate and aspartate ADP-ribosylation by directing PARP1 catalytic activity to glutamate and aspartate residues on histones (PubMed:32822587). Protects against axonal degeneration following mechanical or toxic insults (PubMed:15310905, PubMed:16914673, PubMed:19403820, PubMed:22425156). Delays axonal degeneration after axotomy; results in a >10-fold increase in intact neurites 72 hours after injury (PubMed:16914673, PubMed:19403820, PubMed:27735788). Neural protection does not correlate with cellular NAD(+) levels but may still require enzyme activity (PubMed:19403820)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]; Nmnat1 Deficiency Causes Mitoribosome Excess in Diabetic Nephropathy Mediated by Transcriptional Repressor HIC1. Publication Status: Online-Only, [RefSeq, PubMed]; Nuclear Nicotinamide Adenine Dinucleotide Deficiency by Nmnat1 Deletion Impaired Hepatic Insulin Signaling, Mitochondrial Function, and Hepatokine Expression in Mice Fed a High-Fat Diet., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 3, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 5, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q6B504", "ec_number_list": "2.7.7.1;2.7.7.18", "go_molecular_function": "GO:0005524 ATP binding;GO:0042802 identical protein binding;GO:0004515 nicotinate-nucleotide adenylyltransferase activity;GO:0000309 nicotinamide-nucleotide adenylyltransferase activity;GO:0140768 protein ADP-ribosyltransferase-substrate adaptor activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0016604 nuclear body;GO:0000785 chromatin", "go_biological_process": "GO:0043410 positive regulation of MAPK cascade;GO:0045892 negative regulation of DNA-templated transcription;GO:0043524 negative regulation of neuron apoptotic process;GO:0009611 response to wounding;GO:0009435 NAD+ biosynthetic process", "synthesized_glycan_count": 0, "hit_score": 1.4, "record_id": "Q9EPA7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BMA5-1", "uniprot_id": "NPAT_MOUSE", "mass": 152176.0, "length": 1420, "protein_name": "Protein NPAT", "gene_name": "Npat", "organism": "Mouse", "refseq_name": "protein NPAT isoform 1", "refseq_ac": "NP_001074621", "gene_names_uniprotkb": "Npat", "gene_names_refseq": "6820401K01; Npat", "protein_names_uniprotkb": "Protein NPAT", "protein_names_refseq": "protein NPAT isoform 1; protein NPAT", "tax_id": 10090, "disease": "", "pathway": " (mmu:244879)", "pathway_count": 1, "publication_count": 10, "publication_id_list": "12665581;17003125;21183079;21913724;21952136;31084574;31219806;35820727;35922064;9199343", "class_list": "", "function": "NPAT Supports CD8(+) Immature Single-Positive Thymocyte Proliferation and Thymic Development., [RefSeq, PubMed]; Our data indicates that the function of Npat-dependent Sertoli cells is essential at multiple steps in testis development, and this study also identifies Sertoli cells as a major regulator of germ cell development, which are required to maintain a local growth niche to repress premature mitosis and meiosis of gonocytes., [RefSeq, PubMed]; Transcription regulator required for progression through the G1 and S phases of the cell cycle and for S phase entry (By similarity). Acts as a key transcription regulator of histones (By similarity). Activates transcription of the histone H2A, histone H2B, histone H3 and histone H4 genes in conjunction with GON4L and MIZF (By similarity). Together with CRAMP1, binds to the promoters of H1 genes (H1-2, H1-3, H1-4, H1-5 and H1-10/H1x), driving their transcription (By similarity). Also positively regulates the ATM, MIZF and PRKDC promoters (By similarity). Transcriptional activation may be accomplished at least in part by the recruitment of the NuA4 histone acetyltransferase (HAT) complex to target gene promoters (By similarity)., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 10, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q8BWA9;Q8BY06", "ec_number_list": "", "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0003714 transcription corepressor activity;GO:0003712 transcription coregulator activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0016604 nuclear body;GO:0005694 chromosome", "go_biological_process": "GO:0001701 in utero embryonic development;GO:0006351 DNA-templated transcription;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0045893 positive regulation of DNA-templated transcription;GO:0044843 cell cycle G1/S phase transition", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q8BMA5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9QY53-1", "uniprot_id": "NPHP1_MOUSE", "mass": 77035.0, "length": 687, "protein_name": "Nephrocystin-1", "gene_name": "Nphp1", "organism": "Mouse", "refseq_name": "nephrocystin-1 isoform a", "refseq_ac": "NP_058598", "gene_names_uniprotkb": "Nphp1; Nph1", "gene_names_refseq": "Nphp1", "protein_names_uniprotkb": "Nephrocystin-1", "protein_names_refseq": "nephrocystin-1 isoform a; nephrocystin-1", "tax_id": 10090, "disease": "Senior-Loken syndrome (Disease Ontology:DOID:0050576); Joubert syndrome 4 (Disease Ontology:DOID:0110999); nephronophthisis 1 (Disease Ontology:DOID:0111112); nephronophthisis (Disease Ontology:DOID:12712); Bardet-Biedl syndrome (Disease Ontology:DOID:1935)", "pathway": " (mmu:53885); (R-MMU-5620912)", "pathway_count": 2, "publication_count": 16, "publication_id_list": "10665934;10739664;11493697;12006559;16885411;18477472;18684731;19208653;20856870;21565611;21750661;25671767;29899041;33961633;34415307;40021952", "class_list": "", "function": "An Nphp1 knockout mouse model targeting exon 2-20 demonstrates characteristic phenotypes of human nephronophthisis., [RefSeq, PubMed]; Differential requirement of NPHP1 for compartmentalized protein localization during photoreceptor outer segment development and maintenance. Publication Status: Online-Only, [RefSeq, PubMed]; Together with BCAR1 it may play a role in the control of epithelial cell polarity. Involved in the organization of apical junctions in kidney cells, together with NPHP4 and RPGRIP1L/NPHP8 (PubMed:21565611). Does not seem to be strictly required for ciliogenesis (PubMed:19208653). Seems to help to recruit PTK2B/PYK2 to cell matrix adhesions, thereby initiating phosphorylation of PTK2B/PYK2 and PTK2B/PYK2-dependent signaling (PubMed:11493697). May play a role in the regulation of intraflagellar transport (IFT) during cilia assembly (PubMed:19208653). Required for normal retina development (PubMed:19208653). In connecting photoreceptor cilia influences the movement of some IFT proteins such as IFT88 and WDR19 (PubMed:19208653). Involved in spermatogenesis; required for the differentiation of early elongating spermatids into spermatozoa (PubMed:18684731)., [UniProtKB, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 5, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q9D7G8;Q9QZP0;Q9WUZ2", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005911 cell-cell junction;GO:0005912 adherens junction;GO:0005923 bicellular tight junction;GO:0005929 cilium", "go_biological_process": "GO:0060041 retina development in camera-type eye;GO:0008104 intracellular protein localization;GO:0035845 photoreceptor cell outer segment organization;GO:0030030 cell projection organization;GO:0048515 spermatid differentiation", "synthesized_glycan_count": 0, "hit_score": 1.9, "record_id": "Q9QY53-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9QZS7-1", "uniprot_id": "NPHN_MOUSE", "mass": 136336.0, "length": 1256, "protein_name": "Nephrin", "gene_name": "Nphs1", "organism": "Mouse", "refseq_name": "nephrin precursor", "refseq_ac": "NP_062332", "gene_names_uniprotkb": "Nphs1; Nphn", "gene_names_refseq": "NephrinB; Nphs1; nephrin", "protein_names_uniprotkb": "Nephrin; Renal glomerulus-specific cell adhesion receptor", "protein_names_refseq": "nephrin 1; nephrin precursor; nephrosis 1 homolog, nephrin; renal glomerulus-specific cell adhesion receptor", "tax_id": 10090, "disease": "nephrotic syndrome type 1 (Disease Ontology:DOID:0080390); kidney failure (Disease Ontology:DOID:1074); membranous glomerulonephritis (Disease Ontology:DOID:10976); nephrotic syndrome (Disease Ontology:DOID:1184); kidney disease (Disease Ontology:DOID:557); proteinuria (Disease Ontology:DOID:576); end stage renal disease (Disease Ontology:DOID:783)", "pathway": " (mmu:54631); (R-MMU-373753)", "pathway_count": 2, "publication_count": 17, "publication_id_list": "10504499;10820162;11136707;11733379;11733557;12039968;12424224;12538735;12660326;15843475;17537921;18752272;19470472;19887377;21750661;28179596;35820727", "class_list": "", "function": "Seems to play a role in the development or function of the kidney glomerular filtration barrier. Regulates glomerular vascular permeability. May anchor the podocyte slit diaphragm to the actin cytoskeleton. Plays a role in skeletal muscle formation through regulation of myoblast fusion., [UniProtKB, PubMed, PubMed, PubMed]", "predicted_glycosites": 10, "predicted_n_glycosites": 10, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 5, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 4, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 7, "glyco_site_count": 10, "binding_glycan_count": 0, "secondary_ac_list": "D2KXA7;Q811S5;Q925S5;Q9ESC6;Q9ET59;Q9JIX1", "ec_number_list": "", "go_molecular_function": "GO:0019904 protein domain specific binding;GO:0051393 alpha-actinin binding;GO:0030507 spectrin binding;GO:0050839 cell adhesion molecule binding;GO:0017022 myosin binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0005911 cell-cell junction;GO:0005925 focal adhesion;GO:0016020 membrane;GO:0071944 cell periphery", "go_biological_process": "GO:0036060 slit diaphragm assembly;GO:0007155 cell adhesion;GO:0000165 MAPK cascade;GO:0007254 JNK cascade;GO:0098609 cell-cell adhesion", "synthesized_glycan_count": 0, "hit_score": 1.8, "record_id": "Q9QZS7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BK35-1", "uniprot_id": "NOP53_MOUSE", "mass": 55793.0, "length": 484, "protein_name": "Ribosome biogenesis protein NOP53", "gene_name": "Nop53", "organism": "Mouse", "refseq_name": "ribosome biogenesis protein NOP53", "refseq_ac": "NP_598592", "gene_names_uniprotkb": "Nop53; Gltscr2; Pict1", "gene_names_refseq": "5330430H08Rik; 9430097C02Rik; Gltscr2; Nop53; PICT-1", "protein_names_uniprotkb": "Ribosome biogenesis protein NOP53; Glioma tumor suppressor candidate region gene 2 protein; PreS1-binding protein", "protein_names_refseq": "glioma tumor suppressor candidate region gene 2 protein; preS1-binding protein; ribosome biogenesis protein NOP53", "tax_id": 10090, "disease": "", "pathway": " (mmu:68077)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "16971513;17242355;21183079;21804542;34428180", "class_list": "", "function": "Nucleolar protein which is involved in the integration of the 5S RNP into the ribosomal large subunit during ribosome biogenesis. In ribosome biogenesis, may also play a role in rRNA transcription (By similarity). Also functions as a nucleolar sensor that regulates the activation of p53/TP53 in response to ribosome biogenesis perturbation, DNA damage and other stress conditions. DNA damage or perturbation of ribosome biogenesis disrupt the interaction between NOP53 and RPL11 allowing RPL11 transport to the nucleoplasm where it can inhibit MDM2 and allow p53/TP53 activation (PubMed:21804542). It may also positively regulate the function of p53/TP53 in cell cycle arrest and apoptosis through direct interaction, preventing its MDM2-dependent ubiquitin-mediated proteasomal degradation. Originally identified as a tumor suppressor, it may also play a role in cell proliferation and apoptosis by positively regulating the stability of PTEN, thereby antagonizing the PI3K-AKT/PKB signaling pathway. May also inhibit cell proliferation and increase apoptosis through its interaction with NF2. May negatively regulate NPM1 by regulating its nucleoplasmic localization, oligomerization and ubiquitin-mediated proteasomal degradation. Thereby, may prevent NPM1 interaction with MYC and negatively regulate transcription mediated by the MYC-NPM1 complex. May also regulate cellular aerobic respiration. In the cellular response to viral infection, may play a role in the attenuation of interferon-beta through the inhibition of RIGI (By similarity)., [UniProtKB, UniProtKB, PubMed]; These results suggest that PICT-1 plays a role in phosphatidylinositol 3,4,5-trisphosphate signals through controlling PTEN protein stability., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q8VD18", "ec_number_list": "", "go_molecular_function": "GO:0042802 identical protein binding;GO:0002039 p53 binding;GO:0008097 5S rRNA binding", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005829 cytosol;GO:0001650 fibrillar center;GO:0033553 rDNA heterochromatin", "go_biological_process": "GO:1902570 protein localization to nucleolus;GO:1903006 positive regulation of protein K63-linked deubiquitination;GO:1990173 protein localization to nucleoplasm;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006281 DNA repair", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "Q8BK35-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q99NF2-1", "uniprot_id": "NSMF_MOUSE", "mass": 60293.0, "length": 532, "protein_name": "NMDA receptor synaptonuclear signaling and neuronal migration factor", "gene_name": "Nsmf", "organism": "Mouse", "refseq_name": "NMDA receptor synaptonuclear signaling and neuronal migration factor isoform A", "refseq_ac": "NP_001034475", "gene_names_uniprotkb": "Nsmf; Jac; Nelf", "gene_names_refseq": "Jacob; Nelf; Nsmf", "protein_names_uniprotkb": "NMDA receptor synaptonuclear signaling and neuronal migration factor; Jacob protein; Juxtasynaptic attractor of caldendrin on dendritic boutons protein; Nasal embryonic LHRH factor; Nasal embryonic luteinizing hormone-releasing hormone factor", "protein_names_refseq": "NMDA receptor synaptonuclear signaling and neuronal migration factor isoform A; juxtasynaptic attractor of caldendrin on dendritic boutons protein; nasal embryonic LHRH factor; nasal embryonic luteinizing hormone-releasing hormone factor", "tax_id": 10090, "disease": "hypogonadotropic hypogonadism 7 with or without anosmia (Disease Ontology:DOID:0090078); hypogonadotropic hypogonadism 9 with or without anosmia (Disease Ontology:DOID:0090085); Kallmann syndrome (Disease Ontology:DOID:3614)", "pathway": " (mmu:56876)", "pathway_count": 1, "publication_count": 11, "publication_id_list": "10.1101/2023.09.13.557529;10898796;15018815;19608740;20025934;21183079;21750661;31219806;34428180;36774487;37516276", "class_list": "", "function": "A Jacob/nsmf gene knockout does not protect against acute hypoxia- and NMDA-induced excitotoxic cell death. Publication Status: Online-Only, [RefSeq, PubMed]; Calpain-mediated clipping of the myristoylated N terminus of Jacob is required for its nuclear translocation after N-methyl-d-aspartate receptor activation, [RefSeq, PubMed]; Couples NMDA-sensitive glutamate receptor signaling to the nucleus and triggers long-lasting changes in the cytoarchitecture of dendrites and spine synapse processes. Part of the cAMP response element-binding protein (CREB) shut-off signaling pathway. Stimulates outgrowth of olfactory axons and migration of gonadotropin-releasing hormone (GnRH) and luteinizing-hormone-releasing hormone (LHRH) neuronal cells., [UniProtKB, PubMed]; Investigation of subfertility in the female Nsmf knockout mouse., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "A2AJ93;A2AJ94;Q8BPT0;Q8C9R5;Q9DBF4;Q9ERZ1", "ec_number_list": "", "go_molecular_function": "GO:0048306 calcium-dependent protein binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005634 nucleus;GO:0005635 nuclear envelope;GO:0005654 nucleoplasm;GO:0005737 cytoplasm", "go_biological_process": "GO:0048814 regulation of dendrite morphogenesis;GO:0043523 regulation of neuron apoptotic process;GO:0048168 regulation of neuronal synaptic plasticity;GO:0071230 cellular response to amino acid stimulus;GO:0071257 cellular response to electrical stimulus", "synthesized_glycan_count": 0, "hit_score": 1.4, "record_id": "Q99NF2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O35129-1", "uniprot_id": "PHB2_MOUSE", "mass": 33296.0, "length": 299, "protein_name": "Prohibitin-2", "gene_name": "Phb2", "organism": "Mouse", "refseq_name": "prohibitin-2", "refseq_ac": "NP_031557", "gene_names_uniprotkb": "Phb2; Bap; Bcap37; Rea", "gene_names_refseq": "BAP; Bap37; Bcap37; Phb2; REA", "protein_names_uniprotkb": "Prohibitin-2; B-cell receptor-associated protein BAP37; Repressor of estrogen receptor activity", "protein_names_refseq": "B-cell receptor-associated protein 37; B-cell receptor-associated protein BAP37; prohibitin-2; repressor of estrogen receptor activity", "tax_id": 10090, "disease": "", "pathway": " (mmu:12034); (R-MMU-8949664); (R-MMU-9840373)", "pathway_count": 3, "publication_count": 34, "publication_id_list": "10.1101/2023.09.13.557529;11302691;12878603;15140878;17565718;20959514;21689744;21750661;23241883;23576753;24856930;25605945;26495903;28017329;30084848;30779550;31522117;31599954;31819158;33300544;34428180;35820727;36288343;37453647;37507081;37828378;38464826;38763352;38856931;39627609;39927985;8070406;9445485;9798653", "class_list": "", "function": "In the mitochondria, together with PHB, forms large ring complexes (prohibitin complexes) in the inner mitochondrial membrane (IMM) and functions as a chaperone protein that stabilizes mitochondrial respiratory enzymes and maintains mitochondrial integrity in the IMM, which is required for mitochondrial morphogenesis, neuronal survival, and normal lifespan. The prohibitin complex, with DNAJC19, regulates cardiolipin remodeling and the protein turnover of OMA1 in a cardiolipin-binding manner. Also regulates cytochrome-c oxidase assembly (COX) and mitochondrial respiration. Binding to sphingoid 1-phosphate (SPP) modulates its regulator activity. Has a key role of mitophagy receptor involved in targeting mitochondria for autophagic degradation. Involved in mitochondrial-mediated antiviral innate immunity, activates RIG-I-mediated signal transduction and production of IFNB1 and pro-inflammatory cytokine IL6., [UniProtKB, UniProtKB, UniProtKB]; In the mitochondria, together with PHB1, forms large ring complexes (prohibitin complexes) in the inner mitochondrial membrane (IMM) and functions as a chaperone protein that stabilizes mitochondrial respiratory enzymes and maintains mitochondrial integrity in the IMM, which is required for mitochondrial morphogenesis, neuronal survival, and normal lifespan (Probable). The prohibitin complex, with DNAJC19, regulates cardiolipin remodeling and the protein turnover of OMA1 in a cardiolipin-binding manner (PubMed:31819158). Also regulates cytochrome-c oxidase assembly (COX) and mitochondrial respiration. Binding to sphingoid 1-phosphate (SPP) modulates its regulator activity (PubMed:11302691, PubMed:20959514). Has a key role of mitophagy receptor involved in targeting mitochondria for autophagic degradation (PubMed:28017329). Involved in mitochondrial-mediated antiviral innate immunity, activates RIG-I-mediated signal transduction and production of IFNB1 and pro-inflammatory cytokine IL6 (PubMed:31522117)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed]; In the nucleus, serves as transcriptional co-regulator (Probable). Acts as a mediator of transcriptional repression by nuclear hormone receptors via recruitment of histone deacetylases. Functions as an estrogen receptor (ER)-selective coregulator that potentiates the inhibitory activities of antiestrogens and represses the activity of estrogens. Competes with NCOA1 for modulation of ER transcriptional activity (PubMed:12878603, PubMed:15140878)., [UniProtKB, PubMed, PubMed]; In the nucleus, serves as transcriptional co-regulator. Acts as a mediator of transcriptional repression by nuclear hormone receptors via recruitment of histone deacetylases. Functions as an estrogen receptor (ER)-selective coregulator that potentiates the inhibitory activities of antiestrogens and represses the activity of estrogens. Competes with NCOA1 for modulation of ER transcriptional activity., [UniProtKB, UniProtKB, UniProtKB]; In the plasma membrane, is involved in IGFBP6-induced cell migration (By similarity). Cooperates with CD86 to mediate CD86-signaling in B lymphocytes that regulates the level of IgG1 produced through the activation of distal signaling intermediates. Upon CD40 engagement, required to activate NF-kappa-B signaling pathway via phospholipase C and protein kinase C activation (PubMed:23241883)., [UniProtKB, UniProtKB, PubMed]; In the plasma membrane, is involved in IGFBP6-induced cell migration. Cooperates with CD86 to mediate CD86-signaling in B lymphocytes that regulates the level of IgG1 produced through the activation of distal signaling intermediates. Upon CD40 engagement, required to activate NF-kappa-B signaling pathway via phospholipase C and protein kinase C activation., [UniProtKB, UniProtKB, UniProtKB]; PKM2 interacts with and phosphorylates PHB2 to sustain mitochondrial quality control against septic cerebral-cardiac injury. Publication Status: Online-Only, [RefSeq, PubMed]; Prohibitin 2 deficiency in photoreceptors leads to progressive retinal degeneration and facilitated Muller glia engulfing microglia debris., [RefSeq, PubMed]; Protein with pleiotropic attributes mediated in a cell-compartment- and tissue-specific manner, which include the plasma membrane-associated cell signaling functions, mitochondrial chaperone, and transcriptional co-regulator of transcription factors and sex steroid hormones in the nucleus., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, UniProtKB, UniProtKB, UniProtKB]; Pyruvate kinase M2 sustains cardiac mitochondrial quality surveillance in septic cardiomyopathy by regulating prohibitin 2 abundance via S91 phosphorylation. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 3, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "O89075;Q61336", "ec_number_list": "", "go_molecular_function": "GO:0033218 amide binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0046982 protein heterodimerization activity;GO:0046625 sphingolipid binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0098982 GABA-ergic synapse;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005739 mitochondrion", "go_biological_process": "GO:0060762 regulation of branching involved in mammary gland duct morphogenesis;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0016477 cell migration;GO:0043066 negative regulation of apoptotic process", "synthesized_glycan_count": 0, "hit_score": 4.1, "record_id": "O35129-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q501J7-1", "uniprot_id": "PHAR4_MOUSE", "mass": 76632.0, "length": 694, "protein_name": "Phosphatase and actin regulator 4", "gene_name": "Phactr4", "organism": "Mouse", "refseq_name": "phosphatase and actin regulator 4 isoform 2", "refseq_ac": "NP_001155269", "gene_names_uniprotkb": "Phactr4; Kiaa4120", "gene_names_refseq": "3110001B12Rik; C330013F19Rik; Phactr4; mKIAA4120", "protein_names_uniprotkb": "Phosphatase and actin regulator 4; Humdy; Protein Humpty dumpty", "protein_names_refseq": "humdy; phosphatase and actin regulator 4 isoform 2; protein Humpty dumpty", "tax_id": 10090, "disease": "", "pathway": " (mmu:100169)", "pathway_count": 1, "publication_count": 28, "publication_id_list": "15107502;17114649;17242355;17609112;19144319;21183079;21750661;22215812;22517741;22645316;24748504;26495903;28935714;30059200;30679156;31599954;32782141;32848054;34428180;34678516;35061326;35822049;36084651;36852467;37507081;37828378;40021952;40885482", "class_list": "", "function": "Estrogen receptor beta increases clear cell renal cell carcinoma stem cell phenotype via altering the circPHACTR4/miR-34b-5p/c-Myc signaling., [RefSeq, PubMed]; Phactr4 is critical for the spatially and temporally regulated transition in proliferation through differential regulation of PP1 and the cell cycle during neurulation and eye development, [RefSeq, PubMed]; Regulator of protein phosphatase 1 (PP1) required for neural tube and optic fissure closure, and enteric neural crest cell (ENCCs) migration during development. Acts as an activator of PP1 by interacting with PPP1CA and preventing phosphorylation of PPP1CA at 'Thr-320'. During neural tube closure, localizes to the ventral neural tube and activates PP1, leading to down-regulate cell proliferation within cranial neural tissue and the neural retina. Also acts as a regulator of migration of enteric neural crest cells (ENCCs) by activating PP1, leading to dephosphorylation and subsequent activation of cofilin (COF1 or COF2) and repression of the integrin signaling through the RHO/ROCK pathway., [UniProtKB, PubMed, PubMed, UniProtKB, UniProtKB, UniProtKB]; The Phactr4 forms functional associations with intermediate filament networks in adult neural stem cells., [RefSeq, PubMed]", "predicted_glycosites": 3, "predicted_n_glycosites": 0, "predicted_o_glycosites": 3, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 14, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 14, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 14, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 18, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 16, "binding_glycan_count": 0, "secondary_ac_list": "A2ALF7;A2ALG0;F6QNZ3;Q5DTM4;Q6DI97;Q8C7U9", "ec_number_list": "", "go_molecular_function": "GO:0003779 actin binding;GO:0008157 protein phosphatase 1 binding;GO:0004864 protein phosphatase inhibitor activity;GO:0072542 protein phosphatase activator activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0030027 lamellipodium", "go_biological_process": "GO:0048484 enteric nervous system development;GO:0061386 closure of optic fissure;GO:0043085 positive regulation of catalytic activity;GO:0030036 actin cytoskeleton organization;GO:0007266 Rho protein signal transduction", "synthesized_glycan_count": 0, "hit_score": 4.4, "record_id": "Q501J7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VCI5-1", "uniprot_id": "PEX19_MOUSE", "mass": 32733.0, "length": 299, "protein_name": "Peroxisomal biogenesis factor 19", "gene_name": "Pex19", "organism": "Mouse", "refseq_name": "peroxisomal biogenesis factor 19 isoform b", "refseq_ac": "NP_001152997", "gene_names_uniprotkb": "Pex19; Pxf", "gene_names_refseq": "Pex19; Pxf", "protein_names_uniprotkb": "Peroxisomal biogenesis factor 19; Peroxin-19; Peroxisomal farnesylated protein; PxF", "protein_names_refseq": "peroxin-19; peroxisomal biogenesis factor 19 isoform b; peroxisomal farnesylated protein; peroxisome biogenesis factor 19", "tax_id": 10090, "disease": "peroxisome biogenesis disorder 12A (Disease Ontology:DOID:0080486); Zellweger syndrome (Disease Ontology:DOID:905)", "pathway": " (mmu:19298); (R-MMU-1369062); (R-MMU-9603798)", "pathway_count": 3, "publication_count": 2, "publication_id_list": "17242355;21183079", "class_list": "", "function": "Necessary for early peroxisomal biogenesis. Acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Binds and stabilizes newly synthesized PMPs in the cytoplasm by interacting with their hydrophobic membrane-spanning domains, and targets them to the peroxisome membrane by binding to the integral membrane protein PEX3. Excludes CDKN2A from the nucleus and prevents its interaction with MDM2, which results in active degradation of TP53., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q4FJU7;Q8CEE1;Q921H0;Q9CZC1;Q9QUQ1", "ec_number_list": "", "go_molecular_function": "GO:0036105 peroxisome membrane class-1 targeting sequence binding;GO:0033328 peroxisome membrane targeting sequence binding;GO:0051117 ATPase binding;GO:0140597 protein carrier chaperone", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005777 peroxisome;GO:0005778 peroxisomal membrane", "go_biological_process": "GO:0072663 establishment of protein localization to peroxisome;GO:0016559 peroxisome fission;GO:0007031 peroxisome organization;GO:0050821 protein stabilization;GO:0006457 protein folding", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "Q8VCI5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8R4S0-1", "uniprot_id": "PP14C_MOUSE", "mass": 17754.0, "length": 164, "protein_name": "Protein phosphatase 1 regulatory subunit 14C", "gene_name": "Ppp1r14c", "organism": "Mouse", "refseq_name": "protein phosphatase 1 regulatory subunit 14C", "refseq_ac": "NP_597844", "gene_names_uniprotkb": "Ppp1r14c; Kepi", "gene_names_refseq": "6330514J04Rik; KEPI; Ppp1r14c", "protein_names_uniprotkb": "Protein phosphatase 1 regulatory subunit 14C; Kinase-enhanced PP1 inhibitor; PKC-potentiated PP1 inhibitory protein", "protein_names_refseq": "PKC-potentiated PP1 inhibitory protein; kinase-enhanced PP1 inhibitor; protein phosphatase 1 regulatory subunit 14C", "tax_id": 10090, "disease": "Coronavirus infectious disease (Disease Ontology:DOID:0080599)", "pathway": " (mmu:76142)", "pathway_count": 1, "publication_count": 9, "publication_id_list": "11812771;15837133;21750661;24129315;27333042;30016717;32848054;36288343;40885482", "class_list": "", "function": "Inhibitor of PPP1CA., [UniProtKB, UniProtKB]; Inhibitor of the PP1 regulatory subunit PPP1CA., [UniProtKB, PubMed]; Regulation by morphine GeneRIF: PPP1R14C gene encodes a PKC-potentiated inhibitory protein, KEPI, for type-1 Ser/Thr protein phosphatase (PP1). KEPI mRNA and protein are enriched in brain, heart and skeletal muscle., [RefSeq, PubMed]; The data presented in this manuscript demonstrate a critical function of VPS35 in regulating PTH1R trafficking. This event and VPS35-interaction with PPP1R14C appear to be essential for turning off PTH1R's endosomal signaling, and promoting PTH1R-mediated catabolic response and bone remodeling., [RefSeq, PubMed]; The expression patterns point to possible roles for KEPI in regulating protein dephosphorylation by inhibiting PP1 activities in a number of brain pathways., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 4, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 4, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 4, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 4, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0004865 protein serine/threonine phosphatase inhibitor activity;GO:0004864 protein phosphatase inhibitor activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane;GO:0012505 endomembrane system", "go_biological_process": "GO:0007165 signal transduction", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "Q8R4S0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q2M3X8-1", "uniprot_id": "PHAR1_MOUSE", "mass": 66286.0, "length": 580, "protein_name": "Phosphatase and actin regulator 1", "gene_name": "Phactr1", "organism": "Mouse", "refseq_name": "phosphatase and actin regulator 1 isoform 2", "refseq_ac": "NP_001005740", "gene_names_uniprotkb": "Phactr1", "gene_names_refseq": "9630030F18Rik; Phactr1; Rpel1", "protein_names_uniprotkb": "Phosphatase and actin regulator 1", "protein_names_refseq": "RPEL repeat containing 1; phosphatase and actin regulator 1 isoform 2", "tax_id": 10090, "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); developmental and epileptic encephalopathy 70 (Disease Ontology:DOID:0112206); essential hypertension (Disease Ontology:DOID:10825); Moyamoya disease (Disease Ontology:DOID:13099); coronary artery disease (Disease Ontology:DOID:3393); cerebral infarction (Disease Ontology:DOID:3526); coronary stenosis (Disease Ontology:DOID:4248); myocardial infarction (Disease Ontology:DOID:5844); migraine (Disease Ontology:DOID:6364)", "pathway": " (mmu:218194)", "pathway_count": 1, "publication_count": 15, "publication_id_list": "16359841;21183079;21750661;22517741;22645316;22766235;22976292;23041370;25428506;30256902;33300544;36091033;37199156;38272663;40885482", "class_list": "glycogene", "function": "Binds actin monomers (G actin) and plays a role in multiple processes including the regulation of actin cytoskeleton dynamics, actin stress fibers formation, cell motility and survival, formation of tubules by endothelial cells, and regulation of PPP1CA activity. Involved in the regulation of cortical neuron migration and dendrite arborization (PubMed:30256902)., [UniProtKB, PubMed, PubMed, PubMed]; Endothelial PHACTR1 Promotes Endothelial Activation and Atherosclerosis by Repressing PPARgamma Activity Under Disturbed Flow in Mice., [RefSeq, PubMed]; Genotype and phenotype correlation of PHACTR1-related neurological disorders. Publication Status: Online-Only, [RefSeq, PubMed]; PHACTR1, a coronary artery disease risk gene, mediates endothelial dysfunction. Publication Status: Online-Only, [RefSeq, PubMed]; This study demonistrated that Phactr1 appeared to be expressed in post-mitotic neurons in developmental brain., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 5, "reported_mutagensis": 13, "reported_glycation": 0, "reported_snv": 28, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 9, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "B1B1B5;B1B1B6;B1B1B7;G5E8P7;Q80VL9;Q8C873", "ec_number_list": "", "go_molecular_function": "GO:0003779 actin binding;GO:0008157 protein phosphatase 1 binding;GO:0004864 protein phosphatase inhibitor activity", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0098794 postsynapse", "go_biological_process": "GO:0010628 positive regulation of gene expression;GO:0021987 cerebral cortex development;GO:0140059 dendrite arborization;GO:0030036 actin cytoskeleton organization;GO:0031032 actomyosin structure organization", "synthesized_glycan_count": 0, "hit_score": 1.8, "record_id": "Q2M3X8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q80TL4-1", "uniprot_id": "PHF24_MOUSE", "mass": 45223.0, "length": 400, "protein_name": "PHD finger protein 24", "gene_name": "Phf24", "organism": "Mouse", "refseq_name": "PHD finger protein 24 isoform 1", "refseq_ac": "NP_001333455", "gene_names_uniprotkb": "Phf24; Kiaa1045; N28178", "gene_names_refseq": "GINIP; Phf24", "protein_names_uniprotkb": "PHD finger protein 24", "protein_names_refseq": "PHD finger protein 24 isoform 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:230085)", "pathway_count": 1, "publication_count": 7, "publication_id_list": "21183079;21750661;22517741;22645316;24129315;40684658;40885482", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 3, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 3, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 3, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "A2AG28;Q8BH08", "ec_number_list": "", "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003714 transcription corepressor activity", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0030672 synaptic vesicle membrane", "go_biological_process": "GO:0007214 gamma-aminobutyric acid signaling pathway;GO:0050966 detection of mechanical stimulus involved in sensory perception of pain;GO:0032228 regulation of synaptic transmission, GABAergic;GO:0008277 regulation of G protein-coupled receptor signaling pathway", "synthesized_glycan_count": 0, "hit_score": 1.2, "record_id": "Q80TL4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8C351-1", "uniprot_id": "LAYN_MOUSE", "mass": 43269.0, "length": 381, "protein_name": "Layilin", "gene_name": "Layn", "organism": "Mouse", "refseq_name": "layilin precursor", "refseq_ac": "NP_001028706", "gene_names_uniprotkb": "Layn", "gene_names_refseq": "E030012M19Rik; Gm511; Layn", "protein_names_uniprotkb": "Layilin", "protein_names_refseq": "layilin precursor", "tax_id": 10090, "disease": "", "pathway": " (mmu:244864)", "pathway_count": 1, "publication_count": 7, "publication_id_list": "15913605;18638481;19144319;21750661;26410531;32539073;34470859", "class_list": "glycogene", "function": "LAYN is involved in the TNF-alpha-induced epithelial-mesenchymal transformation (EMT) of renal tubular epithelial cells., [RefSeq, PubMed]; Layilin Anchors Regulatory T Cells in Skin., [RefSeq, PubMed]; Layilin augments integrin activation to promote antitumor immunity., [RefSeq, PubMed]; Receptor for hyaluronate., [UniProtKB]; The structure of the talin/layilin complex, which shows that talin binds integrins, PIPK1gamma and layilin in similar although subtly different ways, is reported., [RefSeq, PubMed]", "predicted_glycosites": 2, "predicted_n_glycosites": 1, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 23, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "E9QQ23;Q3TMU7", "ec_number_list": "", "go_molecular_function": "GO:0030246 carbohydrate binding;GO:0005540 hyaluronic acid binding", "go_cellular_component": "GO:0009986 cell surface;GO:0016020 membrane;GO:0001726 ruffle", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q8C351-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P70268-1", "uniprot_id": "PKN1_MOUSE", "mass": 104411.0, "length": 946, "protein_name": "Serine/threonine-protein kinase N1", "gene_name": "Pkn1", "organism": "Mouse", "refseq_name": "serine/threonine-protein kinase N1 isoform 1", "refseq_ac": "NP_001186522", "gene_names_uniprotkb": "Pkn1; Pkn; Prk1; Prkcl1", "gene_names_refseq": "DBK; F730027O18Rik; PAK1; PRK1; Pkn1; Pkn; Prkcl1; Stk3", "protein_names_uniprotkb": "Serine/threonine-protein kinase N1; 2.7.11.13; Protein kinase C-like 1; Protein kinase C-like PKN; Protein-kinase C-related kinase 1; Serine-threonine protein kinase N", "protein_names_refseq": "protein kinase C-like 1; protein kinase C-like PKN; protein-kinase C-related kinase 1; serine-threonine protein kinase N; serine/threonine kinase 3; serine/threonine-protein kinase N1 isoform 1; serine/threonine-protein kinase N1", "tax_id": 10090, "disease": "", "pathway": " (mmu:320795); (R-MMU-5625740); (R-MMU-5625886); (R-MMU-8980692); (R-MMU-9013026); (R-MMU-9013106); (R-MMU-9013149)", "pathway_count": 7, "publication_count": 15, "publication_id_list": "10.1101/2023.09.13.557529;11054541;15345747;19144319;21183079;21750661;29045568;35984892;36897022;37507081;38002281;39266515;39627609;8571127;8858105", "class_list": "", "function": "PKC-related serine/threonine-protein kinase involved in various processes such as regulation of the intermediate filaments of the actin cytoskeleton, cell migration, tumor cell invasion and transcription regulation. Part of a signaling cascade that begins with the activation of the adrenergic receptor ADRA1B and leads to the activation of MAPK14. Regulates the cytoskeletal network by phosphorylating proteins such as VIM and neurofilament proteins NEFH, NEFL and NEFM, leading to inhibit their polymerization. Phosphorylates 'Ser-575', 'Ser-637' and 'Ser-669' of MAPT/Tau, lowering its ability to bind to microtubules, resulting in disruption of tubulin assembly. Acts as a key coactivator of androgen receptor (ANDR)-dependent transcription, by being recruited to ANDR target genes and specifically mediating phosphorylation of 'Thr-11' of histone H3 (H3T11ph), a specific tag for epigenetic transcriptional activation that promotes demethylation of histone H3 'Lys-9' (H3K9me) by KDM4C/JMJD2C. Phosphorylates HDAC5, HDAC7 and HDAC9, leading to impair their import in the nucleus. Phosphorylates 'Thr-38' of PPP1R14A, 'Ser-159', 'Ser-163' and 'Ser-170' of MARCKS, and GFAP. Able to phosphorylate RPS6 in vitro., [UniProtKB, UniProtKB]; PKN1 Exerts Neurodegenerative Effects in an In Vitro Model of Cerebellar Hypoxic-Ischemic Encephalopathy via Inhibition of AKT/GSK3beta Signaling. Publication Status: Online-Only, [RefSeq, PubMed]; Phosphorylation of KRT8 (keratin 8) by excessive mechanical load-activated PKN (protein kinase N) impairs autophagosome initiation and contributes to disc degeneration., [RefSeq, PubMed]; Protein kinase N promotes cardiac fibrosis in heart failure by fibroblast-to-myofibroblast conversion. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 11, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q3UEA6;Q7TST2;Q8BTL8", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;1.14.14.18;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.1.153;2.7.1.137;3.1.3.48;3.6.5.2;2.7.1.40;2.7.11.21;3.1.2.-;7.6.2.-;3.6.4.-;2.7.11.39;2.3.1.-;3.1.4.4;2.7.10.1;2.7.11.31;3.6.5.-;1.6.3.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0035402 histone H3T11 kinase activity;GO:0003682 chromatin binding;GO:0003713 transcription coactivator activity;GO:0004672 protein kinase activity;GO:0004674 protein serine/threonine kinase activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005768 endosome;GO:0031410 cytoplasmic vesicle;GO:0032154 cleavage furrow", "go_biological_process": "GO:0010631 epithelial cell migration;GO:0002637 regulation of immunoglobulin production;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006468 protein phosphorylation", "synthesized_glycan_count": 0, "hit_score": 2.0, "record_id": "P70268-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3UTJ2-1", "uniprot_id": "SRBS2_MOUSE", "mass": 132349.0, "length": 1180, "protein_name": "Sorbin and SH3 domain-containing protein 2", "gene_name": "Sorbs2", "organism": "Mouse", "refseq_name": "sorbin and SH3 domain-containing protein 2 isoform 3", "refseq_ac": "NP_001297636", "gene_names_uniprotkb": "Sorbs2; Argbp2; Kiaa0777", "gene_names_refseq": "2010203O03Rik; 9430041O17Rik; A530071H08; Argbp2; Sorbs2; mKIAA0777; nArgBP2", "protein_names_uniprotkb": "Sorbin and SH3 domain-containing protein 2; Arg-binding protein 2; Arg/Abl-interacting protein 2; ArgBP2", "protein_names_refseq": "Arg/Abl-binding protein 2; Arg/Abl-interacting protein ArgBP2; arg-binding protein 2; arg/Abl-interacting protein 2; sorbin and SH3 domain-containing protein 2 isoform 3; sorbin and SH3 domain-containing protein 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:234214)", "pathway_count": 1, "publication_count": 19, "publication_id_list": "10.1101/2023.09.13.557529;16452087;17242355;18630941;21183079;21750661;22645316;26495903;30059200;33300544;34428180;34678516;35822049;36288343;37507081;37752619;38362769;38555055;39927985", "class_list": "", "function": "Adapter protein that plays a role in the assembling of signaling complexes, being a link between ABL kinases and actin cytoskeleton. Can form complex with ABL1 and CBL, thus promoting ubiquitination and degradation of ABL1 (By similarity). May play a role in the regulation of pancreatic cell adhesion, possibly by acting on WASF1 phosphorylation, enhancing phosphorylation by ABL1, as well as dephosphorylation by PTPN12 (By similarity)., [UniProtKB, UniProtKB]; MiR-484 promotes nonalcoholic fatty liver disease progression in mice via downregulation of Sorbs2., [RefSeq, PubMed]; Sorbs2 Deficiency and Vascular BK Channelopathy in Diabetes., [RefSeq, PubMed]; Sorbs2 regulates seizure activity by influencing AMPAR-mediated excitatory synaptic transmission in temporal lobe epilepsy., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 6, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 6, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 6, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 31, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 3, "disease_count": 0, "glyco_site_count": 7, "binding_glycan_count": 0, "secondary_ac_list": "Q3USC6;Q80TS1;Q8BJL6;Q8BJU3;Q8BLW9;Q8BX47;Q8CHU0", "ec_number_list": "", "go_molecular_function": "GO:0019904 protein domain specific binding;GO:0030674 protein-macromolecule adaptor activity;GO:0042802 identical protein binding", "go_cellular_component": "GO:0005856 cytoskeleton;GO:0005886 plasma membrane;GO:0005925 focal adhesion;GO:0030027 lamellipodium;GO:0030425 dendrite", "go_biological_process": "GO:0007219 Notch signaling pathway;GO:0095500 acetylcholine receptor signaling pathway;GO:0007010 cytoskeleton organization;GO:0061049 cell growth involved in cardiac muscle cell development;GO:1904393 regulation of skeletal muscle acetylcholine-gated channel clustering", "synthesized_glycan_count": 0, "hit_score": 3.1, "record_id": "Q3UTJ2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P28741-1", "uniprot_id": "KIF3A_MOUSE", "mass": 80170.0, "length": 701, "protein_name": "Kinesin-like protein KIF3A", "gene_name": "Kif3a", "organism": "Mouse", "refseq_name": "kinesin-like protein KIF3A isoform 2", "refseq_ac": "NP_001277734", "gene_names_uniprotkb": "Kif3a; Kif3", "gene_names_refseq": "Kif3a; Kif3; Kifl; Kns3", "protein_names_uniprotkb": "Kinesin-like protein KIF3A; 3.6.4.-; Microtubule plus end-directed kinesin motor 3A", "protein_names_refseq": "N-4 kinesin; kinesin-II subunit; kinesin-like protein KIF3A isoform 2; kinesin-like protein KIF3A; microtubule plus end-directed kinesin motor 3A", "tax_id": 10090, "disease": "polycystic kidney disease (Disease Ontology:DOID:0080322); silicosis (Disease Ontology:DOID:10325); allergic disease (Disease Ontology:DOID:1205); dysostosis (Disease Ontology:DOID:1934); asthma (Disease Ontology:DOID:2841)", "pathway": " (mmu:16568); (R-MMU-2132295); (R-MMU-5610787); (R-MMU-5620924); (R-MMU-5635838); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 7, "publication_count": 19, "publication_id_list": "10.1101/2023.09.13.557529;1447303;15345747;18497258;20643351;21183079;21670265;21750661;23386061;25428506;25605945;30084848;31219806;32935890;33300544;34428180;38587639;39138140;7559760", "class_list": "", "function": "Kinesin KIF3A regulates meiotic progression and spindle assembly in oocyte meiosis. Publication Status: Online-Only, [RefSeq, PubMed]; Microtubule-based anterograde translocator for membranous organelles, such as primary cilium and centriole (PubMed:18497258, PubMed:21670265, PubMed:23386061, PubMed:7559760). Shows a plus end-directed microtubule sliding activity in vitro (PubMed:7559760). Plays a role in primary cilia formation, probably by mediating transport of proteins into primary cilia (PubMed:18497258, PubMed:21670265, PubMed:39138140). Mediates smoothened (SMO) translocation into primary cilia in response to hedgehog morphogens (PubMed:18497258, PubMed:39138140). Plays a role in centriole cohesion and subdistal appendage organization and function (PubMed:23386061). Regulates the formation of the subdistal appendage via recruitment of DCTN1 to the centriole (PubMed:23386061). Also required for ciliary basal feet formation and microtubule anchoring to mother centriole (PubMed:23386061)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed]; Microtubule-based anterograde translocator for membranous organelles. Plus end-directed microtubule sliding activity in vitro. Plays a role in primary cilia formation. Plays a role in centriole cohesion and subdistal appendage organization and function. Regulates the formation of the subdistal appendage via recruitment of DCTN1 to the centriole. Also required for ciliary basal feet formation and microtubule anchoring to mother centriole., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 5, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q7TSZ7", "ec_number_list": "3.6.4.13;3.6.4.10;3.6.4.-;5.6.2.3;5.6.2.4;2.3.2.-;2.3.2.27;3.1.13.1;5.6.2.6;3.1.-.-;7.6.2.1;3.6.1.5;3.4.24.-;3.6.-.-;3.6.5.-;3.1.3.1;3.9.1.1;3.6.1.-;5.6.2.5;4.2.99.18;3.6.4.12;5.6.1.6;5.6.1.3;3.6.4.6;3.6.5.2;3.6.1.15;3.1.4.-;5.6.2.-;7.2.2.-;7.6.2.16;3.4.21.53;2.7.7.7;2.7.7.49;2.7.11.1;2.7.4.3", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0030507 spectrin binding;GO:0044877 protein-containing complex binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0005874 microtubule", "go_biological_process": "GO:0001701 in utero embryonic development;GO:0007507 heart development;GO:0015031 protein transport;GO:0030900 forebrain development;GO:0090316 positive regulation of intracellular protein transport", "synthesized_glycan_count": 0, "hit_score": 2.4, "record_id": "P28741-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P82350-1", "uniprot_id": "SGCA_MOUSE", "mass": 43287.0, "length": 387, "protein_name": "Alpha-sarcoglycan", "gene_name": "Sgca", "organism": "Mouse", "refseq_name": "alpha-sarcoglycan precursor", "refseq_ac": "NP_033187", "gene_names_uniprotkb": "Sgca", "gene_names_refseq": "50DAG; Asg; Sgca", "protein_names_uniprotkb": "Alpha-sarcoglycan; 50 kDa dystrophin-associated glycoprotein; 50DAG; Adhalin; Alpha-SG", "protein_names_refseq": "50 kDa dystrophin-associated glycoprotein; adhalin; alpha-SG; alpha-sarcoglycan precursor; alpha-sarcoglycan", "tax_id": 10090, "disease": "autosomal recessive limb-girdle muscular dystrophy type 2D (Disease Ontology:DOID:0110278); muscular atrophy (Disease Ontology:DOID:767); muscular dystrophy (Disease Ontology:DOID:9884)", "pathway": " (mmu:20391); (R-MMU-9913351)", "pathway_count": 2, "publication_count": 7, "publication_id_list": "10448073;21183079;21750661;36288343;7547961;9196068;9864373", "class_list": "", "function": "Component of the sarcoglycan complex, a subcomplex of the dystrophin-glycoprotein complex which forms a link between the F-actin cytoskeleton and the extracellular matrix., [UniProtKB]; This gene encodes a member of the sarcoglycan alpha/epsilon family of transmembrane proteins. The encoded protein is part of the dystrophin-glycoprotein complex which links the extracellular matrix to the cytoskeleton in muscle fibers. Disruption of this gene results in progressive muscular dystrophy and is associated with the development of embryonal rhabdomysarcoma. [provided by RefSeq, Dec 2012]., [RefSeq]", "predicted_glycosites": 2, "predicted_n_glycosites": 1, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 1, "reported_o_glycosites": 2, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 3, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 3, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 5, "binding_glycan_count": 0, "secondary_ac_list": "O35311;O88490", "ec_number_list": "", "go_molecular_function": "GO:0005509 calcium ion binding", "go_cellular_component": "GO:0005856 cytoskeleton;GO:0005886 plasma membrane;GO:0005911 cell-cell junction;GO:0045121 membrane raft;GO:0042383 sarcolemma", "go_biological_process": "GO:0061024 membrane organization", "synthesized_glycan_count": 0, "hit_score": 1.3, "record_id": "P82350-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6P549-1", "uniprot_id": "SHIP2_MOUSE", "mass": 138973.0, "length": 1257, "protein_name": "Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2", "gene_name": "Inppl1", "organism": "Mouse", "refseq_name": "phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 isoform a", "refseq_ac": "NP_001116211", "gene_names_uniprotkb": "Inppl1; Ship2", "gene_names_refseq": "51C; Inppl1; SHIP2", "protein_names_uniprotkb": "Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2; 3.1.3.86; INPPL-1; Inositol polyphosphate phosphatase-like protein 1; Protein 51C; SH2 domain-containing inositol 5'-phosphatase 2; SH2 domain-containing inositol phosphatase 2; SHIP-2", "protein_names_refseq": "INPPL-1; SH2 domain-containing inositol 5'-phosphatase 2; SH2 domain-containing inositol phosphatase 2; SHIP-2; ablSH3-binding protein; inositol polyphosphate phosphatase-like protein 1; phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 isoform a; phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2; protein 51C", "tax_id": 10090, "disease": "scoliosis (Disease Ontology:DOID:0060249); hypertension (Disease Ontology:DOID:10763); type 2 diabetes mellitus (Disease Ontology:DOID:9352); obesity (Disease Ontology:DOID:9970)", "pathway": " (mmu:16332); (R-MMU-1660499); (R-MMU-1855204); (R-MMU-912526)", "pathway_count": 4, "publication_count": 23, "publication_id_list": "10610720;10789675;10958682;11343120;12145149;14744864;15456754;15492005;15557176;15654325;16179375;17242355;18515860;21624956;21750661;23040614;29749928;30084848;31219806;33953730;34428180;9126384;9485206", "class_list": "", "function": "Association with the insulin resistance of diabetic db/db mice., [RefSeq, PubMed]; Phosphatidylinositol (PtdIns) phosphatase that specifically hydrolyzes the 5-phosphate of phosphatidylinositol-3,4,5-trisphosphate (PtdIns(3,4,5)P3) to produce PtdIns(3,4)P2, thereby negatively regulating the PI3K (phosphoinositide 3-kinase) pathways (PubMed:10958682). Required for correct mitotic spindle orientation and therefore progression of mitosis (By similarity). Plays a central role in regulation of PI3K-dependent insulin signaling, although the precise molecular mechanisms and signaling pathways remain unclear (PubMed:11343120). While overexpression reduces both insulin-stimulated MAP kinase and Akt activation, its absence does not affect insulin signaling or GLUT4 trafficking (PubMed:14744864). Confers resistance to dietary obesity (PubMed:15654325). May act by regulating AKT2, but not AKT1, phosphorylation at the plasma membrane (PubMed:14744864). Part of a signaling pathway that regulates actin cytoskeleton remodeling (By similarity). Required for the maintenance and dynamic remodeling of actin structures as well as in endocytosis, having a major impact on ligand-induced EGFR internalization and degradation (By similarity). Participates in regulation of cortical and submembraneous actin by hydrolyzing PtdIns(3,4,5)P3 thereby regulating membrane ruffling (By similarity). Regulates cell adhesion and cell spreading (PubMed:29749928). Required for HGF-mediated lamellipodium formation, cell scattering and spreading (By similarity). Acts as a negative regulator of EPHA2 receptor endocytosis by inhibiting via PI3K-dependent Rac1 activation (By similarity). Acts as a regulator of neuritogenesis by regulating PtdIns(3,4,5)P3 level and is required to form an initial protrusive pattern, and later, maintain proper neurite outgrowth (By similarity). Acts as a negative regulator of the FC-gamma-RIIA receptor (FCGR2A) (By similarity). Mediates signaling from the FC-gamma-RIIB receptor (FCGR2B), playing a central role in terminating signal transduction from activating immune/hematopoietic cell receptor systems (PubMed:10789675, PubMed:15456754). Upon stimulation by EGF, it is recruited by EGFR and dephosphorylates PtdIns(3,4,5)P3 (By similarity). Plays a negative role in regulating the PI3K-PKB pathway, possibly by inhibiting PKB activity (By similarity). Down-regulates Fc-gamma-R-mediated phagocytosis in macrophages independently of INPP5D/SHIP1 (PubMed:15557176, PubMed:16179375). In macrophages, down-regulates NF-kappa-B-dependent gene transcription by regulating macrophage colony-stimulating factor (M-CSF)-induced signaling (PubMed:15557176, PubMed:16179375). Plays a role in the localization of AURKA and NEDD9/HEF1 to the basolateral membrane at interphase in polarized cysts, thereby mediates cell cycle homeostasis, cell polarization and cilia assembly (By similarity). Additionally promotion of cilia growth is also facilitated by hydrolysis of (PtdIns(3,4,5)P3) to PtdIns(3,4)P2 (By similarity). Promotes formation of apical membrane-initiation sites during the initial stages of lumen formation via Rho family-induced actin filament organization and CTNNB1 localization to cell-cell contacts (By similarity). May also hydrolyze PtdIns(1,3,4,5)P4, and could thus affect the levels of the higher inositol polyphosphates like InsP6. Involved in endochondral ossification (By similarity)., [UniProtKB, PubMed, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, UniProtKB, PubMed, UniProtKB, PubMed]; The 5-Phosphatase SHIP2 Promotes Neutrophil Chemotaxis and Recruitment. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 11, "reported_mutagensis": 8, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 4, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "O08611;Q0VDX5;Q80YB9;Q9JLL7", "ec_number_list": "2.7.1.153;2.7.1.137;2.7.10.2;2.7.10.1;3.1.3.67;3.1.3.86;3.1.3.95;3.1.3.36;2.3.2.27;3.1.3.48;2.7.11.1;3.1.3.56;2.7.1.134;2.7.1.159;3.1.3.-;3.1.4.11;3.1.3.16", "go_molecular_function": "GO:0003779 actin binding;GO:0005547 phosphatidylinositol-3,4,5-trisphosphate binding;GO:0017124 SH3 domain binding;GO:0042169 SH2 domain binding;GO:0004445 inositol-polyphosphate 5-phosphatase activity", "go_cellular_component": "GO:0000922 spindle pole;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0005829 cytosol", "go_biological_process": "GO:0046627 negative regulation of insulin receptor signaling pathway;GO:0006629 lipid metabolic process;GO:0006897 endocytosis;GO:0007015 actin filament organization;GO:0007155 cell adhesion", "synthesized_glycan_count": 0, "hit_score": 2.4, "record_id": "Q6P549-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P63087-1", "uniprot_id": "PP1G_MOUSE", "mass": 36984.0, "length": 323, "protein_name": "Serine/threonine-protein phosphatase PP1-gamma catalytic subunit", "gene_name": "Ppp1cc", "organism": "Mouse", "refseq_name": "serine/threonine-protein phosphatase PP1-gamma catalytic subunit isoform 1", "refseq_ac": "NP_038664", "gene_names_uniprotkb": "Ppp1cc", "gene_names_refseq": "PP-1G; PP1; Ppp1cc; dis2m1", "protein_names_uniprotkb": "Serine/threonine-protein phosphatase PP1-gamma catalytic subunit; 3.1.3.16; PP-1G; Protein phosphatase 1C catalytic subunit", "protein_names_refseq": "PP1C gamma 1; PP1C gamma 2; protein phosphatase 1C catalytic subunit; serine/threonine-protein phosphatase PP1-gamma catalytic subunit isoform 1; serine/threonine-protein phosphatase PP1-gamma catalytic subunit", "tax_id": 10090, "disease": "cancer (Disease Ontology:DOID:162); congestive heart failure (Disease Ontology:DOID:6000); type 2 diabetes mellitus (Disease Ontology:DOID:9352)", "pathway": " (mmu:19047); (R-MMU-141430); (R-MMU-141444); (R-MMU-2467813); (R-MMU-2500257); (R-MMU-5663220); (R-MMU-5673000); (R-MMU-68877); (R-MMU-9648025)", "pathway_count": 9, "publication_count": 20, "publication_id_list": "14638860;15226296;16835242;17381077;19282287;19886865;21712997;21750661;21930935;23082183;2544298;25605614;33300544;34428180;36764308;37085815;37340734;38326336;9339378;9882500", "class_list": "", "function": "Crosstalk of HDAC4, PP1, and GSDMD in controlling pyroptosis. Publication Status: Online-Only, [RefSeq, PubMed]; Oscillations in PP1 activity are essential for accurate progression through mammalian oocyte meiosis., [RefSeq, PubMed]; PP1gamma regulates neuronal insulin signaling and aggravates insulin resistance leading to AD-like phenotypes. Publication Status: Online-Only, [RefSeq, PubMed]; Protein Phosphatase 1 gamma Modulates Steady-State BAD Phosphorylation and Murine Platelet Survival., [RefSeq, PubMed]; Protein phosphatase that associates with over 200 regulatory proteins to form highly specific holoenzymes which dephosphorylate hundreds of biological targets. Protein phosphatase 1 (PP1) is essential for cell division, and participates in the regulation of glycogen metabolism, muscle contractility and protein synthesis. Dephosphorylates RPS6KB1. Involved in regulation of ionic conductances and long-term synaptic plasticity. May play an important role in dephosphorylating substrates such as the postsynaptic density-associated Ca(2+)/calmodulin dependent protein kinase II. Component of the PTW/PP1 phosphatase complex, which plays a role in the control of chromatin structure and cell cycle progression during the transition from mitosis into interphase (By similarity). In balance with CSNK1D and CSNK1E, determines the circadian period length, through the regulation of the speed and rhythmicity of PER1 and PER2 phosphorylation (PubMed:21712997, PubMed:21930935). May dephosphorylate CSNK1D and CSNK1E (PubMed:21930935). Regulates the recruitment of the SKA complex to kinetochores (By similarity). Core component of the SHOC2-MRAS-PP1c (SMP) holophosphatase complex that regulates the MAPK pathway activation (By similarity). Dephosphorylates MKI67 at the onset of anaphase (By similarity). The SMP complex specifically dephosphorylates the inhibitory phosphorylation at 'Ser-259' of RAF1 kinase, 'Ser-365' of BRAF kinase and 'Ser-214' of ARAF kinase, stimulating their kinase activities (By similarity). The SMP complex enhances the dephosphorylation activity and substrate specificity of PP1c (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed]; Required for normal male fertility., [UniProtKB, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "O09186;O09189;P37139;Q64679", "ec_number_list": "3.1.3.67;3.1.3.-;3.1.3.16;3.1.3.48;2.7.11.1;3.6.5.2;3.6.5.-;2.7.11.22;2.7.11.23;3.4.22.49;3.1.3.74;3.1.3.53;2.7.11.21;3.1.3.27;3.4.21.-;3.6.4.12;3.1.3.52;3.1.3.86;3.1.3.36;2.7.11.26;2.3.2.-", "go_molecular_function": "GO:0019901 protein kinase binding;GO:0019904 protein domain specific binding;GO:0046872 metal ion binding;GO:0004722 protein serine/threonine phosphatase activity;GO:0044877 protein-containing complex binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0000164 protein phosphatase type 1 complex;GO:0005634 nucleus;GO:0005730 nucleolus;GO:0005737 cytoplasm", "go_biological_process": "GO:0060252 positive regulation of glial cell proliferation;GO:0007283 spermatogenesis;GO:0046822 regulation of nucleocytoplasmic transport;GO:0051301 cell division;GO:0005977 glycogen metabolic process", "synthesized_glycan_count": 0, "hit_score": 2.3, "record_id": "P63087-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q924W5-1", "uniprot_id": "SMC6_MOUSE", "mass": 127198.0, "length": 1097, "protein_name": "Structural maintenance of chromosomes protein 6", "gene_name": "Smc6", "organism": "Mouse", "refseq_name": "structural maintenance of chromosomes protein 6 isoform 2", "refseq_ac": "NP_001311405", "gene_names_uniprotkb": "Smc6; Kiaa4103; Smc6l1", "gene_names_refseq": "2810489L22Rik; 3830418C19Rik; SMC-6; Smc6l1; Smc6; mKIAA4103", "protein_names_uniprotkb": "Structural maintenance of chromosomes protein 6; SMC protein 6; SMC-6; mSMC6", "protein_names_refseq": "SMC protein 6; SMC6 structural maintenance of chromosomes 6-like 1; structural maintenance of chromosomes protein 6 isoform 2; structural maintenance of chromosomes protein 6", "tax_id": 10090, "disease": "", "pathway": " (mmu:67241); (R-MMU-3108214)", "pathway_count": 2, "publication_count": 11, "publication_id_list": "11408570;21750661;23518413;23907463;25428506;28302748;28528544;30084848;30281394;31219806;33200984", "class_list": "", "function": "Age-dependent depletion of the SMC5/6 complex in oocytes could contribute to increased incidence of oocyte aneuploidy and spontaneous abortion in aging females., [RefSeq, PubMed]; Core component of the SMC5-SMC6 complex, a complex involved in repair of DNA double-strand breaks by homologous recombination. The complex may promote sister chromatid homologous recombination by recruiting the SMC1-SMC3 cohesin complex to double-strand breaks. The complex is required for telomere maintenance via recombination and mediates sumoylation of shelterin complex (telosome) components (By similarity)., [UniProtKB]; Mice deleted for the SMC6 gene are inviable, and mice mutated at Ser-994 in the SMC6 ATPase domain have a mild phenotype., [RefSeq, PubMed]; SMC5/6 complex is essential only when meiotic DNA processing events are perturbed during mouse spermatogenesis, [RefSeq, PubMed]; SMC5/6 is required for replication fork stability and faithful chromosome segregation during neurogenesis. Publication Status: Online-Only, [RefSeq, PubMed]; Smc6 has a role in the prevention of aberrant recombination events between pericentromeric regions during the first meiotic prophase. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3UFI5;Q3UX54;Q499E1;Q5DTN2;Q8BFU9;Q8R0T4;Q9CSK7;Q9CV94;Q9CZZ5;Q9D169;Q9D6B2", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0003684 damaged DNA binding;GO:0016887 ATP hydrolysis activity;GO:0031625 ubiquitin protein ligase binding;GO:0003697 single-stranded DNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016607 nuclear speck;GO:0000775 chromosome, centromeric region;GO:0016605 PML body", "go_biological_process": "GO:0051984 positive regulation of chromosome segregation;GO:0006974 DNA damage response;GO:0000724 double-strand break repair via homologous recombination;GO:0090398 cellular senescence;GO:0000722 telomere maintenance via recombination", "synthesized_glycan_count": 0, "hit_score": 1.4, "record_id": "Q924W5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q80W14-1", "uniprot_id": "PR40B_MOUSE", "mass": 99300.0, "length": 870, "protein_name": "Pre-mRNA-processing factor 40 homolog B", "gene_name": "Prpf40b", "organism": "Mouse", "refseq_name": "pre-mRNA-processing factor 40 homolog B isoform 1", "refseq_ac": "NP_001335185", "gene_names_uniprotkb": "Prpf40b; Hypc", "gene_names_refseq": "2610317D23Rik; Hypc; Prpf40b", "protein_names_uniprotkb": "Pre-mRNA-processing factor 40 homolog B; Huntingtin yeast partner C; Huntingtin-interacting protein C", "protein_names_refseq": "PRP40 pre-mRNA processing factor 40 homolog A; PRP40 pre-mRNA processing factor 40 homolog B; huntingtin yeast partner C; huntingtin-interacting protein C; huntington yeast partner C; pre-mRNA-processing factor 40 homolog B isoform 1; pre-mRNA-processing factor 40 homolog B", "tax_id": 10090, "disease": "", "pathway": " (mmu:54614)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "21183079;21750661;25428506;34428180;40997131", "class_list": "", "function": "May be involved in pre-mRNA splicing., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q5XKB4;Q9CS39;Q9WVC9", "ec_number_list": "", "go_molecular_function": "GO:0003723 RNA binding;GO:0070063 RNA polymerase binding", "go_cellular_component": "GO:0005685 U1 snRNP;GO:0016607 nuclear speck;GO:0016604 nuclear body;GO:0016363 nuclear matrix;GO:0071004 U2-type prespliceosome", "go_biological_process": "GO:0000398 mRNA splicing, via spliceosome;GO:0045292 mRNA cis splicing, via spliceosome", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q80W14-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P23506-1", "uniprot_id": "PIMT_MOUSE", "mass": 24634.0, "length": 227, "protein_name": "Protein-L-isoaspartate(D-aspartate) O-methyltransferase", "gene_name": "Pcmt1", "organism": "Mouse", "refseq_name": "protein-L-isoaspartate(D-aspartate) O-methyltransferase isoform 1", "refseq_ac": "NP_001334157", "gene_names_uniprotkb": "Pcmt1", "gene_names_refseq": "PIMT; Pcmt1", "protein_names_uniprotkb": "Protein-L-isoaspartate(D-aspartate) O-methyltransferase; 2.1.1.77; L-isoaspartyl protein carboxyl methyltransferase; PIMT; Protein L-isoaspartyl/D-aspartyl methyltransferase; Protein-beta-aspartate methyltransferase", "protein_names_refseq": "L-isoaspartyl protein carboxyl methyltransferase; protein L-isoaspartyl/D-aspartyl methyltransferase; protein-L-isoaspartate(D-aspartate) O-methyltransferase isoform 1; protein-L-isoaspartate(D-aspartate) O-methyltransferase; protein-beta-aspartate methyltransferase", "tax_id": 10090, "disease": "Alzheimer's disease (Disease Ontology:DOID:10652); malignant astrocytoma (Disease Ontology:DOID:3069); high grade glioma (Disease Ontology:DOID:3070)", "pathway": " (mmu:18537); (R-MMU-5676934)", "pathway_count": 2, "publication_count": 12, "publication_id_list": "12023972;1511895;16923807;20424163;21750661;24955845;25428506;25465735;31219806;36288343;37070640;8037467", "class_list": "", "function": "Initiates the repair of damaged proteins by catalyzing methyl esterification of L-isoaspartyl and D-aspartyl residues produced by spontaneous isomerization and racemization of L-aspartyl and L-asparaginyl residues in aging peptides and proteins (PubMed:12023972, PubMed:16923807, PubMed:20424163). Acts on EIF4EBP2, microtubule-associated protein 2, calreticulin, clathrin light chains a and b, Ubiquitin C-terminal hydrolase isozyme L1, phosphatidylethanolamine-binding protein 1, stathmin, beta-synuclein and alpha-synuclein (PubMed:16923807, PubMed:20424163)., [UniProtKB, PubMed, PubMed, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Loss of normal CKB structure and function contributes to the mechanisms by which isoaspartate accumulation leads to central nervous system dysfunction in the PIMT-Knockout mouse. Erratum:[PLoS One. 2014;9(12):e116556] Publication Status: Online-Only, [RefSeq, PubMed]; PIMT is a novel and potent suppressor of endothelial activation. Publication Status: Online-Only, [RefSeq, PubMed]; PIMT levels may significantly influence the course of age-related central nervous system dysfunction., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q810R4", "ec_number_list": "2.1.1.77", "go_molecular_function": "GO:0008757 S-adenosylmethionine-dependent methyltransferase activity;GO:0004719 protein-L-isoaspartate (D-aspartate) O-methyltransferase activity", "go_cellular_component": "GO:0005615 extracellular space;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0016323 basolateral plasma membrane;GO:0043204 perikaryon", "go_biological_process": "GO:0006479 protein methylation;GO:0010667 negative regulation of cardiac muscle cell apoptotic process;GO:0046498 S-adenosylhomocysteine metabolic process;GO:0046500 S-adenosylmethionine metabolic process;GO:0032259 methylation", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "P23506-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q62230-1", "uniprot_id": "SN_MOUSE", "mass": 182979.0, "length": 1695, "protein_name": "Sialoadhesin", "gene_name": "Siglec1", "organism": "Mouse", "refseq_name": "sialoadhesin precursor", "refseq_ac": "NP_035556", "gene_names_uniprotkb": "Siglec1; Sa; Sn", "gene_names_refseq": "Cd169; Siglec-1; Siglec1; Sn", "protein_names_uniprotkb": "Sialoadhesin; SER; Sheep erythrocyte receptor; Sialic acid-binding Ig-like lectin 1; Siglec-1", "protein_names_refseq": "SER; sheep erythrocyte receptor; sialic acid-binding Ig-like lectin 1; sialoadhesin precursor; sialoadhesin", "tax_id": 10090, "disease": "", "pathway": " (mmu:20612); (R-MMU-198933)", "pathway_count": 2, "publication_count": 24, "publication_id_list": "10.1101/2023.09.13.557529;10393093;11238599;12737821;15364954;15488769;16449664;17137591;2050106;21750661;24788876;26370074;26740625;28011936;30084848;30779550;31219806;34428180;35820727;40885482;7533044;7925291;9383289;9660955", "class_list": "glycogene", "function": "Macrophage-restricted adhesion molecule that mediates sialic-acid dependent binding to lymphocytes, including granulocytes, monocytes, natural killer cells, B-cells and CD8 T-cells. Plays a crucial role in limiting bacterial dissemination by engaging sialylated bacteria to promote effective phagocytosis and antigen presentation for the adaptive immune response (PubMed:24788876). Mediates the uptake of various enveloped viruses via sialic acid recognition and subsequently induces the formation of intracellular compartments filled with virions (VCCs) (PubMed:26370074). In turn, enhances macrophage-to-T-cell transmission of several viruses including murine leukemia virus (PubMed:26370074). Acts as an endocytic receptor mediating clathrin dependent endocytosis. Preferentially binds to alpha-2,3-linked sialic acid (By similarity). Binds to SPN/CD43 on T-cells (By similarity). May play a role in hemopoiesis. Plays a role in the inhibition of antiviral innate immune by promoting TBK1 degradation via TYROBP and TRIM27-mediated ubiquitination (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed]", "predicted_glycosites": 14, "predicted_n_glycosites": 14, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 1, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 3, "reported_glycation": 0, "reported_snv": 5, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 16, "binding_glycan_count": 0, "secondary_ac_list": "D3YVZ3;D3YVZ4;O55216;Q62228;Q62229", "ec_number_list": "", "go_molecular_function": "GO:0030246 carbohydrate binding;GO:0046790 virion binding", "go_cellular_component": "GO:0005576 extracellular region;GO:0005769 early endosome;GO:0005886 plasma membrane;GO:0005770 late endosome;GO:0016020 membrane", "go_biological_process": "GO:0007155 cell adhesion;GO:2001238 positive regulation of extrinsic apoptotic signaling pathway;GO:0032481 positive regulation of type I interferon production;GO:0070234 positive regulation of T cell apoptotic process;GO:0032480 negative regulation of type I interferon production", "synthesized_glycan_count": 0, "hit_score": 2.9, "record_id": "Q62230-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3TLH4-1", "uniprot_id": "PRC2C_MOUSE", "mass": 310892.0, "length": 2846, "protein_name": "Protein PRRC2C", "gene_name": "Prrc2c", "organism": "Mouse", "refseq_name": "protein PRRC2C", "refseq_ac": "NP_001074759", "gene_names_uniprotkb": "Prrc2c; Bat2d1; Bat2d; Bat2l2; Kiaa1096", "gene_names_refseq": "1810043M20Rik; 9630039I18Rik; A630006J20; Bat2d1; Bat2d; Bat2l2; E130112L15Rik; Prrc2c; Prrc3; mKIAA1096", "protein_names_uniprotkb": "Protein PRRC2C; BAT2 domain-containing protein 1; HLA-B-associated transcript 2-like 2; Proline-rich and coiled-coil-containing protein 2C", "protein_names_refseq": "BAT2 domain containing 1; BAT2 domain-containing protein 1; HLA-B-associated transcript 2-like 2; proline-rich and coiled-coil-containing protein 2C; protein BAT2-like 2; protein PRRC2C", "tax_id": 10090, "disease": "", "pathway": " (mmu:226562)", "pathway_count": 1, "publication_count": 44, "publication_id_list": "10.1101/2023.09.13.557529;10.3389/fragi.2021.757801;17242355;19131326;19144319;19892989;21183079;21540332;21750661;21952136;22517741;22645316;24129315;25428506;25605945;26192747;26495903;27669760;28011936;28528544;29237092;30059200;30084848;31219806;32782141;32848054;33300544;33725478;34428180;34678516;34887587;35820727;35822049;36064721;36210013;36288343;36852467;37507081;37828378;39627609;39927985;40021952;40885482;40997131", "class_list": "", "function": "Required for efficient formation of stress granules., [UniProtKB, UniProtKB]", "predicted_glycosites": 5, "predicted_n_glycosites": 0, "predicted_o_glycosites": 5, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 52, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 52, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 52, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 29, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 5, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 57, "binding_glycan_count": 0, "secondary_ac_list": "E9QKG5;Q05CS4;Q05DM5;Q3TKF3;Q3UXU5;Q4FZE4;Q66K03;Q6P3F4;Q80TK3;Q80YR0;Q8BMJ4;Q8C1K7;Q8CGH3", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005829 cytosol;GO:0010494 cytoplasmic stress granule", "go_biological_process": "GO:0002244 hematopoietic progenitor cell differentiation;GO:0034063 stress granule assembly", "synthesized_glycan_count": 0, "hit_score": 10.0, "record_id": "Q3TLH4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8K135-1", "uniprot_id": "K319L_MOUSE", "mass": 115312.0, "length": 1048, "protein_name": "Dyslexia-associated protein KIAA0319-like protein", "gene_name": "AU040320; Kiaa0319l", "organism": "Mouse", "refseq_name": "dyslexia-associated protein KIAA0319-like protein isoform 1", "refseq_ac": "NP_001030602", "gene_names_uniprotkb": "AU040320; Kiaa0319l; Aavr", "gene_names_refseq": "A730047D20Rik; AAVR; AU040320; Kiaa0319l", "protein_names_uniprotkb": "Dyslexia-associated protein KIAA0319-like protein; AAVR; Adeno-associated virus receptor", "protein_names_refseq": "adeno-associated virus receptor; dyslexia-associated protein KIAA0319-like protein isoform 1; dyslexia-associated protein KIAA0319-like protein; likely ortholog of H. sapiens polycystic kidney disease 1-like (PKD1-like)", "tax_id": 10090, "disease": "", "pathway": " (mmu:100317)", "pathway_count": 1, "publication_count": 13, "publication_id_list": "10.1101/2023.09.13.557529;16075062;21183079;21750661;26495903;26814968;29045729;29991750;30899004;31219806;33300544;35820727;39627609", "class_list": "", "function": "(Microbial infection) Acts as a receptor for adeno-associated virus and is involved in adeno-associated virus infection through endocytosis system., [UniProtKB, PubMed]; Analyses of Kiaa0319L (AU040320) and double Kiaa0319;AU040320 knockouts (dKO) revealed no evidence for impaired cortical lamination, neuronal migration, neurogenesis or other anatomical abnormalities. However, dKO mice displayed an auditory deficit in a behavioral gap-in-noise detection task. Recordings of click-evoked auditory brainstem responses revealed suprathreshold deficits in wave III amplitude in AU040320-KO mice., [RefSeq, PubMed]; Genetic ablation of AAVR renders a wide range of mammalian cell types highly resistant to AAV2 infection Erratum:[Nature. 2016 Nov 17;539(7629):456. doi: 10.1038/nature19835. PMID: 27680708], [RefSeq, PubMed]; Possible role in axon guidance through interaction with RTN4R., [UniProtKB, UniProtKB]; Results suggest AU040320 may be necessary for the normal formation of proacrosomal vesicles or the recruitment of cargo proteins required for downstream events leading to acrosomal fusion. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 2, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 8, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 8, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 8, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 5, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 14, "disease_count": 0, "glyco_site_count": 9, "binding_glycan_count": 0, "secondary_ac_list": "A2A790;Q3TTA3;Q8BHR5;Q8BHU7;Q8BHZ3;Q8VBZ9", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0016020 membrane;GO:0032588 trans-Golgi network membrane", "go_biological_process": "GO:0001764 neuron migration;GO:0010996 response to auditory stimulus", "synthesized_glycan_count": 0, "hit_score": 3.7, "record_id": "Q8K135-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9WVI9-1", "uniprot_id": "JIP1_MOUSE", "mass": 77282.0, "length": 707, "protein_name": "C-Jun-amino-terminal kinase-interacting protein 1", "gene_name": "Mapk8ip1", "organism": "Mouse", "refseq_name": "C-Jun-amino-terminal kinase-interacting protein 1 isoform 1", "refseq_ac": "NP_035292", "gene_names_uniprotkb": "Mapk8ip1; Ib1; Jip1; Mapk8ip; Prkm8ip", "gene_names_refseq": "IB1; JIP-1; Jip1; Mapk8ip1; Prkm8ip; Skip; mjip-2a", "protein_names_uniprotkb": "C-Jun-amino-terminal kinase-interacting protein 1; IB-1; Islet-brain-1; JIP-1; JNK MAP kinase scaffold protein 1; JNK-interacting protein 1; Mitogen-activated protein kinase 8-interacting protein 1", "protein_names_refseq": "C-Jun-amino-terminal kinase-interacting protein 1 isoform 1; C-jun-amino-terminal kinase-interacting protein 1; IB-1; JNK MAP kinase scaffold protein 1; JNK-interacting protein 1; islet-brain-1; protein kinase, mitogen-activated 8 interacting protein", "tax_id": 10090, "disease": "type 2 diabetes mellitus (Disease Ontology:DOID:9352)", "pathway": " (mmu:19099)", "pathway_count": 1, "publication_count": 18, "publication_id_list": "10098834;10490659;10574993;10712642;10827173;11238452;11471062;11562351;11912189;16628014;21183079;22645316;23963642;27084103;31219806;32782141;40885482;9235893", "class_list": "", "function": "The JNK-interacting protein (JIP) group of scaffold proteins selectively mediates JNK signaling by aggregating specific components of the MAPK cascade to form a functional JNK signaling module. Required for JNK activation in response to excitotoxic stress. Cytoplasmic MAPK8IP1 causes inhibition of JNK-regulated activity by retaining JNK in the cytoplasm and thus inhibiting the JNK phosphorylation of c-Jun. May also participate in ApoER2-specific reelin signaling. Directly, or indirectly, regulates GLUT2 gene expression and beta-cell function. Appears to have a role in cell signaling in mature and developing nerve terminals. May function as a regulator of vesicle transport, through interactions with the JNK-signaling components and motor proteins. Functions as an anti-apoptotic protein and whose level seems to influence the beta-cell death or survival response (By similarity). Acts as a scaffold protein that coordinates with SH3RF1 in organizing different components of the JNK pathway, including RAC1 or RAC2, MAP3K11/MLK3 or MAP3K7/TAK1, MAP2K7/MKK7, MAPK8/JNK1 and/or MAPK9/JNK2 into a functional multiprotein complex to ensure the effective activation of the JNK signaling pathway. Regulates the activation of MAPK8/JNK1 and differentiation of CD8(+) T-cells (PubMed:23963642)., [UniProtKB, PubMed, PubMed]", "predicted_glycosites": 2, "predicted_n_glycosites": 0, "predicted_o_glycosites": 2, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 29, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "O35145;Q925J8;Q9R1H9;Q9R1Z1;Q9WVI7;Q9WVI8", "ec_number_list": "", "go_molecular_function": "GO:0019901 protein kinase binding;GO:0042802 identical protein binding;GO:0031434 mitogen-activated protein kinase kinase binding;GO:0019894 kinesin binding;GO:0005078 MAP-kinase scaffold activity", "go_cellular_component": "GO:0044302 dentate gyrus mossy fiber;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane", "go_biological_process": "GO:0007258 JUN phosphorylation;GO:2000564 regulation of CD8-positive, alpha-beta T cell proliferation;GO:0007165 signal transduction;GO:0043066 negative regulation of apoptotic process;GO:0046330 positive regulation of JNK cascade", "synthesized_glycan_count": 0, "hit_score": 2.1, "record_id": "Q9WVI9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P12023-1", "uniprot_id": "A4_MOUSE", "mass": 86722.0, "length": 770, "protein_name": "Amyloid-beta precursor protein", "gene_name": "App", "organism": "Mouse", "refseq_name": "amyloid-beta precursor protein isoform 1 precursor", "refseq_ac": "NP_001185752", "gene_names_uniprotkb": "App; A4; AD1", "gene_names_refseq": "Abeta; Abpp; Adap; Ag; App; Cvap; E030013M08Rik; betaApp", "protein_names_uniprotkb": "Amyloid-beta precursor protein; ABPP; AG; AID(50); AID(57); AID(59); APP-C57; APP-C59; APP-C99; APP; Alpha-CTF; Alpha-secretase C-terminal fragment; Alzheimer disease amyloid A4 protein homolog; Alzheimer disease amyloid protein; Amyloid intracellular domain 50; Amyloid intracellular domain 57; Amyloid intracellular domain 59; Amyloid precursor protein; Amyloid-beta (A4) precursor protein; Amyloid-beta A4 protein; Amyloidogenic glycoprotein; Beta-APP40; Beta-APP42; Beta-CTF; Beta-secretase C-terminal fragment; Gamma-CTF(50); Gamma-CTF(57); Gamma-CTF(59)", "protein_names_refseq": "alzheimer disease amyloid A4 protein homolog; alzheimer disease amyloid protein; amyloid beta (A4) precursor protein; amyloid beta A4 protein; amyloid precursor protein; amyloid-beta precursor protein isoform 1 precursor; amyloidogenic glycoprotein; appican; beta-amyloid precursor protein; protease nexin II", "tax_id": 10090, "disease": "alcohol dependence (Disease Ontology:DOID:0050741); diabetic encephalopathy (Disease Ontology:DOID:0050850); APP-related cerebral amyloid angiopathy (Disease Ontology:DOID:0070028); Alzheimer's disease 1 (Disease Ontology:DOID:0080348); traumatic brain injury (Disease Ontology:DOID:0081292); Alzheimer's disease (Disease Ontology:DOID:10652); hypertension (Disease Ontology:DOID:10763); iron deficiency anemia (Disease Ontology:DOID:11758); alcoholic hepatitis (Disease Ontology:DOID:12351); cognitive disorder (Disease Ontology:DOID:1561); alcohol use disorder (Disease Ontology:DOID:1574); middle cerebral artery infarction (Disease Ontology:DOID:3525); periodontitis (Disease Ontology:DOID:824); obesity (Disease Ontology:DOID:9970)", "pathway": " (mmu:11820); (R-MMU-114608); (R-MMU-3000178); (R-MMU-381426); (R-MMU-416476); (R-MMU-418594); (R-MMU-432720); (R-MMU-444473); (R-MMU-445989); (R-MMU-879415); (R-MMU-8957275); (R-MMU-933542); (R-MMU-9609523); (R-MMU-9769739); (R-MMU-9837999)", "pathway_count": 15, "publication_count": 38, "publication_id_list": "10.1101/2023.09.13.557529;11144355;11235921;11247302;11279131;11517249;11553691;11912189;12011466;12634421;1555768;15677459;16174740;16314516;16407538;1756177;18650440;21084623;21183079;21750661;22645316;23931995;2493250;25168729;25592972;2569710;25757569;26260791;26495903;28720718;30429473;32152506;3322280;34428180;35984892;37828378;7650762;8510506", "class_list": "", "function": "Amyloid-beta peptides are lipophilic metal chelators with metal-reducing activity. Binds transient metals such as copper, zinc and iron. Rat and mouse amyloid-beta peptides bind only weakly transient metals and have little reducing activity due to substitutions of transient metal chelating residues. Amyloid-beta protein 42 may activate mononuclear phagocytes in the brain and elicit inflammatory responses. Promotes both tau aggregation and TPK II-mediated phosphorylation. Also binds GPC1 in lipid rafts (By similarity)., [UniProtKB]; Functions as a cell surface receptor and performs physiological functions on the surface of neurons relevant to neurite growth, neuronal adhesion and axonogenesis. Interaction between APP molecules on neighboring cells promotes synaptogenesis. Involved in cell mobility and transcription regulation through protein-protein interactions. Can promote transcription activation through binding to APBB1-KAT5 and inhibit Notch signaling through interaction with Numb. Couples to apoptosis-inducing pathways such as those mediated by G(o) and JIP. Inhibits G(o)-alpha ATPase activity (By similarity). Acts as a kinesin I membrane receptor, mediating the axonal transport of beta-secretase and presenilin 1 (By similarity). By acting as a kinesin I membrane receptor, plays a role in axonal anterograde transport of cargo towards synapses in axons (By similarity). May be involved in copper homeostasis/oxidative stress through copper ion reduction. Can regulate neurite outgrowth through binding to components of the extracellular matrix such as heparin and collagen I and IV (By similarity). The splice isoforms that contain the BPTI domain possess protease inhibitor activity. Induces a AGER-dependent pathway that involves activation of p38 MAPK, resulting in internalization of amyloid-beta peptide and leading to mitochondrial dysfunction in cultured cortical neurons (By similarity). Provides Cu(2+) ions for GPC1 which are required for release of nitric oxide (NO) and subsequent degradation of the heparan sulfate chains on GPC1., [UniProtKB, UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; The gamma-CTF peptides as well as the caspase-cleaved peptides, including C31, are potent enhancers of neuronal apoptosis., [UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 2, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 3, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 3, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 3, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 8, "reported_mutagensis": 34, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 14, "glyco_site_count": 4, "binding_glycan_count": 0, "secondary_ac_list": "P97487;P97942;Q99K32", "ec_number_list": "", "go_molecular_function": "GO:0050786 RAGE receptor binding;GO:0003682 chromatin binding;GO:0004867 serine-type endopeptidase inhibitor activity;GO:0005102 signaling receptor binding;GO:0005109 frizzled binding", "go_cellular_component": "GO:0097708 intracellular vesicle;GO:0098992 neuronal dense core vesicle;GO:0005615 extracellular space;GO:0005634 nucleus;GO:0005641 nuclear envelope lumen", "go_biological_process": "GO:0032224 positive regulation of synaptic transmission, cholinergic;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001774 microglial cell activation;GO:0001878 response to yeast;GO:0001967 suckling behavior", "synthesized_glycan_count": 0, "hit_score": 4.6, "record_id": "P12023-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8CDG1-1", "uniprot_id": "PIWL2_MOUSE", "mass": 109488.0, "length": 971, "protein_name": "Piwi-like protein 2", "gene_name": "Piwil2", "organism": "Mouse", "refseq_name": "piwi-like protein 2 isoform 1", "refseq_ac": "NP_067283", "gene_names_uniprotkb": "Piwil2; Mili", "gene_names_refseq": "Piwil1l; Piwil2; mili", "protein_names_uniprotkb": "Piwi-like protein 2; 3.1.26.-", "protein_names_refseq": "Miwi like; Miwi likw; piwi-like homolog 2; piwi-like protein 2 isoform 1; piwi-like protein 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:57746)", "pathway_count": 1, "publication_count": 34, "publication_id_list": "11279525;11578866;12906857;14736746;16261612;16751777;16787967;17446352;18381894;18404146;18922463;19114715;19345100;19377467;19465913;19584108;19918066;20439430;20534472;20547853;21750661;22020280;22996915;23611983;23706823;24067652;26669262;28254886;28633017;28903391;31219806;32381626;34428180;36472244", "class_list": "", "function": "Endoribonuclease that plays a central role during spermatogenesis by repressing transposable elements and preventing their mobilization, which is essential for the germline integrity (PubMed:11578866, PubMed:14736746, PubMed:17446352, PubMed:18381894, PubMed:18922463, PubMed:26669262). Plays an essential role in meiotic differentiation of spermatocytes, germ cell differentiation and in self-renewal of spermatogonial stem cells (PubMed:11578866, PubMed:14736746, PubMed:17446352, PubMed:18381894, PubMed:18922463, PubMed:26669262). Its presence in oocytes suggests that it may participate in similar functions during oogenesis in females (PubMed:11578866, PubMed:14736746, PubMed:17446352, PubMed:18381894, PubMed:18922463, PubMed:26669262). Acts via the piRNA metabolic process, which mediates the repression of transposable elements during meiosis by forming complexes composed of piRNAs and Piwi proteins and govern the methylation and subsequent repression of transposons (PubMed:11578866, PubMed:14736746, PubMed:17446352, PubMed:18381894, PubMed:18922463, PubMed:26669262). During piRNA biosynthesis, plays a key role in the piRNA amplification loop, also named ping-pong amplification cycle, by acting as a 'slicer-competent' piRNA endoribonuclease that cleaves primary piRNAs, which are then loaded onto 'slicer-incompetent' PIWIL4 (PubMed:22020280, PubMed:23706823, PubMed:26669262). PIWIL2 slicing produces a pre-miRNA intermediate, which is then processed in mature piRNAs, and as well as a 16 nucleotide by-product that is degraded (PubMed:28633017). Required for PIWIL4/MIWI2 nuclear localization and association with secondary piRNAs antisense (PubMed:18381894, PubMed:18922463, PubMed:26669262). Besides their function in transposable elements repression, piRNAs are probably involved in other processes during meiosis such as translation regulation (PubMed:19114715). Indirectly modulates expression of genes such as PDGFRB, SLC2A1, ITGA6, GJA7, THY1, CD9 and STRA8 (PubMed:16261612). Represses circadian rhythms by promoting the stability and activity of core clock components BMAL1 and CLOCK by inhibiting GSK3B-mediated phosphorylation and ubiquitination-dependent degradation of these proteins (PubMed:28903391)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]; Piwil2 (Mili) sustains neurogenesis and prevents cellular senescence in the postnatal hippocampus., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 5, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "A6H617;Q3TQE8;Q99MV6;Q9JMB6", "ec_number_list": "3.6.4.10;3.6.4.13;2.1.1.386;3.1.26.-;5.6.2.5", "go_molecular_function": "GO:0003729 mRNA binding;GO:0016787 hydrolase activity;GO:0046872 metal ion binding;GO:0004521 RNA endonuclease activity;GO:0034584 piRNA binding", "go_cellular_component": "GO:0010370 perinucleolar chromocenter;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0097433 dense body", "go_biological_process": "GO:2000767 positive regulation of cytoplasmic translation;GO:0007283 spermatogenesis;GO:0048511 rhythmic process;GO:0031047 regulatory ncRNA-mediated gene silencing;GO:0048477 oogenesis", "synthesized_glycan_count": 0, "hit_score": 3.5, "record_id": "Q8CDG1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P07310-1", "uniprot_id": "KCRM_MOUSE", "mass": 43045.0, "length": 381, "protein_name": "Creatine kinase M-type", "gene_name": "Ckm", "organism": "Mouse", "refseq_name": "creatine kinase M-type", "refseq_ac": "NP_031736", "gene_names_uniprotkb": "Ckm; Ckmm", "gene_names_refseq": "CPK-M; Ckmm; Ckm; M-CK; MCK", "protein_names_uniprotkb": "Creatine kinase M-type; 2.7.3.2; CPK-M; Creatine kinase M chain; Creatine phosphokinase M-type; M-CK", "protein_names_refseq": "creatine kinase M chain; creatine kinase M-type; creatine phosphokinase M-type", "tax_id": 10090, "disease": "left ventricular failure (Disease Ontology:DOID:0051064)", "pathway": " (mmu:12715); (R-MMU-71288)", "pathway_count": 2, "publication_count": 8, "publication_id_list": "21183079;21750661;25605945;3003372;30084848;36288343;37507081;39927985", "class_list": "", "function": "Reversibly catalyzes the transfer of phosphate between ATP and various phosphogens (e.g. creatine phosphate). Creatine kinase isoenzymes play a central role in energy transduction in tissues with large, fluctuating energy demands, such as skeletal muscle, heart, brain and spermatozoa., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 8, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "2.7.3.2", "go_molecular_function": "GO:0004111 creatine kinase activity;GO:0005524 ATP binding", "go_cellular_component": "GO:0005615 extracellular space;GO:0005737 cytoplasm", "go_biological_process": "GO:0046314 phosphocreatine biosynthetic process;GO:0009408 response to heat;GO:0006603 phosphocreatine metabolic process", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "P07310-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q60603-1", "uniprot_id": "KCNH1_MOUSE", "mass": 111282.0, "length": 989, "protein_name": "Voltage-gated delayed rectifier potassium channel KCNH1", "gene_name": "Kcnh1", "organism": "Mouse", "refseq_name": "voltage-gated delayed rectifier potassium channel KCNH1 isoform 1", "refseq_ac": "NP_034730", "gene_names_uniprotkb": "Kcnh1; Eag1", "gene_names_refseq": "EAG1; Kcnh1; Kv10.1; M-eag; mEAG1", "protein_names_uniprotkb": "Voltage-gated delayed rectifier potassium channel KCNH1; EAG channel 1; Ether-a-go-go potassium channel 1; Potassium voltage-gated channel subfamily H member 1; Voltage-gated potassium channel subunit Kv10.1; m-eag; mEAG1", "protein_names_refseq": "EAG channel 1; ether a go-go; ether-a-go-go potassium channel 1; potassium voltage-gated channel subfamily H member 1; voltage-gated delayed rectifier potassium channel KCNH1 isoform 1; voltage-gated delayed rectifier potassium channel KCNH1; voltage-gated potassium channel subunit Kv10.1", "tax_id": 10090, "disease": "colorectal adenocarcinoma (Disease Ontology:DOID:0050861); epilepsy (Disease Ontology:DOID:1826); renal cell carcinoma (Disease Ontology:DOID:4450); hepatocellular carcinoma (Disease Ontology:DOID:684)", "pathway": " (mmu:16510); (R-MMU-1296072)", "pathway_count": 2, "publication_count": 16, "publication_id_list": "10.1101/2023.09.13.557529;10559392;19671703;21183079;21750661;22732247;22841712;23424202;23555008;23975098;25556795;27029528;27113750;27618660;34678516;8159766", "class_list": "", "function": "Both M-eag and its C. elegans homolog egl-2 are inhibited by the tricyclic antidepressant imipramine., [RefSeq, PubMed]; Expression of Kv10.1 driven by phosphorylated Rb/E2F1 contributes to G2/M progression of cancer and non-transformed cells., [RefSeq, PubMed]; KV10.1 localizes to the centrosome and the primary cilium and promotes ciliary disassembly. Interference with KV10.1 ciliary localization abolishes not only the effects on ciliary disassembly, but also KV10.1-induced tumor progression in vivo Conversely., [RefSeq, PubMed]; Pore-forming (alpha) subunit of a voltage-gated delayed rectifier potassium channel that mediates outward-rectifying potassium currents which, on depolarization, reaches a steady-state level and do not inactivate (PubMed:19671703, PubMed:23975098). The activation kinetics depend on the prepulse potential and external divalent cation concentration. With negative prepulses, the current activation is delayed and slowed down several fold, whereas more positive prepulses speed up activation. The time course of activation is biphasic with a fast and a slowly activating current component. Activates at more positive membrane potentials and exhibit a steeper activation curve (By similarity). Channel properties are modulated by subunit assembly. Mediates IK(NI) current in myoblasts. Involved in the regulation of cell proliferation and differentiation, in particular adipogenic and osteogenic differentiation in bone marrow-derived mesenchymal stem cells (MSCs) (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 1, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 1, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 3, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 3, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 3, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 3, "reported_mutagensis": 17, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 4, "glyco_site_count": 4, "binding_glycan_count": 0, "secondary_ac_list": "Q32MR6;Q3USQ9", "ec_number_list": "1.8.-.-", "go_molecular_function": "GO:0005251 delayed rectifier potassium channel activity;GO:1902936 phosphatidylinositol bisphosphate binding;GO:0005516 calmodulin binding;GO:0019901 protein kinase binding;GO:0042802 identical protein binding", "go_cellular_component": "GO:0034705 potassium channel complex;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0030424 axon;GO:0030425 dendrite", "go_biological_process": "GO:0001964 startle response;GO:0042127 regulation of cell population proliferation;GO:0042391 regulation of membrane potential;GO:0034220 monoatomic ion transmembrane transport;GO:0071277 cellular response to calcium ion", "synthesized_glycan_count": 0, "hit_score": 2.3, "record_id": "Q60603-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A6BLY7-1", "uniprot_id": "K1C28_MOUSE", "mass": 50346.0, "length": 462, "protein_name": "Keratin, type I cytoskeletal 28", "gene_name": "Krt28", "organism": "Mouse", "refseq_name": "keratin, type I cytoskeletal 28", "refseq_ac": "NP_081850", "gene_names_uniprotkb": "Krt28; Krt25d", "gene_names_refseq": "4733401L19Rik; CK-28; K25D; K28; Krt25d; Krt28", "protein_names_uniprotkb": "Keratin, type I cytoskeletal 28; CK-28; Cytokeratin-28; K25D; K28; Keratin-25D; Keratin-28; Type I inner root sheath-specific keratin-K25irs4", "protein_names_refseq": "cytokeratin-28; keratin 25D; keratin, type I cytoskeletal 28; type I inner root sheath-specific keratin-K25irs4", "tax_id": 10090, "disease": "", "pathway": " (mmu:70843); (R-MMU-6805567); (R-MMU-6809371)", "pathway_count": 3, "publication_count": 5, "publication_id_list": "14996088;17920809;34428180;34887587;41018975", "class_list": "", "function": "Essential for the proper assembly of types I and II keratin protein complexes and the formation of keratin intermediate filaments in the inner root sheath (irs)., [UniProtKB, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q9D637", "ec_number_list": "", "go_molecular_function": "GO:0030280 structural constituent of skin epidermis", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005856 cytoskeleton;GO:0045095 keratin filament", "go_biological_process": "GO:0030855 epithelial cell differentiation;GO:0045109 intermediate filament organization;GO:0031069 hair follicle morphogenesis;GO:0002009 morphogenesis of an epithelium", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "A6BLY7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q61179-1", "uniprot_id": "IRF9_MOUSE", "mass": 44610.0, "length": 399, "protein_name": "Interferon regulatory factor 9", "gene_name": "Irf9", "organism": "Mouse", "refseq_name": "interferon regulatory factor 9 isoform 1", "refseq_ac": "NP_001152889", "gene_names_uniprotkb": "Irf9; Isgf3g", "gene_names_refseq": "Irf-9; Irf9; Isgf3g; p48", "protein_names_uniprotkb": "Interferon regulatory factor 9; IFN-alpha-responsive transcription factor subunit; IRF-9; ISGF-3 gamma; ISGF3 p48 subunit; Interferon-stimulated gene factor 3 gamma; Transcriptional regulator ISGF3 subunit gamma", "protein_names_refseq": "IFN-alpha-responsive transcription factor subunit; ISGF-3 gamma; ISGF3 p48 subunit; interferon dependent positive acting transcription factor 3 gamma; interferon regulatory factor 9 isoform 1; interferon-stimulated gene factor 3 gamma; transcriptional regulator ISGF3 subunit gamma", "tax_id": 10090, "disease": "immunodeficiency 65 (Disease Ontology:DOID:0111978); familial hyperlipidemia (Disease Ontology:DOID:1168); hepatitis C (Disease Ontology:DOID:1883); acute pancreatitis (Disease Ontology:DOID:2913)", "pathway": " (mmu:16391); (R-MMU-909733)", "pathway_count": 2, "publication_count": 7, "publication_id_list": "17242355;17332413;21183079;21750661;30084848;7843405;8882710", "class_list": "", "function": "Transcription factor that plays an essential role in anti-viral immunity. It mediates signaling by type I IFNs (IFN-alpha and IFN-beta). Following type I IFN binding to cell surface receptors, Jak kinases (TYK2 and JAK1) are activated, leading to tyrosine phosphorylation of STAT1 and STAT2. IRF9/ISGF3G associates with the phosphorylated STAT1:STAT2 dimer to form a complex termed ISGF3 transcription factor, that enters the nucleus. ISGF3 binds to the IFN stimulated response element (ISRE) to activate the transcription of interferon stimulated genes, which drive the cell in an antiviral state., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 4, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0000976 transcription cis-regulatory region binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol;GO:0070721 ISGF3 complex", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0042832 defense response to protozoan;GO:0002376 immune system process", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q61179-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9WUR9-1", "uniprot_id": "KAD4_MOUSE", "mass": 25062.0, "length": 223, "protein_name": "Adenylate kinase 4, mitochondrial", "gene_name": "Ak4", "organism": "Mouse", "refseq_name": "adenylate kinase 4, mitochondrial isoform 1", "refseq_ac": "NP_001171073", "gene_names_uniprotkb": "Ak4; Ak-4; Ak3b; Ak3l1", "gene_names_refseq": "AK 4; Ak-3; Ak-4; Ak3l1; Ak3; Ak4; D4Ertd274e", "protein_names_uniprotkb": "Adenylate kinase 4, mitochondrial; 2.7.4.4; 2.7.4.6; Adenylate kinase 3-like; GTP:AMP phosphotransferase AK4", "protein_names_refseq": "ATP-AMP transphosphorylase; GTP:AMP phosphotransferase AK4, mitochondrial; adenylate kinase 3 alpha-like 1; adenylate kinase 3-like 1; adenylate kinase 4, mitochondrial isoform 1; adenylate kinase isoenzyme 4, mitochondrial", "tax_id": 10090, "disease": "acute kidney tubular necrosis (Disease Ontology:DOID:12556)", "pathway": " (mmu:11639); (R-MMU-499943)", "pathway_count": 2, "publication_count": 10, "publication_id_list": "19130895;19492028;21750661;23576753;23806337;25605945;33790902;34428180;37507081;9813319", "class_list": "", "function": "Adenylate Kinase 4 Promotes Inflammatory Gene Expression via Hif1alpha and AMPK in Macrophages. Publication Status: Online-Only, [RefSeq, PubMed]; Broad-specificity mitochondrial nucleoside phosphate kinase involved in cellular nucleotide homeostasis by catalyzing nucleoside-phosphate interconversions. Similar to other adenylate kinases, preferentially catalyzes the phosphorylation of the nucleoside monophosphate AMP with ATP as phosphate donor to produce ADP. Phosphorylates only AMP when using GTP as phosphate donor. In vitro, can also catalyze the phosphorylation of CMP, dAMP and dCMP and use GTP as an alternate phosphate donor. Moreover, exhibits a diphosphate kinase activity, producing ATP, CTP, GTP, UTP, TTP, dATP, dCTP and dGTP from the corresponding diphosphate substrates with either ATP or GTP as phosphate donors. Plays a role in controlling cellular ATP levels by regulating phosphorylation and activation of the energy sensor protein kinase AMPK. Plays a protective role in the cellular response to oxidative stress., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q9R1X7", "ec_number_list": "2.7.4.6;2.7.4.4;3.1.11.-;2.7.11.1;2.7.13.3;2.7.4.18;3.1.24.-;2.7.4.3;2.7.4.14;2.7.4.10", "go_molecular_function": "GO:0004017 AMP kinase activity;GO:0046899 nucleoside triphosphate adenylate kinase activity;GO:0005524 ATP binding;GO:0005525 GTP binding;GO:0004550 nucleoside diphosphate kinase activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix", "go_biological_process": "GO:0006172 ADP biosynthetic process;GO:0046033 AMP metabolic process;GO:0071456 cellular response to hypoxia;GO:0046034 ATP metabolic process;GO:0046039 GTP metabolic process", "synthesized_glycan_count": 0, "hit_score": 1.3, "record_id": "Q9WUR9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q69ZK6-1", "uniprot_id": "JHD2C_MOUSE", "mass": 281594.0, "length": 2531, "protein_name": "Jumonji domain-containing protein 1C", "gene_name": "Jmjd1c", "organism": "Mouse", "refseq_name": "jumonji domain-containing protein 1C isoform 2", "refseq_ac": "NP_001229325", "gene_names_uniprotkb": "Jmjd1c; Jhdm2c; Kiaa1380", "gene_names_refseq": "5430433L24Rik; D630035I23Rik; Jmjd1c; Jmjdic; TRIP8", "protein_names_uniprotkb": "Jumonji domain-containing protein 1C; 1.14.11.-", "protein_names_refseq": "jumonji domain-containing protein 1C isoform 2; jumonji domain-containing protein 1C; probable JmjC domain-containing histone demethylation protein 2C", "tax_id": 10090, "disease": "alcohol use disorder (Disease Ontology:DOID:1574)", "pathway": " (mmu:108829); (R-MMU-983231)", "pathway_count": 2, "publication_count": 10, "publication_id_list": "19144319;20530532;21183079;21750661;24006281;32034158;32782141;34887587;35995859;36852467", "class_list": "", "function": "Demethylates lysine in proteins, such as STAT3 or MDC1 (By similarity) (PubMed:35995859). Demethylates MDC1, thereby promoting MDC1-RNF8 interaction and facilitating RNF8-dependent MDC1 ubiquitination essential for double-strand break (DSB) repair (By similarity). Demethylation of STAT3 at 'Lys-140', facilitates its interactions with the phosphatase PTPN6 and restrains STAT3 activation (PubMed:35995859). It is uncertain whether JMJD1C removes methyl groups from histone proteins as the other JMJD1/KDM3 proteins do (PubMed:20530532, PubMed:24006281, PubMed:32034158, PubMed:35995859). Nevertheless, JMJD1C may act as a context-specific histone demethylase. Implicated in lipogenic gene transcription in the liver, where USF1 recruits JMJD1C to lipogenic promoters in response to insulin or feeding stimuli, thereby potentially promoting H3K9me2 demethylation and enhancing chromatin accessibility (PubMed:32034158). Post-translational modifications may regulate JMJD1C's enzymatic activity, contributing to its context-specific functions (PubMed:32034158). Alternatively, JMJD1C may influence chromatin regulation indirectly, acting as a scaffold or co-regulator that recruits or stabilizes other active demethylase complexes modifying histone marks (By similarity). Plays an indispensable role in spermatogenesis (PubMed:20530532, PubMed:24006281)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed, PubMed]; JMJD1C promotes lipogenesis to increase hepatic and plasma triglyceride levels, showing its role in metabolic adaption for activation of the lipogenic program in response to feeding/insulin, and its contribution to development of hepatosteatosis resulting in insulin resistance. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 3, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 3, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 3, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 19, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 3, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "E9QMM8;G3UZM1;Q6NV48;Q8BUF5;Q8C4I5;Q8C5Q9", "ec_number_list": "1.14.11.-", "go_molecular_function": "GO:0008270 zinc ion binding;GO:0031490 chromatin DNA binding;GO:0051213 dioxygenase activity;GO:0003712 transcription coregulator activity;GO:0032454 histone H3K9 demethylase activity", "go_cellular_component": "GO:0005634 nucleus;GO:0000785 chromatin;GO:0000118 histone deacetylase complex", "go_biological_process": "GO:0098727 maintenance of cell number;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0008610 lipid biosynthetic process;GO:0008584 male gonad development", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "Q69ZK6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O35173-1", "uniprot_id": "KCNS1_MOUSE", "mass": 54918.0, "length": 497, "protein_name": "Delayed-rectifier potassium channel regulatory subunit KCNS1", "gene_name": "Kcns1", "organism": "Mouse", "refseq_name": "delayed-rectifier potassium channel regulatory subunit KCNS1", "refseq_ac": "NP_032461", "gene_names_uniprotkb": "Kcns1", "gene_names_refseq": "Kcns1; Kv9.1", "protein_names_uniprotkb": "Delayed-rectifier potassium channel regulatory subunit KCNS1; Delayed-rectifier K(+) channel alpha subunit 1; Delayed-rectifier potassium channel subunit Kv9.1; Potassium voltage-gated channel modifier subfamily S member 1", "protein_names_refseq": "delayed-rectifier K(+) channel alpha subunit 1; delayed-rectifier potassium channel regulatory subunit KCNS1; delayed-rectifier potassium channel subunit Kv9.1; potassium voltage-gated channel modifier subfamily S member 1; potassium voltage-gated channel subfamily S member 1; voltage-gated potassium channel subunit Kv9.1", "tax_id": 10090, "disease": "intracranial hypertension (Disease Ontology:DOID:9428)", "pathway": " (mmu:16538); (R-MMU-1296072)", "pathway_count": 2, "publication_count": 2, "publication_id_list": "29697531;9305895", "class_list": "", "function": "After neuropathic injury, Kcns1 KO mice exhibited exaggerated mechanical pain responses and hypersensitivity to both noxious and innocuous cold, consistent with increased A-fiber activity. Interestingly, Kcns1 deletion also improved locomotor performance in the rotarod test, indicative of augmented proprioceptive signalling., [RefSeq, PubMed]; Potassium channel regulatory subunit that modulate the delayed rectifier voltage-gated potassium channel activity of KCNB1 and KCNB2 by altering their kinetics, expression levels, and shifting the half-inactivation potential to more polarized values (PubMed:9305895). While it does not form functional channels on its own, it can form functional heterotetrameric channels with KCNB1 and KCNB2 (PubMed:9305895). Each regulatory subunit has unique regulatory properties that can lead to extensive inhibition, significant changes in kinetics, and/or substantial shifts in the voltage dependencies of the inactivation process (PubMed:9305895)., [UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "A2A5M1", "ec_number_list": "", "go_molecular_function": "GO:0015459 potassium channel regulator activity;GO:0005249 voltage-gated potassium channel activity", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005886 plasma membrane;GO:0016020 membrane;GO:0048471 perinuclear region of cytoplasm;GO:0008076 voltage-gated potassium channel complex", "go_biological_process": "GO:1901379 regulation of potassium ion transmembrane transport;GO:0051260 protein homooligomerization;GO:0001508 action potential;GO:0006813 potassium ion transport;GO:0071805 potassium ion transmembrane transport", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "O35173-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O35219-1", "uniprot_id": "KCNH2_MOUSE", "mass": 126886.0, "length": 1162, "protein_name": "Voltage-gated inwardly rectifying potassium channel KCNH2", "gene_name": "Kcnh2", "organism": "Mouse", "refseq_name": "voltage-gated inwardly rectifying potassium channel KCNH2 isoform 2", "refseq_ac": "NP_001281091", "gene_names_uniprotkb": "Kcnh2; Erg; Merg1", "gene_names_refseq": "ERG1; Kcnh2; LQT; Lqt2; M-erg; Merg1; merg1a; merg1b", "protein_names_uniprotkb": "Voltage-gated inwardly rectifying potassium channel KCNH2; ERG-1; Eag-related protein 1; Ether-a-go-go-related gene potassium channel 1; Ether-a-go-go-related protein 1; MERG; Potassium voltage-gated channel subfamily H member 2; Voltage-gated potassium channel subunit Kv11.1", "protein_names_refseq": "eag-related protein 1; ether-a-go-go-related gene potassium channel 1; ether-a-go-go-related protein 1; potassium voltage-gated channel subfamily H member 2; voltage-gated inwardly rectifying potassium channel KCNH2 isoform 2; voltage-gated inwardly rectifying potassium channel KCNH2; voltage-gated potassium channel subunit Kv11.1", "tax_id": 10090, "disease": "short QT syndrome (Disease Ontology:DOID:0050793); long QT syndrome 2 (Disease Ontology:DOID:0110645); heart conduction disease (Disease Ontology:DOID:10273); epilepsy (Disease Ontology:DOID:1826); long QT syndrome (Disease Ontology:DOID:2843)", "pathway": " (mmu:16511); (R-MMU-1296072); (R-MMU-5576890)", "pathway_count": 3, "publication_count": 8, "publication_id_list": "10.1101/2023.09.13.557529;21183079;21750661;24129315;31484079;34363662;9351446;9351462", "class_list": "", "function": "Identification and Characterization of a Transcribed Distal Enhancer Involved in Cardiac Kcnh2 Regulation., [RefSeq, PubMed]; MERG1A Protein Abundance Increases in the Atrophied Skeletal Muscle of Denervated Mice, But Does Not Affect NFkappaB Activity., [RefSeq, PubMed]; Pore-forming (alpha) subunit of voltage-gated inwardly rectifying potassium channel (PubMed:9351446, PubMed:9351462). Characterized by unusual gating kinetics by producing relatively small outward currents during membrane depolarization and large inward currents during subsequent repolarization which reflect a rapid inactivation during depolarization and quick recovery from inactivation but slow deactivation (closing) during repolarization. Channel properties are modulated by cAMP and subunit assembly (PubMed:9351446, PubMed:9351462). Forms a stable complex with KCNE1 or KCNE2, and that this heteromultimerization regulates inward rectifier potassium channel activity (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 1, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 10, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 5, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "O35220;O35221;O35989", "ec_number_list": "1.8.-.-", "go_molecular_function": "GO:0005251 delayed rectifier potassium channel activity;GO:1902282 voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization;GO:0005216 monoatomic ion channel activity;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity", "go_cellular_component": "GO:1902937 inward rectifier potassium channel complex;GO:0005635 nuclear envelope;GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0009986 cell surface", "go_biological_process": "GO:1901379 regulation of potassium ion transmembrane transport;GO:1901380 negative regulation of potassium ion transmembrane transport;GO:0086011 membrane repolarization during action potential;GO:0098915 membrane repolarization during ventricular cardiac muscle cell action potential;GO:1903765 negative regulation of potassium ion export across plasma membrane", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "O35219-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P11679-1", "uniprot_id": "K2C8_MOUSE", "mass": 54565.0, "length": 490, "protein_name": "Keratin, type II cytoskeletal 8", "gene_name": "Krt8", "organism": "Mouse", "refseq_name": "keratin, type II cytoskeletal 8", "refseq_ac": "NP_112447", "gene_names_uniprotkb": "Krt8; Krt2-8", "gene_names_refseq": "Card2; EndoA; K8; Krt-2.8; Krt2-8; Krt8; TROMA-1", "protein_names_uniprotkb": "Keratin, type II cytoskeletal 8; CK-8; Cytokeratin endo A; Cytokeratin-8; K8; Keratin-8; Type-II keratin Kb8", "protein_names_refseq": "CK-8; cytokeratin endo A; cytokeratin-8; keratin complex 2, basic, gene 8; keratin, type II cytoskeletal 8; type-II keratin Kb8", "tax_id": 10090, "disease": "liver cirrhosis (Disease Ontology:DOID:5082)", "pathway": " (mmu:16691); (R-MMU-6805567); (R-MMU-6809371)", "pathway_count": 3, "publication_count": 25, "publication_id_list": "10.1101/2023.09.13.557529;11514590;12857878;1717348;17242355;18630941;20724476;21183079;2454862;2464527;2467842;24940650;25617501;30042374;30059200;30084848;34428180;36064721;36583994;36852467;37453647;37507081;39627609;41018975;9864371", "class_list": "", "function": "Structural component of intermediate filaments in simple epithelial cells. Together with its obligate type I partner KRT18, contributes to the formation of the keratin intermediate filament network that provides mechanical stability and resilience to epithelial cells (PubMed:11514590). Also involved in maintaining epithelial integrity and protecting cells from non-mechanical stress, such as apoptosis (PubMed:11514590). Also required for ARHGEF40-mediated actin stress fiber formation and tensional force-induced stress fiber formation and reinforcement (By similarity). In striated muscle, together with KRT19, may contribute to linking the contractile apparatus to dystrophin at the costameres (By similarity)., [UniProtKB, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 30, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 1, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q3KQK5;Q3TGI1;Q3TJE1;Q3TKY7;Q61463;Q61518;Q61519", "ec_number_list": "", "go_molecular_function": "GO:0044877 protein-containing complex binding;GO:0097110 scaffold protein binding", "go_cellular_component": "GO:0016010 dystrophin-associated glycoprotein complex;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005911 cell-cell junction;GO:0005882 intermediate filament", "go_biological_process": "GO:0060706 cell differentiation involved in embryonic placenta development;GO:0051707 response to other organism;GO:0097191 extrinsic apoptotic signaling pathway;GO:0045214 sarcomere organization;GO:0033209 tumor necrosis factor-mediated signaling pathway", "synthesized_glycan_count": 0, "hit_score": 3.0, "record_id": "P11679-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P48542-1", "uniprot_id": "KCNJ6_MOUSE", "mass": 48652.0, "length": 425, "protein_name": "G protein-activated inward rectifier potassium channel 2", "gene_name": "Kcnj6", "organism": "Mouse", "refseq_name": "G protein-activated inward rectifier potassium channel 2 isoform Girk2B", "refseq_ac": "NP_001020756", "gene_names_uniprotkb": "Kcnj6; Girk2; Kcnj7; W", "gene_names_refseq": "BIR1; GIRK2; KATP2; KCNJ7; Kcnj6; Kir3.2; weaver; wv", "protein_names_uniprotkb": "G protein-activated inward rectifier potassium channel 2; GIRK-2; Inward rectifier K(+) channel Kir3.2; Potassium channel, inwardly rectifying subfamily J member 6", "protein_names_refseq": "G protein-activated inward rectifier potassium channel 2 isoform Girk2B; G-protein-coupled inward rectifier K+ channel 2-1; G-protein-coupled inward rectifier K+ channel 2-A; G-protein-coupled inward rectifier K+ channel 2-B; G-protein-coupled inward rectifier K+ channel 2-C; GIRK-2; g protein-activated inward rectifier potassium channel 2; inward rectifier K(+) channel Kir3.2; potassium channel, inwardly rectifying subfamily J member 6; potassium inwardly-rectifying channel J6", "tax_id": 10090, "disease": "alcohol use disorder (Disease Ontology:DOID:1574); heroin dependence (Disease Ontology:DOID:9976)", "pathway": " (mmu:16522); (R-MMU-1296041); (R-MMU-997272)", "pathway_count": 3, "publication_count": 10, "publication_id_list": "10341034;10562331;21183079;21750661;37594983;7499385;7550338;7926018;8573147;9721208", "class_list": "", "function": "GIRK2 potassium channels expressed by the AgRP neurons decrease adiposity and body weight in mice. Publication Status: Online-Only, [RefSeq, PubMed]; Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is regulated by the concentration of extracellular potassium; as external potassium is raised, the voltage range of the channel opening shifts to more positive voltages. The inward rectification is mainly due to the blockage of outward current by internal magnesium. This potassium channel is controlled by G proteins., [UniProtKB, PubMed, PubMed, PubMed, PubMed, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "O70290;P70216;P70306;P70307;P70308;P70309;P70454;Q9QYH5", "ec_number_list": "1.8.-.-", "go_molecular_function": "GO:0015467 G-protein activated inward rectifier potassium channel activity;GO:0001965 G-protein alpha-subunit binding;GO:0005267 potassium channel activity;GO:0005242 inward rectifier potassium channel activity;GO:0099508 voltage-gated monoatomic ion channel activity involved in regulation of presynaptic membrane potential", "go_cellular_component": "GO:1902937 inward rectifier potassium channel complex;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0016020 membrane;GO:0030424 axon", "go_biological_process": "GO:0046676 negative regulation of insulin secretion;GO:1990573 potassium ion import across plasma membrane", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "P48542-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P50446-1", "uniprot_id": "K2C6A_MOUSE", "mass": 59335.0, "length": 553, "protein_name": "Keratin, type II cytoskeletal 6A", "gene_name": "Krt6a", "organism": "Mouse", "refseq_name": "keratin, type II cytoskeletal 6A", "refseq_ac": "NP_032502", "gene_names_uniprotkb": "Krt6a; Ker2; Krt2-6a; Krt2-6; Krt6", "gene_names_refseq": "2310016L08Rik; CK-6A; K6A; K6[a]; Krt2-6a; Krt2-6c; Krt6a; MK6a; mK6[a]", "protein_names_uniprotkb": "Keratin, type II cytoskeletal 6A; CK-6A; Cytokeratin-6A; K6A; Keratin-6-alpha; Keratin-6A; mK6-alpha", "protein_names_refseq": "60-kDa keratin; K6-alpha; cytokeratin-6A; keratin complex 2, basic, gene 6a; keratin complex 2, basic, gene 6c; keratin, type II cytoskeletal 6A; keratin-6-alpha; mK6-alpha", "tax_id": 10090, "disease": "pachyonychia congenita (Disease Ontology:DOID:0050449); focal or diffuse nonepidermolytic palmoplantar keratoderma (Disease Ontology:DOID:0111710)", "pathway": " (mmu:16687); (R-MMU-6805567); (R-MMU-6809371)", "pathway_count": 3, "publication_count": 15, "publication_id_list": "10866680;11069616;1713533;22529101;26495903;30389720;34428180;34887587;36583994;37453647;39627609;41018975;6207530;8636216;9790766", "class_list": "", "function": "Structural component of intermediate filaments in epithelial keratinocytes. Forms heteropolymers with the type I keratins KRT16 and KRT17, assembling keratin intermediate filament networks that contributes to the structural integrity and stress resilience of stratified epithelia, particularly in epidermis, nail bed and oral mucosa. Rapidly induced in wound-edge keratinocytes and participates in the reorganization of the cytoskeleton during re-epithelialization (PubMed:10866680, PubMed:8636216). Negatively regulates collective keratinocyte migration by stabilizing myosin IIA/MYH2 and desmoplakin, thereby altering cell-cell and cell-matrix adhesion and reducing the speed and directionality of epithelial sheet movement during wound repair (PubMed:30389720). Also limits epithelial migration by inhibiting the activity of SRC during wound repair (PubMed:22529101). Required for normal palmoplantar and nail unit integrity (By similarity)., [UniProtKB, PubMed, PubMed, PubMed, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q9Z332", "ec_number_list": "", "go_molecular_function": "GO:0030280 structural constituent of skin epidermis", "go_cellular_component": "GO:0045111 intermediate filament cytoskeleton;GO:0045095 keratin filament", "go_biological_process": "GO:0031424 keratinization;GO:0050830 defense response to Gram-positive bacterium;GO:0061844 antimicrobial humoral immune response mediated by antimicrobial peptide;GO:0016055 Wnt signaling pathway;GO:0045109 intermediate filament organization", "synthesized_glycan_count": 0, "hit_score": 1.8, "record_id": "P50446-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P63143-1", "uniprot_id": "KCAB1_MOUSE", "mass": 44723.0, "length": 401, "protein_name": "Voltage-gated potassium channel subunit beta-1", "gene_name": "Kcnab1", "organism": "Mouse", "refseq_name": "voltage-gated potassium channel subunit beta-1 isoform 1", "refseq_ac": "NP_034727", "gene_names_uniprotkb": "Kcnab1; Kvb1", "gene_names_refseq": "Akr8a8; Kcnab1; Kvbeta1.1; mKv(beta)1", "protein_names_uniprotkb": "Voltage-gated potassium channel subunit beta-1; 1.1.1.-; K(+) channel subunit beta-1; Kv-beta-1", "protein_names_refseq": "K(+) channel subunit beta-1; voltage dependent potassium channel subunit beta-1; voltage-gated potassium channel subunit beta-1 isoform 1; voltage-gated potassium channel subunit beta-1", "tax_id": 10090, "disease": "hypertension (Disease Ontology:DOID:10763); temporal lobe epilepsy (Disease Ontology:DOID:3328)", "pathway": " (mmu:16497); (R-MMU-1296072)", "pathway_count": 2, "publication_count": 9, "publication_id_list": "10454353;14511342;15530391;21750661;33300544;33499656;35820727;8824288;9468385", "class_list": "", "function": "Myocardial Blood Flow Control by Oxygen Sensing Vascular Kvbeta Proteins., [RefSeq, PubMed]; Regulatory subunit of the voltage-gated potassium (Kv) Shaker channels composed of pore-forming and potassium-conducting alpha subunits and of regulatory beta subunits (PubMed:10454353). The beta-1/KCNAB1 cytoplasmic subunit mediates closure of delayed rectifier potassium channels by physically obstructing the pore via its N-terminal domain and increases the speed of channel closure for other family members. Promotes the inactivation of KCNA1, KCNA2, KCNA4, KCNA5 and KCNA6 alpha subunit-containing channels (By similarity). Displays nicotinamide adenine dinucleotide phosphate (NADPH)-dependent aldoketoreductase activity by catalyzing the NADPH-dependent reduction of a variety of endogenous aldehydes and ketones (By similarity). The binding of NADPH is required for efficient down-regulation of potassium channel activity (By similarity). Oxidation of the bound NADPH restrains N-terminal domain from blocking the channel, thereby decreasing N-type inactivation of potassium channel activity (By similarity)., [UniProtKB, UniProtKB, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "P97380;Q61763;Q63277;Q91WM5", "ec_number_list": "1.1.1.184;1.1.1.189;1.1.1.197;1.1.1.196;1.1.1.71;1.1.1.-;1.6.5.10;1.1.1.300;1.1.1.2;1.6.-.-;1.1.1.19;1.1.1.20;1.1.1.372;1.1.1.54", "go_molecular_function": "GO:0019904 protein domain specific binding;GO:0015459 potassium channel regulator activity;GO:0044325 transmembrane transporter binding;GO:0008106 alcohol dehydrogenase (NADP+) activity;GO:0070402 NADPH binding", "go_cellular_component": "GO:0034705 potassium channel complex;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0030424 axon;GO:0043025 neuronal cell body", "go_biological_process": "GO:1901379 regulation of potassium ion transmembrane transport;GO:0007611 learning or memory;GO:1902260 negative regulation of delayed rectifier potassium channel activity;GO:0071805 potassium ion transmembrane transport", "synthesized_glycan_count": 0, "hit_score": 1.2, "record_id": "P63143-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q059U7-1", "uniprot_id": "INTU_MOUSE", "mass": 104821.0, "length": 942, "protein_name": "Protein inturned", "gene_name": "Intu", "organism": "Mouse", "refseq_name": "protein inturned isoform 1", "refseq_ac": "NP_780724", "gene_names_uniprotkb": "Intu; Kiaa1284; Pdzd6", "gene_names_refseq": "9230116I04Rik; 9430087H23Rik; Intu; Pdzd6; Pdzk6; mKIAA1284", "protein_names_uniprotkb": "Protein inturned; Inturned planar cell polarity effector homolog; PDZ domain-containing protein 6", "protein_names_refseq": "PDZ domain-containing protein 6; inturned planar cell polarity effector homolog; protein inturned isoform 1; protein inturned", "tax_id": 10090, "disease": "asphyxiating thoracic dystrophy (Disease Ontology:DOID:0050592); orofaciodigital syndrome XVII (Disease Ontology:DOID:0080289)", "pathway": " (mmu:380614); (R-MMU-5610787)", "pathway_count": 2, "publication_count": 10, "publication_id_list": "20067783;21183079;21750661;21761479;22935613;27158779;29038301;29581513;35427153;39029571", "class_list": "", "function": "CPLANE protein INTU regulates growth and patterning of the mouse lungs through cilia-dependent Hh signaling., [RefSeq, PubMed]; Data show that the functions of both Inturned and Fuzzy in neural tube patterning are dependent on the presence of cilia., [RefSeq, PubMed]; Plays a key role in ciliogenesis and embryonic development. Regulator of cilia formation by controlling the organization of the apical actin cytoskeleton and the positioning of the basal bodies at the apical cell surface, which in turn is essential for the normal orientation of elongating ciliary microtubules. Plays a key role in definition of cell polarity via its role in ciliogenesis but not via conversion extension. Has an indirect effect on hedgehog signaling (PubMed:20067783, PubMed:21761479). Proposed to function as core component of the CPLANE (ciliogenesis and planar polarity effectors) complex involved in the recruitment of peripheral IFT-A proteins to basal bodies (By similarity). Required for recruitment of CPLANE2 to the mother centriole (PubMed:29038301). Binds phosphatidylinositol 3-phosphate with highest affinity, followed by phosphatidylinositol 4-phosphate and phosphatidylinositol 5-phosphate (PubMed:35427153)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed, PubMed]; Propose a role for Intu in protecting cells and tissues after injury by targeting STAT1 for degradation and maintaining primary cilia Publication Status: Online-Only, [RefSeq, PubMed]; Targeting Intu in the epidermis resulted in almost complete loss of primary cilia in epidermal and follicular keratinocytes, and a suppressed hedgehog signaling pathway., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q80TG0;Q8BS60;Q8C9Y0", "ec_number_list": "", "go_molecular_function": "GO:0035091 phosphatidylinositol binding", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005929 cilium;GO:0009986 cell surface;GO:0031514 motile cilium", "go_biological_process": "GO:0045880 positive regulation of smoothened signaling pathway;GO:0021513 spinal cord dorsal/ventral patterning;GO:0007399 nervous system development;GO:0030216 keratinocyte differentiation;GO:0021915 neural tube development", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q059U7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q61781-1", "uniprot_id": "K1C14_MOUSE", "mass": 52867.0, "length": 484, "protein_name": "Keratin, type I cytoskeletal 14", "gene_name": "Krt14", "organism": "Mouse", "refseq_name": "keratin, type I cytoskeletal 14 isoform 3", "refseq_ac": "NP_001300886", "gene_names_uniprotkb": "Krt14; Krt1-14", "gene_names_refseq": "CK-14; K14; Krt-1.14; Krt1-14; Krt14", "protein_names_uniprotkb": "Keratin, type I cytoskeletal 14; CK-14; Cytokeratin-14; K14; Keratin-14", "protein_names_refseq": "cytokeratin 14; keratin complex 1, acidic, gene 14; keratin, type I cytoskeletal 14 isoform 3; keratin, type I cytoskeletal 14", "tax_id": 10090, "disease": "generalized severe epidermolysis bullosa simplex 1A (Disease Ontology:DOID:0060735); dermatopathia pigmentosa reticularis (Disease Ontology:DOID:0111342); Naegeli-Franceschetti-Jadassohn syndrome (Disease Ontology:DOID:0111528); epidermolysis bullosa simplex (Disease Ontology:DOID:4644); esophagus small cell carcinoma (Disease Ontology:DOID:7134)", "pathway": " (mmu:16664); (R-MMU-446107); (R-MMU-6805567); (R-MMU-6809371)", "pathway_count": 4, "publication_count": 15, "publication_id_list": "11408584;12657653;16702408;17227889;18285451;19267394;21183079;22705788;2433272;24940650;26758872;27033150;28935714;34428180;36583994", "class_list": "", "function": "Structural component of intermediate filaments in basal keratinocytes of stratified epithelia. Forms obligate heteropolymers with the type II keratin KRT5, contributing to the keratin intermediate filament network that confers mechanical strength and structural integrity to the basal layer of the epidermis and other stratified epithelial. The nonhelical tail domain is involved in promoting KRT5-KRT14 filaments to self-organize into large bundles and enhances the mechanical properties involved in resilience of keratin intermediate filaments in vitro., [UniProtKB, PubMed]; This gene encodes a member of the keratin family, the most diverse group of intermediate filaments. This gene product, a type I keratin, is usually found as a heterotetramer with two keratin 5 molecules, a type II keratin. Together they form the cytoskeleton of epithelial cells. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2015]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 5, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "A2A4G4;Q91VQ4;Q99LE0", "ec_number_list": "", "go_molecular_function": "GO:1990254 keratin filament binding;GO:0030280 structural constituent of skin epidermis", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005856 cytoskeleton;GO:0045178 basal part of cell;GO:0005882 intermediate filament", "go_biological_process": "GO:0045110 intermediate filament bundle assembly;GO:0030855 epithelial cell differentiation;GO:0030216 keratinocyte differentiation;GO:0045109 intermediate filament organization;GO:0009314 response to radiation", "synthesized_glycan_count": 0, "hit_score": 1.6, "record_id": "Q61781-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q80U59-1", "uniprot_id": "K0232_MOUSE", "mass": 154778.0, "length": 1396, "protein_name": "Uncharacterized protein KIAA0232", "gene_name": "D5Ertd579e; Kiaa0232", "organism": "Mouse", "refseq_name": "uncharacterized protein KIAA0232", "refseq_ac": "NP_001074701", "gene_names_uniprotkb": "D5Ertd579e; Kiaa0232; D5Ertd579e", "gene_names_refseq": "9030221A05Rik; A930018H20Rik; D5Ertd579e; Kiaa0232", "protein_names_uniprotkb": "Uncharacterized protein KIAA0232", "protein_names_refseq": "uncharacterized protein KIAA0232", "tax_id": 10090, "disease": "", "pathway": " (mmu:320661)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "21183079;21750661;30084848;30779550;34428180", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3U6T9;Q3UTK1;Q3UYU6;Q504Z4;Q80XC4;Q8BJI7;Q8BZV3", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding", "go_cellular_component": "", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "Q80U59-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8K114-1", "uniprot_id": "INT9_MOUSE", "mass": 74078.0, "length": 658, "protein_name": "Integrator complex subunit 9", "gene_name": "Ints9", "organism": "Mouse", "refseq_name": "integrator complex subunit 9 isoform 2", "refseq_ac": "NP_001240660", "gene_names_uniprotkb": "Ints9; D14Ertd231e", "gene_names_refseq": "D14Ertd231e; Ints9", "protein_names_uniprotkb": "Integrator complex subunit 9; Int9", "protein_names_refseq": "int9; integrator complex subunit 9 isoform 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:210925); (R-MMU-6807505)", "pathway_count": 2, "publication_count": 4, "publication_id_list": "21750661;26206133;31219806;34428180", "class_list": "", "function": "Component of the integrator complex, a multiprotein complex that terminates RNA polymerase II (Pol II) transcription in the promoter-proximal region of genes. The integrator complex provides a quality checkpoint during transcription elongation by driving premature transcription termination of transcripts that are unfavorably configured for transcriptional elongation: the complex terminates transcription by (1) catalyzing dephosphorylation of the C-terminal domain (CTD) of Pol II subunit POLR2A/RPB1 and SUPT5H/SPT5, (2) degrading the exiting nascent RNA transcript via endonuclease activity and (3) promoting the release of Pol II from bound DNA. The integrator complex is also involved in terminating the synthesis of non-coding Pol II transcripts, such as enhancer RNAs (eRNAs), small nuclear RNAs (snRNAs), telomerase RNAs and long non-coding RNAs (lncRNAs). Mediates recruitment of cytoplasmic dynein to the nuclear envelope, probably as component of the integrator complex., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q8BP62;Q8CAE4", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0032039 integrator complex", "go_biological_process": "GO:0034243 regulation of transcription elongation by RNA polymerase II;GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway;GO:0016180 snRNA processing;GO:0034472 snRNA 3'-end processing;GO:0160240 RNA polymerase II transcription initiation surveillance", "synthesized_glycan_count": 0, "hit_score": 0.5, "record_id": "Q8K114-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8R0S2-1", "uniprot_id": "IQEC1_MOUSE", "mass": 108015.0, "length": 961, "protein_name": "IQ motif and SEC7 domain-containing protein 1", "gene_name": "Iqsec1", "organism": "Mouse", "refseq_name": "IQ motif and SEC7 domain-containing protein 1 isoform a", "refseq_ac": "NP_001127855", "gene_names_uniprotkb": "Iqsec1; Kiaa0763", "gene_names_refseq": "BRAG2; D6Ertd349e; Iqsec1; cI-43", "protein_names_uniprotkb": "IQ motif and SEC7 domain-containing protein 1", "protein_names_refseq": "IQ motif and SEC7 domain-containing protein 1 isoform a; IQ motif and SEC7 domain-containing protein 1", "tax_id": 10090, "disease": "intellectual developmental disorder with short stature and behavioral abnormalities (Disease Ontology:DOID:0111674); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung adenocarcinoma (Disease Ontology:DOID:3910)", "pathway": " (mmu:232227)", "pathway_count": 1, "publication_count": 14, "publication_id_list": "10.1101/2023.09.13.557529;16452087;17114649;17242355;19144319;20173027;20547133;21183079;21750661;22645316;31607425;32341099;33300544;34428180", "class_list": "", "function": "BRAG2a Mediates mGluR-Dependent AMPA Receptor Internalization at Excitatory Postsynapses through the Interaction with PSD-95 and Endophilin 3., [RefSeq, PubMed]; Guanine nucleotide exchange factor for ARF1 and ARF6. Guanine nucleotide exchange factor activity is enhanced by lipid binding. Accelerates GTP binding by ARFs of all three classes. Guanine nucleotide exchange protein for ARF6, mediating internalization of beta-1 integrin (By similarity). Involved in neuronal development (PubMed:31607425). In neurons, plays a role in the control of vesicle formation by endocytoc cargo. Upon long term depression, interacts with GRIA2 and mediates the activation of ARF6 to internalize synaptic AMPAR receptors (By similarity)., [UniProtKB, UniProtKB, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 12, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 3, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q3TZC3;Q5DU15", "ec_number_list": "", "go_molecular_function": "GO:0019901 protein kinase binding;GO:0008289 lipid binding;GO:0005085 guanyl-nucleotide exchange factor activity", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005654 nucleoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0008021 synaptic vesicle", "go_biological_process": "GO:0051549 positive regulation of keratinocyte migration;GO:0060996 dendritic spine development;GO:0051965 positive regulation of synapse assembly;GO:0016192 vesicle-mediated transport;GO:0032012 regulation of ARF protein signal transduction", "synthesized_glycan_count": 0, "hit_score": 2.0, "record_id": "Q8R0S2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VCW2-1", "uniprot_id": "K1C25_MOUSE", "mass": 48921.0, "length": 446, "protein_name": "Keratin, type I cytoskeletal 25", "gene_name": "Krt25", "organism": "Mouse", "refseq_name": "keratin, type I cytoskeletal 25", "refseq_ac": "NP_598491", "gene_names_uniprotkb": "Krt25", "gene_names_refseq": "4631426H08Rik; CK-25; K25; Ka38; Krt25a; Krt25; mIRSa1", "protein_names_uniprotkb": "Keratin, type I cytoskeletal 25; CK-25; Cytokeratin-25; K25; Keratin-25; Type I inner root sheath-specific keratin-K25irs1; mIRSa1", "protein_names_refseq": "cytokeratin-25; keratin 25A; keratin, type I cytoskeletal 25; type I inner root sheath-specific keratin-K25irs1; type I keratin KA38", "tax_id": 10090, "disease": "autosomal recessive woolly hair 3 (Disease Ontology:DOID:0111574)", "pathway": " (mmu:70810); (R-MMU-6805567); (R-MMU-6809371)", "pathway_count": 3, "publication_count": 3, "publication_id_list": "14996088;17920809;34428180", "class_list": "", "function": "Essential for the proper assembly of type I and type II keratin protein complexes and formation of keratin intermediate filaments in the inner root sheath (irs) (PubMed:14996088, PubMed:17920809). Plays a role in the cytoskeleton organization (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 2, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0046982 protein heterodimerization activity;GO:0030280 structural constituent of skin epidermis", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005856 cytoskeleton;GO:0045095 keratin filament", "go_biological_process": "GO:0030855 epithelial cell differentiation;GO:0007010 cytoskeleton organization;GO:0045109 intermediate filament organization;GO:0031069 hair follicle morphogenesis;GO:0002009 morphogenesis of an epithelium", "synthesized_glycan_count": 0, "hit_score": 0.4, "record_id": "Q8VCW2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9D9J7-1", "uniprot_id": "IZUM1_MOUSE", "mass": 44885.0, "length": 397, "protein_name": "Izumo sperm-egg fusion protein 1", "gene_name": "Izumo1", "organism": "Mouse", "refseq_name": "izumo sperm-egg fusion protein 1 isoform 1 precursor", "refseq_ac": "NP_001018013", "gene_names_uniprotkb": "Izumo1", "gene_names_refseq": "1700058F15Rik; Izumo1; Izumo", "protein_names_uniprotkb": "Izumo sperm-egg fusion protein 1; OBF; Oocyte binding/fusion factor; Sperm-specific protein izumo", "protein_names_refseq": "OBF; izumo sperm-egg fusion protein 1 isoform 1 precursor; izumo sperm-egg fusion protein 1; oocyte binding/fusion factor; sperm-specific protein Izumo", "tax_id": 10090, "disease": "", "pathway": " (mmu:73456); (R-MMU-1300645)", "pathway_count": 2, "publication_count": 22, "publication_id_list": "15759005;18952059;19239425;19288544;19658160;20421979;24739963;25209248;26568141;26782177;27309808;27374339;27624483;29954238;30517645;31599954;31672133;32393636;35096839;35618043;35960805;36394541", "class_list": "", "function": "A novel function for the sperm adhesion protein IZUMO1 in cell-cell fusion., [RefSeq, PubMed]; Data indicate that the Ig-like domain of Izumo plays an important role in the fertilization process, as verified by the dose-dependent reduction in fertilization rates in mouse IVF trials and mouse mating assay. Erratum:[Mol Reprod Dev. 2009 Aug;76(8):802], [RefSeq, PubMed]; Essential sperm cell-surface protein required for fertilization by acting as a ligand for IZUMO1R/JUNO receptor on egg (PubMed:15759005, PubMed:24739963, PubMed:27309808). The IZUMO1:IZUMO1R/JUNO interaction is a necessary adhesion event between sperm and egg that is required for fertilization but is not sufficient for cell fusion (PubMed:15759005, PubMed:24739963, PubMed:27309808). The ligand-receptor interaction probably does not act as a membrane 'fusogen' (PubMed:15759005, PubMed:24739963, PubMed:27309808). Plays a critical role in sperm-oolemma binding prior to plasma membrane fusion (PubMed:35096839). Can mediate cell-cell fusion in cultured mammalian cells independently of its binding to IZUMO1R/JUNO (PubMed:36394541)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed]; Identification of a mouse sperm fusion-related antigen and show that the antigen is a novel immunoglobulin superfamily protein, [RefSeq, PubMed]; PCXN2-mIzumo plasmid possesses appreciable anti-fertility potential., [RefSeq, PubMed]; These data suggest that glycosylation is not essential for the function of IZUMO, but has a role in protecting it from fragmentation in cauda epididymis., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 1, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 10, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005102 signaling receptor binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0048018 receptor ligand activity;GO:0086080 protein binding involved in heterotypic cell-cell adhesion", "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0005789 endoplasmic reticulum membrane;GO:0001669 acrosomal vesicle;GO:0002080 acrosomal membrane", "go_biological_process": "GO:0035036 sperm-egg recognition;GO:0000768 syncytium formation by plasma membrane fusion;GO:0007155 cell adhesion;GO:0007339 binding of sperm to zona pellucida;GO:0007342 fusion of sperm to egg plasma membrane involved in single fertilization", "synthesized_glycan_count": 0, "hit_score": 2.4, "record_id": "Q9D9J7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9JHD2-1", "uniprot_id": "KAT2A_MOUSE", "mass": 93394.0, "length": 830, "protein_name": "Histone acetyltransferase KAT2A", "gene_name": "Kat2a", "organism": "Mouse", "refseq_name": "histone acetyltransferase KAT2A isoform a", "refseq_ac": "NP_064388", "gene_names_uniprotkb": "Kat2a; Gcn5l2", "gene_names_refseq": "1110051E14Rik; Gcn5l2; Gcn5; Kat2a; mmGCN5", "protein_names_uniprotkb": "Histone acetyltransferase KAT2A; 2.3.1.-; 2.3.1.48; General control of amino acid synthesis protein 5-like 2; Histone acetyltransferase GCN5; Histone glutaryltransferase KAT2A; Histone succinyltransferase KAT2A; Lysine acetyltransferase 2A; MmGCN5; Protein lactyltransferase KAT2A", "protein_names_refseq": "GCN5 general control of amino acid synthesis-like 2; PCAF-B/GCN5; general control of amino acid synthesis 5-like 2; general control of amino acid synthesis protein 5-like 2; general control of amino acid synthesis, yeast homolog-like 2; histone acetyltransferase GCN5; histone acetyltransferase KAT2A isoform a; histone acetyltransferase KAT2A; histone glutaryltransferase KAT2A; histone succinyltransferase KAT2A; lysine acetyltransferase 2A", "tax_id": 10090, "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); familial nephrotic syndrome (Disease Ontology:DOID:2590); lung non-small cell carcinoma (Disease Ontology:DOID:3908)", "pathway": " (mmu:14534); (R-MMU-2122947); (R-MMU-350054); (R-MMU-5250924); (R-MMU-5689880); (R-MMU-8941856); (R-MMU-9772755)", "pathway_count": 7, "publication_count": 19, "publication_id_list": "11017084;17301242;19224205;20173027;22886304;25024434;25428506;25428507;28424240;30084848;30270482;30424580;30779550;35053209;35490166;35820727;36112854;37828378;9742083", "class_list": "", "function": "Acetyltransferases GCN5 and PCAF Are Required for B Lymphocyte Maturation in Mice. Publication Status: Online-Only, [RefSeq, PubMed]; GCN5-mediated regulation of pathological cardiac hypertrophy via activation of the TAK1-JNK/p38 signaling pathway. Publication Status: Online-Only, [RefSeq, PubMed]; Protein lysine acyltransferase that catalyzes acetylation of histone and non-histone proteins using acetyl-CoA (PubMed:28424240). Also catalyzes acyl-CoA-dependent acylation of lysine residues in proteins using alternative acyl-CoA donors, including propionyl-CoA, butyryl-CoA, succinyl-CoA, glutaryl-CoA, crotonyl-CoA and lactoyl-CoA (By similarity). Acts as a histone lysine succinyltransferase: catalyzes succinylation of histone H3 on 'Lys-79' (H3K79succ), with a maximum frequency around the transcription start sites of genes (By similarity). Succinylation of histones gives a specific tag for epigenetic transcription activation (By similarity). Association with the 2-oxoglutarate dehydrogenase complex, which provides succinyl-CoA, is required for histone succinylation (By similarity). In different complexes, functions either as an acetyltransferase (HAT) or as a succinyltransferase: in the SAGA and ATAC complexes, acts as a histone acetyltransferase (By similarity). Has significant histone acetyltransferase activity with core histones, but not with nucleosome core particles (By similarity). Has a a strong preference for acetylation of H3 at 'Lys-9' (H3K9ac) (By similarity). Also catalyzes acetylation of histone H1.4 (H1-4) at 'Lys-34' (H1.4K34ac), a modification enriched at promoters of active genes (By similarity). Acetylation of histones gives a specific tag for epigenetic transcription activation (PubMed:28424240). Recruited by the XPC complex at promoters, where it specifically mediates acetylation of histone variant H2A.Z.1/H2A.Z, thereby promoting expression of target genes (By similarity). Involved in long-term memory consolidation and synaptic plasticity: acts by promoting expression of a hippocampal gene expression network linked to neuroactive receptor signaling (PubMed:25024434). Acts as a positive regulator of T-cell activation: upon TCR stimulation, recruited to the IL2 promoter following interaction with NFATC2 and catalyzes acetylation of histone H3 at 'Lys-9' (H3K9ac), leading to promote IL2 expression (PubMed:28424240). Required for growth and differentiation of craniofacial cartilage and bone by regulating acetylation of histone H3 at 'Lys-9' (H3K9ac) (PubMed:30424580). Regulates embryonic stem cell (ESC) pluripotency and differentiation (PubMed:30270482). Also acetylates non-histone proteins, such as CEBPB, MRE11, PPARGC1A, PLK4 and TBX5 (PubMed:17301242). Involved in heart and limb development by mediating acetylation of TBX5, acetylation regulating nucleocytoplasmic shuttling of TBX5 (By similarity). Acts as a negative regulator of centrosome amplification by mediating acetylation of PLK4 (By similarity). Acts as a negative regulator of gluconeogenesis by mediating acetylation and subsequent inactivation of PPARGC1A (By similarity). Also acts as a histone glutaryltransferase: catalyzes glutarylation of histone H4 on 'Lys-91' (H4K91glu), a mark that destabilizes nucleosomes by promoting dissociation of the H2A-H2B dimers from nucleosomes (By similarity). Catalyzes histone H3 lactylation at 'Lys-14' and 'Lys-18' in a lactyl-CoA-dependent manner (By similarity). Lactyl-CoA for this reaction can be generated by ACSS2 (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 4, "predicted_n_glycosites": 0, "predicted_o_glycosites": 4, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 3, "glyco_site_count": 4, "binding_glycan_count": 0, "secondary_ac_list": "Q3TZ59", "ec_number_list": "2.3.1.48;2.3.1.-;3.6.4.-;3.5.1.-;3.5.1.98;2.7.7.6;2.3.2.27;2.3.2.-;2.1.1.-;2.1.1.364;2.3.1.21;3.4.19.12;2.7.11.1;2.3.1.259;2.3.1.57;3.6.4.13;2.3.1.80;4.2.1.-;2.7.10.2", "go_molecular_function": "GO:0061733 protein-lysine-acetyltransferase activity;GO:0043997 histone H4K12 acetyltransferase activity;GO:0106078 histone succinyltransferase activity;GO:0003682 chromatin binding;GO:0003713 transcription coactivator activity", "go_cellular_component": "GO:0033276 transcription factor TFTC complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005813 centrosome;GO:0000785 chromatin", "go_biological_process": "GO:0090043 regulation of tubulin deacetylation;GO:1903010 regulation of bone development;GO:0022037 metencephalon development;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001701 in utero embryonic development", "synthesized_glycan_count": 0, "hit_score": 2.0, "record_id": "Q9JHD2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6ZPY2-1", "uniprot_id": "SMG5_MOUSE", "mass": 114071.0, "length": 1017, "protein_name": "Nonsense-mediated mRNA decay factor SMG5", "gene_name": "Smg5", "organism": "Mouse", "refseq_name": "nonsense-mediated mRNA decay factor SMG5", "refseq_ac": "NP_839977", "gene_names_uniprotkb": "Smg5; Est1b; Kiaa1089", "gene_names_refseq": "LPTS-RP1; Smg5; mKIAA1089", "protein_names_uniprotkb": "Nonsense-mediated mRNA decay factor SMG5; EST1-like protein B; LPTS-RP1; LPTS-interacting protein; SMG-5 homolog", "protein_names_refseq": "EST1-like protein B; LPTS-interacting protein; Smg-5 homolog, nonsense mediated mRNA decay factor; nonsense-mediated mRNA decay factor SMG5; protein SMG5", "tax_id": 10090, "disease": "", "pathway": " (mmu:229512); (R-MMU-975957)", "pathway_count": 2, "publication_count": 8, "publication_id_list": "21183079;21750661;25428506;30084848;30779550;31219806;34428180;39199410", "class_list": "", "function": "Plays a role in nonsense-mediated mRNA decay. Does not have RNase activity by itself. Promotes dephosphorylation of UPF1. Together with SMG7 is thought to provide a link to the mRNA degradation machinery involving exonucleolytic pathways, and to serve as an adapter for UPF1 to protein phosphatase 2A (PP2A), thereby triggering UPF1 dephosphorylation. Necessary for TERT activity (By similarity)., [UniProtKB]; RNA Surveillance Factor SMG5 Is Essential for Mouse Embryonic Stem Cell Differentiation. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q497S2;Q8R3S4", "ec_number_list": "", "go_molecular_function": "GO:0031625 ubiquitin protein ligase binding;GO:0042826 histone deacetylase binding;GO:0042162 telomeric DNA binding;GO:0051721 protein phosphatase 2A binding;GO:0070034 telomerase RNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0036464 cytoplasmic ribonucleoprotein granule;GO:0005697 telomerase holoenzyme complex", "go_biological_process": "GO:0032204 regulation of telomere maintenance;GO:0035303 regulation of dephosphorylation;GO:0000184 nuclear-transcribed mRNA catabolic process, nonsense-mediated decay", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "Q6ZPY2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O70546-1", "uniprot_id": "KDM6A_MOUSE", "mass": 154355.0, "length": 1401, "protein_name": "Lysine-specific demethylase 6A", "gene_name": "Kdm6a", "organism": "Mouse", "refseq_name": "lysine-specific demethylase 6A isoform 2", "refseq_ac": "NP_001297373", "gene_names_uniprotkb": "Kdm6a; Utx", "gene_names_refseq": "Kdm6a; Utx", "protein_names_uniprotkb": "Lysine-specific demethylase 6A; 1.14.11.68; Histone demethylase UTX; Ubiquitously transcribed TPR protein on the X chromosome; Ubiquitously transcribed X chromosome tetratricopeptide repeat protein; [histone H3]-trimethyl-L-lysine(27) demethylase 6A", "protein_names_refseq": "[histone H3]-trimethyl-L-lysine(27) demethylase 6A; histone demethylase UTX; lysine-specific demethylase 6A isoform 2; lysine-specific demethylase 6A; ubiquitously transcribed TPR protein on the X chromosome; ubiquitously transcribed X chromosome tetratricopeptide repeat protein; ubiquitously transcribed tetratricopeptide repeat gene, X chromosome", "tax_id": 10090, "disease": "triple-receptor negative breast cancer (Disease Ontology:DOID:0060081); Kabuki syndrome (Disease Ontology:DOID:0060473); chronic myelomonocytic leukemia (Disease Ontology:DOID:0080188); adenoid cystic carcinoma (Disease Ontology:DOID:0080202); prostate cancer (Disease Ontology:DOID:10283); stomach cancer (Disease Ontology:DOID:10534); alcohol use disorder (Disease Ontology:DOID:1574); breast cancer (Disease Ontology:DOID:1612); rectum adenocarcinoma (Disease Ontology:DOID:1996); colon adenocarcinoma (Disease Ontology:DOID:234); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); lung non-small cell carcinoma (Disease Ontology:DOID:3908); bladder urothelial carcinoma (Disease Ontology:DOID:4006); renal cell carcinoma (Disease Ontology:DOID:4450); lung small cell carcinoma (Disease Ontology:DOID:5409); myocardial infarction (Disease Ontology:DOID:5844); hepatocellular carcinoma (Disease Ontology:DOID:684); malignant pleural mesothelioma (Disease Ontology:DOID:7474); colorectal cancer (Disease Ontology:DOID:9256); acute lymphoblastic leukemia (Disease Ontology:DOID:9952)", "pathway": " (mmu:22289); (R-MMU-3214842); (R-MMU-9772755); (R-MMU-9818564)", "pathway_count": 4, "publication_count": 19, "publication_id_list": "10.1101/2023.09.13.557529;15345747;21095589;21183079;21750661;22645316;23503590;24129315;25605945;30059200;31219806;32782141;34428180;34678516;36852467;40885482;40997131;9499428;9854018", "class_list": "", "function": "Histone demethylase that specifically demethylates 'Lys-27' of histone H3, thereby playing a central role in histone code. Demethylates trimethylated and dimethylated but not monomethylated H3 'Lys-27'. Plays a central role in regulation of posterior development, by regulating HOX gene expression. Demethylation of 'Lys-27' of histone H3 is concomitant with methylation of 'Lys-4' of histone H3, and regulates the recruitment of the PRC1 complex and monoubiquitination of histone H2A (By similarity). Plays a demethylase-independent role in chromatin remodeling to regulate T-box family member-dependent gene expression (PubMed:21095589)., [UniProtKB, UniProtKB, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 5, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 5, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 5, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 3, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 20, "glyco_site_count": 7, "binding_glycan_count": 0, "secondary_ac_list": "A2AID2;Q6DI80;Q7TSG4", "ec_number_list": "2.3.1.48;2.3.1.-;3.1.1.23;1.14.11.68;2.7.11.2;2.7.11.-;3.5.1.-;3.5.1.98;2.3.2.-;3.1.13.-;2.7.7.48;2.7.7.6;3.1.1.32;3.1.1.34;1.14.19.1;6.2.1.3;6.2.1.24;6.2.1.15;3.1.1.79;6.2.1.1;6.2.1.17;1.14.11.65;2.1.1.356;2.3.1.15;2.1.1.364;2.3.1.199;3.1.1.4;3.1.1.3;2.3.1.51;2.7.11.22;2.7.11.23;3.1.3.4;2.3.1.20;2.3.1.76", "go_molecular_function": "GO:0042802 identical protein binding;GO:0046872 metal ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0031490 chromatin DNA binding;GO:0071558 histone H3K27me2/H3K27me3 demethylase activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0035097 histone methyltransferase complex;GO:0044666 MLL3/4 complex", "go_biological_process": "GO:0072359 circulatory system development;GO:0048570 notochord morphogenesis;GO:0001701 in utero embryonic development;GO:0003016 respiratory system process;GO:0006338 chromatin remodeling", "synthesized_glycan_count": 0, "hit_score": 2.8, "record_id": "O70546-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BWW9-1", "uniprot_id": "PKN2_MOUSE", "mass": 111607.0, "length": 983, "protein_name": "Serine/threonine-protein kinase N2", "gene_name": "Pkn2", "organism": "Mouse", "refseq_name": "serine/threonine-protein kinase N2", "refseq_ac": "NP_848769", "gene_names_uniprotkb": "Pkn2; Prk2; Prkcl2", "gene_names_refseq": "6030436C20Rik; PRK2; Pkn2; Prkcl2; Stk7", "protein_names_uniprotkb": "Serine/threonine-protein kinase N2; 2.7.11.13; PKN gamma; Protein kinase C-like 2; Protein-kinase C-related kinase 2", "protein_names_refseq": "PKN gamma; protein kinase C-like 2; protein-kinase C-related kinase 2; serine/threonine kinase 7; serine/threonine-protein kinase N2", "tax_id": 10090, "disease": "", "pathway": " (mmu:109333); (R-MMU-5625740); (R-MMU-8980692); (R-MMU-9013026); (R-MMU-9013106); (R-MMU-9013149); (R-MMU-9856530)", "pathway_count": 7, "publication_count": 18, "publication_id_list": "10.1101/2023.09.13.557529;10818102;11777936;17242355;17403031;19144319;20515922;20974804;21183079;21750661;23806337;31219806;32127582;34428180;34499618;35730579;8910519;9121475", "class_list": "", "function": "Novel roles of PRK1 and PRK2 in cilia and cancer biology. Publication Status: Online-Only, [RefSeq, PubMed]; PKC-related serine/threonine-protein kinase and Rho/Rac effector protein that participates in specific signal transduction responses in the cell. Plays a role in the regulation of cell cycle progression, actin cytoskeleton assembly, cell migration, cell adhesion, tumor cell invasion and transcription activation signaling processes. Phosphorylates CTTN in hyaluronan-induced astrocytes and hence decreases CTTN ability to associate with filamentous actin. Phosphorylates HDAC5, therefore lead to impair HDAC5 import. Direct RhoA target required for the regulation of the maturation of primordial junctions into apical junction formation in bronchial epithelial cells. Required for G2/M phases of the cell cycle progression and abscission during cytokinesis in a ECT2-dependent manner. Stimulates FYN kinase activity that is required for establishment of skin cell-cell adhesion during keratinocytes differentiation. Regulates epithelial bladder cells speed and direction of movement during cell migration and tumor cell invasion. Inhibits Akt pro-survival-induced kinase activity. Mediates Rho protein-induced transcriptional activation via the c-fos serum response factor (SRF). Involved in the negative regulation of ciliogenesis (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed]; PKN2 deficiency leads both to prenatal 'congenital' cardiomyopathy and defective angiotensin II stress responses., [RefSeq, PubMed]; Protein kinase N2 mediates flow-induced endothelial NOS activation and vascular tone regulation., [RefSeq, PubMed]; Yersinia pseudotuberculosis mutants expressing YopM proteins unable to interact with either RSK1 or PRK2 were defective for virulence in this assay, indicating that both interaction domains are important for YopM to promote pathogenesis., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 14, "reported_mutagensis": 4, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q3TBR3;Q80WS2;Q8BJL7;Q8BL62", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;1.14.14.18;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.1.153;2.7.1.137;3.6.5.2;2.7.1.40;2.7.11.21;3.1.2.-;7.6.2.-;3.6.4.-;1.14.13.39;2.7.11.39;2.3.1.-;3.1.4.4;2.7.10.1;2.7.11.31;3.6.5.-;1.6.3.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0042826 histone deacetylase binding;GO:0031267 small GTPase binding;GO:0070063 RNA polymerase binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol", "go_biological_process": "GO:0043297 apical junction assembly;GO:0010631 epithelial cell migration;GO:0006351 DNA-templated transcription;GO:0006468 protein phosphorylation;GO:0007155 cell adhesion", "synthesized_glycan_count": 0, "hit_score": 2.1, "record_id": "Q8BWW9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8CIM8-1", "uniprot_id": "INT4_MOUSE", "mass": 108193.0, "length": 964, "protein_name": "Integrator complex subunit 4", "gene_name": "Ints4", "organism": "Mouse", "refseq_name": "integrator complex subunit 4 isoform 1", "refseq_ac": "NP_081532", "gene_names_uniprotkb": "Ints4", "gene_names_refseq": "2610034N24Rik; Ints4", "protein_names_uniprotkb": "Integrator complex subunit 4; Int4", "protein_names_refseq": "int4; integrator complex subunit 4 isoform 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:101861); (R-MMU-6807505)", "pathway_count": 2, "publication_count": 5, "publication_id_list": "21750661;23806337;31219806;34428180;39627609", "class_list": "", "function": "Component of the integrator complex, a multiprotein complex that terminates RNA polymerase II (Pol II) transcription in the promoter-proximal region of genes. The integrator complex provides a quality checkpoint during transcription elongation by driving premature transcription termination of transcripts that are unfavorably configured for transcriptional elongation: the complex terminates transcription by (1) catalyzing dephosphorylation of the C-terminal domain (CTD) of Pol II subunit POLR2A/RPB1 and SUPT5H/SPT5, (2) degrading the exiting nascent RNA transcript via endonuclease activity and (3) promoting the release of Pol II from bound DNA. The integrator complex is also involved in terminating the synthesis of non-coding Pol II transcripts, such as enhancer RNAs (eRNAs), small nuclear RNAs (snRNAs), telomerase RNAs and long non-coding RNAs (lncRNAs). Within the integrator complex, INTS4 acts as an scaffold that links INTS9 and INTS11. Mediates recruitment of cytoplasmic dynein to the nuclear envelope, probably as component of the integrator complex., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3TQQ4;Q8C2H1;Q91YV5;Q9CSY4", "ec_number_list": "", "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0032039 integrator complex;GO:0160232 INTAC complex", "go_biological_process": "GO:0034243 regulation of transcription elongation by RNA polymerase II;GO:0016180 snRNA processing;GO:0160240 RNA polymerase II transcription initiation surveillance", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q8CIM8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8R104-1", "uniprot_id": "SIR3_MOUSE", "mass": 36615.0, "length": 334, "protein_name": "NAD-dependent protein deacetylase sirtuin-3", "gene_name": "Sirt3", "organism": "Mouse", "refseq_name": "NAD-dependent protein deacetylase sirtuin-3 isoform 1", "refseq_ac": "NP_001120823", "gene_names_uniprotkb": "Sirt3; Sir2l3", "gene_names_refseq": "2310003L23Rik; Sir2l3; Sirt3", "protein_names_uniprotkb": "NAD-dependent protein deacetylase sirtuin-3; 2.3.1.-; 2.3.1.286; NAD-dependent protein delactylase sirtuin-3; Regulatory protein SIR2 homolog 3; SIR2-like protein 3; mSIR2L3", "protein_names_refseq": "NAD-dependent deacetylase sirtuin-3; NAD-dependent protein deacetylase sirtuin-3 isoform 1; NAD-dependent protein deacetylase sirtuin-3; NAD-dependent protein delactylase sirtuin-3; SIR2-like protein 3; SIRT3L mitochondrial; mSIR2L3; mitochondrial protein lysine deacetylase; regulatory protein SIR2 homolog 3; silent mating type information regulation 2, (S.cerevisiae, homolog)-like 3", "tax_id": 10090, "disease": "abdominal obesity-metabolic syndrome (Disease Ontology:DOID:0060611); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); Alzheimer's disease (Disease Ontology:DOID:10652); prediabetes syndrome (Disease Ontology:DOID:11716); myocardial infarction (Disease Ontology:DOID:5844); congestive heart failure (Disease Ontology:DOID:6000); type 2 diabetes mellitus (Disease Ontology:DOID:9352); obesity (Disease Ontology:DOID:9970)", "pathway": " (mmu:64384); (R-MMU-2151201); (R-MMU-9617629); (R-MMU-9841251); (R-MMU-9854311)", "pathway_count": 5, "publication_count": 21, "publication_id_list": "10.1101/2023.09.13.557529;11056054;15653680;16790548;17923681;18794531;19241369;19333382;21172655;21750661;21858060;23283301;23438705;23806337;23835326;24252090;26620563;34428180;35959657;36804859;39425510", "class_list": "", "function": "Knockout of Sirtuin 3 in endothelial cells impairs endothelial-dependent relaxation and myogenic response in mice., [RefSeq, PubMed]; NAD-dependent protein deacetylase (PubMed:17923681, PubMed:18794531, PubMed:21172655, PubMed:23835326, PubMed:26620563). Activates or deactivates mitochondrial target proteins by deacetylating key lysine residues (PubMed:17923681, PubMed:18794531, PubMed:21172655, PubMed:23835326). Known targets include ACSS1, IDH, GDH, PDHA1, SOD2, LCAD, SDHA, MRPL12 and the ATP synthase subunit ATP5PO (PubMed:16790548, PubMed:18794531, PubMed:21172655). Contributes to the regulation of the cellular energy metabolism (PubMed:23835326, PubMed:36804859). Important for regulating tissue-specific ATP levels (PubMed:18794531, PubMed:24252090). In response to metabolic stress, deacetylates transcription factor FOXO3 and recruits FOXO3 and mitochondrial RNA polymerase POLRMT to mtDNA to promote mtDNA transcription (PubMed:23283301). Acts as a regulator of ceramide metabolism by mediating deacetylation of ceramide synthases CERS1, CERS2 and CERS6, thereby increasing their activity and promoting mitochondrial ceramide accumulation (PubMed:26620563). Regulates hepatic lipogenesis (PubMed:36804859). Uses NAD(+) substrate imported by SLC25A47, triggering downstream activation of PRKAA1/AMPK-alpha signaling cascade that ultimately downregulates sterol regulatory element-binding protein (SREBP) transcriptional activities and ATP-consuming lipogenesis to restore cellular energy balance (PubMed:36804859). In addition to protein deacetylase activity, also acts as a protein-lysine deacylase by recognizing other acyl groups, such as benzoyl and lactoyl, leading to protein debenzoylation and delactylation, respectively (By similarity). Catalyzes debenzoylation of PPIF and ACLY (By similarity). Mediates delactylation of CCNE2 and 'Lys-16' of histone H4 (H4K16la) (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]; NAD-dependent protein deacetylase., [UniProtKB, UniProtKB]; Results demonstrate that SIRT3 activates mitochondria and plays an important role in adaptive thermogenesis in brown adipose tissue. GeneRIF: Caloric restriction and cold exposure elevate SIRT3 expression in brown adipose to regulate thermogenesis through PGC-1alpha and UCP1., [RefSeq, PubMed]; These results extend the recent finding of lysine acetylation of mitochondrial proteins and demonstrate that SIRT3 has evolved to control reversible lysine acetylation in this organelle., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 8, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "B9W0A9;C6ZII7;Q9EPA8", "ec_number_list": "1.15.1.1;1.4.1.3;1.1.1.42;2.4.2.-;2.3.1.-;2.3.1.286;6.2.1.-;6.2.1.1;6.2.1.17", "go_molecular_function": "GO:0008270 zinc ion binding;GO:0019899 enzyme binding;GO:0070403 NAD+ binding;GO:0043565 sequence-specific DNA binding;GO:0017136 histone deacetylase activity, NAD-dependent", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0005759 mitochondrial matrix", "go_biological_process": "GO:1902553 positive regulation of catalase activity;GO:0032024 positive regulation of insulin secretion;GO:2000378 negative regulation of reactive oxygen species metabolic process;GO:0070373 negative regulation of ERK1 and ERK2 cascade;GO:1903862 positive regulation of oxidative phosphorylation", "synthesized_glycan_count": 0, "hit_score": 2.4, "record_id": "Q8R104-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9CZ42-1", "uniprot_id": "NNRD_MOUSE", "mass": 36717.0, "length": 343, "protein_name": "ATP-dependent (S)-NAD(P)H-hydrate dehydratase", "gene_name": "Naxd", "organism": "Mouse", "refseq_name": "ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform 2", "refseq_ac": "NP_001177286", "gene_names_uniprotkb": "Naxd; CARKD; Carkd", "gene_names_refseq": "0710008K08Rik; 2810407E01Rik; Carkd; Naxd", "protein_names_uniprotkb": "ATP-dependent (S)-NAD(P)H-hydrate dehydratase; 4.2.1.93; ATP-dependent NAD(P)HX dehydratase; Carbohydrate kinase domain-containing protein; NAD(P)HX dehydratase", "protein_names_refseq": "ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform 2; ATP-dependent (S)-NAD(P)H-hydrate dehydratase; ATP-dependent NAD(P)HX dehydratase; carbohydrate kinase domain containing; carbohydrate kinase domain-containing protein", "tax_id": 10090, "disease": "", "pathway": " (mmu:69225); (R-MMU-196807)", "pathway_count": 2, "publication_count": 13, "publication_id_list": "10.1101/2023.09.13.557529;17947660;18034455;18614015;21183079;21750661;21994945;22645316;23576753;30899004;31219806;34428180;37828378", "class_list": "", "function": "Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ATP, which is converted to ADP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration., [UniProtKB, HAMAP, UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 4, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q9CQX9;Q9D7G7;Q9DC93", "ec_number_list": "4.2.1.93", "go_molecular_function": "GO:0047453 ATP-dependent NAD(P)H-hydrate dehydratase activity;GO:0005524 ATP binding", "go_cellular_component": "GO:0005739 mitochondrion;GO:0005783 endoplasmic reticulum;GO:0005829 cytosol", "go_biological_process": "GO:0046496 nicotinamide nucleotide metabolic process;GO:0110051 metabolite repair", "synthesized_glycan_count": 0, "hit_score": 2.0, "record_id": "Q9CZ42-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q80XM9-1", "uniprot_id": "S66A2_MOUSE", "mass": 30580.0, "length": 271, "protein_name": "Solute carrier family 66 member 2", "gene_name": "Slc66a2", "organism": "Mouse", "refseq_name": "solute carrier family 66 member 2 isoform b", "refseq_ac": "NP_001157892", "gene_names_uniprotkb": "Slc66a2; Pqlc1", "gene_names_refseq": "2310009N05Rik; 4933425L21Rik; 5730564E11Rik; Pqlc1; Slc66a2", "protein_names_uniprotkb": "Solute carrier family 66 member 2; PQ-loop repeat-containing protein 1", "protein_names_refseq": "PQ loop repeat containing 1; PQ-loop repeat-containing protein 1; solute carrier family 66 member 2 isoform b", "tax_id": 10090, "disease": "", "pathway": " (mmu:66943)", "pathway_count": 1, "publication_count": 3, "publication_id_list": "21183079;21750661;35820727", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3U6E6;Q9CYA7;Q9D2D3;Q9D2V1;Q9D7G6", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005829 cytosol;GO:0032588 trans-Golgi network membrane;GO:0010008 endosome membrane;GO:0016020 membrane", "go_biological_process": "GO:0045332 phospholipid translocation;GO:0042147 retrograde transport, endosome to Golgi", "synthesized_glycan_count": 0, "hit_score": 0.4, "record_id": "Q80XM9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9R112-1", "uniprot_id": "SQOR_MOUSE", "mass": 50282.0, "length": 450, "protein_name": "Sulfide:quinone oxidoreductase, mitochondrial", "gene_name": "Sqor", "organism": "Mouse", "refseq_name": "sulfide:quinone oxidoreductase, mitochondrial", "refseq_ac": "NP_001155975", "gene_names_uniprotkb": "Sqor; Sqrdl", "gene_names_refseq": "0610039J17Rik; 4930557M22Rik; Sqor; Sqrdl", "protein_names_uniprotkb": "Sulfide:quinone oxidoreductase, mitochondrial; 1.8.5.8; SQOR; Sulfide quinone oxidoreductase", "protein_names_refseq": "flavo-binding protein; sulfide quinone reductase-like; sulfide:quinone oxidoreductase, mitochondrial", "tax_id": 10090, "disease": "", "pathway": " (mmu:59010); (R-MMU-1614517)", "pathway_count": 2, "publication_count": 12, "publication_id_list": "10.1101/2023.09.13.557529;21183079;21750661;21950400;23576753;25130143;30084848;34035265;34428180;37453647;37507081;38376922", "class_list": "", "function": "Catalyzes the oxidation of hydrogen sulfide with the help of a quinone, such as ubiquinone-10, giving rise to thiosulfate and ultimately to sulfane (molecular sulfur) atoms. Requires an additional electron acceptor; can use sulfite, sulfide or cyanide (in vitro). It is believed the in vivo electron acceptor is glutathione., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Levels of mRNA encoding SQR were higher in the colonic muscularis externa and the liver than in the brain., [RefSeq, PubMed]; Sulfide catabolism ameliorates hypoxic brain injury. Publication Status: Online-Only, [RefSeq, PubMed]; Sulfide quinone oxidoreductase contributes to voltage sensing of the mitochondrial permeability transition pore., [RefSeq, PubMed]; The present report demonstrates the presence and specific localization of SQRDL in various mammalian tissues., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q8BW20;Q91XA1;Q9D891", "ec_number_list": "1.13.11.18;1.8.5.8", "go_molecular_function": "GO:0070224 sulfide:quinone oxidoreductase activity;GO:0071949 FAD binding;GO:0048038 quinone binding;GO:0106436 glutathione-dependent sulfide quinone oxidoreductase activity", "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane", "go_biological_process": "GO:0070221 sulfide oxidation, using sulfide:quinone oxidoreductase;GO:0006790 sulfur compound metabolic process", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "Q9R112-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9JK45-1", "uniprot_id": "KCNQ5_MOUSE", "mass": 102258.0, "length": 933, "protein_name": "Potassium voltage-gated channel subfamily KQT member 5", "gene_name": "Kcnq5", "organism": "Mouse", "refseq_name": "potassium voltage-gated channel subfamily KQT member 5 isoform 2", "refseq_ac": "NP_076361", "gene_names_uniprotkb": "Kcnq5", "gene_names_refseq": "7730402H11; 9230107O05Rik; D1Mgi1; Kcnq5", "protein_names_uniprotkb": "Potassium voltage-gated channel subfamily KQT member 5; KQT-like 5; Potassium channel subunit alpha KvLQT5; Voltage-gated potassium channel subunit Kv7.5", "protein_names_refseq": "KQT-like 5; potassium channel subunit alpha KvLQT5; potassium voltage-gated channel subfamily KQT member 5 isoform 2; potassium voltage-gated channel subfamily KQT member 5; voltage-gated potassium channel subunit Kv7.5; voltage-gated potassium channel type Kv7.5", "tax_id": 10090, "disease": "autosomal dominant intellectual developmental disorder 46 (Disease Ontology:DOID:0080237); developmental and epileptic encephalopathy 7 (Disease Ontology:DOID:0080462); developmental and epileptic encephalopathy (Disease Ontology:DOID:0112202); heart conduction disease (Disease Ontology:DOID:10273); long QT syndrome (Disease Ontology:DOID:2843)", "pathway": " (mmu:226922); (R-MMU-1296072)", "pathway_count": 2, "publication_count": 10, "publication_id_list": "15963599;17519950;18457656;18536747;21183079;21750661;26495903;30084848;35320039;38354270", "class_list": "", "function": "Data show that murine KCNQ5 channels are tightly regulated by changes in extracellular Zn2+, pH, and tonicity, thus adding to the complex regulation of these channels., [RefSeq, PubMed]; KCNQ2 and KCNQ5 form heteromeric channels independent of KCNQ3., [RefSeq, PubMed]; KCNQ5 Controls Perivascular Adipose Tissue-Mediated Vasodilation., [RefSeq, PubMed]; Murine blood vessels exhibit a distinctive expression profile of KCNQ1, KCNQ4, and KCNQ5, with 'neuronal' KCNQ4 dominating, [RefSeq, PubMed]; Pore-forming subunit of the voltage-gated potassium (Kv) channel broadly expressed in brain and skeletal muscle and involved in the regulation of neuronal excitability (PubMed:15963599). Associates with KCNQ3/Kv7.3 pore-forming subunit to form a potassium channel which contributes to M-type current, a slowly activating and deactivating potassium conductance which plays a critical role in determining the subthreshold electrical excitability of neurons (By similarity). Contributes, with other potassium channels, to the molecular diversity of a heterogeneous population of M-channels, varying in kinetic and pharmacological properties, which underlie this physiologically important current (PubMed:15963599). Also forms a functional channel with KCNQ1/Kv7.1 subunit that may contribute to vasoconstriction and hypertension. Channel may be selectively permeable in vitro to other cations besides potassium, in decreasing order of affinity K(+) = Rb(+) > Cs(+) > Na(+) (By similarity)., [UniProtKB, UniProtKB, PubMed]; Results provide support for KCNQ4- or KCNQ5-encoded channels having an important functional impact in the vasculature., [RefSeq, PubMed]; These data represent an exhaustive characterisation of a truncated KCNQ5 splice variant that may contribute to the native XE991-sensitive channel in murine vasculature., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 5, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q4QXS5;Q8BSF6", "ec_number_list": "1.8.-.-", "go_molecular_function": "GO:0005249 voltage-gated potassium channel activity;GO:0099508 voltage-gated monoatomic ion channel activity involved in regulation of presynaptic membrane potential", "go_cellular_component": "GO:0030118 clathrin coat;GO:0044305 calyx of Held;GO:0005886 plasma membrane;GO:0008076 voltage-gated potassium channel complex;GO:0042734 presynaptic membrane", "go_biological_process": "GO:0006813 potassium ion transport;GO:0071805 potassium ion transmembrane transport;GO:0007605 sensory perception of sound", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q9JK45-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O70551-1", "uniprot_id": "SRPK1_MOUSE", "mass": 73088.0, "length": 648, "protein_name": "SRSF protein kinase 1", "gene_name": "Srpk1", "organism": "Mouse", "refseq_name": "SRSF protein kinase 1", "refseq_ac": "NP_058075", "gene_names_uniprotkb": "Srpk1", "gene_names_refseq": "Srpk1", "protein_names_uniprotkb": "SRSF protein kinase 1; 2.7.11.1; SFRS protein kinase 1; SR-protein-specific kinase 1; Serine/arginine-rich protein-specific kinase 1", "protein_names_refseq": "SFRS protein kinase 1; SR-protein-specific kinase 1; SRSF protein kinase 1; serine/threonine-protein kinase SRPK1", "tax_id": 10090, "disease": "", "pathway": " (mmu:20815)", "pathway_count": 1, "publication_count": 26, "publication_id_list": "10.1101/2023.09.13.557529;10390541;15345747;17242355;18299400;19224205;20173027;21183079;21750661;21952136;24703948;25153642;25428506;25774502;28135057;28528544;29474929;30059200;30084848;31219806;33080171;34428180;34524595;35820727;37828378;9446799", "class_list": "", "function": "Depletion of endogenous SRPK1 enhanced the development of C3H10T1/2 cells toward brown adipocytes., [RefSeq, PubMed]; Functional Diversification of SRSF Protein Kinase to Control Ubiquitin-Dependent Neurodevelopmental Signaling., [RefSeq, PubMed]; In 2 independent murine models of breast tumor metastasis, stable shRNA-based SRPK1 knockdown suppressed metastasis to distant organs, including lung, liver, and spleen, and inhibited focal adhesion reorganization., [RefSeq, PubMed]; LncRNA Neat1/miR-298-5p/Srpk1 Contributes to Sevoflurane-Induced Neurotoxicity., [RefSeq, PubMed]; SRPK1 overexpression is also tumorigenic because excess SRPK1 squelches PHLPP1., [RefSeq, PubMed]; Serine/arginine-rich protein-specific kinase which specifically phosphorylates its substrates at serine residues located in regions rich in arginine/serine dipeptides, known as RS domains and is involved in the phosphorylation of SR splicing factors and the regulation of splicing. Plays a central role in the regulatory network for splicing, controlling the intranuclear distribution of splicing factors in interphase cells and the reorganization of nuclear speckles during mitosis. Can influence additional steps of mRNA maturation, as well as other cellular activities, such as chromatin reorganization in somatic and sperm cells and cell cycle progression. Phosphorylates SFRS2, ZRSR2, LBR and PRM1. Phosphorylates SRSF1 using a directional (C-terminal to N-terminal) and a dual-track mechanism incorporating both processive phosphorylation (in which the kinase stays attached to the substrate after each round of phosphorylation) and distributive phosphorylation steps (in which the kinase and substrate dissociate after each phosphorylation event). The RS domain of SRSF1 binds first to a docking groove in the large lobe of the kinase domain of SRPK1. This induces certain structural changes in SRPK1 and/or RRM2 domain of SRSF1, allowing RRM2 to bind the kinase and initiate phosphorylation. The cycles continue for several phosphorylation steps in a processive manner (steps 1-8) until the last few phosphorylation steps (approximately steps 9-12). During that time, a mechanical stress induces the unfolding of the beta-4 motif in RRM2, which then docks at the docking groove of SRPK1. This also signals RRM2 to begin to dissociate, which facilitates SRSF1 dissociation after phosphorylation is completed. Can mediate hepatitis B virus (HBV) core protein phosphorylation. It plays a negative role in the regulation of HBV replication through a mechanism not involving the phosphorylation of the core protein but by reducing the packaging efficiency of the pregenomic RNA (pgRNA) without affecting the formation of the viral core particles. Can induce splicing of exon 10 in MAPT/TAU (By similarity). Phosphorylates the N-terminus of ERC1 (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 7, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "O70193;Q99JT3", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;2.7.11.39;2.3.1.-;2.7.11.31;3.6.5.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0106310 protein serine kinase activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane", "go_biological_process": "GO:0006468 protein phosphorylation;GO:0007059 chromosome segregation;GO:0030154 cell differentiation;GO:0035556 intracellular signal transduction;GO:0045071 negative regulation of viral genome replication", "synthesized_glycan_count": 0, "hit_score": 3.1, "record_id": "O70551-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6P5D8-1", "uniprot_id": "SMHD1_MOUSE", "mass": 225648.0, "length": 2007, "protein_name": "Structural maintenance of chromosomes flexible hinge domain-containing protein 1", "gene_name": "Smchd1", "organism": "Mouse", "refseq_name": "structural maintenance of chromosomes flexible hinge domain-containing protein 1", "refseq_ac": "NP_083163", "gene_names_uniprotkb": "Smchd1; Kiaa0650", "gene_names_refseq": "4931400A14Rik; MommeD1; Smchd1; mKIAA0650", "protein_names_uniprotkb": "Structural maintenance of chromosomes flexible hinge domain-containing protein 1; 3.6.1.-; SMC hinge domain-containing protein 1", "protein_names_refseq": "SMC hinge domain-containing protein 1; structural maintenance of chromosomes flexible hinge domain-containing protein 1", "tax_id": 10090, "disease": "facioscapulohumeral muscular dystrophy 2 (Disease Ontology:DOID:0111193); choanal atresia (Disease Ontology:DOID:9574)", "pathway": " (mmu:74355)", "pathway_count": 1, "publication_count": 33, "publication_id_list": "18425126;21183079;21553025;21750661;22645316;22841499;23213215;23754746;23806337;23819640;25153642;25428506;26091879;26391951;26733688;27059856;28067911;28135057;28587678;29187734;29887375;29900695;30084848;30779550;31219806;34203471;34428180;35820727;35879318;36210013;37749075;39627609;41018975", "class_list": "", "function": "Maternal SMCHD1 regulates Hox gene expression and patterning in the mouse embryo. Publication Status: Online-Only, [RefSeq, PubMed]; Non-canonical member of the structural maintenance of chromosomes (SMC) protein family that plays a key role in epigenetic silencing by regulating chromatin architecture (PubMed:26091879, PubMed:29887375). Promotes heterochromatin formation in both autosomes and chromosome X, probably by mediating the merge of chromatin compartments (PubMed:23754746, PubMed:23819640, PubMed:26391951, PubMed:28587678, PubMed:29887375). Plays a key role in chromosome X inactivation in females by promoting the spreading of heterochromatin (PubMed:18425126, PubMed:22841499, PubMed:26391951, PubMed:29887375). Recruited to inactivated chromosome X by Xist RNA and acts by mediating the merge of chromatin compartments: promotes random chromatin interactions that span the boundaries of existing structures, leading to create a compartment-less architecture typical of inactivated chromosome X (PubMed:29887375). Required to facilitate Xist RNA spreading (PubMed:29887375). Also required for silencing of a subset of clustered autosomal loci in somatic cells, such as the DUX4 locus (PubMed:23754746, PubMed:23819640, PubMed:28587678). Has ATPase activity; may participate in structural manipulation of chromatin in an ATP-dependent manner as part of its role in gene expression regulation (PubMed:26391951, PubMed:27059856). Also plays a role in DNA repair: localizes to sites of DNA double-strand breaks in response to DNA damage to promote the repair of DNA double-strand breaks (By similarity). Acts by promoting non-homologous end joining (NHEJ) and inhibiting homologous recombination (HR) repair (By similarity). Required during preimplantation development, probably acts by regulating chromatin architecture (PubMed:29900695)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]; SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in disease. Publication Status: Online-Only, [RefSeq, PubMed]; SmcHD1 is not required for correct Xist expression, but localizes to the inactive X and has a role in the maintenance of X inactivation and the hypermethylation of CpG islands associated with the inactive X., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 3, "reported_mutagensis": 3, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q6PDM8;Q6PE93;Q6ZQ78;Q811H3;Q8BP09;Q9D4M7", "ec_number_list": "3.6.4.13;3.6.4.10;3.6.4.-;5.6.2.3;5.6.2.4;2.3.2.-;2.3.2.27;3.1.13.1;5.6.2.6;3.1.-.-;7.6.2.1;3.6.1.5;3.4.24.-;3.6.-.-;3.1.3.1;3.9.1.1;3.6.1.-;5.6.2.5;4.2.99.18;3.6.4.12;5.6.1.6;3.6.4.6;3.6.5.-;3.6.1.15;3.1.4.-;5.6.2.-;7.2.2.-;7.6.2.16;3.4.21.53;2.7.7.7;2.7.7.49;2.7.11.1;2.7.4.3", "go_molecular_function": "GO:0003677 DNA binding;GO:0005524 ATP binding;GO:0042803 protein homodimerization activity;GO:0016887 ATP hydrolysis activity", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0016604 nuclear body;GO:0035861 site of double-strand break;GO:0000781 chromosome, telomeric region;GO:0001740 Barr body", "go_biological_process": "GO:0043584 nose development;GO:2000042 negative regulation of double-strand break repair via homologous recombination;GO:2001034 positive regulation of double-strand break repair via nonhomologous end joining;GO:0006302 double-strand break repair;GO:0045739 positive regulation of DNA repair", "synthesized_glycan_count": 0, "hit_score": 3.6, "record_id": "Q6P5D8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9Q3L2-1", "uniprot_id": "PI4KA_MOUSE", "mass": 237042.0, "length": 2105, "protein_name": "Phosphatidylinositol 4-kinase alpha", "gene_name": "Pi4ka", "organism": "Mouse", "refseq_name": "phosphatidylinositol 4-kinase alpha isoform 2", "refseq_ac": "NP_001001983", "gene_names_uniprotkb": "Pi4ka; Pik4ca; Pik4", "gene_names_refseq": "PI4K-alpha; Pi4ka; Pik4ca", "protein_names_uniprotkb": "Phosphatidylinositol 4-kinase alpha; 2.7.1.67; PI4-kinase alpha; PI4K-alpha; PtdIns-4-kinase alpha", "protein_names_refseq": "PI4-kinase alpha; phosphatidylinositol 4-kinase alpha isoform 2; phosphatidylinositol 4-kinase, catalytic, alpha polypeptide; ptdIns-4-kinase alpha", "tax_id": 10090, "disease": "chromosome 22q11.2 deletion syndrome, distal (Disease Ontology:DOID:0060413); hereditary spastic paraplegia 84 (Disease Ontology:DOID:0112347)", "pathway": " (mmu:224020); (R-MMU-1483248); (R-MMU-1660514)", "pathway_count": 3, "publication_count": 14, "publication_id_list": "10.1101/2023.09.13.557529;17242355;19581584;21183079;21750661;23229899;29386109;29874576;31219806;33300544;34203471;34428180;36210013;37390900", "class_list": "", "function": "Actin dynamics regulation by TTC7A/PI4KIIIalpha limits DNA damage and cell death under confinement., [RefSeq, PubMed]; Acts on phosphatidylinositol (PtdIns) in the first committed step in the production of the second messenger inositol-1,4,5,-trisphosphate., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Loss of phosphatidylinositol 4-kinase 2alpha activity causes late onset degeneration of spinal cord axons., [RefSeq, PubMed]; Mutation of Pi4ka found to promote myeloid and erythroid dysfunction. Subsequent validation experiments showed that targeted inactivation of the Pi4ka catalytic domain or reduction in mRNA expression inhibited myeloid and erythroid cell differentiation in vitro and promoted anemia in vivo, [RefSeq, PubMed]; These studies define a role for PI4KA in myelin formation primarily affecting metabolism of key phospholipids and the actin cytoskeleton., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 3, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 3, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 3, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 9, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 3, "disease_count": 2, "glyco_site_count": 4, "binding_glycan_count": 0, "secondary_ac_list": "Q3UVT5;Q6DIC7;Q7TNG2;Q80Y45", "ec_number_list": "2.7.1.67", "go_molecular_function": "GO:0005524 ATP binding;GO:0004430 1-phosphatidylinositol 4-kinase activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0030660 Golgi-associated vesicle membrane", "go_biological_process": "GO:0030036 actin cytoskeleton organization;GO:0048015 phosphatidylinositol-mediated signaling;GO:0022011 myelination in peripheral nervous system;GO:0036135 Schwann cell migration;GO:0046854 phosphatidylinositol phosphate biosynthetic process", "synthesized_glycan_count": 0, "hit_score": 2.2, "record_id": "E9Q3L2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q62137-1", "uniprot_id": "JAK3_MOUSE", "mass": 122641.0, "length": 1100, "protein_name": "Tyrosine-protein kinase JAK3", "gene_name": "Jak3", "organism": "Mouse", "refseq_name": "tyrosine-protein kinase JAK3", "refseq_ac": "NP_001177759", "gene_names_uniprotkb": "Jak3", "gene_names_refseq": "Jak3; fae; wil", "protein_names_uniprotkb": "Tyrosine-protein kinase JAK3; 2.7.10.2; JAK-3; Janus kinase 3", "protein_names_refseq": "tyrosine-protein kinase JAK3", "tax_id": 10090, "disease": "juvenile myelomonocytic leukemia (Disease Ontology:DOID:0050458); adult T-cell leukemia/lymphoma (Disease Ontology:DOID:0050523); tongue squamous cell carcinoma (Disease Ontology:DOID:0050865); T-cell prolymphocytic leukemia (Disease Ontology:DOID:0081042); graft-versus-host disease (Disease Ontology:DOID:0081267); T-cell non-Hodgkin lymphoma (Disease Ontology:DOID:0081312); severe combined immunodeficiency 104 (Disease Ontology:DOID:0090014); disease of cellular proliferation (Disease Ontology:DOID:14566); cancer (Disease Ontology:DOID:162); hematologic cancer (Disease Ontology:DOID:2531); T-cell acute lymphoblastic leukemia (Disease Ontology:DOID:5603); severe combined immunodeficiency (Disease Ontology:DOID:627); acute megakaryocytic leukemia (Disease Ontology:DOID:8761)", "pathway": " (mmu:16453); (R-MMU-1266695); (R-MMU-201556); (R-MMU-5673001); (R-MMU-6785807); (R-MMU-8854691); (R-MMU-8983432); (R-MMU-8985947); (R-MMU-9020558); (R-MMU-9020958); (R-MMU-912526)", "pathway_count": 11, "publication_count": 17, "publication_id_list": "10733938;15121872;18250455;20696842;21183079;21750661;26495903;31219806;34428180;36210013;7481767;7481769;7518579;8022486;8605329;9016869;9620658", "class_list": "", "function": "Non-receptor tyrosine kinase involved in various processes such as cell growth, development, or differentiation (PubMed:20696842). Mediates essential signaling events in both innate and adaptive immunity and plays a crucial role in hematopoiesis during T-cells development. In the cytoplasm, plays a pivotal role in signal transduction via its association with type I receptors sharing the common subunit gamma such as IL2R, IL4R, IL7R, IL9R, IL15R and IL21R. Following ligand binding to cell surface receptors, phosphorylates specific tyrosine residues on the cytoplasmic tails of the receptor, creating docking sites for STATs proteins. Subsequently, phosphorylates the STATs proteins once they are recruited to the receptor. Phosphorylated STATs then form homodimer or heterodimers and translocate to the nucleus to activate gene transcription. For example, upon IL2R activation by IL2, JAK1 and JAK3 molecules bind to IL2R beta (IL2RB) and gamma chain (IL2RG) subunits inducing the tyrosine phosphorylation of both receptor subunits on their cytoplasmic domain. Then, STAT5A and STAT5B are recruited, phosphorylated and activated by JAK1 and JAK3. Once activated, dimerized STAT5 translocates to the nucleus and promotes the transcription of specific target genes in a cytokine-specific fashion., [UniProtKB, PubMed, PubMed]", "predicted_glycosites": 2, "predicted_n_glycosites": 0, "predicted_o_glycosites": 2, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 6, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 13, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "A2RRI3;Q0D2M8;Q61746;Q61747;Q8BTY6;Q8BYU2", "ec_number_list": "2.7.12.2;2.7.10.1;3.2.1.31;2.7.12.1;2.7.1.153;2.7.1.137;2.7.1.32;2.7.1.82;2.7.10.2;2.7.11.1;3.6.5.2;2.7.11.17;3.1.3.48;2.7.11.13;2.7.10.4;2.7.1.40;2.7.11.23;3.1.3.86;3.1.3.56;3.1.3.36", "go_molecular_function": "GO:0004713 protein tyrosine kinase activity;GO:0004715 non-membrane spanning protein tyrosine kinase activity;GO:0005524 ATP binding;GO:0019903 protein phosphatase binding;GO:0005131 growth hormone receptor binding", "go_cellular_component": "GO:0005829 cytosol;GO:0031234 extrinsic component of cytoplasmic side of plasma membrane;GO:0012505 endomembrane system;GO:0005737 cytoplasm;GO:0005856 cytoskeleton", "go_biological_process": "GO:0035771 interleukin-4-mediated signaling pathway;GO:0038110 interleukin-2-mediated signaling pathway;GO:0070669 response to interleukin-2;GO:0071104 response to interleukin-9;GO:0032693 negative regulation of interleukin-10 production", "synthesized_glycan_count": 0, "hit_score": 1.8, "record_id": "Q62137-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q80ZQ5-1", "uniprot_id": "JAZF1_MOUSE", "mass": 27098.0, "length": 243, "protein_name": "Juxtaposed with another zinc finger protein 1", "gene_name": "Jazf1", "organism": "Mouse", "refseq_name": "juxtaposed with another zinc finger protein 1 isoform 2", "refseq_ac": "NP_001161749", "gene_names_uniprotkb": "Jazf1", "gene_names_refseq": "C820002C15; Jaz1; Jazf1; Tip27", "protein_names_uniprotkb": "Juxtaposed with another zinc finger protein 1", "protein_names_refseq": "juxtaposed with another zinc finger protein 1 isoform 2; juxtaposed with another zinc finger protein 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:231986)", "pathway_count": 1, "publication_count": 9, "publication_id_list": "10.1101/2023.09.13.557529;20580384;21183079;24380856;24930994;25428506;25614086;34910364;36442127", "class_list": "", "function": "Acts as a transcriptional corepressor of orphan nuclear receptor NR2C2 (By similarity). Inhibits expression of the gluconeogenesis enzyme PCK2 through inhibition of NR2C2 activity (PubMed:24380856). Also involved in transcriptional activation of NAMPT by promoting expression of PPARA and PPARD (PubMed:24930994). Plays a role in lipid metabolism by suppressing lipogenesis, increasing lipolysis and decreasing lipid accumulation in adipose tissue (PubMed:24380856, PubMed:25614086). Plays a role in glucose homeostasis by improving glucose metabolism and insulin sensitivity (PubMed:24380856, PubMed:25614086)., [UniProtKB, PubMed, PubMed, UniProtKB, PubMed]; Deletion of Jazf1 gene causes early growth retardation and insulin resistance in mice., [RefSeq, PubMed]; MicroRNA-19b-3p-containing extracellular vesicles derived from macrophages promote the development of atherosclerosis by targeting JAZF1., [RefSeq, PubMed]; These results showed that JAZF1 in adipocytes and liver cells reduces lipid synthesis and increases lipolysis, [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q8BLQ8;Q8BWN4", "ec_number_list": "", "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003714 transcription corepressor activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0001650 fibrillar center;GO:0017053 transcription repressor complex", "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006629 lipid metabolic process", "synthesized_glycan_count": 0, "hit_score": 1.2, "record_id": "Q80ZQ5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q99PT3-1", "uniprot_id": "IN80B_MOUSE", "mass": 40565.0, "length": 375, "protein_name": "INO80 complex subunit B", "gene_name": "Ino80b", "organism": "Mouse", "refseq_name": "INO80 complex subunit B", "refseq_ac": "NP_076036", "gene_names_uniprotkb": "Ino80b; Hmga1l4; Papa1; Znhit4", "gene_names_refseq": "2510009I23Rik; HMG1YL4; Hmga1l4; Ino80b; Papa1; Znhit4", "protein_names_uniprotkb": "INO80 complex subunit B; High mobility group AT-hook 1-like 4; PAP-1-associated protein 1; PAPA-1; Zinc finger HIT domain-containing protein 4", "protein_names_refseq": "INO80 complex subunit B; PAP-1 binding protein; PAP-1-associated protein 1; PAPA-1; high mobility group AT-hook 1-like 4; zinc finger HIT domain-containing protein 4; zinc finger, HIT type 4", "tax_id": 10090, "disease": "", "pathway": " (mmu:70020); (R-MMU-5689603); (R-MMU-5696394)", "pathway_count": 3, "publication_count": 4, "publication_id_list": "15556297;19095771;21183079;21750661", "class_list": "", "function": "Proposed core component of the chromatin remodeling INO80 complex which is involved in transcriptional regulation, DNA replication and probably DNA repair., [UniProtKB, PubMed]; Results suggest that the growth-promoting role of IGFBP-2 in prostate cancer is inhibited by its intracellular interaction with PAPA-1., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 5, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q9CY38", "ec_number_list": "", "go_molecular_function": "GO:0008270 zinc ion binding", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0031011 Ino80 complex;GO:0016604 nuclear body", "go_biological_process": "GO:0060382 regulation of DNA strand elongation;GO:0033044 regulation of chromosome organization;GO:0006281 DNA repair;GO:0006310 DNA recombination;GO:0006338 chromatin remodeling", "synthesized_glycan_count": 0, "hit_score": 0.5, "record_id": "Q99PT3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q61414-1", "uniprot_id": "K1C15_MOUSE", "mass": 49138.0, "length": 452, "protein_name": "Keratin, type I cytoskeletal 15", "gene_name": "Krt15", "organism": "Mouse", "refseq_name": "keratin, type I cytoskeletal 15", "refseq_ac": "NP_032495", "gene_names_uniprotkb": "Krt15; Krt1-15", "gene_names_refseq": "K15; Krt1-15; Krt15", "protein_names_uniprotkb": "Keratin, type I cytoskeletal 15; CK-15; Cytokeratin-15; K15; Keratin-15", "protein_names_refseq": "CK-15; cytokeratin-15; keratin complex 1, acidic, gene 15; keratin, type I cytoskeletal 15", "tax_id": 10090, "disease": "", "pathway": " (mmu:16665); (R-MMU-6805567); (R-MMU-6809371)", "pathway_count": 3, "publication_count": 10, "publication_id_list": "10623468;11408584;14506658;21183079;21750661;24940650;34428180;34887587;7510260;7539810", "class_list": "", "function": "In the absence of KRT14, makes a bona fide, but ultrastructurally distinct keratin filament network with KRT5., [UniProtKB, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 8, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q6PEQ0", "ec_number_list": "", "go_molecular_function": "GO:0097110 scaffold protein binding;GO:0030280 structural constituent of skin epidermis;GO:0005198 structural molecule activity", "go_cellular_component": "GO:0005856 cytoskeleton;GO:0045111 intermediate filament cytoskeleton;GO:0045095 keratin filament;GO:0005882 intermediate filament", "go_biological_process": "GO:0030855 epithelial cell differentiation;GO:0045109 intermediate filament organization;GO:0002009 morphogenesis of an epithelium", "synthesized_glycan_count": 0, "hit_score": 1.3, "record_id": "Q61414-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9DCL8-1", "uniprot_id": "IPP2_MOUSE", "mass": 23119.0, "length": 206, "protein_name": "Protein phosphatase inhibitor 2", "gene_name": "Ppp1r2", "organism": "Mouse", "refseq_name": "protein phosphatase inhibitor 2", "refseq_ac": "NP_080076", "gene_names_uniprotkb": "Ppp1r2", "gene_names_refseq": "0610025N14Rik; 2310007G06Rik; 4930440J04Rik; 5430408E15Rik; D16Ertd248e; I-2; IPP-2; Ppp1r2", "protein_names_uniprotkb": "Protein phosphatase inhibitor 2; IPP-2", "protein_names_refseq": "protein phosphatase inhibitor 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:66849)", "pathway_count": 1, "publication_count": 10, "publication_id_list": "15345747;17242355;17622165;17636256;19131326;19144319;21183079;21750661;26558779;30144392", "class_list": "", "function": "Inhibitor of protein-phosphatase 1., [UniProtKB, UniProtKB, UniProtKB]; Protein phosphatase-1 inhibitor-2 acts as a memory suppressor through its positive functional influence on type I protein phosphatase., [RefSeq, PubMed]; The three regulators (PPP1R2, PPP1R7, and PPP1R11)share localization with PP1gamma2 in the head and the principal piece of sperm. We show that the association of inhibitors to PP1gamma2 changes during epididymal sperm maturation. In immotile caput epididymal sperm, PPP1R2 and PPP1R7 are not bound to PP1gamma2, whereas in motile caudal sperm, all three inhibitors are bound as heterodimers or heterotrimers., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 9, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3UD25;Q8C1A6", "ec_number_list": "", "go_molecular_function": "GO:0019904 protein domain specific binding;GO:0004864 protein phosphatase inhibitor activity;GO:0140678 molecular function inhibitor activity", "go_cellular_component": "GO:0030426 growth cone;GO:0043197 dendritic spine", "go_biological_process": "GO:0035556 intracellular signal transduction;GO:0005977 glycogen metabolic process;GO:0009966 regulation of signal transduction", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q9DCL8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O88792-1", "uniprot_id": "JAM1_MOUSE", "mass": 32424.0, "length": 300, "protein_name": "Junctional adhesion molecule A", "gene_name": "F11r", "organism": "Mouse", "refseq_name": "junctional adhesion molecule A precursor", "refseq_ac": "NP_766235", "gene_names_uniprotkb": "F11r; Jam1; Jcam1; Jcam", "gene_names_refseq": "9130004G24; ESTM33; F11r; JAM-1; JAM-A; JAM; Jcam1; Jcam; Ly106", "protein_names_uniprotkb": "Junctional adhesion molecule A; JAM-1; JAM-A; Junctional adhesion molecule 1", "protein_names_refseq": "BV11 antigen; F11 receptor/F11R; junction cell adhesion molecule A; junction cell adhesion molecule1; junctional adhesion molecule 1; junctional adhesion molecule A precursor; junctional adhesion molecule A", "tax_id": 10090, "disease": "hypertension (Disease Ontology:DOID:10763); peptic esophagitis (Disease Ontology:DOID:13976); breast cancer (Disease Ontology:DOID:1612); transient cerebral ischemia (Disease Ontology:DOID:224); systemic scleroderma (Disease Ontology:DOID:418)", "pathway": " (mmu:16456); (R-MMU-202733); (R-MMU-216083); (R-MMU-2173791); (R-MMU-420029)", "pathway_count": 5, "publication_count": 18, "publication_id_list": "10.1101/2023.09.13.557529;11036763;11447115;11500366;12810109;17242355;19349973;19656770;21183079;28062807;34428180;35819838;35820727;36531986;37453647;37828378;38566526;9660867", "class_list": "", "function": "Junctional adhesion molecule-A deficient mice are protected from severe experimental autoimmune encephalomyelitis., [RefSeq, PubMed]; Junctional adhesion molecule-A deletion increases phagocytosis and improves survival in a murine model of sepsis. Publication Status: Online-Only, [RefSeq, PubMed]; Junctional adhesion molecule-A is dispensable for myeloid cell recruitment and diversification in the tumor microenvironment. Publication Status: Online-Only, [RefSeq, PubMed]; Seems to play a role in epithelial tight junction formation. Appears early in primordial forms of cell junctions and recruits PARD3 (PubMed:11447115). The association of the PARD6-PARD3 complex may prevent the interaction of PARD3 with JAM1, thereby preventing tight junction assembly (PubMed:11447115). Plays a role in regulating monocyte transmigration involved in integrity of epithelial barrier (PubMed:9660867). Ligand for integrin alpha-L/beta-2 involved in memory T-cell and neutrophil transmigration (By similarity). Involved in platelet activation (By similarity)., [UniProtKB, PubMed, PubMed, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 2, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 3, "disease_count": 5, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q8VC39", "ec_number_list": "", "go_molecular_function": "GO:0005178 integrin binding;GO:0042803 protein homodimerization activity;GO:0030165 PDZ domain binding", "go_cellular_component": "GO:0005886 plasma membrane;GO:0005911 cell-cell junction;GO:0005923 bicellular tight junction;GO:0030054 cell junction;GO:0032991 protein-containing complex", "go_biological_process": "GO:0090559 regulation of membrane permeability;GO:0007155 cell adhesion;GO:0030855 epithelial cell differentiation;GO:0032956 regulation of actin cytoskeleton organization;GO:0045777 positive regulation of blood pressure", "synthesized_glycan_count": 0, "hit_score": 2.5, "record_id": "O88792-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P59997-1", "uniprot_id": "KDM2A_MOUSE", "mass": 132680.0, "length": 1161, "protein_name": "Lysine-specific demethylase 2A", "gene_name": "Kdm2a", "organism": "Mouse", "refseq_name": "lysine-specific demethylase 2A", "refseq_ac": "NP_001001984", "gene_names_uniprotkb": "Kdm2a; Fbl11; Fbxl11; Jhdm1a; Kiaa1004", "gene_names_refseq": "100043628; 5530401A10Rik; Cxxc8; Fbl11; Fbl7; Fbxl11; Gm4560; Jhdm1a; Jhdm1; Kdm2a; lalina", "protein_names_uniprotkb": "Lysine-specific demethylase 2A; 1.14.11.27; F-box and leucine-rich repeat protein 11; F-box/LRR-repeat protein 11; JmjC domain-containing histone demethylation protein 1A; [Histone-H3]-lysine-36 demethylase 1A", "protein_names_refseq": "F-box and leucine-rich repeat protein 11; F-box protein containing leucine repeats; F-box/LRR-repeat protein 11; [Histone-H3]-lysine-36 demethylase 1A; jmjC domain-containing histone demethylation protein 1A; lysine-specific demethylase 2A", "tax_id": 10090, "disease": "melanoma (Disease Ontology:DOID:1909); lung non-small cell carcinoma (Disease Ontology:DOID:3908)", "pathway": " (mmu:225876); (R-MMU-3214842)", "pathway_count": 2, "publication_count": 8, "publication_id_list": "17242355;17525332;21183079;21750661;32584788;34428180;34887587;38745315", "class_list": "", "function": "Histone demethylase that specifically demethylates 'Lys-36' of histone H3, thereby playing a central role in histone code (PubMed:32584788). Preferentially demethylates dimethylated H3 'Lys-36' residue while it has weak or no activity for mono- and tri-methylated H3 'Lys-36'. May also recognize and bind to some phosphorylated proteins and promote their ubiquitination and degradation. Required to maintain the heterochromatic state. Associates with centromeres and represses transcription of small non-coding RNAs that are encoded by the clusters of satellite repeats at the centromere. Required to sustain centromeric integrity and genomic stability, particularly during mitosis (By similarity). Regulates circadian gene expression by repressing the transcriptional activator activity of CLOCK-BMAL1 heterodimer and RORA in a catalytically-independent manner (By similarity)., [UniProtKB, UniProtKB, PubMed]; MicroRNA-721 regulates gluconeogenesis via KDM2A-mediated epigenetic modulation in diet-induced insulin resistance in C57BL/6J mice. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 14, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q3U1M5;Q3UR56;Q3V3Q1;Q69ZT4", "ec_number_list": "1.14.11.27;1.14.11.69;1.14.11.66;1.14.11.79", "go_molecular_function": "GO:0051864 histone H3K36 demethylase activity;GO:0008270 zinc ion binding;GO:0003712 transcription coregulator activity;GO:0032452 histone demethylase activity;GO:0045322 unmethylated CpG binding", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0000785 chromatin;GO:0005634 nucleus", "go_biological_process": "GO:0001701 in utero embryonic development;GO:0006338 chromatin remodeling;GO:0006357 regulation of transcription by RNA polymerase II;GO:0010628 positive regulation of gene expression;GO:0010629 negative regulation of gene expression", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "P59997-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q50H33-1", "uniprot_id": "KCTD8_MOUSE", "mass": 52768.0, "length": 476, "protein_name": "BTB/POZ domain-containing protein KCTD8", "gene_name": "Kctd8", "organism": "Mouse", "refseq_name": "BTB/POZ domain-containing protein KCTD8", "refseq_ac": "NP_780728", "gene_names_uniprotkb": "Kctd8", "gene_names_refseq": "A730087N02Rik; Kctd8", "protein_names_uniprotkb": "BTB/POZ domain-containing protein KCTD8", "protein_names_refseq": "BTB/POZ domain-containing protein KCTD8", "tax_id": 10090, "disease": "", "pathway": " (mmu:243043)", "pathway_count": 1, "publication_count": 7, "publication_id_list": "20400944;21183079;21452234;24129315;33300544;33913808;35017224", "class_list": "", "function": "Auxiliary subunit of GABA-B receptors that determine the pharmacology and kinetics of the receptor response. Increases agonist potency and markedly alter the G protein signaling of the receptors by accelerating onset and promoting desensitization., [UniProtKB, PubMed]; Data suggest that the distinct spatial and temporal distribution patterns of KCTD8, 12, 12b, and 16 underlie functional differences in native GABA(B) responses., [RefSeq, PubMed]; GABAB receptor auxiliary subunits modulate Cav2.3-mediated release from medial habenula terminals. Publication Status: Online-Only, [RefSeq, PubMed]; KCTD8 and KCTD12 Facilitate Axonal Expression of GABAB Receptors in Habenula Cholinergic Neurons., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q8BR74;Q8C4C2;Q8C906;Q8C9B0;Q8CAA9", "ec_number_list": "", "go_molecular_function": "GO:0150047 G protein-coupled neurotransmitter receptor activity involved in regulation of presynaptic membrane potential", "go_cellular_component": "GO:0048787 presynaptic active zone membrane;GO:0043235 receptor complex;GO:0045211 postsynaptic membrane;GO:0098794 postsynapse;GO:0042734 presynaptic membrane", "go_biological_process": "GO:0051260 protein homooligomerization;GO:0008277 regulation of G protein-coupled receptor signaling pathway", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "Q50H33-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q69ZS8-1", "uniprot_id": "KAZRN_MOUSE", "mass": 86717.0, "length": 779, "protein_name": "Kazrin", "gene_name": "Kazn", "organism": "Mouse", "refseq_name": "kazrin isoform 2", "refseq_ac": "NP_001103154", "gene_names_uniprotkb": "Kazn; Kaz; Kiaa1026", "gene_names_refseq": "2310007B04Rik; 9030409G11Rik; Kazn; Kazrin; Kaz", "protein_names_uniprotkb": "Kazrin", "protein_names_refseq": "kazrin isoform 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:71529); (R-MMU-6809371)", "pathway_count": 2, "publication_count": 8, "publication_id_list": "15337775;16086310;21183079;21750661;22513779;22645316;34428180;37096882", "class_list": "", "function": "Component of the cornified envelope of keratinocytes. May be involved in the interplay between adherens junctions and desmosomes. The function in the nucleus is not known., [UniProtKB, UniProtKB, UniProtKB]; Exons 5-15 of kazrin, encoding the nuclear localization signal and C-terminal domain, are not required for epidermal development and function, [RefSeq, PubMed]; Kazrin promotes dynein/dynactin-dependent traffic from early to recycling endosomes. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "A2AC34;B1B0N1;Q8BIY2;Q8R1X4", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005856 cytoskeleton;GO:0016607 nuclear speck;GO:0001533 cornified envelope", "go_biological_process": "GO:0031424 keratinization", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q69ZS8-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q920E3-1", "uniprot_id": "KCNH5_MOUSE", "mass": 111810.0, "length": 988, "protein_name": "Voltage-gated delayed rectifier potassium channel KCNH5", "gene_name": "Kcnh5", "organism": "Mouse", "refseq_name": "voltage-gated delayed rectifier potassium channel KCNH5", "refseq_ac": "NP_766393", "gene_names_uniprotkb": "Kcnh5; Eag2", "gene_names_refseq": "Eag2; Kcnh5; mEag2", "protein_names_uniprotkb": "Voltage-gated delayed rectifier potassium channel KCNH5; Ether-a-go-go potassium channel 2; Potassium voltage-gated channel subfamily H member 5; Voltage-gated potassium channel subunit Kv10.2; mEag2", "protein_names_refseq": "ether-a-go-go potassium channel 2; potassium voltage-gated channel subfamily H member 5; voltage-gated delayed rectifier potassium channel KCNH5; voltage-gated potassium channel subunit Kv10.2", "tax_id": 10090, "disease": "developmental and epileptic encephalopathy (Disease Ontology:DOID:0112202); epilepsy (Disease Ontology:DOID:1826)", "pathway": " (mmu:238271); (R-MMU-1296072)", "pathway_count": 2, "publication_count": 3, "publication_id_list": "19580749;21183079;22855790", "class_list": "", "function": "Disruption of EAG2 expression results in G2 arrest and mitotic catastrophe associated with failure of premitotic cytoplasmic condensation, [RefSeq, PubMed]; Our results suggest close conformational conservation between closed EAG (Kv12.1 and Kv10.2) and Shaker family channels, despite large differences in voltage sensitivity, activation rates, and activation threshold, [RefSeq, PubMed]; Pore-forming (alpha) subunit of a voltage-gated delayed rectifier potassium channel that mediates outward-rectifying potassium currents which, on depolarization, reaches a steady-state level and do not inactivate. The kinetic is characterized by a slow activation time course and a small voltage dependence of the activation time constants, therefore, starts to open at more negative voltages. The activation kinetics depend on the prepulse potential and external divalent cation concentration. The time course of activation is biphasic with a fast and a slowly activating current component. With negative prepulses, the current activation is delayed and slowed down several fold, whereas more positive prepulses speed up activation, therefore the activation rate depends on holding potential., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 1, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "E9QPM0;Q8C035", "ec_number_list": "1.8.-.-", "go_molecular_function": "GO:0005251 delayed rectifier potassium channel activity;GO:0005516 calmodulin binding;GO:0044325 transmembrane transporter binding;GO:0044877 protein-containing complex binding;GO:0005249 voltage-gated potassium channel activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0008076 voltage-gated potassium channel complex", "go_biological_process": "GO:0042391 regulation of membrane potential;GO:0010389 regulation of G2/M transition of mitotic cell cycle;GO:0006813 potassium ion transport;GO:0071805 potassium ion transmembrane transport", "synthesized_glycan_count": 0, "hit_score": 0.4, "record_id": "Q920E3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9ERE9-1", "uniprot_id": "JIP2_MOUSE", "mass": 89900.0, "length": 830, "protein_name": "C-Jun-amino-terminal kinase-interacting protein 2", "gene_name": "Mapk8ip2", "organism": "Mouse", "refseq_name": "C-Jun-amino-terminal kinase-interacting protein 2", "refseq_ac": "NP_068740", "gene_names_uniprotkb": "Mapk8ip2; Ib2; Jip2", "gene_names_refseq": "3230402N03Rik; IB2; Jip2; Mapk8ip2", "protein_names_uniprotkb": "C-Jun-amino-terminal kinase-interacting protein 2; IB-2; Islet-brain-2; JIP-2; JNK MAP kinase scaffold protein 2; JNK-interacting protein 2; Mitogen-activated protein kinase 8-interacting protein 2", "protein_names_refseq": "C-Jun-amino-terminal kinase-interacting protein 2; IB-2; JIP-2; JNK MAP kinase scaffold protein 2; JNK-interacting protein 2; islet-brain-2", "tax_id": 10090, "disease": "", "pathway": " (mmu:60597)", "pathway_count": 1, "publication_count": 7, "publication_id_list": "10.1101/2023.09.13.557529;10827199;11378392;16628014;19893486;21183079;35820727", "class_list": "", "function": "The JNK-interacting protein (JIP) group of scaffold proteins selectively mediates JNK signaling by aggregating specific components of the MAPK cascade to form a functional JNK signaling module. JIP2 inhibits IL1 beta-induced apoptosis in insulin-secreting cells (By similarity)., [UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q9CXI4", "ec_number_list": "", "go_molecular_function": "GO:0019901 protein kinase binding;GO:0030295 protein kinase activator activity;GO:0044877 protein-containing complex binding;GO:0019894 kinesin binding;GO:0005078 MAP-kinase scaffold activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0014069 postsynaptic density;GO:0043025 neuronal cell body;GO:0032991 protein-containing complex", "go_biological_process": "GO:0046958 nonassociative learning;GO:0007617 mating behavior;GO:0098815 modulation of excitatory postsynaptic potential;GO:0000165 MAPK cascade;GO:0007254 JNK cascade", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "Q9ERE9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9QWL7-1", "uniprot_id": "K1C17_MOUSE", "mass": 48162.0, "length": 433, "protein_name": "Keratin, type I cytoskeletal 17", "gene_name": "Krt17", "organism": "Mouse", "refseq_name": "keratin, type I cytoskeletal 17", "refseq_ac": "NP_034793", "gene_names_uniprotkb": "Krt17; Krt1-17", "gene_names_refseq": "K17; Krt1-17; Krt17", "protein_names_uniprotkb": "Keratin, type I cytoskeletal 17; CK-17; Cytokeratin-17; K17; Keratin-17", "protein_names_refseq": "CK-17; cytokeratin-17; keratin complex 1, acidic, gene 17; keratin, type I cytoskeletal 17", "tax_id": 10090, "disease": "pachyonychia congenita (Disease Ontology:DOID:0050449); steatocystoma multiplex (Disease Ontology:DOID:0111556); ectodermal dysplasia (Disease Ontology:DOID:2121)", "pathway": " (mmu:16667); (R-MMU-6805567); (R-MMU-6809371)", "pathway_count": 3, "publication_count": 18, "publication_id_list": "10087197;10844551;11408584;12050118;14714564;16702408;16710422;20871598;21183079;22006917;2433272;34428180;34887587;36210013;37453647;39159283;39627609;9786956", "class_list": "", "function": "Repeated stress to the skin amplifies neutrophil infiltration in a keratin 17- and PKCalpha-dependent manner. Publication Status: Online-Only, [RefSeq, PubMed]; The protein encoded by this gene is a member of the type I keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The encoded protein is a cytokeratin required for the normal growth of hair follicles and may act in psoriasis as an immunopathogenic autoantigen. [provided by RefSeq, Sep 2015]., [RefSeq]; Type I keratin involved in the formation and maintenance of various skin appendages, specifically in determining shape and orientation of hair (PubMed:14714564, PubMed:16702408). Required for the correct growth of hair follicles, in particular for the persistence of the anagen (growth) state (PubMed:16702408). Modulates the function of TNF in the specific context of hair cycling. Regulates protein synthesis and epithelial cell growth through binding to the adapter protein SFN and by stimulating Akt/mTOR pathway (PubMed:16710422). Involved in tissue repair. May be a marker of basal cell differentiation in complex epithelia and therefore indicative of a certain type of epithelial 'stem cells'. Acts as a promoter of epithelial proliferation by acting a regulator of immune response in skin: promotes Th1/Th17-dominated immune environment contributing to the development of basaloid skin tumors (PubMed:20871598). May act as an autoantigen in the immunopathogenesis of psoriasis, with certain peptide regions being a major target for autoreactive T-cells and hence causing their proliferation., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 10, "reported_mutagensis": 3, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "A2A4G6;Q61783", "ec_number_list": "", "go_molecular_function": "GO:0030280 structural constituent of skin epidermis", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005856 cytoskeleton;GO:0071944 cell periphery;GO:0045111 intermediate filament cytoskeleton;GO:0001533 cornified envelope", "go_biological_process": "GO:0030307 positive regulation of cell growth;GO:0030855 epithelial cell differentiation;GO:0031424 keratinization;GO:0045727 positive regulation of translation;GO:0045109 intermediate filament organization", "synthesized_glycan_count": 0, "hit_score": 2.1, "record_id": "Q9QWL7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9JJZ6-1", "uniprot_id": "KLF13_MOUSE", "mass": 31136.0, "length": 289, "protein_name": "Krueppel-like factor 13", "gene_name": "Klf13", "organism": "Mouse", "refseq_name": "Krueppel-like factor 13", "refseq_ac": "NP_067341", "gene_names_uniprotkb": "Klf13; Bteb3; Fklf2", "gene_names_refseq": "0610043C13Rik; 9430029L20Rik; Bteb3; FKLF-2; Klf13; NSLP1; RFLAT-1", "protein_names_uniprotkb": "Krueppel-like factor 13; BTE-binding protein 3; Basic transcription element-binding protein 3; Erythroid transcription factor FKLF-2; RANTES factor of late activated T-lymphocytes 1; RFLAT-1; Transcription factor BTEB3", "protein_names_refseq": "BTE-binding protein 3; C2-H2 zinc finger protein; Krueppel-like factor 13; Kruppel-like factor 13; RANTES factor of late activated T-lymphocytes 1; basic transcription element-binding protein 3; erythroid transcription factor FKLF-2; transcription factor BTEB3", "tax_id": 10090, "disease": "", "pathway": " (mmu:50794)", "pathway_count": 1, "publication_count": 10, "publication_id_list": "10642511;10828046;11087666;21183079;21750661;26495903;31219806;36318265;36583453;38973459", "class_list": "", "function": "KLF13 overexpression protects sepsis-induced myocardial injury and LPS-induced inflammation and apoptosis., [RefSeq, PubMed]; KLF13 restrains Dll4-muscular Notch2 axis to improve the muscle atrophy., [RefSeq, PubMed]; KLF9 and KLF13 transcription factors boost myelin gene expression in oligodendrocytes as partners of SOX10 and MYRF., [RefSeq, PubMed]; Transcription factor that activates expression from GC-rich minimal promoter regions, including genes in the cells of the erythroid lineage (PubMed:10642511, PubMed:10828046). Represses transcription by binding to the BTE site, a GC-rich DNA element, in competition with the activator SP1. It also represses transcription by interacting with the corepressor Sin3A and HDAC1. Activates RANTES and CCL5 expression in T-cells (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 5, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q9ESX3;Q9JHF8", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific", "go_cellular_component": "GO:0005634 nucleus", "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0008285 negative regulation of cell population proliferation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006366 transcription by RNA polymerase II;GO:0045647 negative regulation of erythrocyte differentiation", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q9JJZ6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P81068-1", "uniprot_id": "IRX1_MOUSE", "mass": 50169.0, "length": 480, "protein_name": "Iroquois-class homeodomain protein IRX-1", "gene_name": "Irx1", "organism": "Mouse", "refseq_name": "iroquois-class homeodomain protein IRX-1", "refseq_ac": "NP_034703", "gene_names_uniprotkb": "Irx1; Irxa1", "gene_names_refseq": "Irx1", "protein_names_uniprotkb": "Iroquois-class homeodomain protein IRX-1; Homeodomain protein IRXA1; Iroquois homeobox protein 1", "protein_names_refseq": "Iroquois related homeobox 1; homeodomain protein IRXA1; iroquois homeobox protein 1; iroquois-class homeodomain protein IRX-1", "tax_id": 10090, "disease": "congenital heart disease (Disease Ontology:DOID:1682); congestive heart failure (Disease Ontology:DOID:6000)", "pathway": " (mmu:16371)", "pathway_count": 1, "publication_count": 7, "publication_id_list": "10704856;10926765;17875669;21183079;21750661;34428180;9486539", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "G5E8H6;O55120;Q3UZB9;Q9JLL6", "ec_number_list": "", "go_molecular_function": "GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0043565 sequence-specific DNA binding;GO:1990837 sequence-specific double-stranded DNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm", "go_biological_process": "GO:0072086 specification of loop of Henle identity;GO:0072272 proximal/distal pattern formation involved in metanephric nephron development;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0010628 positive regulation of gene expression", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "P81068-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9DBC7-1", "uniprot_id": "KAP0_MOUSE", "mass": 43185.0, "length": 381, "protein_name": "cAMP-dependent protein kinase type I-alpha regulatory subunit", "gene_name": "Prkar1a", "organism": "Mouse", "refseq_name": "cAMP-dependent protein kinase type I-alpha regulatory subunit", "refseq_ac": "NP_001300902", "gene_names_uniprotkb": "Prkar1a", "gene_names_refseq": "1300018C22Rik; Prkar1a; RIalpha; Tse-1; Tse1", "protein_names_uniprotkb": "cAMP-dependent protein kinase type I-alpha regulatory subunit", "protein_names_refseq": "cAMP-dependent protein kinase type I-alpha regulatory subunit; protein kinase, cAMP dependent regulatory, type 1, alpha", "tax_id": 10090, "disease": "Carney complex (Disease Ontology:DOID:0050471); primary pigmented nodular adrenocortical disease (Disease Ontology:DOID:0060280); primary pigmented nodular adrenocortical disease 1 (Disease Ontology:DOID:0070546); acrodysostosis (Disease Ontology:DOID:14669); follicular thyroid carcinoma (Disease Ontology:DOID:3962)", "pathway": " (mmu:19084); (R-MMU-163615); (R-MMU-164378); (R-MMU-180024); (R-MMU-432040); (R-MMU-442720); (R-MMU-5610787); (R-MMU-9634597); (R-MMU-983231); (R-MMU-9856530)", "pathway_count": 10, "publication_count": 20, "publication_id_list": "10913627;15345747;17242355;18630941;19131326;20138877;21183079;21750661;25153642;27357676;28135057;28528544;31219806;34087234;34428180;34850745;35820727;37507081;37828378;9852104", "class_list": "", "function": "Loss of PKA regulatory subunit 1alpha aggravates cardiomyocyte necrosis and myocardial ischemia/reperfusion injury., [RefSeq, PubMed]; Protein kinase A drives paracrine crisis and WNT4-dependent testis tumor in Carney complex., [RefSeq, PubMed]; Regulatory subunit of the cAMP-dependent protein kinases involved in cAMP signaling in cells., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; The encoded protein is a regulatory subunit of the cAMP-dependent protein kinase (PKA) complex, which is responsible for transducing most of the cAMP signals in eukaryotic cells. The inactive PKA complex contains two regulatory and two catalytic subunits. Binding of cAMP dissociates the complex, allowing monomeric catalytic subunits to phosphorylate cytosolic proteins or induce gene expression in the nucleus. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Sep 2015]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 6, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 5, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3UKU7;Q9JHR5;Q9JHR6", "ec_number_list": "", "go_molecular_function": "GO:0034236 protein kinase A catalytic subunit binding;GO:0019904 protein domain specific binding;GO:0004862 cAMP-dependent protein kinase inhibitor activity;GO:0008603 cAMP-dependent protein kinase regulator activity;GO:0031625 ubiquitin protein ligase binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0005886 plasma membrane", "go_biological_process": "GO:0006468 protein phosphorylation;GO:0007189 adenylate cyclase-activating G protein-coupled receptor signaling pathway;GO:0007507 heart development;GO:0008283 cell population proliferation;GO:0010629 negative regulation of gene expression", "synthesized_glycan_count": 0, "hit_score": 2.3, "record_id": "Q9DBC7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P63250-1", "uniprot_id": "KCNJ3_MOUSE", "mass": 56573.0, "length": 501, "protein_name": "G protein-activated inward rectifier potassium channel 1", "gene_name": "Kcnj3", "organism": "Mouse", "refseq_name": "G protein-activated inward rectifier potassium channel 1 isoform 1", "refseq_ac": "NP_032452", "gene_names_uniprotkb": "Kcnj3; Girk1", "gene_names_refseq": "GIRK-1; GIRK1; Kcnf3; Kcnj1; Kcnj3; Kir3.1", "protein_names_uniprotkb": "G protein-activated inward rectifier potassium channel 1; GIRK-1; Inward rectifier K(+) channel Kir3.1; Potassium channel, inwardly rectifying subfamily J member 3", "protein_names_refseq": "G protein-activated inward rectifier potassium channel 1 isoform 1; G protein-gated K+ channel subunit 1 GIRK1; g protein-activated inward rectifier potassium channel 1; inward rectifier K(+) channel Kir3.1; potassium channel, inwardly rectifying subfamily J member 3", "tax_id": 10090, "disease": "", "pathway": " (mmu:16519); (R-MMU-1296041); (R-MMU-997272)", "pathway_count": 3, "publication_count": 11, "publication_id_list": "10341034;12507423;21183079;21750661;22517741;25428506;32617840;34261700;34678516;40885482;7702616", "class_list": "", "function": "G-Protein-Gated Inwardly Rectifying Potassium (Kir3/GIRK) Channels Govern Synaptic Plasticity That Supports Hippocampal-Dependent Cognitive Functions in Male Mice., [RefSeq, PubMed]; Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is regulated by the concentration of extracellular potassium; as external potassium is raised, the voltage range of the channel opening shifts to more positive voltages. The inward rectification is mainly due to the blockage of outward current by internal magnesium. This potassium channel is controlled by G proteins (PubMed:32617840). This receptor plays a crucial role in regulating the heartbeat (By similarity). Forms a functional channel in association with KCNJ5/GIRK4 or KCNJ6/GIRK2 or KCNJ9/GIRK3 (PubMed:10341034)., [UniProtKB, PubMed, PubMed, UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 1, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "P35562", "ec_number_list": "1.8.-.-", "go_molecular_function": "GO:0015467 G-protein activated inward rectifier potassium channel activity;GO:0005546 phosphatidylinositol-4,5-bisphosphate binding;GO:0099508 voltage-gated monoatomic ion channel activity involved in regulation of presynaptic membrane potential", "go_cellular_component": "GO:1902937 inward rectifier potassium channel complex;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0009897 external side of plasma membrane;GO:0008076 voltage-gated potassium channel complex", "go_biological_process": "GO:0051602 response to electrical stimulus;GO:1990573 potassium ion import across plasma membrane;GO:0071805 potassium ion transmembrane transport", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "P63250-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8K1S5-1", "uniprot_id": "KLF11_MOUSE", "mass": 54054.0, "length": 502, "protein_name": "Krueppel-like factor 11", "gene_name": "Klf11", "organism": "Mouse", "refseq_name": "Krueppel-like factor 11", "refseq_ac": "NP_848134", "gene_names_uniprotkb": "Klf11; Tieg2b; Tieg3", "gene_names_refseq": "9830142A17; D12Ertd427e; Klf11; Tieg2b; Tieg2; Tieg3", "protein_names_uniprotkb": "Krueppel-like factor 11; TGFB-inducible early growth response protein 2b; TGFB-inducible early growth response protein 3; TIEG-3; Transforming growth factor-beta-inducible early growth response protein 3", "protein_names_refseq": "Krueppel-like factor 11; Kruppel-like factor 11; TGFB inducible early growth response 2; TGFB inducible early growth response 3; TGFB-inducible early growth response protein 2b; TGFB-inducible early growth response protein 3; TIEG-3; transforming growth factor-beta-inducible early growth response protein 3", "tax_id": 10090, "disease": "maturity-onset diabetes of the young type 7 (Disease Ontology:DOID:0111106); type 2 diabetes mellitus (Disease Ontology:DOID:9352)", "pathway": " (mmu:194655)", "pathway_count": 1, "publication_count": 9, "publication_id_list": "12970187;14697507;15607700;18189266;20385766;21750661;35820727;36403074;37321514", "class_list": "", "function": "Genetic deletion of Kruppel-like factor 11 aggravates traumatic brain injury. Publication Status: Online-Only, [RefSeq, PubMed]; Host immunity and KLF 11 deficiency together promote fibrosis in a mouse model of endometriosis. Erratum:[Biochim Biophys Acta Mol Basis Dis. 2024 Mar;1870(3):166923. doi: 10.1016/j.bbadis.2023.166923. PMID: 37949756], [RefSeq, PubMed]; KLF11 is downregulated in human cancers, inhibits cell growth in vitro and in vivo, and suppresses neoplastic transformation, [RefSeq, PubMed]; Results from genetic knockout suggest that KLF11 is not absolutely required for hematopoiesis, growth, and development, [RefSeq, PubMed]; Transcription factor. Activates the epsilon- and gamma-globin gene promoters and, to a much lower degree, the beta-globin gene and represses promoters containing SP1-like binding sites inhibiting cell growth (By similarity). Represses transcription of SMAD7 which enhances TGF-beta signaling. Induces apoptosis., [UniProtKB, PubMed, UniProtKB, PubMed]", "predicted_glycosites": 2, "predicted_n_glycosites": 0, "predicted_o_glycosites": 2, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q8BHJ1;Q8BI37;Q8BI70", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0000976 transcription cis-regulatory region binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005925 focal adhesion;GO:0016604 nuclear body", "go_biological_process": "GO:1990859 cellular response to endothelin;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0008285 negative regulation of cell population proliferation", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "Q8K1S5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O88986-1", "uniprot_id": "KBL_MOUSE", "mass": 44931.0, "length": 416, "protein_name": "2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial", "gene_name": "Gcat", "organism": "Mouse", "refseq_name": "2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial isoform a", "refseq_ac": "NP_038875", "gene_names_uniprotkb": "Gcat; Kbl", "gene_names_refseq": "Gcat; Kbl", "protein_names_uniprotkb": "2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial; 2.3.1.29; AKB ligase; Aminoacetone synthase; Glycine acetyltransferase", "protein_names_refseq": "2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial isoform a; 2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial; AKB ligase; aminoacetone synthase; glycine acetyltransferase", "tax_id": 10090, "disease": "", "pathway": " (mmu:26912)", "pathway_count": 1, "publication_count": 8, "publication_id_list": "10712613;17688197;21750661;23576753;23806337;29323231;34428180;37507081", "class_list": "", "function": "Nuclear translocation of 2-amino-3-ketobutyrate coenzyme A ligase (KBL) was detected in response to cold and osmotic stresses., [RefSeq, PubMed]; Pyridoxal phosphate (PLP) dependent enzyme, which catalyzes the cleavage of 2-amino-3-oxobutanoate to glycine and acetyl-CoA. Catalyzes the second reaction step on the main metabolic degradation pathway for L-threonine., [UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "2.3.1.29", "go_molecular_function": "GO:0030170 pyridoxal phosphate binding;GO:0008890 glycine C-acetyltransferase activity;GO:0003870 5-aminolevulinate synthase activity;GO:0016746 acyltransferase activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0016607 nuclear speck", "go_biological_process": "GO:0019518 L-threonine catabolic process to glycine;GO:0006567 L-threonine catabolic process", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "O88986-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P05132-1", "uniprot_id": "KAPCA_MOUSE", "mass": 40571.0, "length": 351, "protein_name": "cAMP-dependent protein kinase catalytic subunit alpha", "gene_name": "Prkaca", "organism": "Mouse", "refseq_name": "cAMP-dependent protein kinase catalytic subunit alpha isoform 2", "refseq_ac": "NP_001264827", "gene_names_uniprotkb": "Prkaca; Pkaca", "gene_names_refseq": "PKCD; Pkaca; Prkaca", "protein_names_uniprotkb": "cAMP-dependent protein kinase catalytic subunit alpha; 2.7.11.11; PKA C-alpha", "protein_names_refseq": "PKA C-alpha; cAMP-dependent protein kinase catalytic subunit alpha isoform 2; sperm cAMP-dependent protein kinase catalytic subunit", "tax_id": 10090, "disease": "adrenal cortical adenoma (Disease Ontology:DOID:0050891); primary pigmented nodular adrenocortical disease 4 (Disease Ontology:DOID:0070549); alcohol use disorder (Disease Ontology:DOID:1574); brain ischemia (Disease Ontology:DOID:2316); fibrolamellar carcinoma (Disease Ontology:DOID:5015); congestive heart failure (Disease Ontology:DOID:6000); amphetamine abuse (Disease Ontology:DOID:670)", "pathway": " (mmu:18747); (R-MMU-163615); (R-MMU-164378); (R-MMU-180024); (R-MMU-2565942); (R-MMU-380259); (R-MMU-380270); (R-MMU-380284); (R-MMU-380320); (R-MMU-381676); (R-MMU-392517); (R-MMU-422356); (R-MMU-432040); (R-MMU-4420097); (R-MMU-442720); (R-MMU-512988); (R-MMU-5578775); (R-MMU-5610785); (R-MMU-5610787); (R-MMU-5620912); (R-MMU-5621575); (R-MMU-5687128); (R-MMU-8853659); (R-MMU-8854518); (R-MMU-8963896); (R-MMU-9634597); (R-MMU-983231); (R-MMU-9837999); (R-MMU-9856530)", "pathway_count": 29, "publication_count": 41, "publication_id_list": "10805756;10982398;11141074;11875122;14705934;14757059;15340140;16611981;17889648;17932298;18367160;1862342;19122195;19223768;19560455;19748511;20173027;20890288;21866565;22323819;25428507;26495903;27105888;27802388;28011936;2833513;31131693;33300544;33886552;34428180;3456589;35984892;37507081;37828378;39138140;39927985;8395513;8443157;9109651;9261084;9707564", "class_list": "", "function": "Calpha(2) null males are infertile despite normal mating behavior, [RefSeq, PubMed]; Phosphorylates a large number of substrates in the cytoplasm and the nucleus (By similarity). Phosphorylates CDC25B, ABL1, NFKB1, CLDN3, histone H1.4 (H1-4), PSMC5/RPT6, PJA2, RYR2, RORA, SLC6A6, SOX9, UHRF1 and VASP (PubMed:10805756, PubMed:19223768). Regulates the abundance of compartmentalized pools of its regulatory subunits through phosphorylation of PJA2 which binds and ubiquitinates these subunits, leading to their subsequent proteolysis (By similarity). RORA is activated by phosphorylation. Required for glucose-mediated adipogenic differentiation increase and osteogenic differentiation inhibition from osteoblasts (By similarity). Involved in chondrogenesis by mediating phosphorylation of SOX9 (PubMed:10805756). Involved in the regulation of platelets in response to thrombin and collagen; maintains circulating platelets in a resting state by phosphorylating proteins in numerous platelet inhibitory pathways when in complex with NF-kappa-B (NFKB1 and NFKB2) and I-kappa-B-alpha (NFKBIA), but thrombin and collagen disrupt these complexes and free active PRKACA stimulates platelets and leads to platelet aggregation by phosphorylating VASP. RYR2 channel activity is potentiated by phosphorylation in presence of luminal Ca(2+), leading to reduced amplitude and increased frequency of store overload-induced Ca(2+) release (SOICR) characterized by an increased rate of Ca(2+) release and propagation velocity of spontaneous Ca(2+) waves, despite reduced wave amplitude and resting cytosolic Ca(2+). PSMC5/RPT6 activation by phosphorylation stimulates proteasome. Negatively regulates tight junctions (TJs) in ovarian cancer cells via CLDN3 phosphorylation. NFKB1 phosphorylation promotes NF-kappa-B p50-p50 DNA binding. Acts as a key inhibitor of smoothened signaling pathway by mediating phosphorylation of GLI (GLI1, GLI2 and GLI3) transcription factors in absence of hedgehog (DHH, IHH or SHH) morphogens: GLI phosphorylation promotes their processing and prevents transcriptional activation of smoothened target genes (PubMed:33886552). GLI transcription factor phosphorylation is inhibited by interaction of PRKACA with SMO which sequesters PRKACA at the cell membrane (PubMed:33886552, PubMed:39138140). Also inhibits the smoothened signaling pathway in embryonic development by catalyzing phosphorylation of OFD1 in ciliogenesis (By similarity). Prevents meiosis resumption in prophase-arrested oocytes via CDC25B inactivation by phosphorylation (PubMed:19223768). May also regulate rapid eye movement (REM) sleep in the pedunculopontine tegmental (PPT) (By similarity). Phosphorylates APOBEC3G and AICDA. Phosphorylates HSF1; this phosphorylation promotes HSF1 nuclear localization and transcriptional activity upon heat shock (By similarity). Acts as a negative regulator of mTORC1 by mediating phosphorylation of RPTOR (By similarity). Phosphorylates AKAP19 (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed, UniProtKB, PubMed, PubMed, PubMed]; Phosphorylates and activates ABL1 in sperm flagellum to promote spermatozoa capacitation., [UniProtKB, PubMed, PubMed]; This gene encodes a member of the serine/threonine protein kinase family. The holoenzyme, protein kinase A (also known as cyclic-AMP dependent protein kinase), mediates cellular response to changes in cyclic-AMP levels. This gene encodes the alpha catalytic subunit of protein kinase A. Protein kinase A-mediated signaling is transduced via phosphorylation of target proteins, and is important for many cellular functions, including mammalian sperm maturation and motility. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been defined on the X chromosome. [provided by RefSeq, Apr 2013]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 8, "reported_mutagensis": 7, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 7, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q9JID0", "ec_number_list": "2.7.11.1;2.7.11.25;3.1.4.-;3.1.4.53;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;2.7.11.10;2.7.11.11;3.6.5.-;3.6.4.10;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.10.1;7.6.2.1;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;3.6.5.2;1.14.13.39;2.7.11.39;2.3.1.-;2.7.11.31;7.2.2.10;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0019870 potassium channel inhibitor activity;GO:0000287 magnesium ion binding;GO:0004672 protein kinase activity;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005739 mitochondrion", "go_biological_process": "GO:0038110 interleukin-2-mediated signaling pathway;GO:0043457 regulation of cellular respiration;GO:0070417 cellular response to cold;GO:1904539 negative regulation of glycolytic process through fructose-6-phosphate;GO:0006397 mRNA processing", "synthesized_glycan_count": 0, "hit_score": 4.4, "record_id": "P05132-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P16054-1", "uniprot_id": "KPCE_MOUSE", "mass": 83561.0, "length": 737, "protein_name": "Protein kinase C epsilon type", "gene_name": "Prkce", "organism": "Mouse", "refseq_name": "protein kinase C epsilon type", "refseq_ac": "NP_035234", "gene_names_uniprotkb": "Prkce; Pkcea; Pkce", "gene_names_refseq": "5830406C15Rik; PKC[e]; PKCepsilon; Pkce; Prkce", "protein_names_uniprotkb": "Protein kinase C epsilon type; 2.7.11.13; nPKC-epsilon", "protein_names_refseq": "PCK epsilon; nPKC-epsilon; protein kinase C epsilon type", "tax_id": 10090, "disease": "hypertension (Disease Ontology:DOID:10763); alcohol use disorder (Disease Ontology:DOID:1574); type 2 diabetes mellitus (Disease Ontology:DOID:9352)", "pathway": " (mmu:18754); (R-MMU-114508); (R-MMU-1250196); (R-MMU-1489509); (R-MMU-2029485)", "pathway_count": 5, "publication_count": 27, "publication_id_list": "11062054;11746497;12407104;15345747;15548766;15949469;16270034;16445938;16757566;17611075;18237277;18566587;18604201;19954762;21183079;2917656;31219806;31657718;33300544;33850054;34428180;35820727;37336688;37828378;38497285;38656553;9467942", "class_list": "", "function": "Brain-specific serine/threonine-protein kinase 1 is a substrate of protein kinase C epsilon involved in sex-specific ethanol and anxiety phenotypes., [RefSeq, PubMed]; Calcium-independent, phospholipid- and diacylglycerol (DAG)-dependent serine/threonine-protein kinase that plays essential roles in the regulation of multiple cellular processes linked to cytoskeletal proteins, such as cell adhesion, motility, migration and cell cycle, functions in neuron growth and ion channel regulation, and is involved in immune response, cancer cell invasion and regulation of apoptosis. Mediates cell adhesion to the extracellular matrix via integrin-dependent signaling, by mediating angiotensin-2-induced activation of integrin beta-1 (ITGB1) in cardiac fibroblasts. Phosphorylates MARCKS, which phosphorylates and activates PTK2/FAK, leading to the spread of cardiomyocytes. Involved in the control of the directional transport of ITGB1 in mesenchymal cells by phosphorylating vimentin (VIM), an intermediate filament (IF) protein. In epithelial cells, associates with and phosphorylates keratin-8 (KRT8), which induces targeting of desmoplakin at desmosomes and regulates cell-cell contact. Phosphorylates IQGAP1, which binds to CDC42, mediating epithelial cell-cell detachment prior to migration. During cytokinesis, forms a complex with YWHAB, which is crucial for daughter cell separation, and facilitates abscission by a mechanism which may implicate the regulation of RHOA. In cardiac myocytes, regulates myofilament function and excitation coupling at the Z-lines, where it is indirectly associated with F-actin via interaction with COPB1. During endothelin-induced cardiomyocyte hypertrophy, mediates activation of PTK2/FAK, which is critical for cardiomyocyte survival and regulation of sarcomere length. Plays a role in the pathogenesis of dilated cardiomyopathy via persistent phosphorylation of troponin I (TNNI3). Involved in nerve growth factor (NFG)-induced neurite outgrowth and neuron morphological change independently of its kinase activity, by inhibition of RHOA pathway, activation of CDC42 and cytoskeletal rearrangement. May be involved in presynaptic facilitation by mediating phorbol ester-induced synaptic potentiation. Phosphorylates gamma-aminobutyric acid receptor subunit gamma-2 (GABRG2), which reduces the response of GABA receptors to ethanol and benzodiazepines and may mediate acute tolerance to the intoxicating effects of ethanol. Upon PMA treatment, phosphorylates the capsaicin- and heat-activated cation channel TRPV1, which is required for bradykinin-induced sensitization of the heat response in nociceptive neurons. Is able to form a complex with PDLIM5 and N-type calcium channel, and may enhance channel activities and potentiates fast synaptic transmission by phosphorylating the pore-forming alpha subunit CACNA1B (CaV2.2). Downstream of TLR4, plays an important role in the lipopolysaccharide (LPS)-induced immune response by phosphorylating and activating TICAM2/TRAM, which in turn activates the transcription factor IRF3 and subsequent cytokines production. In differentiating erythroid progenitors, is regulated by EPO and controls the protection against the TNFSF10/TRAIL-mediated apoptosis, via BCL2. May be involved in the regulation of the insulin-induced phosphorylation and activation of AKT1. Phosphorylates NLRP5/MATER and may thereby modulate AKT pathway activation in cumulus cells (By similarity). Phosphorylates and activates LRRK1, which phosphorylates RAB proteins involved in intracellular trafficking (By similarity)., [UniProtKB, PubMed, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed]; Hepatocyte NLRP3 interacts with PKCepsilon to drive hepatic insulin resistance and steatosis., [RefSeq, PubMed]; The binding of PKCepsilon and MEG2 to STAT3 regulates IL-6-mediated microglial hyperalgesia during inflammatory pain., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 18, "reported_mutagensis": 5, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;2.7.11.39;2.3.1.-;2.7.11.31;3.6.5.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0004699 diacylglycerol-dependent, calcium-independent serine/threonine kinase activity;GO:0003785 actin monomer binding;GO:0004672 protein kinase activity;GO:0004674 protein serine/threonine kinase activity;GO:0005102 signaling receptor binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0000139 Golgi membrane;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005739 mitochondrion", "go_biological_process": "GO:0051562 negative regulation of mitochondrial calcium ion concentration;GO:0035669 TRAM-dependent toll-like receptor 4 signaling pathway;GO:0051280 negative regulation of release of sequestered calcium ion into cytosol;GO:0006468 protein phosphorylation;GO:0007155 cell adhesion", "synthesized_glycan_count": 0, "hit_score": 3.0, "record_id": "P16054-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3UXZ9-1", "uniprot_id": "KDM5A_MOUSE", "mass": 192216.0, "length": 1690, "protein_name": "Lysine-specific demethylase 5A", "gene_name": "Kdm5a", "organism": "Mouse", "refseq_name": "lysine-specific demethylase 5A", "refseq_ac": "NP_666109", "gene_names_uniprotkb": "Kdm5a; Jarid1a; Rbp2", "gene_names_refseq": "Jarid1a; Kdm5a; RBP2; Rbbp2", "protein_names_uniprotkb": "Lysine-specific demethylase 5A; 1.14.11.67; Histone demethylase JARID1A; Jumonji/ARID domain-containing protein 1A; RBBP-2; Retinoblastoma-binding protein 2; [histone H3]-trimethyl-L-lysine(4) demethylase 5A", "protein_names_refseq": "RBBP-2; [histone H3]-trimethyl-L-lysine(4) demethylase 5A; histone demethylase JARID1A; jumonji, AT rich interactive domain 1A (Rbp2 like); jumonji/ARID domain-containing protein 1A; lysine (K)-specific demethylase 5A; lysine-specific demethylase 5A; retinoblastoma binding protein 2", "tax_id": 10090, "disease": "syndromic intellectual disability (Disease Ontology:DOID:0050888); autism spectrum disorder (Disease Ontology:DOID:0060041); syndromic X-linked intellectual disability Claes-Jensen type (Disease Ontology:DOID:0060809); prostate cancer (Disease Ontology:DOID:10283); intellectual disability (Disease Ontology:DOID:1059); cryptorchidism (Disease Ontology:DOID:11383); alcohol use disorder (Disease Ontology:DOID:1574); breast cancer (Disease Ontology:DOID:1612); lung non-small cell carcinoma (Disease Ontology:DOID:3908); stomach carcinoma (Disease Ontology:DOID:5517); ankylosing spondylitis (Disease Ontology:DOID:7147); alopecia areata (Disease Ontology:DOID:986)", "pathway": " (mmu:214899); (R-MMU-3214842)", "pathway_count": 2, "publication_count": 10, "publication_id_list": "15081428;17320161;17320163;19144319;20064375;21183079;21750661;21960634;31219806;34428180", "class_list": "", "function": "Histone demethylase that specifically demethylates 'Lys-4' of histone H3, thereby playing a central role in histone code. Does not demethylate histone H3 'Lys-9', H3 'Lys-27', H3 'Lys-36', H3 'Lys-79' or H4 'Lys-20'. Demethylates trimethylated and dimethylated but not monomethylated H3 'Lys-4' (PubMed:17320161, PubMed:17320163). Regulates specific gene transcription through DNA-binding on 5'-CCGCCC-3' motif. May stimulate transcription mediated by nuclear receptors. Involved in transcriptional regulation of Hox proteins during cell differentiation (By similarity). May participate in transcriptional repression of cytokines such as CXCL12. Plays a role in the regulation of the circadian rhythm and in maintaining the normal periodicity of the circadian clock. In a histone demethylase-independent manner, acts as a coactivator of the CLOCK-BMAL1-mediated transcriptional activation of PER1/2 and other clock-controlled genes and increases histone acetylation at PER1/2 promoters by inhibiting the activity of HDAC1 (PubMed:21960634). Seems to act as a transcriptional corepressor for some genes such as MT1F and to favor the proliferation of cancer cells (By similarity)., [UniProtKB, PubMed, PubMed, UniProtKB, PubMed]; Mutation can downregulate cardiac cell proliferation by repressing cyclin D1 expression in the same way as jumonji, [RefSeq, PubMed]; Study reports that RBP2 is a demethylase that specifically catalyzes demethylation on histone H3 lysine 4, whose methylation is normally associated with transcriptionally active genes., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 12, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 12, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3TM94;Q3UMI5;Q66JZ3", "ec_number_list": "1.14.11.67", "go_molecular_function": "GO:0034647 histone H3K4me/H3K4me2/H3K4me3 demethylase activity;GO:0032453 histone H3K4 demethylase activity;GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0003713 transcription coactivator activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0016604 nuclear body;GO:0000785 chromatin", "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006338 chromatin remodeling;GO:0007283 spermatogenesis;GO:0006355 regulation of DNA-templated transcription;GO:0008584 male gonad development", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q3UXZ9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q80Y84-1", "uniprot_id": "KDM5B_MOUSE", "mass": 175555.0, "length": 1544, "protein_name": "Lysine-specific demethylase 5B", "gene_name": "Kdm5b", "organism": "Mouse", "refseq_name": "lysine-specific demethylase 5B", "refseq_ac": "NP_690855", "gene_names_uniprotkb": "Kdm5b; Jarid1b; Kiaa4034; Plu1", "gene_names_refseq": "2010009J12Rik; 2210016I17Rik; D1Ertd202e; Jarid1b; Kdm5b; PLU-1; PUT1; Plu1; RBBP2H1A; Rb-Bp2; mKIAA4034", "protein_names_uniprotkb": "Lysine-specific demethylase 5B; 1.14.11.67; Histone demethylase JARID1B; Jumonji/ARID domain-containing protein 1B; PLU-1; [histone H3]-trimethyl-L-lysine(4) demethylase 5B", "protein_names_refseq": "[histone H3]-trimethyl-L-lysine(4) demethylase 5B; histone demethylase JARID1B; jumonji, AT rich interactive domain 1B (Rbp2 like); jumonji/ARID domain-containing protein 1B; lysine (K)-specific demethylase 5B; lysine-specific demethylase 5B; putative DNA/chromatin binding motif 1", "tax_id": 10090, "disease": "syndromic intellectual disability (Disease Ontology:DOID:0050888); autism spectrum disorder (Disease Ontology:DOID:0060041); syndromic X-linked intellectual disability Claes-Jensen type (Disease Ontology:DOID:0060809); autosomal recessive intellectual developmental disorder 65 (Disease Ontology:DOID:0081226); prostate cancer (Disease Ontology:DOID:10283); intellectual disability (Disease Ontology:DOID:1059); urinary bladder cancer (Disease Ontology:DOID:11054); alcohol use disorder (Disease Ontology:DOID:1574); breast cancer (Disease Ontology:DOID:1612); high grade glioma (Disease Ontology:DOID:3070); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); uveal melanoma (Disease Ontology:DOID:6039)", "pathway": " (mmu:75605); (R-MMU-3214842); (R-MMU-8866911)", "pathway_count": 3, "publication_count": 17, "publication_id_list": "10.1101/2023.09.13.557529;12237901;14516692;14579128;15201984;17310255;17320160;21369698;21960634;22872234;23806337;24802759;30084848;30409806;34203471;34428180;38575342", "class_list": "", "function": "Histone demethylase that demethylates 'Lys-4' of histone H3, thereby playing a central role in histone code. Does not demethylate histone H3 'Lys-9' or H3 'Lys-27'. Demethylates trimethylated, dimethylated and monomethylated H3 'Lys-4'. Acts as a transcriptional corepressor for FOXG1B and PAX9. Represses the CLOCK-BMAL1 heterodimer-mediated transcriptional activation of the core clock component PER2., [UniProtKB, PubMed, PubMed, PubMed]; Mechanistically, JARID1B was required for GATA3 recruitment to the Foxa1 promoter to activate Foxa1 expression., [RefSeq, PubMed]; PLU-1/JARID1B/KDM5B is required for embryonic survival and contributes to cell proliferation in the mammary gland and in ER+ breast cancer cells., [RefSeq, PubMed]; Regions upstream of the promoter repress transcription more effectively in a non-malignant breast cell line as compared to breast cancer cell lines., [RefSeq, PubMed]; The Intellectual Disability Risk Gene Kdm5b Regulates Long-Term Memory Consolidation in the Hippocampus. Publication Status: Online-Only, [RefSeq, PubMed]; This gene encodes a lysine-specific histone demethylase that belongs to the jumonji/ARID domain-containing family of histone demethylases. The encoded protein is capable of demethylating tri-, di- and monomethylated lysine 4 of histone H3. This protein plays a role in the transcriptional repression or certain tumor suppressor genes and is upregulated in certain cancer cells. This protein may also play a role in genome stability and DNA repair. Homozygous mutant mice display decreased body weight, decreased female fertility, lower uterine weight, and a delay in mammary development. Knockout of this gene has also been associated with embryonic lethality. [provided by RefSeq, Dec 2016]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 3, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 12, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q5DTR9;Q8BLU1;Q8JZL8", "ec_number_list": "1.14.11.67", "go_molecular_function": "GO:0034647 histone H3K4me/H3K4me2/H3K4me3 demethylase activity;GO:0032453 histone H3K4 demethylase activity;GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0003714 transcription corepressor activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0000785 chromatin;GO:1990904 ribonucleoprotein complex", "go_biological_process": "GO:2000864 regulation of estradiol secretion;GO:0006338 chromatin remodeling;GO:0006351 DNA-templated transcription;GO:0010628 positive regulation of gene expression;GO:0006355 regulation of DNA-templated transcription", "synthesized_glycan_count": 0, "hit_score": 2.0, "record_id": "Q80Y84-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BZ03-1", "uniprot_id": "KPCD2_MOUSE", "mass": 96542.0, "length": 875, "protein_name": "Serine/threonine-protein kinase D2", "gene_name": "Prkd2", "organism": "Mouse", "refseq_name": "serine/threonine-protein kinase D2", "refseq_ac": "NP_001239387", "gene_names_uniprotkb": "Prkd2", "gene_names_refseq": "PKD2; Prkd2", "protein_names_uniprotkb": "Serine/threonine-protein kinase D2; 2.7.11.13; nPKC-D2", "protein_names_refseq": "nPKC-D2; serine/threonine-protein kinase D2", "tax_id": 10090, "disease": "candidiasis (Disease Ontology:DOID:1508)", "pathway": " (mmu:101540)", "pathway_count": 1, "publication_count": 6, "publication_id_list": "17226786;17242355;20819079;21183079;34428180;37730136", "class_list": "", "function": "Data demonstrate that, unlike PKD1, PKD2 catalytic activity is dispensable for normal embryogenesis., [RefSeq, PubMed]; PKD2, like PKD, facilitates mitogenesis in 3T3 cells, [RefSeq, PubMed]; Protein kinase D2 confers neuroprotection by promoting AKT and CREB activation in ischemic stroke., [RefSeq, PubMed]; Serine/threonine-protein kinase that converts transient diacylglycerol (DAG) signals into prolonged physiological effects downstream of PKC, and is involved in the regulation of cell proliferation via MAPK1/3 (ERK1/2) signaling, oxidative stress-induced NF-kappa-B activation, inhibition of HDAC7 transcriptional repression, signaling downstream of T-cell antigen receptor (TCR) and cytokine production, and plays a role in Golgi membrane trafficking, angiogenesis, secretory granule release and cell adhesion (PubMed:17226786, PubMed:20819079). May potentiate mitogenesis induced by the neuropeptide bombesin by mediating an increase in the duration of MAPK1/3 (ERK1/2) signaling, which leads to accumulation of immediate-early gene products including FOS that stimulate cell cycle progression (PubMed:17226786). In response to oxidative stress, is phosphorylated at Tyr-438 and Tyr-718 by ABL1, which leads to the activation of PRKD2 without increasing its catalytic activity, and mediates activation of NF-kappa-B (By similarity). In response to the activation of the gastrin receptor CCKBR, is phosphorylated at Ser-244 by CSNK1D and CSNK1E, translocates to the nucleus, phosphorylates HDAC7, leading to nuclear export of HDAC7 and inhibition of HDAC7 transcriptional repression of NR4A1/NUR77 (By similarity). Upon TCR stimulation, is activated independently of ZAP70, translocates from the cytoplasm to the nucleus and is required for interleukin-2 (IL2) promoter up-regulation. During adaptive immune responses, is required in peripheral T-lymphocytes for the production of the effector cytokines IL2 and IFNG after TCR engagement and for optimal induction of antibody responses to antigens (PubMed:20819079). In epithelial cells stimulated with lysophosphatidic acid (LPA), is activated through a PKC-dependent pathway and mediates LPA-stimulated interleukin-8 (IL8) secretion via a NF-kappa-B-dependent pathway (By similarity). During TCR-induced T-cell activation, interacts with and is activated by the tyrosine kinase LCK, which results in the activation of the NFAT transcription factors (By similarity). In the trans-Golgi network (TGN), regulates the fission of transport vesicles that are on their way to the plasma membrane and in polarized cells is involved in the transport of proteins from the TGN to the basolateral membrane (By similarity). Plays an important role in endothelial cell proliferation and migration prior to angiogenesis, partly through modulation of the expression of KDR/VEGFR2 and FGFR1, two key growth factor receptors involved in angiogenesis (By similarity). In secretory pathway, is required for the release of chromogranin-A (CHGA)-containing secretory granules from the TGN (By similarity). Downstream of PRKCA, plays important roles in angiotensin-2-induced monocyte adhesion to endothelial cells (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 21, "reported_mutagensis": 2, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3TCE5;Q3TDF0;Q3U4V4", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;2.7.11.39;2.3.1.-;2.7.11.31;3.6.5.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0004672 protein kinase activity;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0008270 zinc ion binding;GO:0005080 protein kinase C binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0005829 cytosol", "go_biological_process": "GO:0070232 regulation of T cell apoptotic process;GO:2001028 positive regulation of endothelial cell chemotaxis;GO:0001525 angiogenesis;GO:0006468 protein phosphorylation;GO:0007155 cell adhesion", "synthesized_glycan_count": 0, "hit_score": 0.7, "record_id": "Q8BZ03-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q922U2-1", "uniprot_id": "K2C5_MOUSE", "mass": 61767.0, "length": 580, "protein_name": "Keratin, type II cytoskeletal 5", "gene_name": "Krt5", "organism": "Mouse", "refseq_name": "keratin, type II cytoskeletal 5", "refseq_ac": "NP_081287", "gene_names_uniprotkb": "Krt5; Krt2-5", "gene_names_refseq": "3300001P10Rik; CK5; K5; Krt2-5; Krt5; Tfip8", "protein_names_uniprotkb": "Keratin, type II cytoskeletal 5; CK-5; Cytokeratin-5; K5; Keratin-5; Type-II keratin Kb5", "protein_names_refseq": "58 kDa cytokeratin; cytokeratin 5; keratin complex 2, basic, gene 5; keratin, type II cytoskeletal 5; tuftelin interacting protein 8; type-II keratin Kb5", "tax_id": 10090, "disease": "Dowling-Degos disease (Disease Ontology:DOID:0060256); generalized severe epidermolysis bullosa simplex 1A (Disease Ontology:DOID:0060735); epidermolysis bullosa simplex 2F with mottled pigmentation (Disease Ontology:DOID:0111346); urinary bladder cancer (Disease Ontology:DOID:11054); epidermolysis bullosa simplex (Disease Ontology:DOID:4644)", "pathway": " (mmu:110308); (R-MMU-446107); (R-MMU-6805567); (R-MMU-6809371)", "pathway_count": 4, "publication_count": 17, "publication_id_list": "11408584;12657653;18285451;18299400;19267394;21183079;22645316;24129315;24751727;24940650;26758872;29518391;32758484;34428180;34887587;36288343;39627609", "class_list": "", "function": "Structural component of intermediate filaments in basal keratinocytes of stratified epithelia (PubMed:11408584). Together with its obligate type I partner KRT14, contributes to the formation of the keratin intermediate filament network that provides mechanical stability and resilience to the basal layer of the epidermis (PubMed:11408584). Regulates the recruitment of Langerhans cells to the epidermis, potentially by modulation of the abundance of macrophage chemotactic cytokines, macrophage inflammatory cytokines and CTNND1 localization in keratinocytes (PubMed:19267394)., [UniProtKB, PubMed, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 15, "reported_mutagensis": 4, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 5, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q920F2;Q9CRS6", "ec_number_list": "", "go_molecular_function": "GO:0097110 scaffold protein binding;GO:0030280 structural constituent of skin epidermis", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005886 plasma membrane;GO:0005882 intermediate filament;GO:0001533 cornified envelope", "go_biological_process": "GO:0031424 keratinization;GO:0009612 response to mechanical stimulus;GO:0032880 regulation of protein localization;GO:0030334 regulation of cell migration;GO:0045109 intermediate filament organization", "synthesized_glycan_count": 0, "hit_score": 2.1, "record_id": "Q922U2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9DBS5-1", "uniprot_id": "KLC4_MOUSE", "mass": 68613.0, "length": 619, "protein_name": "Kinesin light chain 4", "gene_name": "Klc4", "organism": "Mouse", "refseq_name": "kinesin light chain 4 isoform 1", "refseq_ac": "NP_083367", "gene_names_uniprotkb": "Klc4; Knsl8", "gene_names_refseq": "1200014P03Rik; Klc4; Knsl8", "protein_names_uniprotkb": "Kinesin light chain 4; KLC 4; Kinesin-like protein 8", "protein_names_refseq": "KLC 4; kinesin light chain 4 isoform 1; kinesin-like 8; kinesin-like protein 8", "tax_id": 10090, "disease": "Alzheimer's disease 1 (Disease Ontology:DOID:0080348)", "pathway": " (mmu:74764); (R-MMU-2132295); (R-MMU-5625970); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 5, "publication_count": 9, "publication_id_list": "15345747;17242355;18630941;21183079;26495903;30084848;31219806;34428180;36210013", "class_list": "", "function": "Kinesin is a microtubule-associated force-producing protein that may play a role in organelle transport. The light chain may function in coupling of cargo to the heavy chain or in the modulation of its ATPase activity (By similarity)., [UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 6, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3TCC5", "ec_number_list": "", "go_molecular_function": "GO:0019894 kinesin binding", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005874 microtubule;GO:0035253 ciliary rootlet;GO:0005871 kinesin complex;GO:0043005 neuron projection", "go_biological_process": "GO:0008088 axo-dendritic transport;GO:0007018 microtubule-based movement", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "Q9DBS5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9ET77-1", "uniprot_id": "JPH3_MOUSE", "mass": 81229.0, "length": 744, "protein_name": "Junctophilin-3", "gene_name": "Jph3", "organism": "Mouse", "refseq_name": "junctophilin-3", "refseq_ac": "NP_065630", "gene_names_uniprotkb": "Jph3; Jp3", "gene_names_refseq": "JP-3; Jp3; Jph3", "protein_names_uniprotkb": "Junctophilin-3; JP-3; Junctophilin type 3", "protein_names_refseq": "junctophilin type 3; junctophilin-3", "tax_id": 10090, "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); Huntington's disease-like 2 (Disease Ontology:DOID:0090104)", "pathway": " (mmu:57340)", "pathway_count": 1, "publication_count": 9, "publication_id_list": "10949023;11906164;16452087;16809425;17904530;21183079;27336719;31219806;31461656", "class_list": "", "function": "Gene expression was slightly altered in the JP-3 and JP-4 Knockout cerebellum., [RefSeq, PubMed]; Junctophilin Proteins Tether a Cav1-RyR2-KCa3.1 Tripartite Complex to Regulate Neuronal Excitability., [RefSeq, PubMed]; Junctophilins contribute to the formation of junctional membrane complexes (JMCs) which link the plasma membrane with the endoplasmic or sarcoplasmic reticulum in excitable cells. Provides a structural foundation for functional cross-talk between the cell surface and intracellular calcium release channels. JPH3 is brain-specific and appears to have an active role in certain neurons involved in motor coordination and memory., [UniProtKB, PubMed, PubMed]; Motor discoordination in mutant mice lacking junctophilin type 3, [RefSeq, PubMed]; The expression of JPH isoforms was examined in human and mouse pancreatic tissues, and JPH3 expression was found in both the beta cells. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 8, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3ZAS3;Q8BNM7;Q9EQZ2", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005886 plasma membrane;GO:0016020 membrane;GO:0005789 endoplasmic reticulum membrane;GO:0030314 junctional membrane complex", "go_biological_process": "GO:0007612 learning;GO:0007613 memory;GO:0050885 neuromuscular process controlling balance;GO:0035640 exploration behavior;GO:0048167 regulation of synaptic plasticity", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "Q9ET77-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9WTP6-1", "uniprot_id": "KAD2_MOUSE", "mass": 26469.0, "length": 239, "protein_name": "Adenylate kinase 2, mitochondrial", "gene_name": "Ak2", "organism": "Mouse", "refseq_name": "adenylate kinase 2, mitochondrial isoform a", "refseq_ac": "NP_001029138", "gene_names_uniprotkb": "Ak2", "gene_names_refseq": "Ak-2; Ak2; D4Ertd220e", "protein_names_uniprotkb": "Adenylate kinase 2, mitochondrial; 2.7.4.3; AK 2; ATP-AMP transphosphorylase 2; ATP:AMP phosphotransferase; Adenylate monophosphate kinase", "protein_names_refseq": "AK 2; ATP-AMP transphosphorylase 2; ATP:AMP phosphotransferase; adenylate kinase 2, mitochondrial isoform a; adenylate kinase 2, mitochondrial; adenylate monophosphate kinase", "tax_id": 10090, "disease": "reticular dysgenesis (Disease Ontology:DOID:0060020); temporal lobe epilepsy (Disease Ontology:DOID:3328)", "pathway": " (mmu:11637); (R-MMU-499943)", "pathway_count": 2, "publication_count": 18, "publication_id_list": "19043416;21183079;21750661;22645316;23576753;23806337;24788674;28135057;28528544;31219806;31780678;33571905;34428180;35585049;36210013;36288343;36804949;37507081", "class_list": "", "function": "AK2 is an AMP-sensing negative regulator of BRAF in tumorigenesis. Publication Status: Online-Only, [RefSeq, PubMed]; Adenylate kinase AK2 isoform integral in embryo and adult heart homeostasis., [RefSeq, PubMed]; Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism. Adenylate kinase activity is critical for regulation of the phosphate utilization and the AMP de novo biosynthesis pathways. Plays a key role in hematopoiesis., [UniProtKB, HAMAP]; Prognostic and therapeutic potential of Adenylate kinase 2 in lung adenocarcinoma. Publication Status: Online-Only, [RefSeq, PubMed]; The association of ODF4 with AK1 and AK2 in mice is essential for fertility through its contribution to flagellar shape. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "A2A820;Q3THT3;Q3TI11;Q3TKI6;Q8C7I9;Q9CY37", "ec_number_list": "2.7.4.6;2.7.4.4;2.7.4.3;2.7.4.14", "go_molecular_function": "GO:0004017 AMP kinase activity;GO:0005524 ATP binding;GO:0019205 nucleobase-containing compound kinase activity", "go_cellular_component": "GO:0097226 sperm mitochondrial sheath;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0005758 mitochondrial intermembrane space", "go_biological_process": "GO:0006172 ADP biosynthetic process;GO:0046033 AMP metabolic process;GO:0046034 ATP metabolic process;GO:0006139 nucleobase-containing compound metabolic process", "synthesized_glycan_count": 0, "hit_score": 2.1, "record_id": "Q9WTP6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9WU01-1", "uniprot_id": "KHDR2_MOUSE", "mass": 38866.0, "length": 349, "protein_name": "KH domain-containing, RNA-binding, signal transduction-associated protein 2", "gene_name": "Khdrbs2", "organism": "Mouse", "refseq_name": "KH domain-containing, RNA-binding, signal transduction-associated protein 2", "refseq_ac": "NP_573498", "gene_names_uniprotkb": "Khdrbs2; Slm1", "gene_names_refseq": "6330586C16Rik; Khdrbs2; Slim1; Slm-1; Slm1; TG-RP135; Tg(LRRK2*R1441G)135Cjli; mSLM-1", "protein_names_uniprotkb": "KH domain-containing, RNA-binding, signal transduction-associated protein 2; SLM-1; Sam68-like mammalian protein 1; mSLM-1", "protein_names_refseq": "KH domain-containing, RNA-binding, signal transduction-associated protein 2; LRRK2; Sam68-like mammalian protein 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:170771); (R-MMU-8849468)", "pathway_count": 2, "publication_count": 8, "publication_id_list": "10077576;12397030;15471878;21540332;21750661;22196734;24129315;24469635", "class_list": "", "function": "Expression of active BRK/Sik results in increased SLM-1 and SLM-2 phosphorylation which has functional relevance and leads to inhibition of their RNA-binding, [RefSeq, PubMed]; RNA-binding protein that plays a role in the regulation of alternative splicing and influences mRNA splice site selection and exon inclusion (By similarity). Binds both poly(A) and poly(U) homopolymers. Phosphorylation by PTK6 inhibits its RNA-binding ability. Induces an increased concentration-dependent incorporation of exon in CD44 pre-mRNA by direct binding to purine-rich exonic enhancer (By similarity). Can regulate alternative splicing of neurexins NRXN1-3 in the laminin G-like domain 6 containing the evolutionary conserved neurexin alternative spliced segment 4 (AS4) involved in neurexin selective targeting to postsynaptic partners. Regulates cell-type specific alternative splicing of NRXN1 at AS4 and acts synergystically with SAM68 in exon skipping. In contrast acts antagonistically with SAM68 in NRXN3 exon skipping at AS4 (PubMed:22196734, PubMed:24469635). Its phosphorylation by FYN inhibits its ability to regulate splice site selection (By similarity). May function as an adapter protein for Src kinases during mitosis (PubMed:10077576)., [UniProtKB, PubMed, PubMed, PubMed, UniProtKB, PubMed]; SLIM1 localizes in an integrin-dependent manner to the nucleus and focal adhesions where it functions downstream of integrin activation to promote cell spreading and migration., [RefSeq, PubMed]; The protein encoded by this gene is similar to the src associated in mitosis, 68 kDa protein, which is an RNA-binding protein and a substrate for Src-family tyrosine kinases during mitosis. This protein has a KH RNA-binding motif and proline-rich motifs which may be SH2 and SH3 domain binding sites. A similar rat protein is an RNA-binding protein which is tyrosine phosphorylated by Src during mitosis. These studies also suggest that the rat protein may function as an adaptor protein for Src by binding the SH2 and SH3 domains of various other proteins. [provided by RefSeq, Jul 2008]., [RefSeq]", "predicted_glycosites": 3, "predicted_n_glycosites": 0, "predicted_o_glycosites": 3, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "Q6NXZ3", "ec_number_list": "", "go_molecular_function": "GO:0003729 mRNA binding;GO:0017124 SH3 domain binding;GO:0042169 SH2 domain binding;GO:0008143 poly(A) binding;GO:0008266 poly(U) RNA binding", "go_cellular_component": "GO:0005634 nucleus", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006397 mRNA processing;GO:0048024 regulation of mRNA splicing, via spliceosome;GO:0000381 regulation of alternative mRNA splicing, via spliceosome", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q9WU01-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A2APT9-1", "uniprot_id": "KLD7A_MOUSE", "mass": 83590.0, "length": 773, "protein_name": "Kelch domain-containing protein 7A", "gene_name": "Klhdc7a", "organism": "Mouse", "refseq_name": "kelch domain-containing protein 7A", "refseq_ac": "NP_775603", "gene_names_uniprotkb": "Klhdc7a", "gene_names_refseq": "B230308G19Rik; Klhdc7a", "protein_names_uniprotkb": "Kelch domain-containing protein 7A", "protein_names_refseq": "kelch domain-containing protein 7A; novel kelch domain containing protein", "tax_id": 10090, "disease": "", "pathway": " (mmu:242721)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "17242355;21183079;30084848;34428180;39145457", "class_list": "", "function": "", "predicted_glycosites": 3, "predicted_n_glycosites": 2, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "Q80SV4;Q8C706", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0016020 membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.6, "record_id": "A2APT9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P28738-1", "uniprot_id": "KIF5C_MOUSE", "mass": 109275.0, "length": 956, "protein_name": "Kinesin heavy chain isoform 5C", "gene_name": "Kif5c", "organism": "Mouse", "refseq_name": "kinesin heavy chain isoform 5C", "refseq_ac": "NP_032475", "gene_names_uniprotkb": "Kif5c; Nkhc2", "gene_names_refseq": "KINN; Khc; Kif5c; NKHC2; NKHC", "protein_names_uniprotkb": "Kinesin heavy chain isoform 5C; 3.6.4.-; Kinesin heavy chain neuron-specific 2; Kinesin-1", "protein_names_refseq": "kinesin heavy chain isoform 5C; kinesin heavy chain member 5C; kinesin heavy chain neuron-specific 2; kinesin-1", "tax_id": 10090, "disease": "complex cortical dysplasia with other brain malformations 2 (Disease Ontology:DOID:0090133); Alzheimer's disease 3 (Disease Ontology:DOID:0110042); spinal muscular atrophy (Disease Ontology:DOID:12377); leiomyoma (Disease Ontology:DOID:127); neurodegenerative disease (Disease Ontology:DOID:1289); motor neuron disease (Disease Ontology:DOID:231); hereditary spastic paraplegia (Disease Ontology:DOID:2476); schizophrenia (Disease Ontology:DOID:5419)", "pathway": " (mmu:16574)", "pathway_count": 1, "publication_count": 12, "publication_id_list": "10.1101/2023.09.13.557529;11986669;12106288;15286375;19608740;21183079;21750661;21976701;27669760;34372599;34966180;9782088", "class_list": "", "function": "Deletion of Kif5c Does Not Alter Prion Disease Tempo or Spread in Mouse Brain. Publication Status: Online-Only, [RefSeq, PubMed]; KIF5C deficiency causes abnormal cortical neuronal migration, dendritic branching, and spine morphology in mice., [RefSeq, PubMed]; Microtubule-associated force-producing protein that may play a role in organelle transport. Has ATPase activity (By similarity). Involved in synaptic transmission (By similarity). Mediates dendritic trafficking of mRNAs (PubMed:19608740). Required for anterograde axonal transportation of MAPK8IP3/JIP3 which is essential for MAPK8IP3/JIP3 function in axon elongation (By similarity)., [UniProtKB, UniProtKB, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 8, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q6NXI9;Q9Z2F8", "ec_number_list": "3.6.4.13;3.6.4.10;3.6.4.-;5.6.2.3;5.6.2.4;2.3.2.-;2.3.2.27;3.1.13.1;5.6.2.6;3.1.-.-;7.6.2.1;3.6.1.5;3.4.24.-;3.6.-.-;3.1.3.1;3.9.1.1;3.6.1.-;5.6.2.5;4.2.99.18;3.6.4.12;5.6.1.6;3.6.4.6;3.6.5.-;3.6.1.15;3.1.4.-;5.6.2.-;7.2.2.-;7.6.2.16;3.4.21.53;2.7.7.7;2.7.7.49;2.7.11.1;2.7.4.3", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0034190 apolipoprotein receptor binding;GO:0003777 microtubule motor activity", "go_cellular_component": "GO:0098982 GABA-ergic synapse;GO:0005737 cytoplasm;GO:0005874 microtubule;GO:0035253 ciliary rootlet;GO:0043025 neuronal cell body", "go_biological_process": "GO:0099641 anterograde axonal protein transport;GO:0007411 axon guidance;GO:0098971 anterograde dendritic transport of neurotransmitter receptor complex;GO:0008045 motor neuron axon guidance;GO:0008298 intracellular mRNA localization", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "P28738-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VBY2-1", "uniprot_id": "KKCC1_MOUSE", "mass": 55838.0, "length": 505, "protein_name": "Calcium/calmodulin-dependent protein kinase kinase 1", "gene_name": "Camkk1", "organism": "Mouse", "refseq_name": "calcium/calmodulin-dependent protein kinase kinase 1", "refseq_ac": "NP_061371", "gene_names_uniprotkb": "Camkk1; Camkk", "gene_names_refseq": "CaMKKalpha; Camkk1; Camkk; caM-KK 1; caM-KK alpha; caMKK 1; caMKK alpha", "protein_names_uniprotkb": "Calcium/calmodulin-dependent protein kinase kinase 1; 2.7.11.17; CaM-KK 1; CaM-KK alpha; CaM-kinase IV kinase; CaM-kinase kinase 1; CaM-kinase kinase alpha; CaMKK 1; CaMKK alpha; Calcium/calmodulin-dependent protein kinase kinase alpha", "protein_names_refseq": "caM-kinase IV kinase; caM-kinase kinase 1; caM-kinase kinase alpha; calcium calmodulin dependent protein kinase kinase alpha; calcium/calmodulin-dependent protein kinase kinase 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:55984); (R-MMU-111932); (R-MMU-442729); (R-MMU-9619229)", "pathway_count": 4, "publication_count": 15, "publication_id_list": "10560916;12637513;12654522;15150258;17015467;17114649;21183079;21750661;22872234;24101676;24129315;25159322;26772170;30084848;30779550", "class_list": "", "function": "CaCaMKKalpha stimulates glucose uptake additively with insulin, and in insulin-resistant muscle, and alters the phosphorylation of TBC1D1/TBC1D4., [RefSeq, PubMed]; Calcium/calmodulin-dependent protein kinase that belongs to a proposed calcium-triggered signaling cascade involved in a number of cellular processes. Phosphorylates CAMK1, CAMK1D, CAMK1G and CAMK4. Involved in regulating cell apoptosis. Promotes cell survival by phosphorylating AKT1/PKB that inhibits pro-apoptotic BAD/Bcl2-antagonist of cell death., [UniProtKB, PubMed]; Data (including data from knockout mice) suggest that up-regulation of Camkk1 and calcium signaling stimulates muscle growth via up-regulation of mTORC1 (mammalian target of rapamycin complex 1) signaling and muscle protein biosynthesis., [RefSeq, PubMed]; ERK activation and neurite outgrowth in response to depolarization are mediated by CaMKK activation of CaMKI, [RefSeq, PubMed]; The CaMKK-CaMKIalpha cascade is required for the axonal growth effect of Wnt5a during neuronal polarization. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 7, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q9R054", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;2.7.11.39;2.3.1.-;2.7.11.31;3.6.5.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0005516 calmodulin binding;GO:0005524 ATP binding;GO:0004683 calcium/calmodulin-dependent protein kinase activity;GO:0106310 protein serine kinase activity", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol", "go_biological_process": "GO:0035556 intracellular signal transduction;GO:0045860 positive regulation of protein kinase activity;GO:0032147 activation of protein kinase activity", "synthesized_glycan_count": 0, "hit_score": 1.6, "record_id": "Q8VBY2-1", "record_type": "protein" }, { "uniprot_canonical_ac": "B7ZNG0-1", "uniprot_id": "KIF7_MOUSE", "mass": 151624.0, "length": 1348, "protein_name": "Kinesin-like protein KIF7", "gene_name": "Kif7", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Kif7", "gene_names_refseq": "", "protein_names_uniprotkb": "Kinesin-like protein KIF7", "protein_names_refseq": "", "tax_id": 10090, "disease": "hydrolethalus syndrome (Disease Ontology:DOID:0050779); idiopathic scoliosis (Disease Ontology:DOID:0060250); ciliopathy (Disease Ontology:DOID:0060340); hydrolethalus syndrome 2 (Disease Ontology:DOID:0111356); congenital diaphragmatic hernia (Disease Ontology:DOID:3827); acrocallosal syndrome (Disease Ontology:DOID:9250); cleft lip (Disease Ontology:DOID:9296)", "pathway": " (mmu:16576); (R-MMU-5610787); (R-MMU-5632684)", "pathway_count": 3, "publication_count": 14, "publication_id_list": "19549984;19592253;19666503;20485683;21183079;21633164;21750661;21795282;23034632;24952464;25644602;27195754;31219806;36852467", "class_list": "", "function": "Essential for hedgehog signaling regulation: acts both as a negative and a positive regulator of sonic hedgehog (Shh) and Indian hedgehog (Ihh) pathways, acting downstream of SMO, through both SUFU-dependent and -independent mechanisms. Involved in the regulation of microtubular dynamics. Required for proper organization of the ciliary tip and control of ciliary localization of SUFU-GLI2 complexes. Required for localization of GLI3 to cilia in response to Shh. Negatively regulates Shh signaling by preventing inappropriate activation of the transcriptional activator GLI2 in the absence of ligand. Positively regulates Shh signaling by preventing the processing of the transcription factor GLI3 into its repressor form. In keratinocytes, promotes the dissociation of SUFU-GLI2 complexes, GLI2 nuclear translocation and Shh signaling activation. Involved in the regulation of epidermal differentiation and chondrocyte development., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 1, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 7, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "B2RUB1", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0042802 identical protein binding;GO:0016887 ATP hydrolysis activity;GO:0003777 microtubule motor activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005874 microtubule;GO:0005929 cilium;GO:0001650 fibrillar center", "go_biological_process": "GO:0045880 positive regulation of smoothened signaling pathway;GO:0007018 microtubule-based movement;GO:0035904 aorta development;GO:0060976 coronary vasculature development;GO:0003279 cardiac septum development", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "B7ZNG0-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P12849-1", "uniprot_id": "KAP1_MOUSE", "mass": 43224.0, "length": 381, "protein_name": "cAMP-dependent protein kinase type I-beta regulatory subunit", "gene_name": "Prkar1b", "organism": "Mouse", "refseq_name": "cAMP-dependent protein kinase type I-beta regulatory subunit isoform a", "refseq_ac": "NP_001240819", "gene_names_uniprotkb": "Prkar1b", "gene_names_refseq": "Prkar1b; RIbeta", "protein_names_uniprotkb": "cAMP-dependent protein kinase type I-beta regulatory subunit", "protein_names_refseq": "cAMP-dependent protein kinase type I-beta regulatory subunit isoform a; cAMP-dependent protein kinase type I-beta regulatory subunit", "tax_id": 10090, "disease": "", "pathway": " (mmu:19085); (R-MMU-163615); (R-MMU-164378); (R-MMU-180024); (R-MMU-432040); (R-MMU-442720); (R-MMU-5610787); (R-MMU-9634597); (R-MMU-983231); (R-MMU-9856530)", "pathway_count": 10, "publication_count": 9, "publication_id_list": "21183079;21750661;24129315;25605945;27357676;30541888;3375237;34428180;35984892", "class_list": "", "function": "EZH2 ensures normal cortical differentiation by repression of phosphodiesterases PDE1B, 3A, and 7A and of PRKAR1B., [RefSeq, PubMed]; Regulatory subunit of the cAMP-dependent protein kinases involved in cAMP signaling in cells., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0034236 protein kinase A catalytic subunit binding;GO:0004862 cAMP-dependent protein kinase inhibitor activity;GO:0008603 cAMP-dependent protein kinase regulator activity;GO:0030552 cAMP binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0045202 synapse", "go_biological_process": "GO:0006468 protein phosphorylation;GO:0007189 adenylate cyclase-activating G protein-coupled receptor signaling pathway;GO:0007611 learning or memory;GO:1900273 positive regulation of long-term synaptic potentiation;GO:2000463 positive regulation of excitatory postsynaptic potential", "synthesized_glycan_count": 0, "hit_score": 1.0, "record_id": "P12849-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E9PVX6-1", "uniprot_id": "KI67_MOUSE", "mass": 350864.0, "length": 3177, "protein_name": "Proliferation marker protein Ki-67", "gene_name": "Mki67", "organism": "Mouse", "refseq_name": "proliferation marker protein Ki-67", "refseq_ac": "NP_001074586", "gene_names_uniprotkb": "Mki67", "gene_names_refseq": "D630048A14Rik; Ki-67; Ki67; Mki67", "protein_names_uniprotkb": "Proliferation marker protein Ki-67; Antigen KI-67 homolog; Antigen Ki67 homolog; Antigen identified by monoclonal antibody Ki-67 homolog", "protein_names_refseq": "antigen KI-67 homolog; antigen Ki67 homolog; antigen identified by monoclonal antibody Ki-67 homolog; proliferation marker protein Ki-67", "tax_id": 10090, "disease": "diffuse large B-cell lymphoma (Disease Ontology:DOID:0050745); mucositis (Disease Ontology:DOID:0080178); graft-versus-host disease (Disease Ontology:DOID:0081267); prostate carcinoma (Disease Ontology:DOID:10286); stomach cancer (Disease Ontology:DOID:10534); urinary bladder cancer (Disease Ontology:DOID:11054); neutropenia (Disease Ontology:DOID:1227); leiomyoma (Disease Ontology:DOID:127); lung cancer (Disease Ontology:DOID:1324); interstitial cystitis (Disease Ontology:DOID:13949); alcohol use disorder (Disease Ontology:DOID:1574); breast cancer (Disease Ontology:DOID:1612); pancreatic cancer (Disease Ontology:DOID:1793); colon cancer (Disease Ontology:DOID:219); high grade glioma (Disease Ontology:DOID:3070); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung adenocarcinoma (Disease Ontology:DOID:3910); cholangiocarcinoma (Disease Ontology:DOID:4947); adult pineal parenchymal tumor (Disease Ontology:DOID:5031); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); kidney disease (Disease Ontology:DOID:557); hepatoblastoma (Disease Ontology:DOID:687); in situ carcinoma (Disease Ontology:DOID:8719); Crohn's disease (Disease Ontology:DOID:8778); psoriasis (Disease Ontology:DOID:8893); systemic lupus erythematosus (Disease Ontology:DOID:9074); Barrett's esophagus (Disease Ontology:DOID:9206); colorectal cancer (Disease Ontology:DOID:9256); type 2 diabetes mellitus (Disease Ontology:DOID:9352)", "pathway": " (mmu:17345)", "pathway_count": 1, "publication_count": 18, "publication_id_list": "12355204;19144319;21183079;21750661;22645316;23806337;25428506;26495903;26949251;27362226;30779550;34428180;34887587;35820727;36852467;39003739;39627609;8834799", "class_list": "", "function": "Protein that associates with the surface of mitotic chromosomes and acts both as a chromosome repellent during early mitosis and chromosome attractant during late mitosis (PubMed:27362226). Required to maintain individual mitotic chromosomes dispersed in the cytoplasm following nuclear envelope disassembly (PubMed:27362226). During early mitosis, relocalizes from nucleoli to the chromosome surface where it forms extended brush structures that cover a substantial fraction of the chromosome surface (PubMed:27362226). The MKI67 brush structure prevents chromosomes from collapsing into a single chromatin mass by forming a steric and electrostatic charge barrier: the protein has a high net electrical charge and acts as a surfactant, dispersing chromosomes and enabling independent chromosome motility (PubMed:27362226). During mitotic anaphase, the MKI67 brush structure collapses and MKI67 switches from a chromosome repellent to a chromosome attractant to promote chromosome clustering and facilitate the exclusion of large cytoplasmic particles from the future nuclear space (By similarity). Mechanistically, dephosphorylation during mitotic exit and simultaneous exposure of a conserved basic patch induce the RNA-dependent formation of a liquid-like condensed phase on the chromosome surface, promoting coalescence of neighboring chromosome surfaces and clustering of chromosomes (By similarity). Binds premature ribosomal RNAs during anaphase; promoting liquid-liquid phase separation. Binds DNA, with a preference for supercoiled DNA and AT-rich DNA (By similarity). Does not contribute to the internal structure of mitotic chromosomes (PubMed:26949251). May play a role in chromatin organization; it is however unclear whether it plays a direct role in chromatin organization or whether it is an indirect consequence of its function in mitotic chromosome (PubMed:26949251)., [UniProtKB, UniProtKB, PubMed, PubMed]", "predicted_glycosites": 3, "predicted_n_glycosites": 0, "predicted_o_glycosites": 3, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 95, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 3, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 29, "glyco_site_count": 5, "binding_glycan_count": 0, "secondary_ac_list": "Q61769;Q7TSF6", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0003723 RNA binding;GO:0005524 ATP binding;GO:0140693 molecular condensate scaffold activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0000775 chromosome, centromeric region", "go_biological_process": "GO:0072574 hepatocyte proliferation;GO:0007059 chromosome segregation;GO:0008283 cell population proliferation;GO:0007088 regulation of mitotic nuclear division;GO:0051321 meiotic cell cycle", "synthesized_glycan_count": 0, "hit_score": 2.2, "record_id": "E9PVX6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O08550-1", "uniprot_id": "KMT2B_MOUSE", "mass": 294821.0, "length": 2713, "protein_name": "Histone-lysine N-methyltransferase 2B", "gene_name": "Kmt2b", "organism": "Mouse", "refseq_name": "histone-lysine N-methyltransferase 2B isoform 2", "refseq_ac": "NP_083550", "gene_names_uniprotkb": "Kmt2b; Mll2; Trx2; Wbp7", "gene_names_refseq": "2610014H22Rik; Kmt2b; Mll2; Wbp7; mKIAA0304", "protein_names_uniprotkb": "Histone-lysine N-methyltransferase 2B; 2.1.1.364; Lysine N-methyltransferase 2B; Myeloid/lymphoid or mixed-lineage leukemia protein 4 homolog; Trithorax homolog 2; WBP-7; WW domain-binding protein 7", "protein_names_refseq": "WBP-7; WW domain binding protein 7; histone-lysine N-methyltransferase 2B isoform 2; histone-lysine N-methyltransferase 2B; histone-lysine N-methyltransferase MLL4; lysine N-methyltransferase 2B; mixed lineage leukemia 2; myeloid/lymphoid or mixed-lineage leukemia protein 4 homolog; trithorax homolog 2", "tax_id": 10090, "disease": "colorectal adenocarcinoma (Disease Ontology:DOID:0050861); dystonia 28, childhood-onset (Disease Ontology:DOID:0060936); autosomal dominant intellectual developmental disorder 68 (Disease Ontology:DOID:0061041); prostate cancer (Disease Ontology:DOID:10283); breast cancer (Disease Ontology:DOID:1612); congenital heart disease (Disease Ontology:DOID:1682); hepatocellular carcinoma (Disease Ontology:DOID:684)", "pathway": " (mmu:75410); (R-MMU-201722); (R-MMU-3214841); (R-MMU-8936459); (R-MMU-9772755)", "pathway_count": 5, "publication_count": 9, "publication_id_list": "17242355;20808952;21183079;21750661;22872234;31219806;35820727;36852467;9171351", "class_list": "", "function": "Histone methyltransferase that catalyzes methyl group transfer from S-adenosyl-L-methionine to the epsilon-amino group of 'Lys-4' of histone H3 (H3K4) via a non-processive mechanism. Part of chromatin remodeling machinery predominantly forms H3K4me1 and H3K4me2 methylation marks at active chromatin sites where transcription and DNA repair take place (By similarity). Likely plays a redundant role with KMT2C in enriching H3K4me1 marks on primed and active enhancer elements (By similarity). Plays a central role in beta-globin locus transcription regulation by being recruited by NFE2 (By similarity). Plays an important role in controlling bulk H3K4me during oocyte growth and preimplantation development (PubMed:20808952). Required during the transcriptionally active period of oocyte growth for the establishment and/or maintenance of bulk H3K4 trimethylation (H3K4me3), global transcriptional silencing that preceeds resumption of meiosis, oocyte survival and normal zygotic genome activation (PubMed:20808952)., [UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 6, "predicted_n_glycosites": 0, "predicted_o_glycosites": 6, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 17, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 4, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 7, "glyco_site_count": 7, "binding_glycan_count": 0, "secondary_ac_list": "E9QKF4;Q5NU09", "ec_number_list": "2.3.1.48;2.3.1.-;2.1.1.364;2.1.1.-;2.1.1.370;2.1.1.371;3.4.25.-;2.1.1.85;2.1.1.359;2.1.1.355;2.1.1.354;2.1.1.362;2.1.1.361;2.3.1.57;2.1.1.319", "go_molecular_function": "GO:0008270 zinc ion binding;GO:0042800 histone H3K4 methyltransferase activity;GO:0045322 unmethylated CpG binding;GO:0140945 histone H3K4 monomethyltransferase activity;GO:0003677 DNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol;GO:0035097 histone methyltransferase complex;GO:0044665 MLL1/2 complex", "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0045893 positive regulation of DNA-templated transcription;GO:0032259 methylation;GO:0006346 DNA methylation-dependent constitutive heterochromatin formation;GO:0006355 regulation of DNA-templated transcription", "synthesized_glycan_count": 0, "hit_score": 1.2, "record_id": "O08550-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P28740-3", "uniprot_id": "KIF2A_MOUSE", "mass": 79756.0, "length": 705, "protein_name": "Kinesin-like protein KIF2A", "gene_name": "Kif2a", "organism": "Mouse", "refseq_name": "kinesin-like protein KIF2A isoform 2", "refseq_ac": "NP_001139251", "gene_names_uniprotkb": "Kif2a; Kif2; Kns2", "gene_names_refseq": "C530030B14Rik; Kif2a; Kif2; Kns2; M-kinesin", "protein_names_uniprotkb": "Kinesin-like protein KIF2A; Kinesin-2", "protein_names_refseq": "kinesin heavy chain member 2; kinesin-2; kinesin-like protein KIF2A isoform 2; kinesin-like protein KIF2A", "tax_id": 10090, "disease": "complex cortical dysplasia with other brain malformations 3 (Disease Ontology:DOID:0090134)", "pathway": " (mmu:16563); (R-MMU-141430); (R-MMU-141444); (R-MMU-2132295); (R-MMU-2467813); (R-MMU-2500257); (R-MMU-5663220); (R-MMU-6811434); (R-MMU-68877); (R-MMU-9648025); (R-MMU-983189)", "pathway_count": 11, "publication_count": 12, "publication_id_list": "10.1101/2023.09.13.557529;12887924;1447303;15345747;21183079;23806337;24339785;25428506;34428180;36343267;39627609;9774330", "class_list": "", "function": "KIF2A deficiency causes early-onset neurodegeneration., [RefSeq, PubMed]; Plus end-directed microtubule-dependent motor required for normal brain development. May regulate microtubule dynamics during axonal growth. Required for normal progression through mitosis. Required for normal congress of chromosomes at the metaphase plate. Required for normal spindle dynamics during mitosis. Promotes spindle turnover. Implicated in formation of bipolar mitotic spindles. Has microtubule depolymerization activity (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 6, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 1, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "O54744;Q91W03", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0003777 microtubule motor activity;GO:0120283 protein serine/threonine kinase binding", "go_cellular_component": "GO:0097227 sperm annulus;GO:0098982 GABA-ergic synapse;GO:0000922 spindle pole;GO:0005654 nucleoplasm;GO:0005730 nucleolus", "go_biological_process": "GO:0007399 nervous system development;GO:0030154 cell differentiation;GO:0051301 cell division;GO:0090307 mitotic spindle assembly;GO:0030334 regulation of cell migration", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "P28740-3", "record_type": "protein" }, { "uniprot_canonical_ac": "P33174-1", "uniprot_id": "KIF4_MOUSE", "mass": 139519.0, "length": 1231, "protein_name": "Chromosome-associated kinesin KIF4", "gene_name": "Kif4", "organism": "Mouse", "refseq_name": "chromosome-associated kinesin KIF4", "refseq_ac": "NP_032472", "gene_names_uniprotkb": "Kif4; Kif4a; Kns4", "gene_names_refseq": "D330050K22Rik; Kif4; Kns4", "protein_names_uniprotkb": "Chromosome-associated kinesin KIF4; Chromokinesin", "protein_names_refseq": "N-5 kinesin; chromokinesin; chromosome-associated kinesin KIF4; kinesin heavy chain member 4", "tax_id": 10090, "disease": "non-syndromic X-linked intellectual disability 100 (Disease Ontology:DOID:0112040); epilepsy (Disease Ontology:DOID:1826)", "pathway": " (mmu:16571); (R-MMU-2132295); (R-MMU-437239); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 5, "publication_count": 13, "publication_id_list": "1447303;17242355;21183079;28125646;28528544;31486502;34887587;35579738;35820727;36482480;39627609;40021952;7929562", "class_list": "", "function": "CircKIF4A enhances osteosarcoma proliferation and metastasis by sponging MiR-515-5p and upregulating SLC7A11., [RefSeq, PubMed]; Iron-sulfur (Fe-S) cluster binding motor protein that has a role in chromosome segregation during mitosis (By similarity). Required for mitotic chromosomal positioning and bipolar spindle stabilization., [UniProtKB, PubMed, UniProtKB]; KIF4 regulates neuronal morphology and seizure susceptibility via the PARP1 signaling pathway., [RefSeq, PubMed]; Whole genome expression microarray reveals novel roles for Kif4 in monocyte/macrophage cells., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 7, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 2, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q80YP3", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0046872 metal ion binding;GO:0003777 microtubule motor activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol;GO:0005874 microtubule;GO:0005875 microtubule associated complex;GO:0030496 midbody", "go_biological_process": "GO:0000281 mitotic cytokinesis;GO:0007018 microtubule-based movement;GO:0007052 mitotic spindle organization;GO:0051256 mitotic spindle midzone assembly;GO:0051231 spindle elongation", "synthesized_glycan_count": 0, "hit_score": 1.6, "record_id": "P33174-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q5SXA9-1", "uniprot_id": "KIBRA_MOUSE", "mass": 124110.0, "length": 1104, "protein_name": "Protein KIBRA", "gene_name": "Wwc1", "organism": "Mouse", "refseq_name": "protein KIBRA", "refseq_ac": "NP_740749", "gene_names_uniprotkb": "Wwc1; Kiaa0869", "gene_names_refseq": "Kibra; Wwc1", "protein_names_uniprotkb": "Protein KIBRA; KIBRA; Kidney and brain protein; WW domain-containing protein 1", "protein_names_refseq": "WW domain-containing protein 1; kidney and brain protein; protein KIBRA; protein WWC1", "tax_id": 10090, "disease": "", "pathway": " (mmu:211652); (R-MMU-2028269)", "pathway_count": 2, "publication_count": 12, "publication_id_list": "17242355;18190796;19129633;21183079;21233212;21943600;25428506;31599954;31730661;34428180;38906255;38924398", "class_list": "", "function": "KIBRA anchoring the action of PKMzeta maintains the persistence of memory., [RefSeq, PubMed]; KIBRA associates with and activates Lats (large tumor suppressor) 1 and 2 kinases by stimulating their phosphorylation on the hydrophobic motif, [RefSeq, PubMed]; KIBRA functions in memory performance via interaction with PKMzeta., [RefSeq, PubMed]; Regulator of the Hippo signaling pathway, also known as the Salvador-Warts-Hippo (SWH) pathway. Enhances phosphorylation of LATS1 and YAP1 and negatively regulates cell proliferation and organ growth due to a suppression of the transcriptional activity of YAP1, the major effector of the Hippo pathway. Along with NF2 can synergistically induce the phosphorylation of LATS1 and LATS2 and function in the regulation of Hippo signaling pathway. Acts as a transcriptional coactivator of ESR1 which plays an essential role in DYNLL1-mediated ESR1 transactivation. Modulates directional migration of podocytes. May be associated with memory performance (By similarity). Regulates collagen-stimulated activation of the ERK/MAPK cascade (PubMed:18190796). Plays an important role in regulating AMPA-selective glutamate receptors (AMPARs) trafficking (PubMed:21943600, PubMed:31730661)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed]; WWC1 upregulation accelerates hyperuricemia by reduction in renal uric acid excretion through Hippo signaling pathway., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 11, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q571D0;Q8K1Y3;Q8VD17;Q922W3", "ec_number_list": "", "go_molecular_function": "GO:0060090 molecular adaptor activity;GO:0003713 transcription coactivator activity;GO:0030674 protein-macromolecule adaptor activity;GO:0019900 kinase binding;GO:0035591 signaling adaptor activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0048471 perinuclear region of cytoplasm;GO:0032587 ruffle membrane", "go_biological_process": "GO:0046621 negative regulation of organ growth;GO:0035330 regulation of hippo signaling;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0008285 negative regulation of cell population proliferation", "synthesized_glycan_count": 0, "hit_score": 1.3, "record_id": "Q5SXA9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q61771-1", "uniprot_id": "KIF3B_MOUSE", "mass": 85288.0, "length": 747, "protein_name": "Kinesin-like protein KIF3B", "gene_name": "Kif3b", "organism": "Mouse", "refseq_name": "kinesin-like protein KIF3B", "refseq_ac": "NP_032470", "gene_names_uniprotkb": "Kif3b", "gene_names_refseq": "Kif3b; mKIAA0359", "protein_names_uniprotkb": "Kinesin-like protein KIF3B; Microtubule plus end-directed kinesin motor 3B", "protein_names_refseq": "kinesin-like protein KIF3B; microtubule plus end-directed kinesin motor 3B", "tax_id": 10090, "disease": "chromosome 16p11.2 deletion syndrome, 593-kb (Disease Ontology:DOID:0070515); retinitis pigmentosa 89 (Disease Ontology:DOID:0112146); schizophrenia (Disease Ontology:DOID:5419)", "pathway": " (mmu:16569); (R-MMU-2132295); (R-MMU-5620924); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 5, "publication_count": 11, "publication_id_list": "10.1101/2023.09.13.557529;12821668;25243405;31746486;33300544;33852848;34428180;36220081;7559760;8710890;9865700", "class_list": "", "function": "Betaine ameliorates schizophrenic traits by functionally compensating for KIF3-based CRMP2 transport., [RefSeq, PubMed]; KIF3B promotes a PI3K signaling gradient causing changes in a Shh protein gradient and suppressing polydactyly in mice., [RefSeq, PubMed]; Kif3b mutation reduces NMDAR subunit NR2A trafficking and causes schizophrenia-like phenotypes., [RefSeq, PubMed]; Microtubule-based molecular motor that transport intracellular cargos, such as vesicles, organelles and protein complexes. Uses ATP hydrolysis to generate force to bind and move along the microtubule (PubMed:7559760). Plays a role in cilia formation (PubMed:9865700). Involved in photoreceptor integrity and opsin trafficking in rod photoreceptors (By similarity). Transports vesicles containing N-methyl-D-aspartate (NMDA) receptor subunit GRIN2A into neuronal dendrites (PubMed:31746486)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 3, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q3UFZ8;Q8BNH4", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0031267 small GTPase binding;GO:0003777 microtubule motor activity", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0005874 microtubule", "go_biological_process": "GO:0090307 mitotic spindle assembly;GO:0060271 cilium assembly;GO:0016192 vesicle-mediated transport;GO:0007018 microtubule-based movement;GO:0042073 intraciliary transport", "synthesized_glycan_count": 0, "hit_score": 1.6, "record_id": "Q61771-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6ZQ58-1", "uniprot_id": "LARP1_MOUSE", "mass": 121125.0, "length": 1072, "protein_name": "La-related protein 1", "gene_name": "Larp1", "organism": "Mouse", "refseq_name": "la-related protein 1", "refseq_ac": "NP_082727", "gene_names_uniprotkb": "Larp1; Kiaa0731; Larp", "gene_names_refseq": "1810024J12Rik; 3110040D16Rik; Larp1; Larp; mKIAA0731", "protein_names_uniprotkb": "La-related protein 1; La ribonucleoprotein domain family member 1", "protein_names_refseq": "La ribonucleoprotein domain family, member 1; la related protein; la-related protein 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:73158)", "pathway_count": 1, "publication_count": 23, "publication_id_list": "10878606;17242355;18630941;19131326;19144319;21183079;21750661;22645316;24129315;25153642;26495903;28135057;28528544;31219806;32782141;33483593;34428180;34887587;35716596;35863436;36852467;39627609;40885482", "class_list": "", "function": "Lysophosphatidic acid stimulates pericyte migration via LPA receptor 1., [RefSeq, PubMed]; RNA-binding protein that regulates the translation of specific target mRNA species downstream of the mTORC1 complex, in function of growth signals and nutrient availability. Interacts on the one hand with the 3' poly-A tails that are present in all mRNA molecules, and on the other hand with the 7-methylguanosine cap structure of mRNAs containing a 5' terminal oligopyrimidine (5'TOP) motif, which is present in mRNAs encoding ribosomal proteins and several components of the translation machinery. The interaction with the 5' end of mRNAs containing a 5'TOP motif leads to translational repression by preventing the binding of EIF4G1. When mTORC1 is activated, LARP1 is phosphorylated and dissociates from the 5' untranslated region (UTR) of mRNA. Does not prevent binding of EIF4G1 to mRNAs that lack a 5'TOP motif. Interacts with the free 40S ribosome subunit and with ribosomes, both monosomes and polysomes. Under normal nutrient availability, interacts primarily with the 3' untranslated region (UTR) of mRNAs encoding ribosomal proteins and increases protein synthesis. Associates with actively translating ribosomes and stimulates translation of mRNAs containing a 5'TOP motif, thereby regulating protein synthesis, and as a consequence, cell growth and proliferation. Stabilizes mRNAs species with a 5'TOP motif, which is required to prevent apoptosis., [UniProtKB, UniProtKB]; The RNA-binding protein LARP1 is dispensable for pancreatic beta-cell function and mass. Publication Status: Online-Only, [RefSeq, PubMed]; The amino acid sensor GCN2 suppresses terminal oligopyrimidine (TOP) mRNA translation via La-related protein 1 (LARP1)., [RefSeq, PubMed]", "predicted_glycosites": 4, "predicted_n_glycosites": 0, "predicted_o_glycosites": 4, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 3, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 3, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 3, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 39, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 7, "binding_glycan_count": 0, "secondary_ac_list": "A2AFQ8;J3QNB1;Q7TSF7", "ec_number_list": "", "go_molecular_function": "GO:0003723 RNA binding;GO:0043024 ribosomal small subunit binding;GO:0008190 eukaryotic initiation factor 4E binding;GO:0008494 translation activator activity;GO:0000340 RNA 7-methylguanosine cap binding", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0010494 cytoplasmic stress granule;GO:0031931 TORC1 complex", "go_biological_process": "GO:0072752 cellular response to rapamycin;GO:0008283 cell population proliferation;GO:0048255 mRNA stabilization;GO:0010608 post-transcriptional regulation of gene expression;GO:0006413 translational initiation", "synthesized_glycan_count": 0, "hit_score": 2.8, "record_id": "Q6ZQ58-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9QWT9-1", "uniprot_id": "KIFC1_MOUSE", "mass": 74153.0, "length": 674, "protein_name": "Kinesin-like protein KIFC1", "gene_name": "Kifc1", "organism": "Mouse", "refseq_name": "kinesin-like protein KIFC1 isoform 1", "refseq_ac": "NP_001182227", "gene_names_uniprotkb": "Kifc1; Kifc4; Kifc5a; Kifc5b", "gene_names_refseq": "100042970; Gm4137; HSET; KNSL2; Kifc1; Kifc5a; Knsl2a; Tctex-7A; Tctex-7; Tctex7a; Tctex7", "protein_names_uniprotkb": "Kinesin-like protein KIFC1", "protein_names_refseq": "kinesin family c-terminal 5A; kinesin motor protein KIFC4; kinesin-like 2a; kinesin-like protein KIFC1 isoform 1; kinesin-like protein KIFC1; kinesin-related protein KIFC5A", "tax_id": 10090, "disease": "", "pathway": " (mmu:100502766); (mmu:16580); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 4, "publication_count": 18, "publication_id_list": "10775188;16638812;17360972;18237440;20173027;21750661;22872234;23807208;25428506;30084848;30779550;31219806;31599954;34203471;35142352;35259401;9115736;9339368", "class_list": "", "function": "Kinesin motor KIFC1 is required for tubulin acetylation and actin-dependent spindle migration in mouse oocyte meiosis., [RefSeq, PubMed]; Kinesin-14 KIFC1 modulates spindle assembly and chromosome segregation in mouse spermatocytes., [RefSeq, PubMed]; Minus end-directed microtubule-dependent motor required for bipolar spindle formation (PubMed:16638812). May contribute to movement of early endocytic vesicles (PubMed:17360972). Regulates cilium formation and structure (PubMed:23807208)., [UniProtKB, PubMed, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "O08671;O35230;Q497Y3;Q4A1N2;Q6PG90;Q8BV06;Q99L84;Q9JKZ0", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0003777 microtubule motor activity;GO:0008569 minus-end-directed microtubule motor activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005769 early endosome;GO:0005874 microtubule;GO:0005871 kinesin complex", "go_biological_process": "GO:0072382 minus-end-directed vesicle transport along microtubule;GO:0051301 cell division;GO:0090307 mitotic spindle assembly;GO:0007018 microtubule-based movement;GO:0007080 mitotic metaphase chromosome alignment", "synthesized_glycan_count": 0, "hit_score": 1.9, "record_id": "Q9QWT9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q60749-1", "uniprot_id": "KHDR1_MOUSE", "mass": 48371.0, "length": 443, "protein_name": "KH domain-containing, RNA-binding, signal transduction-associated protein 1", "gene_name": "Khdrbs1", "organism": "Mouse", "refseq_name": "KH domain-containing, RNA-binding, signal transduction-associated protein 1", "refseq_ac": "NP_035447", "gene_names_uniprotkb": "Khdrbs1", "gene_names_refseq": "Khdrbs1; Sam68; p62; p68", "protein_names_uniprotkb": "KH domain-containing, RNA-binding, signal transduction-associated protein 1; GAP-associated tyrosine phosphoprotein p62; Sam68; Src-associated in mitosis 68 kDa protein; p21 Ras GTPase-activating protein-associated p62; p68", "protein_names_refseq": "GAP-associated tyrosine phosphoprotein p62; KH domain-containing, RNA-binding, signal transduction-associated protein 1; p21 Ras GTPase-activating protein-associated p62; src associated in mitosis, 68 kDa; src-associated in mitosis 68 kDa protein", "tax_id": 10090, "disease": "", "pathway": " (mmu:20218); (R-MMU-8849468)", "pathway_count": 2, "publication_count": 28, "publication_id_list": "10077576;12478298;12496368;12529443;19457263;22196734;23637638;23806337;24129315;24469635;24788674;25153642;25428506;28135057;28528544;29187734;31219806;33300544;34099657;34252225;34428180;34693458;36232770;37828378;7512695;7541765;7799925;9315629", "class_list": "", "function": "Ablation of Sam68 in adult mice increases thermogenesis and energy expenditure., [RefSeq, PubMed]; Hepatic Sam68 Regulates Systemic Glucose Homeostasis and Insulin Sensitivity. Publication Status: Online-Only, [RefSeq, PubMed]; Recruited and tyrosine phosphorylated by several receptor systems, for example the T-cell, leptin and insulin receptors. Once phosphorylated, functions as an adapter protein in signal transduction cascades by binding to SH2 and SH3 domain-containing proteins. Role in G2-M progression in the cell cycle. Represses CBP-dependent transcriptional activation apparently by competing with other nuclear factors for binding to CBP. Also acts as a putative regulator of mRNA stability and/or translation rates and mediates mRNA nuclear export. Positively regulates the association of constitutive transport element (CTE)-containing mRNA with large polyribosomes and translation initiation. May not be involved in the nucleocytoplasmic export of unspliced (CTE)-containing RNA species. RNA-binding protein that plays a role in the regulation of alternative splicing and influences mRNA splice site selection and exon inclusion. Binds to RNA containing 5'-[AU]UAA-3' as a bipartite motif spaced by more than 15 nucleotides. Binds poly(A). In cooperation with HNRNPA1 modulates alternative splicing of BCL2L1 by promoting splicing toward isoform Bcl-X(S), and of SMN1 (By similarity). Can regulate CD44 alternative splicing in a Ras pathway-dependent manner. Can regulate alternative splicing of NRXN1 and NRXN3 in the laminin G-like domain 6 containing the evolutionary conserved neurexin alternative spliced segment 4 (AS4) involved in neurexin selective targeting to postsynaptic partners. In a neuronal activity-dependent manner cooperates synergistically with KHDRBS2/SLIM-1 in regulation of NRXN1 exon skipping at AS4. The cooperation with KHDRBS2/SLIM-1 is antagonistic for regulation of NXRN3 alternative splicing at AS4 (PubMed:12478298, PubMed:22196734, PubMed:24469635)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, UniProtKB, PubMed]; Sam68 contributes to intestinal inflammation in experimental and human colitis., [RefSeq, PubMed]; Sam68 promotes hepatic gluconeogenesis via CRTC2. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 2, "predicted_n_glycosites": 0, "predicted_o_glycosites": 2, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 15, "reported_mutagensis": 4, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "A2ACH3;B2KG38;Q3U8T3;Q60735;Q7M4N5;Q99M33", "ec_number_list": "", "go_molecular_function": "GO:0003723 RNA binding;GO:0003729 mRNA binding;GO:0017124 SH3 domain binding;GO:0019904 protein domain specific binding;GO:0042802 identical protein binding", "go_cellular_component": "GO:0070618 Grb2-Sos complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0016020 membrane", "go_biological_process": "GO:0046833 positive regulation of RNA export from nucleus;GO:0046831 regulation of RNA export from nucleus;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006397 mRNA processing", "synthesized_glycan_count": 0, "hit_score": 3.1, "record_id": "Q60749-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7M6Z4-1", "uniprot_id": "KIF27_MOUSE", "mass": 158956.0, "length": 1394, "protein_name": "Kinesin-like protein KIF27", "gene_name": "Kif27", "organism": "Mouse", "refseq_name": "kinesin-like protein KIF27 isoform 1", "refseq_ac": "NP_780423", "gene_names_uniprotkb": "Kif27", "gene_names_refseq": "4930517I18Rik; Kif27", "protein_names_uniprotkb": "Kinesin-like protein KIF27", "protein_names_refseq": "kinesin-like protein KIF27 isoform 1; kinesin-like protein KIF27; kinesin-related protein KIF27", "tax_id": 10090, "disease": "hydrocephalus (Disease Ontology:DOID:10908)", "pathway": " (mmu:75050); (R-MMU-6811434); (R-MMU-983189)", "pathway_count": 3, "publication_count": 7, "publication_id_list": "12783626;17971504;19305393;21183079;21746835;21750661;29351996", "class_list": "", "function": "Congenital hydrocephalus, suppurative rhinosinusitis and otitis media in Kif27 null mice is indicative of primary ciliary dyskinesis, [RefSeq, PubMed]; Kif27 is most abundantly expressed in tissues rich in highly ciliated cells, such as olfactory sensory neurons, and is predicted to be important to cilia., [RefSeq, PubMed]; Plays an essential role in motile ciliogenesis., [UniProtKB, PubMed]; Slow processive KIF27 behavior arises from a slow adenosine triphosphatase rate and a high affinity for both adenosine triphosphate and microtubules., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 8, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q14AX5;Q8BMB9", "ec_number_list": "", "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0003777 microtubule motor activity", "go_cellular_component": "GO:0005576 extracellular region;GO:0005737 cytoplasm;GO:0005874 microtubule;GO:0005929 cilium;GO:0005871 kinesin complex", "go_biological_process": "GO:0003351 epithelial cilium movement involved in extracellular fluid movement;GO:0060271 cilium assembly;GO:0007018 microtubule-based movement;GO:0021591 ventricular system development", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q7M6Z4-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9Z1M7-1", "uniprot_id": "LARG1_MOUSE", "mass": 87964.0, "length": 756, "protein_name": "Xylosyl- and glucuronyltransferase LARGE1", "gene_name": "Large1", "organism": "Mouse", "refseq_name": "xylosyl- and glucuronyltransferase LARGE1 isoform 1", "refseq_ac": "NP_001304320", "gene_names_uniprotkb": "Large1; Kiaa0609; Large", "gene_names_refseq": "BPFD#36; Gyltl1a; Large1; Large; Mbp-1; Mbp1; enr; fg; froggy; myd", "protein_names_uniprotkb": "Xylosyl- and glucuronyltransferase LARGE1; 2.4.-.-; Acetylglucosaminyltransferase-like 1A; Glycosyltransferase-like protein; LARGE xylosyl- and glucuronyltransferase 1", "protein_names_refseq": "acetylglucosaminyltransferase-like 1A; glycosyltransferase-like protein LARGE1; like-glycosyltransferase; myodystrophy; xylosyl- and glucuronyltransferase LARGE1 isoform 1; xylosyl- and glucuronyltransferase LARGE1", "tax_id": 10090, "disease": "muscular dystrophy-dystroglycanopathy type B1 (Disease Ontology:DOID:0050588); muscular dystrophy-dystroglycanopathy type B6 (Disease Ontology:DOID:0110637); congenital muscular dystrophy-dystroglycanopathy type A6 (Disease Ontology:DOID:0111242); facioscapulohumeral muscular dystrophy (Disease Ontology:DOID:11727)", "pathway": " (mmu:16795); (R-MMU-9939291)", "pathway_count": 2, "publication_count": 13, "publication_id_list": "10.1101/2023.09.13.557529;11381262;15184894;15210115;15958417;23125099;23135544;24132234;25138275;31219806;32975514;36723429;9892679", "class_list": "glycogene;glycosyltransferase", "function": "Bifunctional glycosyltransferase with both alpha-1,3-xylosyltransferase and beta-1,3-glucuronyltransferase activities involved in the maturation of alpha-dystroglycan (DAG1) by glycosylation leading to DAG1 binding to laminin G-like domain-containing extracellular proteins with high affinity (PubMed:23125099, PubMed:23135544, PubMed:25138275, PubMed:32975514). Elongates the glucuronyl-beta-1,4-xylose-beta disaccharide primer structure initiated by B4GAT1 by adding repeating units [-3-Xylose-alpha-1,3-GlcA-beta-1-] to produce a heteropolysaccharide (By similarity). Requires the phosphorylation of core M3 (O-mannosyl trisaccharide) by POMK to elongate the glucuronyl-beta-1,4-xylose-beta disaccharide primer (PubMed:32975514). Plays a key role in skeletal muscle function and regeneration (PubMed:15184894, PubMed:24132234)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed]; N-terminal domain on dystroglycan enables LARGE1 to extend matriglycan on alpha-dystroglycan and prevents muscular dystrophy. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 1, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 3, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 3, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 3, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 3, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 29, "reported_interactions": 0, "missing_score": 9562, "biomarker_type": "", "glycan_count": 3, "disease_count": 4, "glyco_site_count": 4, "binding_glycan_count": 0, "secondary_ac_list": "Q497S9;Q6P7U2;Q80TW0", "ec_number_list": "2.4.2.-;2.4.1.-;2.4.-.-", "go_molecular_function": "GO:0042285 xylosyltransferase activity;GO:0030145 manganese ion binding;GO:0016757 glycosyltransferase activity;GO:0015020 glucuronosyltransferase activity;GO:0016758 hexosyltransferase activity", "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0031594 neuromuscular junction;GO:0032991 protein-containing complex", "go_biological_process": "GO:0043403 skeletal muscle tissue regeneration;GO:0060538 skeletal muscle organ development;GO:0048708 astrocyte differentiation;GO:0006468 protein phosphorylation;GO:0006886 intracellular protein transport", "synthesized_glycan_count": 0, "hit_score": 2.0, "record_id": "Q9Z1M7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P28656-1", "uniprot_id": "NP1L1_MOUSE", "mass": 45345.0, "length": 391, "protein_name": "Nucleosome assembly protein 1-like 1", "gene_name": "Nap1l1", "organism": "Mouse", "refseq_name": "nucleosome assembly protein 1-like 1 isoform 2", "refseq_ac": "NP_056596", "gene_names_uniprotkb": "Nap1l1; Nrp", "gene_names_refseq": "D10Ertd68e; NAP-1; Nap1l1", "protein_names_uniprotkb": "Nucleosome assembly protein 1-like 1; Brain protein DN38; Histone H2A-H2B chaperone NAP1L1; NAP-1-related protein", "protein_names_refseq": "NAP-1-related protein; brain protein DN38; histone H2A-H2B chaperone NAP1L1; nucleosome assembly protein 1-like 1 isoform 2; nucleosome assembly protein-1", "tax_id": 10090, "disease": "appendiceal neoplasm (Disease Ontology:DOID:11240); pancreatic cancer (Disease Ontology:DOID:1793); hepatoblastoma (Disease Ontology:DOID:687)", "pathway": " (mmu:53605)", "pathway_count": 1, "publication_count": 16, "publication_id_list": "12106288;15345747;17499049;18331838;21183079;21333655;23806337;24893663;25428506;26824453;29490266;33300544;34076483;34428180;36148951;37507081", "class_list": "", "function": "Histone chaperone that plays a role in the nuclear import of H2A-H2B and nucleosome assembly. Also participates in several important DNA repair mechanisms: greatly enhances ERCC6-mediated chromatin remodeling which is essential for transcription-coupled nucleotide excision DNA repair. Also stimulates homologous recombination (HR) by RAD51 and RAD54 which is essential in mitotic DNA double strand break (DSB) repair (By similarity). Plays a key role in the regulation of embryonic neurogenesis (PubMed:29490266). Promotes the proliferation of neural progenitors and inhibits neuronal differentiation during cortical development (PubMed:29490266). Regulates neurogenesis via the modulation of RASSF10; regulates RASSF10 expression by promoting SETD1A-mediated H3K4 methylation at the RASSF10 promoter (PubMed:29490266)., [UniProtKB, UniProtKB, PubMed]; NAP1L1 and NAP1L4 Binding to Hypervariable Domain of Chikungunya Virus nsP3 Protein Is Bivalent and Requires Phosphorylation., [RefSeq, PubMed]; NAP1L1 promotes the growth of colon cancer by activating HDGF/DDX5., [RefSeq, PubMed]; Nap1l1 promotes the proliferation of iPSC attributable to G2/M transition caused by downregulation of p27 and p21, and upregulation of cyclin B1, the activation of AKT or ERK is involved in the process., [RefSeq, PubMed]; The molecular interaction between DGKzeta and Nap1l1 was attenuated after hypoxic stress., [RefSeq, PubMed]; These findings reveal an essential role for the Nap1l1 histone chaperone in cortical neurogenesis during early embryonic brain development., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 5, "reported_mutagensis": 2, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3UL14", "ec_number_list": "", "go_molecular_function": "GO:0003682 chromatin binding;GO:0019900 kinase binding;GO:0042393 histone binding;GO:0140713 histone chaperone activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0042470 melanosome;GO:0000785 chromatin", "go_biological_process": "GO:0007399 nervous system development;GO:0006334 nucleosome assembly;GO:2000179 positive regulation of neural precursor cell proliferation;GO:0050769 positive regulation of neurogenesis", "synthesized_glycan_count": 0, "hit_score": 1.9, "record_id": "P28656-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P51954-1", "uniprot_id": "NEK1_MOUSE", "mass": 136690.0, "length": 1203, "protein_name": "Serine/threonine-protein kinase Nek1", "gene_name": "Nek1", "organism": "Mouse", "refseq_name": "serine/threonine-protein kinase Nek1 isoform 1", "refseq_ac": "NP_001280566", "gene_names_uniprotkb": "Nek1", "gene_names_refseq": "D8Ertd790e; Nek1; kat", "protein_names_uniprotkb": "Serine/threonine-protein kinase Nek1; 2.7.11.1; Never in mitosis A-related kinase 1; NimA-related protein kinase 1", "protein_names_refseq": "NIMA-related kinase 1; NY-REN-55 antigen; Nek1 serine/threonine- and tyrosine-specific protein kinase; kidney, anemia and testis; never in mitosis A-related kinase 1; nimA-related protein kinase 1; serine/threonine-protein kinase Nek1 isoform 1; serine/threonine-protein kinase Nek1", "tax_id": 10090, "disease": "asphyxiating thoracic dystrophy (Disease Ontology:DOID:0050592); orofaciodigital syndrome II (Disease Ontology:DOID:0060959); amyotrophic lateral sclerosis type 24 (Disease Ontology:DOID:0081378); short-rib thoracic dysplasia 6 with or without polydactyly (Disease Ontology:DOID:0110092); autosomal recessive polycystic kidney disease (Disease Ontology:DOID:0110861)", "pathway": " (mmu:18004); (R-MMU-9861718)", "pathway_count": 2, "publication_count": 10, "publication_id_list": "10.1101/2023.09.13.557529;12204287;1382974;15345747;16267153;18843199;21183079;28235073;34376696;39227882", "class_list": "", "function": "ALS-associated C21ORF2 variant disrupts DNA damage repair, mitochondrial metabolism, neuronal excitability and NEK1 levels in human motor neurons. Publication Status: Online-Only, [RefSeq, PubMed]; NEK1-mediated retromer trafficking promotes blood-brain barrier integrity by regulating glucose metabolism and RIPK1 activation. Publication Status: Online-Only, [RefSeq, PubMed]; Phosphorylates serines and threonines, but also appears to possess tyrosine kinase activity (PubMed:1382974). Involved in DNA damage checkpoint control and for proper DNA damage repair (PubMed:18843199). In response to injury that includes DNA damage, NEK1 phosphorylates VDAC1 to limit mitochondrial cell death (By similarity). May be implicated in the control of meiosis (PubMed:1382974). Involved in cilium assembly (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 12, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 5, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;2.7.11.10;2.7.11.11;1.1.1.40;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;2.7.11.39;2.3.1.-;2.7.11.31;3.6.5.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0004672 protein kinase activity;GO:0004674 protein serine/threonine kinase activity;GO:0004713 protein tyrosine kinase activity;GO:0005524 ATP binding;GO:0046872 metal ion binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol", "go_biological_process": "GO:2000001 regulation of DNA damage checkpoint;GO:0006468 protein phosphorylation;GO:0007283 spermatogenesis;GO:0051301 cell division;GO:0001822 kidney development", "synthesized_glycan_count": 0, "hit_score": 1.3, "record_id": "P51954-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q80TM9-1", "uniprot_id": "NISCH_MOUSE", "mass": 175012.0, "length": 1593, "protein_name": "Nischarin", "gene_name": "Nisch", "organism": "Mouse", "refseq_name": "nischarin isoform 1", "refseq_ac": "NP_073147", "gene_names_uniprotkb": "Nisch; Kiaa0975", "gene_names_refseq": "1200007D05Rik; 3202002H23Rik; I-1; Nisch; edsn", "protein_names_uniprotkb": "Nischarin; I-1; I1R; IR1; Imidazoline receptor 1; Imidazoline receptor I-1-like protein; Imidazoline-1 receptor", "protein_names_refseq": "I1R; IR1; imidazoline receptor 1; imidazoline receptor I-1-like protein; imidazoline-1 receptor; nischarin isoform 1", "tax_id": 10090, "disease": "otitis media (Disease Ontology:DOID:10754); hypertension (Disease Ontology:DOID:10763); congestive heart failure (Disease Ontology:DOID:6000)", "pathway": " (mmu:64652); (R-MMU-9013149); (R-MMU-9696264); (R-MMU-9696270)", "pathway_count": 4, "publication_count": 25, "publication_id_list": "11121431;12915132;14535848;15229651;16002401;16678176;17242355;18332102;19144319;21183079;21750661;22872234;25428507;25605945;26495903;31219806;33649389;33725478;34203471;34428180;35820727;36210013;36716956;37443018;37828378", "class_list": "", "function": "Acts either as the functional imidazoline-1 receptor (I1R) candidate or as a membrane-associated mediator of the I1R signaling. Binds numerous imidazoline ligands that induces initiation of cell-signaling cascades triggering to cell survival, growth and migration. Its activation by the agonist rilmenidine induces an increase in phosphorylation of mitogen-activated protein kinases MAPK1 and MAPK3 in rostral ventrolateral medulla (RVLM) neurons that exhibited rilmenidine-evoked hypotension (By similarity). Blocking its activation with efaroxan abolished rilmenidine-induced mitogen-activated protein kinase phosphorylation in RVLM neurons (By similarity). Acts as a modulator of Rac-regulated signal transduction pathways. Suppresses Rac1-stimulated cell migration by interacting with PAK1 and inhibiting its kinase activity. Also blocks Pak-independent Rac signaling by interacting with RAC1 and inhibiting Rac1-stimulated NF-kB response element and cyclin D1 promoter activation. Also inhibits LIMK1 kinase activity by reducing LIMK1 'Tyr-508' phosphorylation. Inhibits Rac-induced cell migration and invasion in breast and colon epithelial cells. Inhibits lamellipodia formation, when overexpressed. Plays a role in protection against apoptosis (By similarity). Involved in association with IRS4 in the enhancement of insulin activation of MAPK1 and MAPK3 (By similarity). When overexpressed, induces a redistribution of cell surface ITGA5 integrin to intracellular endosomal structures (By similarity)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]; Contribution of Nischarin/IRAS in CNS development, injury and diseases. Review article, [RefSeq, PubMed]; Identification of a psychiatric risk gene NISCH at 3p21.1 GWAS locus mediating dendritic spine morphogenesis and cognitive function. Publication Status: Online-Only, [RefSeq, PubMed]; Nisch regulates cell movement by inhibiting PAK., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 5, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 3, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q2YDV7;Q8C354;Q8C4X9;Q8CBH0;Q91XW6;Q99LG6;Q9EPW8;Q9WUM6", "ec_number_list": "", "go_molecular_function": "GO:0005178 integrin binding;GO:0042802 identical protein binding;GO:0035091 phosphatidylinositol binding", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005769 early endosome;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0055037 recycling endosome", "go_biological_process": "GO:0048243 norepinephrine secretion;GO:0006915 apoptotic process;GO:0008217 regulation of blood pressure;GO:0030336 negative regulation of cell migration;GO:0030036 actin cytoskeleton organization", "synthesized_glycan_count": 0, "hit_score": 2.6, "record_id": "Q80TM9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9QZ09-1", "uniprot_id": "PHTF1_MOUSE", "mass": 86779.0, "length": 761, "protein_name": "Protein PHTF1", "gene_name": "Phtf1", "organism": "Mouse", "refseq_name": "protein PHTF1 isoform a", "refseq_ac": "NP_001156939", "gene_names_uniprotkb": "Phtf1; Phtf", "gene_names_refseq": "Phft; Phtf1; Phtf", "protein_names_uniprotkb": "Protein PHTF1", "protein_names_refseq": "protein PHTF1 isoform a; protein PHTF1", "tax_id": 10090, "disease": "", "pathway": " (mmu:18685)", "pathway_count": 1, "publication_count": 10, "publication_id_list": "10729229;15601915;21183079;21750661;25428506;25605945;30084848;31599954;33649389;34428180", "class_list": "", "function": "Neither FEM1B nor PHTF1 are directly implicated in apoptosis in testis tissue, [RefSeq, PubMed]", "predicted_glycosites": 7, "predicted_n_glycosites": 6, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 5, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 7, "binding_glycan_count": 0, "secondary_ac_list": "Q9CS51;Q9CSB9;Q9QZ14", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0033106 cis-Golgi network membrane;GO:0005783 endoplasmic reticulum;GO:0016020 membrane", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q9QZ09-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P97814-1", "uniprot_id": "PPIP1_MOUSE", "mass": 47590.0, "length": 415, "protein_name": "Proline-serine-threonine phosphatase-interacting protein 1", "gene_name": "Pstpip1", "organism": "Mouse", "refseq_name": "proline-serine-threonine phosphatase-interacting protein 1 isoform 1", "refseq_ac": "NP_035323", "gene_names_uniprotkb": "Pstpip1", "gene_names_refseq": "CD2BP1; Pstpip1; def-2", "protein_names_uniprotkb": "Proline-serine-threonine phosphatase-interacting protein 1; PEST phosphatase-interacting protein 1", "protein_names_refseq": "PEST phosphatase-interacting protein 1; proline-serine-threonine phosphatase-interacting protein 1 isoform 1", "tax_id": 10090, "disease": "autoinflammatory syndrome with cytopenia, hyperzincemia, and hypercalprotectinemia (Disease Ontology:DOID:0061185); PAPA syndrome (Disease Ontology:DOID:0080519)", "pathway": " (mmu:19200); (R-MMU-844456)", "pathway_count": 2, "publication_count": 11, "publication_id_list": "11163214;11711533;12530983;18480402;21183079;21750661;23293022;27760174;34428180;9265651;9488710", "class_list": "", "function": "A new PSTPIP1/PTPN6/SHIP1/2-dependent negative feedback mechanism that counterbalances Src and PI(3,4,5)P3 signalling to control osteoclast cell polarity and activity during bone resorption Publication Status: Online-Only, [RefSeq, PubMed]; Analysis of inflammation in mice ectopically expressing human Pyogenic Arthritis, Pyoderma Gangrenosum, and Acne (PAPA) Syndrome-associated PSTPIP1 A230T mutant proteins, [RefSeq, PubMed]; Involved in regulation of the actin cytoskeleton. May regulate WAS actin-bundling activity. Bridges the interaction between ABL1 and PTPN18 leading to ABL1 dephosphorylation. May play a role as a scaffold protein between PTPN12 and WAS and allow PTPN12 to dephosphorylate WAS. Has the potential to physically couple CD2 and CD2AP to WAS. Acts downstream of CD2 and CD2AP to recruit WAS to the T-cell:APC contact site so as to promote the actin polymerization required for synapse induction during T-cell activation. Down-regulates CD2-stimulated adhesion through the coupling of PTPN12 to CD2. Also has a role in innate immunity and the inflammatory response. Recruited to inflammasomes by MEFV. Induces formation of pyroptosomes, large supramolecular structures composed of oligomerized PYCARD dimers which form prior to inflammatory apoptosis. Binding to MEFV allows MEFV to bind to PYCARD and facilitates pyroptosome formation. Regulates endocytosis and cell migration in neutrophils., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, UniProtKB, UniProtKB]; PSTPIP1 is a novel component of the leukocyte uropod that regulates endocytosis and cell migration, [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 3, "reported_mutagensis": 2, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q4V9R4", "ec_number_list": "", "go_molecular_function": "GO:0003779 actin binding;GO:0042802 identical protein binding;GO:0019903 protein phosphatase binding", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0030027 lamellipodium;GO:0048471 perinuclear region of cytoplasm", "go_biological_process": "GO:0006897 endocytosis;GO:0006954 inflammatory response;GO:0007155 cell adhesion;GO:0045087 innate immune response", "synthesized_glycan_count": 0, "hit_score": 1.2, "record_id": "P97814-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3UMT1-1", "uniprot_id": "PP12C_MOUSE", "mass": 84685.0, "length": 782, "protein_name": "Protein phosphatase 1 regulatory subunit 12C", "gene_name": "Ppp1r12c", "organism": "Mouse", "refseq_name": "protein phosphatase 1 regulatory subunit 12C isoform 1", "refseq_ac": "NP_084110", "gene_names_uniprotkb": "Ppp1r12c; Mbs85", "gene_names_refseq": "2410197A17Rik; B430101M08; Mbs85; Ppp1r12c", "protein_names_uniprotkb": "Protein phosphatase 1 regulatory subunit 12C; Protein phosphatase 1 myosin-binding subunit of 85 kDa; Protein phosphatase 1 myosin-binding subunit p85", "protein_names_refseq": "myosin-binding subunit 85; protein phosphatase 1 myosin-binding subunit of 85 kDa; protein phosphatase 1 myosin-binding subunit p85; protein phosphatase 1 regulatory subunit 12C isoform 1; protein phosphatase 1, regulatory (inhibitor) subunit 12C", "tax_id": 10090, "disease": "", "pathway": " (mmu:232807)", "pathway_count": 1, "publication_count": 5, "publication_id_list": "15469989;21183079;21750661;34428180;34887587", "class_list": "", "function": "Regulates myosin phosphatase activity., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 7, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q9CWD5", "ec_number_list": "", "go_molecular_function": "GO:0017020 myosin phosphatase regulator activity;GO:0004857 enzyme inhibitor activity;GO:0019901 protein kinase binding;GO:0019208 phosphatase regulator activity", "go_cellular_component": "GO:0005737 cytoplasm;GO:0001725 stress fiber", "go_biological_process": "GO:0007165 signal transduction;GO:0048812 neuron projection morphogenesis", "synthesized_glycan_count": 0, "hit_score": 0.8, "record_id": "Q3UMT1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q91VJ5-1", "uniprot_id": "PQBP1_MOUSE", "mass": 30597.0, "length": 263, "protein_name": "Polyglutamine-binding protein 1", "gene_name": "Pqbp1", "organism": "Mouse", "refseq_name": "polyglutamine-binding protein 1", "refseq_ac": "NP_001239457", "gene_names_uniprotkb": "Pqbp1; Npw38", "gene_names_refseq": "PQBP-1; Pqbp1; Sfc2; npw38", "protein_names_uniprotkb": "Polyglutamine-binding protein 1; 38 kDa nuclear protein containing a WW domain; Npw38; PQBP-1; Polyglutamine tract-binding protein 1", "protein_names_refseq": "38 kDa nuclear protein containing a WW domain; polyglutamine tract-binding protein 1; polyglutamine-binding protein 1; scurfy candidate 2", "tax_id": 10090, "disease": "Renpenning syndrome (Disease Ontology:DOID:0060179)", "pathway": " (mmu:54633); (R-MMU-72163)", "pathway_count": 2, "publication_count": 6, "publication_id_list": "10332029;21750661;23512658;31219806;34428180;34782623", "class_list": "", "function": "Intrinsically disordered protein that acts as a scaffold, and which is involved in different processes, such as pre-mRNA splicing, transcription regulation, innate immunity and neuron development (By similarity). Interacts with splicing-related factors via the intrinsically disordered region and regulates alternative splicing of target pre-mRNA species (PubMed:23512658). May suppress the ability of POU3F2 to transactivate the DRD1 gene in a POU3F2 dependent manner (By similarity). Can activate transcription directly or via association with the transcription machinery (By similarity). May be involved in ATXN1 mutant-induced cell death (By similarity). The interaction with ATXN1 mutant reduces levels of phosphorylated RNA polymerase II large subunit (By similarity). Involved in the assembly of cytoplasmic stress granule, possibly by participating in the transport of neuronal RNA granules (By similarity). Also acts as an innate immune sensor of infection by retroviruses, by detecting the presence of reverse-transcribed DNA in the cytosol (By similarity). Directly binds retroviral reverse-transcribed DNA in the cytosol and interacts with CGAS, leading to activate the cGAS-STING signaling pathway, triggering type-I interferon production (By similarity)., [UniProtKB, PubMed, UniProtKB]; Tau activates microglia via the PQBP1-cGAS-STING pathway to promote brain inflammation. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q80WW2;Q9ER43;Q9QYY2", "ec_number_list": "", "go_molecular_function": "GO:0043021 ribonucleoprotein complex binding;GO:0003690 double-stranded DNA binding;GO:0051020 GTPase binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol", "go_biological_process": "GO:0071360 cellular response to exogenous dsRNA;GO:0006351 DNA-templated transcription;GO:0031175 neuron projection development;GO:0045087 innate immune response;GO:0048814 regulation of dendrite morphogenesis", "synthesized_glycan_count": 0, "hit_score": 0.7, "record_id": "Q91VJ5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "E2JF22-1", "uniprot_id": "PIEZ1_MOUSE", "mass": 292002.0, "length": 2547, "protein_name": "Piezo-type mechanosensitive ion channel component 1", "gene_name": "Piezo1", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Piezo1; Fam38a", "gene_names_refseq": "", "protein_names_uniprotkb": "Piezo-type mechanosensitive ion channel component 1; Protein FAM38A", "protein_names_refseq": "", "tax_id": 10090, "disease": "hereditary lymphedema (Disease Ontology:DOID:0050580); dehydrated hereditary stomatocytosis (Disease Ontology:DOID:0111575); dehydrated hereditary stomatocytosis 1 (Disease Ontology:DOID:0111576); distal arthrogryposis type 5 (Disease Ontology:DOID:0111608)", "pathway": " (mmu:234839)", "pathway_count": 1, "publication_count": 25, "publication_id_list": "10.1101/2023.09.13.557529;19144319;20485683;20813920;21183079;21750661;22343900;23479567;24157948;24662763;24958852;25119035;26390154;29261642;29799007;30899004;31219806;34418053;34428180;35388220;36210013;36515266;37590348;38184690;38228630", "class_list": "", "function": "Pore-forming subunit of the mechanosensitive non-specific cation Piezo channel required for rapidly adapting mechanically activated (MA) currents and has a key role in sensing touch and tactile pain (PubMed:20813920, PubMed:22343900, PubMed:38184690, PubMed:26390154, PubMed:29261642, PubMed:35388220, PubMed:37590348). Piezo channels are homotrimeric three-blade propeller-shaped structures that utilize a cap-motion and plug-and-latch mechanism to gate their ion-conducting pathways (PubMed:26390154, PubMed:29261642, PubMed:35388220, PubMed:37590348). Generates currents characterized by a linear current-voltage relationship that are sensitive to ruthenium red and gadolinium (PubMed:20813920, PubMed:22343900, PubMed:38228630). Conductance to monovalent alkali ions is highest for K(+), intermediate for Na(+) and lowest for Li(+) (By similarity). Divalent ions except for Mn(2+) permeate the channel but more slowly than the monovalent ions and they also reduce K(+) currents (By similarity). Plays a key role in epithelial cell adhesion by maintaining integrin activation through R-Ras recruitment to the ER, most probably in its activated state, and subsequent stimulation of calpain signaling (By similarity). In inner ear hair cells, PIEZO1/2 subunits may constitute part of the mechanotransducer (MET) non-selective cation channel complex where they may act as pore-forming ion-conducting component in the complex (PubMed:38228630). In the kidney, may contribute to the detection of intraluminal pressure changes and to urine flow sensing (PubMed:24157948). Acts as a shear-stress sensor that promotes endothelial cell organization and alignment in the direction of blood flow through calpain activation (By similarity). Plays a key role in blood vessel formation and vascular structure in both development and adult physiology (PubMed:24958852, PubMed:25119035, PubMed:36515266). Acts as a sensor of phosphatidylserine (PS) flipping at the plasma membrane and governs morphogenesis of muscle cells (PubMed:29799007). In myoblasts, flippase-mediated PS enrichment at the inner leaflet of plasma membrane triggers channel activation and Ca(2+) influx followed by Rho GTPases signal transduction, leading to assembly of cortical actomyosin fibers and myotube formation (PubMed:29799007)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 1, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 3, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 3, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 3, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 6, "reported_mutagensis": 5, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 6, "disease_count": 4, "glyco_site_count": 5, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "1.8.-.-;2.7.11.1", "go_molecular_function": "GO:0042802 identical protein binding;GO:0005261 monoatomic cation channel activity;GO:0008381 mechanosensitive monoatomic ion channel activity;GO:0140135 mechanosensitive monoatomic cation channel activity", "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005886 plasma membrane;GO:0005789 endoplasmic reticulum membrane;GO:0033116 endoplasmic reticulum-Golgi intermediate compartment membrane;GO:0031258 lamellipodium membrane", "go_biological_process": "GO:0010831 positive regulation of myotube differentiation;GO:0042391 regulation of membrane potential;GO:0006812 monoatomic cation transport;GO:0071260 cellular response to mechanical stimulus;GO:0050982 detection of mechanical stimulus", "synthesized_glycan_count": 0, "hit_score": 3.6, "record_id": "E2JF22-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q60829-1", "uniprot_id": "PPR1B_MOUSE", "mass": 21781.0, "length": 194, "protein_name": "Protein phosphatase 1 regulatory subunit 1B", "gene_name": "Ppp1r1b", "organism": "Mouse", "refseq_name": "protein phosphatase 1 regulatory subunit 1B isoform 2", "refseq_ac": "NP_001300899", "gene_names_uniprotkb": "Ppp1r1b", "gene_names_refseq": "DARPP-32; Darpp32; Ppp1r1b", "protein_names_uniprotkb": "Protein phosphatase 1 regulatory subunit 1B; DARPP-32; Dopamine- and cAMP-regulated neuronal phosphoprotein", "protein_names_refseq": "dopamine- and cAMP-regulated neuronal phosphoprotein; protein phosphatase 1 regulatory subunit 1B isoform 2; protein phosphatase 1 regulatory subunit 1B", "tax_id": 10090, "disease": "withdrawal disorder (Disease Ontology:DOID:0060001); Huntington's disease (Disease Ontology:DOID:12858); depressive disorder (Disease Ontology:DOID:1596); status epilepticus (Disease Ontology:DOID:1824); bipolar disorder (Disease Ontology:DOID:3312); brain infarction (Disease Ontology:DOID:3454); schizophrenia (Disease Ontology:DOID:5419)", "pathway": " (mmu:19049); (R-MMU-180024)", "pathway_count": 2, "publication_count": 55, "publication_id_list": "10.1101/2023.09.13.557529;10217279;10604473;10669419;11880651;11880652;12064480;12077213;12181566;12651945;12956723;14529709;14713295;15312165;15657149;15770104;16084497;16123776;16525043;16750892;17010100;18367215;18622401;18823371;18923023;19169672;19538708;19796684;19834457;20236221;20423708;20720111;20888397;21183079;22342812;22564758;22971543;23420105;24312250;24316474;24555476;24663062;25254549;25892655;26465004;26488498;26639316;26657176;27480796;27998980;29221855;31972514;36351540;38132125;7485543", "class_list": "", "function": "Inhibitor of protein-phosphatase 1., [UniProtKB]; Mapping Chromatin Occupancy of Ppp1r1b-lncRNA Genome-Wide Using Chromatin Isolation by RNA Purification (ChIRP)-seq. Publication Status: Online-Only, [RefSeq, PubMed]; This gene encodes a bifunctional signal transduction molecule. Dopaminergic and glutamatergic receptor stimulation regulates its phosphorylation and function as a kinase or phosphatase inhibitor. As a target for dopamine, this gene may serve as a therapeutic target for neurologic and psychiatric disorders in humans. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2015]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 7, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 9671, "biomarker_type": "", "glycan_count": 1, "disease_count": 7, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "A2A564;Q3URF2;Q6DV86;Q91XB5", "ec_number_list": "", "go_molecular_function": "GO:0031752 D5 dopamine receptor binding;GO:0004865 protein serine/threonine phosphatase inhibitor activity;GO:0031751 D4 dopamine receptor binding;GO:0031748 D1 dopamine receptor binding;GO:0004864 protein phosphatase inhibitor activity", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0043025 neuronal cell body;GO:0098794 postsynapse", "go_biological_process": "GO:0007621 negative regulation of female receptivity;GO:0006351 DNA-templated transcription;GO:0007613 memory;GO:0007626 locomotory behavior;GO:0008542 visual learning", "synthesized_glycan_count": 0, "hit_score": 5.8, "record_id": "Q60829-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O55242-1", "uniprot_id": "SGMR1_MOUSE", "mass": 25250.0, "length": 223, "protein_name": "Sigma non-opioid intracellular receptor 1", "gene_name": "Sigmar1", "organism": "Mouse", "refseq_name": "sigma non-opioid intracellular receptor 1 isoform 2", "refseq_ac": "NP_001273467", "gene_names_uniprotkb": "Sigmar1; Oprs1", "gene_names_refseq": "Oprs1; Sig1R; Sigmar1; sigma1R", "protein_names_uniprotkb": "Sigma non-opioid intracellular receptor 1; Sigma 1-type opioid receptor; Sigma1-receptor; Sigma1R", "protein_names_refseq": "opioid receptor, sigma 1; sigma 1 receptor variant SR-1D; sigma 1-type opioid receptor; sigma non-opioid intracellular receptor 1 isoform 2; sigma1-receptor", "tax_id": 10090, "disease": "alcohol dependence (Disease Ontology:DOID:0050741); amyotrophic lateral sclerosis type 16 (Disease Ontology:DOID:0060207); autosomal recessive distal hereditary motor neuronopathy 2 (Disease Ontology:DOID:0111065); sciatic neuropathy (Disease Ontology:DOID:11446); post-traumatic stress disorder (Disease Ontology:DOID:2055); diabetic neuropathy (Disease Ontology:DOID:9743)", "pathway": " (mmu:18391)", "pathway_count": 1, "publication_count": 20, "publication_id_list": "11149946;11207432;11476895;11687279;12730355;14622179;15571673;15777781;20167253;22381068;22619170;23332758;25678561;26792191;28350844;34428180;38763502;39162886;9425306;9603192", "class_list": "", "function": "Activation of the sigma-1 receptor ameliorates neuronal ferroptosis via IRE1alpha after spinal cord injury., [RefSeq, PubMed]; Data indicate that sigma1-receptor short form sigma(1)SR isoform interferes with sigma(1)R function relevant to mitochondrial energy production under endoplasmic reticulum stress conditions, promoting cellular apoptosis., [RefSeq, PubMed]; Functions in lipid transport from the endoplasmic reticulum and is involved in a wide array of cellular functions probably through regulation of the biogenesis of lipid microdomains at the plasma membrane (PubMed:12730355). Involved in the regulation of different receptors it plays a role in BDNF signaling and EGF signaling. Also regulates ion channels like the potassium channel and could modulate neurotransmitter release. Plays a role in calcium signaling through modulation together with ANK2 of the ITP3R-dependent calcium efflux at the endoplasmic reticulum. Plays a role in several other cell functions including proliferation, survival and death. Originally identified for its ability to bind various psychoactive drugs it is involved in learning processes, memory and mood alteration (PubMed:11149946, PubMed:14622179, PubMed:15571673, PubMed:15777781, PubMed:23332758, PubMed:9425306, PubMed:9603192). Necessary for proper mitochondrial axonal transport in motor neurons, in particular the retrograde movement of mitochondria (PubMed:25678561). Plays a role in protecting cells against oxidative stress-induced cell death via its interaction with RNF112 (PubMed:26792191)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]; Novel functions of the sigma-1 receptor, [RefSeq, PubMed]; Sigma-1 Receptors Control Neuropathic Pain and Peripheral Neuroinflammation After Nerve Injury in Female Mice: A Transcriptomic Study. Publication Status: Online-Only, [RefSeq, PubMed]; The sigma-1 receptor may play a role in the regulation of motor behavior., [RefSeq, PubMed]; This gene encodes a transmembrane protein located in the endoplasmic reticulum. The encoded protein is a receptor that binds several endogenous ligands, including N,N-dimethyltryptamine, progesterone and pregnenolone and a variety of of non-opiate compounds. The encoded protein plays a role in regulating the activity of ion channels, acting as a chaperone and protecting cells from oxidative stress. In humans, this receptor has been associated with Alzheimer's and Parkinson's diseases, stroke and numerous disease conditions such as depression, pain and addiction. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Nov 2013]., [RefSeq]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 6, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "A2AMS0;B7ZJH6;B7ZJH7;B7ZJH8;B7ZJH9;Q9JKU9", "ec_number_list": "", "go_molecular_function": "GO:0004985 G protein-coupled opioid receptor activity;GO:0042802 identical protein binding;GO:0031852 mu-type opioid receptor binding;GO:0038023 signaling receptor activity", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005635 nuclear envelope;GO:0005737 cytoplasm;GO:0005783 endoplasmic reticulum;GO:0005811 lipid droplet", "go_biological_process": "GO:0097305 response to alcohol;GO:0006869 lipid transport;GO:0007399 nervous system development;GO:0043524 negative regulation of neuron apoptotic process;GO:0070207 protein homotrimerization", "synthesized_glycan_count": 0, "hit_score": 2.1, "record_id": "O55242-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q3UUV5-1", "uniprot_id": "SKAP1_MOUSE", "mass": 40962.0, "length": 355, "protein_name": "Src kinase-associated phosphoprotein 1", "gene_name": "Skap1", "organism": "Mouse", "refseq_name": "src kinase-associated phosphoprotein 1 isoform 1", "refseq_ac": "NP_001028358", "gene_names_uniprotkb": "Skap1; Scap1", "gene_names_refseq": "1700091G21Rik; Scap1; Skap-55; Skap1", "protein_names_uniprotkb": "Src kinase-associated phosphoprotein 1; Src family-associated phosphoprotein 1", "protein_names_refseq": "ortholog of human src family associated phosphoprotein 1 SCAP1; src kinase-associated phosphoprotein 1 isoform 1; src kinase-associated phosphoprotein 1", "tax_id": 10090, "disease": "", "pathway": " (mmu:78473)", "pathway_count": 1, "publication_count": 8, "publication_id_list": "12681493;17646386;17947660;21750661;25605945;25851535;26905930;27181093", "class_list": "", "function": "In this study, the authors identified that the ADAP-SKAP55 signaling module reduced CD8(+) cytotoxic T lymphocyte cytotoxicity and enhanced PD-1 expression in a Fyn-, Ca(2+)-, and NFATc1-dependent manner., [RefSeq, PubMed]; Positively regulates T-cell receptor signaling by enhancing the MAP kinase pathway (By similarity). Required for optimal conjugation between T-cells and antigen-presenting cells by promoting the clustering of integrin ITGAL on the surface of T-cells (By similarity). May be involved in high affinity immunoglobulin epsilon receptor signaling in mast cells (PubMed:12681493)., [UniProtKB, UniProtKB, PubMed]; Results identify a clear effector role for SKAP-55 in LFA-1 adhesion in peripheral T cells and demonstrate that dependency on SKAP-55 and ADAP differs among T cells and differs with the strength of the TCR signal., [RefSeq, PubMed]; SKAP1 can affect the function of talin in T-cells needed for optimal T-cell/dendritic cell conjugation, [RefSeq, PubMed]; This study shows that Skap1-deficient (skap1-/-) mice are highly resistant to the induction of collagen-induced arthritis, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q3TE54;Q3UUT7;Q3UUX6", "ec_number_list": "", "go_molecular_function": "GO:0019901 protein kinase binding;GO:0044877 protein-containing complex binding;GO:0042169 SH2 domain binding;GO:0019903 protein phosphatase binding", "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0005911 cell-cell junction", "go_biological_process": "GO:0045785 positive regulation of cell adhesion;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0072659 protein localization to plasma membrane;GO:0050852 T cell receptor signaling pathway;GO:0045893 positive regulation of DNA-templated transcription", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "Q3UUV5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "A2AAY5-1", "uniprot_id": "SPD2B_MOUSE", "mass": 101517.0, "length": 908, "protein_name": "SH3 and PX domain-containing protein 2B", "gene_name": "Sh3pxd2b", "organism": "Mouse", "refseq_name": "SH3 and PX domain-containing protein 2B", "refseq_ac": "NP_796338", "gene_names_uniprotkb": "Sh3pxd2b; Fad49; Tks4", "gene_names_refseq": "G431001E03Rik; Sh3pxd2b; TSK4; Tks4; fad49", "protein_names_uniprotkb": "SH3 and PX domain-containing protein 2B; Factor for adipocyte differentiation 49; Tyrosine kinase substrate with four SH3 domains", "protein_names_refseq": "SH3 and PX domain-containing protein 2B; factor for adipocyte differentiation 49; tyrosine kinase substrate with four SH3 domains", "tax_id": 10090, "disease": "Frank-Ter Haar syndrome (Disease Ontology:DOID:0111789); otitis media (Disease Ontology:DOID:10754); glaucoma (Disease Ontology:DOID:1686)", "pathway": " (mmu:268396)", "pathway_count": 1, "publication_count": 15, "publication_id_list": "15592455;18959745;19144319;19144821;19233245;19669234;19755710;20137777;21183079;21750661;28528544;31219806;31387265;31591456;35820727", "class_list": "", "function": "Adapter protein involved in invadopodia and podosome formation and extracellular matrix degradation. Binds matrix metalloproteinases (ADAMs), NADPH oxidases (NOXs) and phosphoinositides. Acts as an organizer protein that allows NOX1- or NOX3-dependent reactive oxygen species (ROS) generation and ROS localization. Plays a role in mitotic clonal expansion during the immediate early stage of adipocyte differentiation., [UniProtKB, PubMed, PubMed, PubMed, UniProtKB, UniProtKB]; Beigeing process was more robust in the WAT of Tks4-KO mice compared to the wild-type animals. Publication Status: Online-Only, [RefSeq, PubMed]; Enhanced endothelial motility and multicellular sprouting is mediated by the scaffold protein TKS4. Erratum:[Sci Rep. 2020 Jul 20;10(1):12293. doi: 10.1038/s41598-020-68536-8. PMID: 32686692] Publication Status: Online-Only, [RefSeq, PubMed]; Induction of the fad49 gene was observed in adipocyte differentiable 3T3-L1 cells, but not in non-adipogenic NIH-3T3 cells., [RefSeq, PubMed]; SH3PXD2B is a podosomal-adaptor protein required for postnatal growth and development., [RefSeq, PubMed]; Silencing of C/EBPdelta impaired the expression of factor for adipocyte differentiation (fad) 49, which is up-regulated and plays a crucial role early in adipogenesis., [RefSeq, PubMed]; These findings establish a role for TKS4 in Frank-Ter Haar syndrome and embryonic development., [RefSeq, PubMed]; Tks4 has a role in the formation and function of podosomes., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 7, "reported_mutagensis": 3, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 3, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "B6F0V1;Q1LZL8;Q1LZM5;Q3TB89;Q8BIC6", "ec_number_list": "", "go_molecular_function": "GO:0010314 phosphatidylinositol-5-phosphate binding;GO:0042169 SH2 domain binding;GO:0080025 phosphatidylinositol-3,5-bisphosphate binding;GO:0070273 phosphatidylinositol-4-phosphate binding;GO:0032266 phosphatidylinositol-3-phosphate binding", "go_cellular_component": "GO:0005737 cytoplasm;GO:0002102 podosome", "go_biological_process": "GO:1904888 cranial skeletal system development;GO:0002051 osteoblast fate commitment;GO:1904179 positive regulation of adipose tissue development;GO:0060378 regulation of brood size;GO:0007507 heart development", "synthesized_glycan_count": 0, "hit_score": 1.8, "record_id": "A2AAY5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O55201-1", "uniprot_id": "SPT5H_MOUSE", "mass": 120664.0, "length": 1082, "protein_name": "Transcription elongation factor SPT5", "gene_name": "Supt5h; Supt5", "organism": "Mouse", "refseq_name": "transcription elongation factor SPT5 isoform a", "refseq_ac": "NP_038704", "gene_names_uniprotkb": "Supt5h; Supt5; Supt5", "gene_names_refseq": "Spt5; Supt5h; Supt5", "protein_names_uniprotkb": "Transcription elongation factor SPT5; DRB sensitivity-inducing factor large subunit; DSIF large subunit", "protein_names_refseq": "DRB sensitivity-inducing factor large subunit; DSIF large subunit; suppressor of Ty 5 homolog; transcription elongation factor SPT5 isoform a; transcription elongation factor SPT5", "tax_id": 10090, "disease": "", "pathway": " (mmu:20924); (R-MMU-112382); (R-MMU-113418); (R-MMU-674695); (R-MMU-6796648); (R-MMU-6807505); (R-MMU-72086); (R-MMU-75955); (R-MMU-77075)", "pathway_count": 9, "publication_count": 13, "publication_id_list": "10.1101/2023.09.13.557529;17242355;21183079;21750661;23806337;24129315;31219806;32782141;34428180;34534457;34678516;39627609;9480761", "class_list": "", "function": "Component of the DRB sensitivity-inducing factor complex (DSIF complex), which regulates mRNA processing and transcription elongation by RNA polymerase II. DSIF positively regulates mRNA capping by stimulating the mRNA guanylyltransferase activity of RNGTT/CAP1A. DSIF also acts cooperatively with the negative elongation factor complex (NELF complex) to enhance transcriptional pausing at sites proximal to the promoter. Transcriptional pausing may facilitate the assembly of an elongation competent RNA polymerase II complex. DSIF and NELF promote pausing by inhibition of the transcription elongation factor TFIIS/S-II. TFIIS/S-II binds to RNA polymerase II at transcription pause sites and stimulates the weak intrinsic nuclease activity of the enzyme. Cleavage of blocked transcripts by RNA polymerase II promotes the resumption of transcription from the new 3' terminus and may allow repeated attempts at transcription through natural pause sites. Following phosphorylation by CDK9, DSIF can also positively regulate transcriptional elongation., [UniProtKB, UniProtKB]; SPT5 stabilizes RNA polymerase II, orchestrates transcription cycles, and maintains the enhancer landscape., [RefSeq, PubMed]", "predicted_glycosites": 3, "predicted_n_glycosites": 0, "predicted_o_glycosites": 3, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 14, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 5, "binding_glycan_count": 0, "secondary_ac_list": "Q3UJ77;Q3UJH1;Q3UKD7;Q3UM54;Q6PB73;Q6PDP0;Q6PFR4", "ec_number_list": "", "go_molecular_function": "GO:0003729 mRNA binding;GO:0019899 enzyme binding;GO:0046982 protein heterodimerization activity;GO:0140870 RNA polymerase inhibitor activity", "go_cellular_component": "GO:0032044 DSIF complex", "go_biological_process": "GO:0032785 negative regulation of DNA-templated transcription, elongation;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0016239 positive regulation of macroautophagy;GO:0006368 transcription elongation by RNA polymerase II;GO:0032968 positive regulation of transcription elongation by RNA polymerase II", "synthesized_glycan_count": 0, "hit_score": 1.9, "record_id": "O55201-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P15508-1", "uniprot_id": "SPTB1_MOUSE", "mass": 245250.0, "length": 2128, "protein_name": "Spectrin beta chain, erythrocytic", "gene_name": "Sptb", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Sptb; Spnb-1; Spnb1; Sptb1", "gene_names_refseq": "", "protein_names_uniprotkb": "Spectrin beta chain, erythrocytic; Beta-I spectrin", "protein_names_refseq": "", "tax_id": 10090, "disease": "spinocerebellar ataxia 5 (Disease Ontology:DOID:0050882); hereditary spherocytosis type 2 (Disease Ontology:DOID:0110917); hereditary spherocytosis (Disease Ontology:DOID:12971)", "pathway": " (R-MMU-375165); (R-MMU-445095); (R-MMU-5673001); (R-MMU-6807878)", "pathway_count": 4, "publication_count": 11, "publication_id_list": "10.1101/2023.09.13.557529;16452087;17242355;21183079;21750661;30084848;3307952;33300544;34428180;35820727;8219239", "class_list": "", "function": "Spectrin is the major constituent of the cytoskeletal network underlying the erythrocyte plasma membrane. It associates with band 4.1 and actin to form the cytoskeletal superstructure of the erythrocyte plasma membrane., [UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 3, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 3, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 3, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 12, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 4, "disease_count": 3, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003779 actin binding;GO:0005200 structural constituent of cytoskeleton;GO:0051015 actin filament binding;GO:0030506 ankyrin binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0016020 membrane", "go_biological_process": "GO:0098885 modification of postsynaptic actin cytoskeleton;GO:0007009 plasma membrane organization;GO:0030036 actin cytoskeleton organization;GO:0030097 hemopoiesis;GO:0006779 porphyrin-containing compound biosynthetic process", "synthesized_glycan_count": 0, "hit_score": 2.0, "record_id": "P15508-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P97454-1", "uniprot_id": "SMAD5_MOUSE", "mass": 52172.0, "length": 465, "protein_name": "SMAD family member 5", "gene_name": "Smad5", "organism": "Mouse", "refseq_name": "SMAD family member 5", "refseq_ac": "NP_001157513", "gene_names_uniprotkb": "Smad5; Madh5; Msmad5", "gene_names_refseq": "1110051M15Rik; Dwf-C; Madh5; MusMLP; Smad5", "protein_names_uniprotkb": "SMAD family member 5; Dwarfin-C; Dwf-C; MAD homolog 5; Mothers against DPP homolog 5; Mothers against decapentaplegic homolog 5; SMAD 5; mSmad5", "protein_names_refseq": "MAD homolog 5; SMAD family member 5; Smad 5; dwarfin-C; mSmad5; mothers against DPP homolog 5; mothers against decapentaplegic homolog 5", "tax_id": 10090, "disease": "juvenile polyposis syndrome (Disease Ontology:DOID:0050787)", "pathway": " (mmu:17129); (R-MMU-201451)", "pathway_count": 2, "publication_count": 15, "publication_id_list": "10079220;10504300;10708952;12370310;12393578;15221015;15331632;16522160;21239498;26304548;31599954;34428180;8799132;9076683;9759503", "class_list": "", "function": "Transcriptional regulator that plays a role in various cellular processes including embryonic development, cell differentiation, angiogenesis and tissue homeostasis (PubMed:10079220, PubMed:12393578). Upon BMP ligand binding to their receptors at the cell surface, is phosphorylated by activated type I BMP receptors (BMPRIs) and associates with SMAD4 to form a heteromeric complex which translocates into the nucleus acting as transcription factor. In turn, the hetero-trimeric complex recognizes cis-regulatory elements containing Smad Binding Elements (SBEs) to modulate the outcome of the signaling network (PubMed:26304548). Non-phosphorylated SMAD5 has a cytoplasmic role in energy metabolism regulation by promoting mitochondrial respiration and glycolysis in response to cytoplasmic pH changes. Mechanistically, interacts with hexokinase 1/HK1 and thereby accelerates glycolysis., [UniProtKB, UniProtKB, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 1, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "P70341;Q810K0", "ec_number_list": "", "go_molecular_function": "GO:0046872 metal ion binding;GO:0031625 ubiquitin protein ligase binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding", "go_cellular_component": "GO:0071144 heteromeric SMAD protein complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005739 mitochondrion", "go_biological_process": "GO:0002051 osteoblast fate commitment;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001525 angiogenesis;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II", "synthesized_glycan_count": 0, "hit_score": 1.6, "record_id": "P97454-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q924S7-1", "uniprot_id": "SPRE2_MOUSE", "mass": 46794.0, "length": 410, "protein_name": "Sprouty-related, EVH1 domain-containing protein 2", "gene_name": "Spred2", "organism": "Mouse", "refseq_name": "sprouty-related, EVH1 domain-containing protein 2", "refseq_ac": "NP_277058", "gene_names_uniprotkb": "Spred2", "gene_names_refseq": "Spred2", "protein_names_uniprotkb": "Sprouty-related, EVH1 domain-containing protein 2; Spred-2", "protein_names_refseq": "sprouty protein with EVH-1 domain 2, related sequence; sprouty-related, EVH1 domain-containing protein 2", "tax_id": 10090, "disease": "Noonan syndrome (Disease Ontology:DOID:3490); achondroplasia (Disease Ontology:DOID:4480)", "pathway": " (mmu:114716); (R-MMU-5658442); (R-MMU-5658623)", "pathway_count": 3, "publication_count": 14, "publication_id_list": "11493923;14981116;15580519;15946934;17974561;19144319;21750661;25576668;28882895;29501879;34626534;35820727;36704943;38892460", "class_list": "", "function": "MicroRNA-141-3p mediates epithelial cell proliferation, apoptosis, and epithelial-mesenchymal transition and alleviates pulmonary fibrosis in mice via Spred2., [RefSeq, PubMed]; Negatively regulates Ras signaling pathways and downstream activation of MAP kinases (PubMed:11493923). Recruits and translocates NF1 to the cell membrane, thereby enabling NF1-dependent hydrolysis of active GTP-bound Ras to inactive GDP-bound Ras (By similarity). Inhibits fibroblast growth factor (FGF)-induced retinal lens fiber differentiation, probably by inhibiting FGF-mediated phosphorylation of ERK1/2 (PubMed:29501879). Inhibits TGFB-induced epithelial-to-mesenchymal transition in lens epithelial cells (PubMed:25576668)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed]; SPRED2 Is a Novel Regulator of Autophagy in Hepatocellular Carcinoma Cells and Normal Hepatocytes. Publication Status: Online-Only, [RefSeq, PubMed]; Spred-2 functions as a negative regulator of aorta-gonad-mesonephros hematopoiesis by inhibiting hematopoietic cytokine signaling., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0005173 stem cell factor receptor binding;GO:0019901 protein kinase binding;GO:0030291 protein serine/threonine kinase inhibitor activity", "go_cellular_component": "GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0030658 transport vesicle membrane;GO:0031410 cytoplasmic vesicle", "go_biological_process": "GO:1902532 negative regulation of intracellular signal transduction;GO:0070373 negative regulation of ERK1 and ERK2 cascade;GO:0043517 positive regulation of DNA damage response, signal transduction by p53 class mediator;GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway;GO:0043409 negative regulation of MAPK cascade", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "Q924S7-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q61142-1", "uniprot_id": "SPIN1_MOUSE", "mass": 29643.0, "length": 262, "protein_name": "Spindlin-1", "gene_name": "Spin1", "organism": "Mouse", "refseq_name": "spindlin-1 isoform 2", "refseq_ac": "NP_001269957", "gene_names_uniprotkb": "Spin1; Spin", "gene_names_refseq": "SSEC P; Spin1; Spin", "protein_names_uniprotkb": "Spindlin-1; 30000 Mr metaphase complex; SSEC P; Spindlin1", "protein_names_refseq": "30000 Mr metaphase complex; spindlin-1 isoform 2; spindlin1", "tax_id": 10090, "disease": "", "pathway": " (mmu:20729)", "pathway_count": 1, "publication_count": 11, "publication_id_list": "16098913;18201843;18543248;18645677;23806337;23894536;34428180;38348706;39294378;40885482;9053325", "class_list": "", "function": "Chromatin reader that specifically recognizes and binds histone H3 both trimethylated at 'Lys-4' and 'Lys-9' (H3K4me3K9me3) and is involved in piRNA-mediated retrotransposon silencing during spermatogenesis (PubMed:39294378). Plays a key role in the initiation of the PIWIL4-piRNA pathway, a pathway that directs transposon DNA methylation and silencing in the male embryonic germ cells, by promoting recruitment of DNA methylation machinery to transposons: binds young, but not old, LINE1 transposons, which are specifically marked with H3K4me3K9me3, and promotes the recruitment of PIWIL4 and SPOCD1 to transposons, leading to piRNA-directed DNA methylation (PubMed:39294378). Also recognizes and binds histone H3 both trimethylated at 'Lys-4' and asymmetrically dimethylated at 'Arg-8' (H3K4me3 and H3R8me2a) and acts as an activator of Wnt signaling pathway downstream of PRMT2 (By similarity). Overexpression induces metaphase arrest and chromosomal instability (PubMed:18543248). Overexpression induces metaphase arrest and chromosomal instability (By similarity). Localizes to active rDNA loci and promotes the expression of rRNA genes (By similarity). May play a role in cell-cycle regulation during the transition from gamete to embryo (PubMed:23894536). Involved in oocyte meiotic resumption, a process that takes place before ovulation to resume meiosis of oocytes blocked in prophase I: may act by regulating maternal transcripts to control meiotic resumption (PubMed:23894536)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed]; Exosome-transported of circ_0081069 induces SPIN1 production by binding to miR-195-5p to inhibit radiosensitivity in esophageal squamous cell carcinoma., [RefSeq, PubMed]; SPINDLIN1 is an important gene for mammalian mitotic chromosome functions, and disrupted regulation results in abnormal cell division, a mechanism that may be involved in tumorigenesis, [RefSeq, PubMed]; Spindlin1 gene may contribute to tumorigenesis, [RefSeq, PubMed]; Two-factor authentication underpins the precision of the piRNA pathway., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q3TLC3;Q3UT05;Q91VG8", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0140566 histone reader activity;GO:0140002 histone H3K4me3 reader activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005819 spindle;GO:0005829 cytosol", "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0045893 positive regulation of DNA-templated transcription;GO:0016055 Wnt signaling pathway;GO:0007143 female meiotic nuclear division;GO:0009303 rRNA transcription", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "Q61142-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q62261-1", "uniprot_id": "SPTB2_MOUSE", "mass": 274223.0, "length": 2363, "protein_name": "Spectrin beta chain, non-erythrocytic 1", "gene_name": "Sptbn1", "organism": "Mouse", "refseq_name": "spectrin beta chain, non-erythrocytic 1 isoform 2", "refseq_ac": "NP_033286", "gene_names_uniprotkb": "Sptbn1; Elf; Spnb-2; Spnb2; Sptb2", "gene_names_refseq": "9930031C03Rik; SPTB2; Spnb-2; Spnb2; Sptbn1; elf1; elf3; mKIAA4049", "protein_names_uniprotkb": "Spectrin beta chain, non-erythrocytic 1; Beta-II spectrin; Embryonic liver fodrin; Fodrin beta chain", "protein_names_refseq": "beta fodrin; beta-II spectrin; beta-spectrin 2, non-erythrocytic; brain spectrin; embryonic liver fodrin; fodrin beta chain; spectrin G; spectrin beta 2; spectrin beta chain, brain 1; spectrin beta chain, non-erythrocytic 1 isoform 2; spectrin beta chain, non-erythrocytic 1; spectrin, non-erythroid beta chain 1", "tax_id": 10090, "disease": "spinocerebellar ataxia 5 (Disease Ontology:DOID:0050882); Beckwith-Wiedemann syndrome (Disease Ontology:DOID:5572)", "pathway": " (mmu:20742); (R-MMU-375165); (R-MMU-445095); (R-MMU-5673001); (R-MMU-6807878); (R-MMU-9013420); (R-MMU-9013424)", "pathway_count": 7, "publication_count": 44, "publication_id_list": "10.1101/2023.09.13.557529;12522145;1281216;15262991;15345747;16452087;16452088;17114649;17242355;18034455;18630941;18683930;19131326;19692427;21183079;21750661;22645316;25428506;26495903;29562282;30016717;30059200;30084848;31219806;31361958;32782141;32848054;34211179;34428180;34678516;36064721;36288343;36852467;37507081;39276238;39627609;40021952;40885482;40997131;7588597;8208297;8479293;9199409;9927192", "class_list": "", "function": "Fodrin, which seems to be involved in secretion, interacts with calmodulin in a calcium-dependent manner and is thus candidate for the calcium-dependent movement of the cytoskeleton at the membrane. Plays a critical role in central nervous system development and function., [UniProtKB, PubMed, UniProtKB, UniProtKB]; Osteocyte Sptbn1 Deficiency Alters Cell Survival and Mechanotransduction Following Formation of Plasma Membrane Disruptions (PMD) from Mechanical Loading., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 1, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 14, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 14, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 14, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 33, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 3, "disease_count": 2, "glyco_site_count": 16, "binding_glycan_count": 0, "secondary_ac_list": "A2AFU1;Q3TEM7;Q5SQL8;Q5SQL9;Q9QWJ7", "ec_number_list": "", "go_molecular_function": "GO:0005200 structural constituent of cytoskeleton;GO:0005516 calmodulin binding;GO:0005543 phospholipid binding;GO:0051015 actin filament binding;GO:0044877 protein-containing complex binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005634 nucleus;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005829 cytosol", "go_biological_process": "GO:0060390 regulation of SMAD protein signal transduction;GO:0007009 plasma membrane organization;GO:0072659 protein localization to plasma membrane;GO:0007417 central nervous system development;GO:0030036 actin cytoskeleton organization", "synthesized_glycan_count": 0, "hit_score": 6.4, "record_id": "Q62261-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6NSW3-1", "uniprot_id": "SPKAP_MOUSE", "mass": 185095.0, "length": 1687, "protein_name": "A-kinase anchor protein SPHKAP", "gene_name": "Sphkap", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Sphkap; Kiaa1678", "gene_names_refseq": "", "protein_names_uniprotkb": "A-kinase anchor protein SPHKAP; SPHK1-interactor and AKAP domain-containing protein", "protein_names_refseq": "", "tax_id": 10090, "disease": "", "pathway": "", "pathway_count": 0, "publication_count": 10, "publication_id_list": "10.1101/2023.09.13.557529;16452087;21183079;21750661;22645316;29237092;31219806;32848054;40021952;40885482", "class_list": "", "function": "Anchoring protein that binds preferentially to the type I regulatory subunit of c-AMP-dependent protein kinase (PKA type I) and targets it to distinct subcellular compartments. May act as a converging factor linking cAMP and sphingosine signaling pathways. Plays a regulatory role in the modulation of SPHK1 (By similarity)., [UniProtKB]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 3, "reported_o_glycosites_with_glycan": 6, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 3, "total_reported_o_glycosites": 6, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 3, "total_o_glycosites": 6, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 8, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 4, "disease_count": 0, "glyco_site_count": 8, "binding_glycan_count": 0, "secondary_ac_list": "Q6PAM6;Q6PAP7;Q80TA7;Q80XT3;Q8BYQ9;Q8BZL6;Q8C1G7", "ec_number_list": "", "go_molecular_function": "GO:0051018 protein kinase A binding", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0030018 Z disc", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 2.4, "record_id": "Q6NSW3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8R3P9-1", "uniprot_id": "SLF1_MOUSE", "mass": 121004.0, "length": 1054, "protein_name": "SMC5-SMC6 complex localization factor protein 1", "gene_name": "Slf1", "organism": "Mouse", "refseq_name": "SMC5-SMC6 complex localization factor protein 1", "refseq_ac": "NP_598832", "gene_names_uniprotkb": "Slf1; Ankrd32; Brctd1; Brctx", "gene_names_refseq": "2700017A04Rik; Ankrd32; Brctd1; Brctx; C730024G01Rik; Slf1", "protein_names_uniprotkb": "SMC5-SMC6 complex localization factor protein 1; Ankyrin repeat domain-containing protein 32; BRCT domain-containing protein 1; Protein BRCTx", "protein_names_refseq": "BRCT domain containing 1; BRCT domain-containing protein 1; SMC5-SMC6 complex localization factor protein 1; ankyrin repeat domain 32; ankyrin repeat domain-containing protein 32; protein BRCTx", "tax_id": 10090, "disease": "", "pathway": " (mmu:105377)", "pathway_count": 1, "publication_count": 6, "publication_id_list": "15632077;21750661;22036607;30084848;34428180;39927985", "class_list": "", "function": "Plays a role in the DNA damage response (DDR) pathway by regulating postreplication repair of UV-damaged DNA and genomic stability maintenance. The SLF1-SLF2 complex acts to link RAD18 with the SMC5-SMC6 complex at replication-coupled interstrand cross-links (ICL) and DNA double-strand breaks (DSBs) sites on chromatin during DNA repair in response to stalled replication forks. Promotes the recruitment of SLF2 and the SMC5-SMC6 complex to DNA lesions., [UniProtKB, UniProtKB]; RAD18 interacts with BRCTx in a phosphorylation-dependent manner, [RefSeq, PubMed]; Results describe the cloning, characterization, and targeted mutagenesis of Brctx, a novel gene with a BRCT motif [Brctx]., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q497V2;Q5XK30;Q8BHY5;Q8BQM6;Q921Y9", "ec_number_list": "", "go_molecular_function": "GO:0031625 ubiquitin protein ligase binding;GO:0044877 protein-containing complex binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0035861 site of double-strand break", "go_biological_process": "GO:1990166 protein localization to site of double-strand break;GO:0006281 DNA repair;GO:0006974 DNA damage response;GO:0031334 positive regulation of protein-containing complex assembly;GO:2000781 positive regulation of double-strand break repair", "synthesized_glycan_count": 0, "hit_score": 0.9, "record_id": "Q8R3P9-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q91WK1-1", "uniprot_id": "SPRY4_MOUSE", "mass": 23275.0, "length": 207, "protein_name": "SPRY domain-containing protein 4", "gene_name": "Spryd4", "organism": "Mouse", "refseq_name": "SPRY domain-containing protein 4", "refseq_ac": "NP_079992", "gene_names_uniprotkb": "Spryd4", "gene_names_refseq": "4633402N23Rik; Spryd4", "protein_names_uniprotkb": "SPRY domain-containing protein 4", "protein_names_refseq": "SPRY domain-containing protein 4", "tax_id": 10090, "disease": "", "pathway": " (mmu:66701)", "pathway_count": 1, "publication_count": 2, "publication_id_list": "23576753;23806337", "class_list": "", "function": "", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "Q8BUS6;Q9D651", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "GO:0005634 nucleus;GO:0005739 mitochondrion", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 0.3, "record_id": "Q91WK1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P17742-1", "uniprot_id": "PPIA_MOUSE", "mass": 17971.0, "length": 164, "protein_name": "Peptidyl-prolyl cis-trans isomerase A", "gene_name": "Ppia", "organism": "Mouse", "refseq_name": "peptidyl-prolyl cis-trans isomerase A", "refseq_ac": "NP_032933", "gene_names_uniprotkb": "Ppia", "gene_names_refseq": "Cphn; CyP-18; CypA; Ppia; SP18", "protein_names_uniprotkb": "Peptidyl-prolyl cis-trans isomerase A; 5.2.1.8; Cyclophilin A; Cyclosporin A-binding protein; PPIase A; Rotamase A; SP18", "protein_names_refseq": "PPIase A; cyclophilin A; cyclosporin A-binding protein; peptidyl-prolyl cis-trans isomerase A; rotamase A", "tax_id": 10090, "disease": "childhood-onset asthma (Disease Ontology:DOID:0080815); Bell's palsy (Disease Ontology:DOID:12506); aggressive periodontitis (Disease Ontology:DOID:1474); epilepsy (Disease Ontology:DOID:1826); cholangiocarcinoma (Disease Ontology:DOID:4947); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); nasopharynx carcinoma (Disease Ontology:DOID:9261)", "pathway": " (mmu:268373); (R-MMU-210991); (R-MMU-6798695)", "pathway_count": 3, "publication_count": 26, "publication_id_list": "10964515;1565646;16352598;21183079;21750661;2197604;23806337;24429998;25678563;25967121;26495903;31219806;32848054;33725478;34428180;35984892;36288343;37453647;37507081;37828378;38427624;38723722;39627609;39927985;40885482;7664883", "class_list": "glycogene", "function": "Catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides (PubMed:24429998). Exerts a strong chemotactic effect on leukocytes partly through activation of one of its membrane receptors BSG/CD147, initiating a signaling cascade that culminates in MAPK/ERK activation (By similarity). Activates endothelial cells (ECs) in a pro-inflammatory manner by stimulating activation of NF-kappa-B and ERK, JNK and p38 MAP-kinases and by inducing expression of adhesion molecules including SELE and VCAM1 (By similarity). Induces apoptosis in ECs by promoting the FOXO1-dependent expression of CCL2 and BCL2L11 which are involved in EC chemotaxis and apoptosis (By similarity). In response to oxidative stress, initiates proapoptotic and antiapoptotic signaling in ECs via activation of NF-kappa-B and AKT1 and up-regulation of antiapoptotic protein BCL2 (By similarity). Negatively regulates MAP3K5/ASK1 kinase activity, autophosphorylation and oxidative stress-induced apoptosis mediated by MAP3K5/ASK1 (By similarity). Necessary for the assembly of TARDBP in heterogeneous nuclear ribonucleoprotein (hnRNP) complexes and regulates TARDBP binding to RNA UG repeats and TARDBP-dependent expression of HDAC6, ATG7 and VCP which are involved in clearance of protein aggregates (PubMed:25678563). Plays an important role in platelet activation and aggregation (PubMed:24429998). Regulates calcium mobilization and integrin ITGA2B:ITGB3 bidirectional signaling via increased ROS production as well as by facilitating the interaction between integrin and the cell cytoskeleton (PubMed:24429998). Binds heparan sulfate glycosaminoglycans (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed]; Intracellular and extracellular Cyclophilin a promote cardiac fibrosis through TGF-beta signaling in response to angiotensin ., [RefSeq, PubMed]; Mice lacking cyclophilin B, but not cyclophilin A, are protected from the development of NASH in a diet and chemical-induced model. Publication Status: Online-Only, [RefSeq, PubMed]; PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides., [UniProtKB, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 1, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 2, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 2, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 2, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 2, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 7, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q9CWJ5;Q9R137", "ec_number_list": "5.2.1.8;2.4.1.25;3.2.1.33;3.5.4.6;1.11.1.24;3.4.22.52;3.4.19.12;3.4.22.27;1.1.1.42;3.4.21.46;4.1.2.13;5.3.1.9;5.1.3.-;3.6.4.10;2.4.2.7;1.16.3.1;3.6.5.-;4.2.1.24;3.4.22.1;3.2.1.31;2.7.1.11;2.7.10.2;3.4.23.5;2.5.1.18;4.2.99.18;5.6.2.4;2.4.2.1;3.2.1.23;1.11.1.6;3.3.2.6;3.4.11.4;1.1.1.205;5.3.2.1;5.3.3.12;3.4.24.35;3.6.1.-;2.7.11.24;1.13.11.-;1.13.11.34;1.11.1.7;3.1.6.12;2.7.11.1;2.7.1.40;3.5.4.5;3.4.25.1;2.7.11.39;2.7.4.6;2.7.13.3;3.6.4.6;2.7.1.1;2.7.1.-;3.1.1.47;3.6.4.13;2.7.11.22;2.7.11.23;2.3.2.26;5.4.2.2;5.4.2.7;2.3.2.27;3.1.6.14;2.7.1.35;3.4.19.1;3.6.1.6;2.3.3.8;4.1.2.4;2.3.2.5;5.4.2.11;5.4.2.4;2.4.1.1;2.4.1.186;3.4.18.1;3.5.1.23;3.5.1.-", "go_molecular_function": "GO:0005178 integrin binding;GO:1904399 heparan sulfate binding;GO:0016018 cyclosporin A binding;GO:0003755 peptidyl-prolyl cis-trans isomerase activity", "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol", "go_biological_process": "GO:2001233 regulation of apoptotic signaling pathway;GO:0001934 positive regulation of protein phosphorylation;GO:0043410 positive regulation of MAPK cascade;GO:0001933 negative regulation of protein phosphorylation;GO:0006469 negative regulation of protein kinase activity", "synthesized_glycan_count": 0, "hit_score": 3.0, "record_id": "P17742-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9JJI6-1", "uniprot_id": "PIGO_MOUSE", "mass": 119156.0, "length": 1093, "protein_name": "GPI ethanolamine phosphate transferase 3, catalytic subunit", "gene_name": "Pigo", "organism": "Mouse", "refseq_name": "", "refseq_ac": "", "gene_names_uniprotkb": "Pigo", "gene_names_refseq": "", "protein_names_uniprotkb": "GPI ethanolamine phosphate transferase 3, catalytic subunit; 2.-.-.-; PIG-O; Phosphatidylinositol-glycan biosynthesis class O protein", "protein_names_refseq": "", "tax_id": 10090, "disease": "hyperphosphatasia with impaired intellectual development syndrome 2 (Disease Ontology:DOID:0070434)", "pathway": " (mmu:56703)", "pathway_count": 1, "publication_count": 4, "publication_id_list": "10.1101/2023.09.13.557529;10781593;21750661;25428506", "class_list": "glycogene", "function": "Catalytic subunit of the ethanolamine phosphate transferase 3 complex that transfers an ethanolamine phosphate (EtNP) from a phosphatidylethanolamine (PE) to the 6-OH position of the third alpha-1,2-linked mannose of the a 2-acyl-6-[alpha-D-mannosyl-(1->2)-alpha-D-mannosyl-(1->6)-2-phosphoethanolamine-alpha-D-mannosyl-(1->4)-alpha-D-glucosaminyl]-1-(1-radyl,2-acyl-sn-glycero-3-phospho)-1D-myo-inositol (also termed H6) intermediate to generate a a 2-acyl-6-[6-phosphoethanolamine-alpha-D-mannosyl-(1->2)-alpha-D-mannosyl-(1->6)-2-phosphoethanolamine-alpha-D-mannosyl-(1->4)-alpha-D-glucosaminyl]-1-(1-radyl,2-acyl-sn-glycero-3-phospho)-1D-myo-inositol (also termed H7) and participates in the tenth step of the glycosylphosphatidylinositol-anchor biosynthesis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, PubMed, UniProtKB]", "predicted_glycosites": 2, "predicted_n_glycosites": 1, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 63, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 3, "binding_glycan_count": 0, "secondary_ac_list": "Q9CRY2", "ec_number_list": "2.-.-.-", "go_molecular_function": "GO:0051377 mannose-ethanolamine phosphotransferase activity", "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane", "go_biological_process": "GO:0006506 GPI anchor biosynthetic process", "synthesized_glycan_count": 0, "hit_score": 0.7, "record_id": "Q9JJI6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P43136-1", "uniprot_id": "NR2F6_MOUSE", "mass": 41968.0, "length": 390, "protein_name": "Nuclear receptor subfamily 2 group F member 6", "gene_name": "Nr2f6", "organism": "Mouse", "refseq_name": "nuclear receptor subfamily 2 group F member 6 isoform 1", "refseq_ac": "NP_034280", "gene_names_uniprotkb": "Nr2f6; Ear-2; Ear2; Erbal2", "gene_names_refseq": "COUP-TF3; EAR2; Erbal2; Nr2f6", "protein_names_uniprotkb": "Nuclear receptor subfamily 2 group F member 6; COUP transcription factor 3; COUP-TF3; EAR-2; V-erbA-related protein 2", "protein_names_refseq": "COUP transcription factor 3; EAR-2; V-erbA-related protein 2; avian erythroblastic leukemia viral (v-erb-a) oncogene homolog-like 2; nuclear receptor subfamily 2 group F member 6 isoform 1", "tax_id": 10090, "disease": "type 2 diabetes mellitus (Disease Ontology:DOID:9352)", "pathway": " (mmu:13864); (R-MMU-383280)", "pathway_count": 2, "publication_count": 14, "publication_id_list": "10.1101/2023.09.13.557529;10318855;11382775;12690040;15741322;17242355;18701084;21183079;21750661;31599954;38682559;38710764;7947324;8194772", "class_list": "", "function": "Concerted regulation of skeletal muscle metabolism and contractile properties by the orphan nuclear receptor Nr2f6., [RefSeq, PubMed]; Transcription factor predominantly involved in transcriptional repression. Binds to promoter/enhancer response elements that contain the imperfect 5'-AGGTCA-3' direct or inverted repeats with various spacings which are also recognized by other nuclear hormone receptors. Involved in modulation of hormonal responses. Represses transcriptional activity of the lutropin-choriogonadotropic hormone receptor/LHCGR gene, the renin/REN gene and the oxytocin-neurophysin/OXT gene. Represses the triiodothyronine-dependent and -independent transcriptional activity of the thyroid hormone receptor gene in a cell type-specific manner. The corepressing function towards thyroid hormone receptor beta/THRB involves at least in part the inhibition of THRB binding to triiodothyronine response elements (TREs) by NR2F6. Inhibits NFATC transcription factor DNA binding and subsequently its transcriptional activity. Acts as transcriptional repressor of IL-17 expression in Th-17 differentiated CD4(+) T cells and may be involved in induction and/or maintenance of peripheral immunological tolerance and autoimmunity. Involved in development of forebrain circadian clock; is required early in the development of the locus coeruleus (LC)., [UniProtKB, PubMed, PubMed, PubMed]; Trefoil factor 3 can stimulate Th17 cell response in the development of type 2 diabetes mellitus. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 3, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q61504;Q922G8", "ec_number_list": "", "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0043565 sequence-specific DNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0016607 nuclear speck", "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0007399 nervous system development;GO:0030154 cell differentiation;GO:0050965 detection of temperature stimulus involved in sensory perception of pain", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "P43136-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8CFH6-1", "uniprot_id": "SIK2_MOUSE", "mass": 104198.0, "length": 931, "protein_name": "Serine/threonine-protein kinase SIK2", "gene_name": "Sik2", "organism": "Mouse", "refseq_name": "serine/threonine-protein kinase SIK2 isoform 1", "refseq_ac": "NP_848825", "gene_names_uniprotkb": "Sik2; Snf1lk2", "gene_names_refseq": "G630080D20Rik; Sik2; Snf1lk2", "protein_names_uniprotkb": "Serine/threonine-protein kinase SIK2; 2.7.11.1; SIK-2; Salt-inducible kinase 2; Serine/threonine-protein kinase SNF1-like kinase 2", "protein_names_refseq": "SIK-2; SNF1-like kinase 2; salt induceable kinase 2; salt-inducible protein kinase 2; serine/threonine-protein kinase SIK2 isoform 1; serine/threonine-protein kinase SIK2; serine/threonine-protein kinase SNF1-like kinase 2", "tax_id": 10090, "disease": "", "pathway": " (mmu:235344)", "pathway_count": 1, "publication_count": 16, "publication_id_list": "12624099;16817901;18239551;19351809;20819186;21183079;21220102;21750661;25088745;29211348;30030465;30546087;32457359;32848054;34732767;36309093", "class_list": "", "function": "Results support a role for SIK2 in adipocyte energy metabolism. SIK2 may function similarly to AMPK for turning off lipogenesis in low-energy state., [RefSeq, PubMed]; SIK2 represses eumelanogenesis in mice., [RefSeq, PubMed]; SIK2-TORC2 cascade may be important for the regulation of PGC-1alpha and UCP-1 gene expression in insulin signaling in brown adipose tissue, [RefSeq, PubMed]; Salt-inducible kinase 2 regulates fibrosis during bleomycin-induced lung injury., [RefSeq, PubMed]; Serine/threonine-protein kinase that plays a role in many biological processes such as fatty acid oxidation, autophagy, immune response or glucose metabolism (PubMed:12624099, PubMed:16817901, PubMed:29211348). Phosphorylates 'Ser-794' of IRS1 in insulin-stimulated adipocytes, potentially modulating the efficiency of insulin signal transduction (PubMed:12624099). Inhibits CREB activity by phosphorylating and repressing TORCs, the CREB-specific coactivators (PubMed:16817901). Phosphorylates EP300 and thus inhibits its histone acetyltransferase activity. In turn, regulates the DNA-binding ability of several transcription factors such as PPARA or MLXIPL (By similarity). Also plays a role in thymic T-cell development (PubMed:34732767)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 8, "reported_mutagensis": 8, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;2.7.11.39;2.3.1.-;2.7.11.31;3.6.5.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0106310 protein serine kinase activity", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005789 endoplasmic reticulum membrane", "go_biological_process": "GO:0006468 protein phosphorylation;GO:0008610 lipid biosynthetic process;GO:0035556 intracellular signal transduction;GO:0046777 protein autophosphorylation;GO:0008286 insulin receptor signaling pathway", "synthesized_glycan_count": 0, "hit_score": 1.9, "record_id": "Q8CFH6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8CD54-1", "uniprot_id": "PIEZ2_MOUSE", "mass": 325628.0, "length": 2822, "protein_name": "Piezo-type mechanosensitive ion channel component 2", "gene_name": "Piezo2", "organism": "Mouse", "refseq_name": "piezo-type mechanosensitive ion channel component 2", "refseq_ac": "NP_001034574", "gene_names_uniprotkb": "Piezo2; Fam38b", "gene_names_refseq": "5930434P17; 9030411M15Rik; 9430028L06Rik; Fam38b2; Fam38b; Piezo2", "protein_names_uniprotkb": "Piezo-type mechanosensitive ion channel component 2; Protein FAM38B", "protein_names_refseq": "family with sequence similarity 38, member B2; piezo-type mechanosensitive ion channel component 2", "tax_id": 10090, "disease": "dehydrated hereditary stomatocytosis (Disease Ontology:DOID:0111575); distal arthrogryposis type 3 (Disease Ontology:DOID:0111607); distal arthrogryposis type 5 (Disease Ontology:DOID:0111608)", "pathway": " (mmu:667742)", "pathway_count": 1, "publication_count": 20, "publication_id_list": "20813920;21183079;21750661;22343900;22921401;23575686;24662763;24717433;25471886;26551544;28002412;31435011;33057202;34428180;37590348;38228630;38568807;39147733;39919739;41349545", "class_list": "", "function": "Data indicate that the Epac1-Piezo2 axis has a role in the development of mechanical allodynia during neuropathic pain, [RefSeq, PubMed]; Overexpression of Piezo1 or Piezo2 induced 2 kinetically distinct mechanically activated (MA) currents; Piezos are expressed in several tissues; propose that Piezos are components of MA cation channels, [RefSeq, PubMed]; Piezo2 sensitization may contribute to PKA- and PKC-mediated mechanical hyperalgesia., [RefSeq, PubMed]; Pore-forming subunit of the mechanosensitive non-specific cation Piezo channel required for rapidly adapting mechanically activated (MA) currents and has a key role in sensing touch and tactile pain (PubMed:20813920, PubMed:24717433, PubMed:31435011, PubMed:37590348). Piezo channels are homotrimeric three-blade propeller-shaped structures that utilize a cap-motion and plug-and-latch mechanism to gate their ion-conducting pathways (PubMed:31435011, PubMed:37590348). Expressed in sensory neurons, is essential for diverse physiological processes, including respiratory control, systemic metabolism, urinary function, and proprioception (PubMed:26551544, PubMed:28002412, PubMed:33057202, PubMed:39919739). Mediates airway stretch sensing, enabling efficient respiration at birth and maintaining normal breathing in adults (PubMed:28002412). It regulates brown and beige adipose tissue morphology and function, preventing systemic hypermetabolism (PubMed:39919739). In the lower urinary tract, acts as a sensor in both the bladder urothelium and innervating sensory neurons and is required for bladder-stretch sensing and urethral micturition reflexes, ensuring proper urinary function (PubMed:33057202). Additionally, Piezo2 serves as the principal mechanotransducer in proprioceptors, facilitating proprioception and coordinated body movements (PubMed:26551544). In inner ear hair cells, PIEZO1/2 subunits may constitute part of the mechanotransducer (MET) non-selective cation channel complex where they may act as pore-forming ion-conducting component in the complex (PubMed:38228630). Required for Merkel-cell mechanotransduction (PubMed:24717433). Plays a major role in light-touch mechanosensation (PubMed:25471886). In kidney, during blood volume challenges, regulates calcium dynamics and maintains renin production, thereby serving as an essential regulator of the renin-angiotensin-aldosterone system (RAAS) and systemic blood volume control (PubMed:41349545)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 3, "predicted_n_glycosites": 2, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 4, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 4, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 4, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 2, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 3, "glyco_site_count": 7, "binding_glycan_count": 0, "secondary_ac_list": "E2JF23;Q8BSM4;Q9D341", "ec_number_list": "2.7.11.1", "go_molecular_function": "GO:0005261 monoatomic cation channel activity;GO:0008381 mechanosensitive monoatomic ion channel activity;GO:0140135 mechanosensitive monoatomic cation channel activity", "go_cellular_component": "GO:0005886 plasma membrane;GO:0032809 neuronal cell body membrane;GO:0032437 cuticular plate;GO:0032420 stereocilium;GO:0016020 membrane", "go_biological_process": "GO:0042391 regulation of membrane potential;GO:0009612 response to mechanical stimulus;GO:0006812 monoatomic cation transport;GO:0071260 cellular response to mechanical stimulus;GO:0050982 detection of mechanical stimulus", "synthesized_glycan_count": 0, "hit_score": 2.5, "record_id": "Q8CD54-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8K2C6-1", "uniprot_id": "SIR5_MOUSE", "mass": 34134.0, "length": 310, "protein_name": "NAD-dependent protein deacylase sirtuin-5, mitochondrial", "gene_name": "Sirt5", "organism": "Mouse", "refseq_name": "NAD-dependent protein deacylase sirtuin-5, mitochondrial", "refseq_ac": "NP_849179", "gene_names_uniprotkb": "Sirt5; SIRT5; Sir2l5", "gene_names_refseq": "0610012J09Rik; 1500032M05Rik; Sirt5", "protein_names_uniprotkb": "NAD-dependent protein deacylase sirtuin-5, mitochondrial; 2.3.1.-; Regulatory protein SIR2 homolog 5; SIR2-like protein 5", "protein_names_refseq": "NAD-dependent deacetylase sirtuin-5; NAD-dependent lysine demalonylase and desuccinylase sirtuin-5, mitochondrial; NAD-dependent protein deacylase sirtuin-5, mitochondrial", "tax_id": 10090, "disease": "", "pathway": " (mmu:68346); (R-MMU-2151201); (R-MMU-70635)", "pathway_count": 3, "publication_count": 14, "publication_id_list": "18054327;19410549;21750661;21908771;22076378;23085393;23438705;23806337;24076663;24315375;24703693;36288343;37507081;39031546", "class_list": "", "function": "NAD-dependent lysine demalonylase, desuccinylase and deglutarylase that specifically removes malonyl, succinyl and glutaryl groups on target proteins. Activates CPS1 and contributes to the regulation of blood ammonia levels during prolonged fasting: acts by mediating desuccinylation and deglutarylation of CPS1, thereby increasing CPS1 activity in response to elevated NAD levels during fasting. Activates SOD1 by mediating its desuccinylation, leading to reduced reactive oxygen species. Modulates ketogenesis through the desuccinylation and activation of HMGCS2. Has weak NAD-dependent protein deacetylase activity; however this activity may not be physiologically relevant in vivo. Can deacetylate cytochrome c (CYCS) and a number of other proteins in vitro such as Uox., [UniProtKB, HAMAP, UniProtKB, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]; Results suggest that the SIRT3, SIRT4, and SIRT5 proteins exert distinct functions in mitochondria., [RefSeq, PubMed]; SIRT5 mutants reveal the role of conserved asparagine and glutamine residues in the NAD[+]-binding pocket., [RefSeq, PubMed]; SIRT5 plays a pivotal role in ammonia detoxification and disposal by activating carbamoyl phosphate synthetase 1, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 0, "reported_mutagensis": 1, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "2.3.1.-;2.3.1.286;6.3.4.16", "go_molecular_function": "GO:0036054 protein-malonyllysine demalonylase activity;GO:0036055 protein-succinyllysine desuccinylase activity;GO:0061697 protein-glutaryllysine deglutarylase activity;GO:0008270 zinc ion binding;GO:0070403 NAD+ binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0005758 mitochondrial intermembrane space;GO:0005759 mitochondrial matrix", "go_biological_process": "GO:0010566 regulation of ketone biosynthetic process;GO:0036046 protein demalonylation;GO:0036047 peptidyl-lysine demalonylation;GO:0036048 protein desuccinylation;GO:0036049 peptidyl-lysine desuccinylation", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "Q8K2C6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q62407-1", "uniprot_id": "SPEG_MOUSE", "mass": 354343.0, "length": 3262, "protein_name": "Striated muscle-specific serine/threonine-protein kinase", "gene_name": "Speg", "organism": "Mouse", "refseq_name": "striated muscle-specific serine/threonine-protein kinase isoform 2", "refseq_ac": "NP_001078839", "gene_names_uniprotkb": "Speg; Apeg1; Kiaa1297", "gene_names_refseq": "APEG-1; Apeg1; BPEG; D1Bwg1450e; SPEGalpha; SPEGbeta; Speg; mKIAA1297", "protein_names_uniprotkb": "Striated muscle-specific serine/threonine-protein kinase; 2.7.11.1; APEG-1; Aortic preferentially expressed protein 1", "protein_names_refseq": "aortic preferentially expressed gene 1; aortic preferentially expressed protein 1; striated muscle-specific serine/threonine-protein kinase isoform 2; striated muscle-specific serine/threonine-protein kinase", "tax_id": 10090, "disease": "centronuclear myopathy 5 (Disease Ontology:DOID:0111222)", "pathway": " (mmu:11790)", "pathway_count": 1, "publication_count": 15, "publication_id_list": "10973969;16452087;19118250;21183079;21750661;24129315;25428506;30059200;34428180;36288343;37709832;38145999;39927985;40885482;8663449", "class_list": "", "function": "Disruption of the striated preferentially expressed gene (Speg) locus leads to cardiac dysfunction and a phenotype consistent with dilated cardiomyopathy., [RefSeq, PubMed]; Isoform 3 may have a role in regulating the growth and differentiation of arterial smooth muscle cells., [UniProtKB]; Speg interactions that regulate the stability of excitation-contraction coupling protein complexes in triads and dyads. Publication Status: Online-Only, [RefSeq, PubMed]; Striated preferentially expressed gene deficiency leads to mitochondrial dysfunction in developing cardiomyocytes., [RefSeq, PubMed]; This gene encodes a protein with similarity to members of the myosin light chain kinase family. This protein family is required for myocyte cytoskeletal development. Studies have determined that a lack of this protein affected myocardial development. Multiple alternatively spliced transcript variants that encode different protein isoforms have been defined. [provided by RefSeq, Mar 2010]., [RefSeq]", "predicted_glycosites": 4, "predicted_n_glycosites": 0, "predicted_o_glycosites": 4, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 5, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 5, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 5, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 39, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 3, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 9, "binding_glycan_count": 0, "secondary_ac_list": "Q3TPH8;Q6P5V1;Q80TF7;Q80ZN0;Q8BZF4;Q9EQJ5", "ec_number_list": "2.7.11.1;2.7.11.25;2.7.11.24;2.7.12.2;2.7.12.1;2.7.11.22;2.7.10.2;2.7.11.-;2.7.11.4;2.7.11.10;2.7.11.11;2.7.11.26;2.7.11.19;2.7.11.17;2.7.2.3;2.7.11.12;2.7.11.23;3.1.11.-;2.7.4.6;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.13;2.7.1.153;2.7.1.137;2.7.1.40;2.7.11.21;2.7.11.39;2.3.1.-;2.7.11.31;3.6.5.-;2.3.1.48;4.1.1.32;2.7.11.38;3.6.1.-;3.6.-.-;3.1.26.-;2.7.11.34;2.7.1.154;2.7.11.8;2.7.1.150", "go_molecular_function": "GO:0004672 protein kinase activity;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0106310 protein serine kinase activity", "go_cellular_component": "GO:0005634 nucleus", "go_biological_process": "GO:0072359 circulatory system development;GO:0001701 in utero embryonic development;GO:0055013 cardiac muscle cell development;GO:0042692 muscle cell differentiation;GO:0060541 respiratory system development", "synthesized_glycan_count": 0, "hit_score": 2.2, "record_id": "Q62407-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9Z0H3-1", "uniprot_id": "SNF5_MOUSE", "mass": 44141.0, "length": 385, "protein_name": "SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1", "gene_name": "Smarcb1", "organism": "Mouse", "refseq_name": "SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1 isoform 1", "refseq_ac": "NP_035548", "gene_names_uniprotkb": "Smarcb1; Baf47; Ini1; Snf5l1", "gene_names_refseq": "Baf47; Ini1; SNF5/INI1; Smarcb1; Snf5", "protein_names_uniprotkb": "SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1; BAF47; BRG1-associated factor 47; Integrase interactor 1 protein; SNF5 homolog; mSNF5", "protein_names_refseq": "BRG1-associated factor 47; SNF5 homolog; SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1; SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1 isoform 1; SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1; integrase interactor 1 protein; mSNF5", "tax_id": 10090, "disease": "colorectal adenocarcinoma (Disease Ontology:DOID:0050861); Coffin-Siris syndrome 3 (Disease Ontology:DOID:0070045); schwannomatosis 1 (Disease Ontology:DOID:0070480); rhabdoid tumor predisposition syndrome 1 (Disease Ontology:DOID:0070618); sinonasal undifferentiated carcinoma (Disease Ontology:DOID:0080799); vestibular schwannomatosis (Disease Ontology:DOID:0111252); atypical teratoid rhabdoid tumor (Disease Ontology:DOID:2129); schwannomatosis (Disease Ontology:DOID:3204); meningioma (Disease Ontology:DOID:3565); rhabdoid cancer (Disease Ontology:DOID:3672); clear cell renal cell carcinoma (Disease Ontology:DOID:4467); synovial sarcoma (Disease Ontology:DOID:5485); epithelioid sarcoma (Disease Ontology:DOID:6193); hepatocellular carcinoma (Disease Ontology:DOID:684)", "pathway": " (mmu:20587); (R-MMU-3214858); (R-MMU-8939243); (R-MMU-9933937); (R-MMU-9933939); (R-MMU-9933946); (R-MMU-9934037)", "pathway_count": 7, "publication_count": 10, "publication_id_list": "10208879;16787967;17640523;20111005;21750661;22952240;26601204;29272704;34428180;39362842", "class_list": "", "function": "Core component of the BAF (SWI/SNF) complex. This ATP-dependent chromatin-remodeling complex plays important roles in cell proliferation and differentiation, in cellular antiviral activities and inhibition of tumor formation. The BAF complex is able to create a stable, altered form of chromatin that constrains fewer negative supercoils than normal. This change in supercoiling would be due to the conversion of up to one-half of the nucleosomes on polynucleosomal arrays into asymmetric structures, termed altosomes, each composed of 2 histones octamers. Stimulates in vitro the remodeling activity of SMARCA4/BRG1/BAF190A. Plays a key role in cell-cycle control and causes cell cycle arrest in G0/G1. Belongs to the neural progenitors-specific chromatin remodeling complex (npBAF complex) and the neuron-specific chromatin remodeling complex (nBAF complex). During neural development a switch from a stem/progenitor to a postmitotic chromatin remodeling mechanism occurs as neurons exit the cell cycle and become committed to their adult state. The transition from proliferating neural stem/progenitor cells to postmitotic neurons requires a switch in subunit composition of the npBAF and nBAF complexes. As neural progenitors exit mitosis and differentiate into neurons, npBAF complexes which contain ACTL6A/BAF53A and PHF10/BAF45A, are exchanged for homologous alternative ACTL6B/BAF53B and DPF1/BAF45B or DPF3/BAF45C subunits in neuron-specific complexes (nBAF). The npBAF complex is essential for the self-renewal/proliferative capacity of the multipotent neural stem cells. The nBAF complex along with CREST plays a role regulating the activity of genes essential for dendrite growth., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed]; Lack of SMARCB1 expression characterizes a subset of human and murine peripheral T-cell lymphomas. Publication Status: Online-Only, [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 14, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0003713 transcription coactivator activity;GO:0042802 identical protein binding;GO:0030957 Tat protein binding;GO:0002039 p53 binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0016514 SWI/SNF complex;GO:0071564 npBAF complex", "go_biological_process": "GO:1902459 positive regulation of stem cell population maintenance;GO:1902661 positive regulation of glucose mediated signaling pathway;GO:0039692 single stranded viral RNA replication via double stranded DNA intermediate;GO:2000819 regulation of nucleotide-excision repair;GO:0006338 chromatin remodeling", "synthesized_glycan_count": 0, "hit_score": 1.1, "record_id": "Q9Z0H3-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O35253-1", "uniprot_id": "SMAD7_MOUSE", "mass": 46442.0, "length": 426, "protein_name": "SMAD family member 7", "gene_name": "Smad7", "organism": "Mouse", "refseq_name": "SMAD family member 7", "refseq_ac": "NP_001036125", "gene_names_uniprotkb": "Smad7; Madh7; Madh8", "gene_names_refseq": "Madh7; Smad7", "protein_names_uniprotkb": "SMAD family member 7; MAD homolog 7; MAD homolog 8; Mothers against DPP homolog 7; Mothers against DPP homolog 8; Mothers against decapentaplegic homolog 7; Mothers against decapentaplegic homolog 8; SMAD 7", "protein_names_refseq": "MAD homolog 7; MAD homolog 8; SMAD 7; SMAD family member 7; madh8; mothers against DPP homolog 7; mothers against DPP homolog 8; mothers against decapentaplegic homolog 7; mothers against decapentaplegic homolog 8", "tax_id": 10090, "disease": "nephritis (Disease Ontology:DOID:10952); endometrial cancer (Disease Ontology:DOID:1380); pancreatic cancer (Disease Ontology:DOID:1793); pancreatic adenocarcinoma (Disease Ontology:DOID:4074); liver cirrhosis (Disease Ontology:DOID:5082); pulmonary hypertension (Disease Ontology:DOID:6432); hepatocellular carcinoma (Disease Ontology:DOID:684); colorectal cancer (Disease Ontology:DOID:9256)", "pathway": " (mmu:17131); (R-MMU-201451); (R-MMU-2173788); (R-MMU-2173796); (R-MMU-5689880)", "pathway_count": 5, "publication_count": 11, "publication_id_list": "10828018;11278814;14657019;15221015;15496141;21750661;23610558;38657333;38899461;39412480;9335507", "class_list": "", "function": "Antagonist of signaling by TGF-beta (transforming growth factor) type 1 receptor superfamily members; has been shown to inhibit TGF-beta (Transforming growth factor) and activin signaling by associating with their receptors thus preventing SMAD2 access. Functions as an adapter to recruit SMURF2 to the TGF-beta receptor complex. Also acts by recruiting the PPP1R15A-PP1 complex to TGFBR1, which promotes its dephosphorylation. Positively regulates PDPK1 kinase activity by stimulating its dissociation from the 14-3-3 protein YWHAQ which acts as a negative regulator., [UniProtKB, UniProtKB]; Fibroblast Smad7 Induction Protects the Remodeling Pressure-Overloaded Heart. Erratum:[Circ Res. 2025 Jun 6;136(12):e129. doi: 10.1161/RES.0000000000000716. PMID: 40472059], [RefSeq, PubMed]; Reduced expression of SMAD7 and consequent reduction of autophagy promotes endometrial stromal-myofibroblast transition and fibrosis., [RefSeq, PubMed]; UHRF1 inhibition mitigates vascular endothelial cell injury and ameliorates atherosclerosis in mice via regulating the SMAD7/YAP1 axis., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 1, "reported_mutagensis": 2, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 8, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "O88709", "ec_number_list": "", "go_molecular_function": "GO:0046872 metal ion binding;GO:0003714 transcription corepressor activity;GO:0031625 ubiquitin protein ligase binding;GO:0005518 collagen binding;GO:0008013 beta-catenin binding", "go_cellular_component": "GO:0071144 heteromeric SMAD protein complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005813 centrosome", "go_biological_process": "GO:0010717 regulation of epithelial to mesenchymal transition;GO:0017015 regulation of transforming growth factor beta receptor signaling pathway;GO:0060373 regulation of ventricular cardiac muscle cell membrane depolarization;GO:2000317 negative regulation of T-helper 17 type immune response;GO:0002725 negative regulation of T cell cytokine production", "synthesized_glycan_count": 0, "hit_score": 1.2, "record_id": "O35253-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8BUN5-1", "uniprot_id": "SMAD3_MOUSE", "mass": 48081.0, "length": 425, "protein_name": "SMAD family member 3", "gene_name": "Smad3", "organism": "Mouse", "refseq_name": "SMAD family member 3", "refseq_ac": "NP_058049", "gene_names_uniprotkb": "Smad3; Madh3", "gene_names_refseq": "Madh3; Smad3", "protein_names_uniprotkb": "SMAD family member 3; MAD homolog 3; Mad3; Mothers against DPP homolog 3; Mothers against decapentaplegic homolog 3; SMAD 3; mMad3", "protein_names_refseq": "MAD homolog 3; SMAD family member 3; Smad 3; mMad3; mad3; mothers against DPP homolog 3; mothers against decapentaplegic homolog 3", "tax_id": 10090, "disease": "pre-malignant neoplasm (Disease Ontology:DOID:0060071); Loeys-Dietz syndrome 3 (Disease Ontology:DOID:0070237); prostate cancer (Disease Ontology:DOID:10283); hypospadias (Disease Ontology:DOID:10892); alcoholic cardiomyopathy (Disease Ontology:DOID:12935); endometrial cancer (Disease Ontology:DOID:1380); alcoholic liver cirrhosis (Disease Ontology:DOID:14018); pancreatic cancer (Disease Ontology:DOID:1793); cervical squamous cell carcinoma (Disease Ontology:DOID:3744); Lynch syndrome (Disease Ontology:DOID:3883); lung non-small cell carcinoma (Disease Ontology:DOID:3908); osteoarthritis (Disease Ontology:DOID:8398); cocaine dependence (Disease Ontology:DOID:9975)", "pathway": " (mmu:17127); (R-MMU-1181150); (R-MMU-1502540); (R-MMU-2173788); (R-MMU-2173789); (R-MMU-2173795); (R-MMU-2173796); (R-MMU-5689880); (R-MMU-8941855); (R-MMU-9617828)", "pathway_count": 10, "publication_count": 44, "publication_id_list": "10197981;10331191;10559937;10681527;10823886;11094085;11585338;12370310;12943993;14617288;14755691;15221015;15241418;15282343;15356634;15464984;15496141;16115198;17341133;17467076;18039968;19106105;19458083;21035443;21145499;21295571;21750661;22045334;22781750;23786998;24391884;25945408;26289811;27207538;27221338;29234059;29581148;30132832;31219806;33232327;34428180;40128797;9380693;9702197", "class_list": "", "function": "Receptor-regulated SMAD (R-SMAD) that is an intracellular signal transducer and transcriptional modulator activated by TGF-beta (transforming growth factor) and activin type 1 receptor kinases. Binds the TRE element in the promoter region of many genes that are regulated by TGF-beta and, on formation of the SMAD3/SMAD4 complex, activates transcription. Also can form a SMAD3/SMAD4/JUN/FOS complex at the AP-1/SMAD site to regulate TGF-beta-mediated transcription. Has an inhibitory effect on wound healing probably by modulating both growth and migration of primary keratinocytes and by altering the TGF-mediated chemotaxis of monocytes. This effect on wound healing appears to be hormone-sensitive. Regulator of chondrogenesis and osteogenesis and inhibits early healing of bone fractures. Positively regulates PDPK1 kinase activity by stimulating its dissociation from the 14-3-3 protein YWHAQ which acts as a negative regulator (By similarity)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, UniProtKB, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 1, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 1, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 1, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 13, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 13, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "O09064;O09144;O14510;O35273;Q8BX84;Q92940;Q93002;Q9GKR4", "ec_number_list": "", "go_molecular_function": "GO:0070410 co-SMAD binding;GO:0031962 nuclear mineralocorticoid receptor binding;GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0003700 DNA-binding transcription factor activity", "go_cellular_component": "GO:0071144 heteromeric SMAD protein complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol", "go_biological_process": "GO:0017015 regulation of transforming growth factor beta receptor signaling pathway;GO:0030878 thyroid gland development;GO:0016202 regulation of striated muscle tissue development;GO:0071559 response to transforming growth factor beta;GO:0050678 regulation of epithelial cell proliferation", "synthesized_glycan_count": 0, "hit_score": 4.7, "record_id": "Q8BUN5-1", "record_type": "protein" }, { "uniprot_canonical_ac": "D3YZU1-1", "uniprot_id": "SHAN1_MOUSE", "mass": 226317.0, "length": 2167, "protein_name": "SH3 and multiple ankyrin repeat domains protein 1", "gene_name": "Shank1", "organism": "Mouse", "refseq_name": "SH3 and multiple ankyrin repeat domains protein 1", "refseq_ac": "NP_001029287", "gene_names_uniprotkb": "Shank1", "gene_names_refseq": "Shank1", "protein_names_uniprotkb": "SH3 and multiple ankyrin repeat domains protein 1; Shank1", "protein_names_refseq": "SH3 and multiple ankyrin repeat domains protein 1; SH3/ankyrin domain gene 1", "tax_id": 10090, "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041)", "pathway": " (mmu:243961); (R-MMU-6794361)", "pathway_count": 2, "publication_count": 20, "publication_id_list": "15033168;16452087;18034455;21183079;21423165;21750661;22645316;22826440;24129315;25428506;32848054;34678516;35181969;35388181;35820727;35822049;37880287;39927985;40021952;40885482", "class_list": "", "function": "A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling. Erratum:[Mol Psychiatry. 2022 Sep;27(9):3922. doi: 10.1038/s41380-022-01605-8. PMID: 35538194], [RefSeq, PubMed]; Downregulation of mGluR1-mediated signaling underlying autistic-like core symptoms in Shank1 P1812L-knock-in mice. Publication Status: Online-Only, [RefSeq, PubMed]; Seems to be an adapter protein in the postsynaptic density (PSD) of excitatory synapses that interconnects receptors of the postsynaptic membrane including NMDA-type and metabotropic glutamate receptors, and the actin-based cytoskeleton. Plays a role in the structural and functional organization of the dendritic spine and synaptic junction. Overexpression promotes maturation of dendritic spines and the enlargement of spine heads via its ability to recruit Homer to postsynaptic sites, and enhances presynaptic function (By similarity)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Suv39h1 regulates memory stability by inhibiting the expression of Shank1 in hippocampal newborn neurons., [RefSeq, PubMed]", "predicted_glycosites": 7, "predicted_n_glycosites": 0, "predicted_o_glycosites": 7, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 3, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 25, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 25, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 25, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 7, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 3, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 1, "glyco_site_count": 32, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0031877 somatostatin receptor binding;GO:0017124 SH3 domain binding;GO:0042802 identical protein binding;GO:0001664 G protein-coupled receptor binding;GO:0044877 protein-containing complex binding", "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0014069 postsynaptic density;GO:0016020 membrane", "go_biological_process": "GO:0042048 olfactory behavior;GO:0046959 habituation;GO:0050894 determination of affect;GO:0008306 associative learning;GO:0030534 adult behavior", "synthesized_glycan_count": 0, "hit_score": 4.7, "record_id": "D3YZU1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q6ZPQ6-1", "uniprot_id": "PITM2_MOUSE", "mass": 148035.0, "length": 1335, "protein_name": "Membrane-associated phosphatidylinositol transfer protein 2", "gene_name": "Pitpnm2", "organism": "Mouse", "refseq_name": "membrane-associated phosphatidylinositol transfer protein 2 isoform 2", "refseq_ac": "NP_001276401", "gene_names_uniprotkb": "Pitpnm2; Kiaa1457; Nir3", "gene_names_refseq": "NIR3; Pitpnm2; RDGBA2; Rdgb2; mKIAA1457", "protein_names_uniprotkb": "Membrane-associated phosphatidylinositol transfer protein 2; Drosophila retinal degeneration B homolog 2; NIR-3; PITPnm 2; Phosphatidylinositol transfer protein, membrane-associated 2; Pyk2 N-terminal domain-interacting receptor 3; RdgB2", "protein_names_refseq": "drosophila retinal degeneration B homolog 2; membrane-associated phosphatidylinositol transfer protein 2 isoform 2; membrane-associated phosphatidylinositol transfer protein 2; pyk2 N-terminal domain-interacting receptor 3; retinal degeneration B2 homolog", "tax_id": 10090, "disease": "", "pathway": " (mmu:19679); (R-MMU-1483226)", "pathway_count": 2, "publication_count": 13, "publication_id_list": "10.1101/2023.09.13.557529;10460238;12522145;16452087;21183079;21750661;24129315;26269578;30084848;31219806;31594866;34428180;36581712", "class_list": "", "function": "Here we found that under high light intensities, RdgB2(-/-) mutant mice showed normal pupillary light responses and circadian photoentrainment, [RefSeq, PubMed]; Membrane-associated phosphatidylinositol (PI) transfer protein that shuttles PI between intracellular membranes and thereby maintains plasma membrane phosphoinositide signaling competence (PubMed:36581712). Upon production of phosphatidic acid (PA), mediates the transfer of phosphatidylinositol from the endoplasmic reticulum to the plasma membrane at endoplasmic reticulum-plasma membrane contact sites. This transfer sustains phospholipase C (PLC)-coupled receptor signaling and replenishing of plasma membrane phosphoinositides following receptor-induced hydrolysis (PubMed:36581712). Promotes PIP2 replenishment following TCR stimulation; plays a critical role in T cell development by supporting calcium signaling in response to weak TCR stimulation during TCRbeta selection and positive selection of thymocytes, as well as maintaining peripheral T cell survival (PubMed:36581712)., [UniProtKB, PubMed]; The VAP-interacting membrane-associated phosphatidylinositol (PtdIns) transfer proteins PYK2 N-terminal domain-interacting receptor 2 (Nir2) and Nir3 specifically associate with Kv2.1 complexes., [RefSeq, PubMed]", "predicted_glycosites": 1, "predicted_n_glycosites": 0, "predicted_o_glycosites": 1, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 1, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 1, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 1, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 9, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 1, "reported_interactions": 0, "missing_score": 9343, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "Q9R1P5", "ec_number_list": "", "go_molecular_function": "GO:0005543 phospholipid binding;GO:0005509 calcium ion binding;GO:0030971 receptor tyrosine kinase binding;GO:0031210 phosphatidylcholine binding;GO:0035091 phosphatidylinositol binding", "go_cellular_component": "GO:0005737 cytoplasm;GO:0005856 cytoskeleton;GO:0012505 endomembrane system;GO:0044297 cell body", "go_biological_process": "", "synthesized_glycan_count": 0, "hit_score": 1.6, "record_id": "Q6ZPQ6-1", "record_type": "protein" }, { "uniprot_canonical_ac": "P15314-1", "uniprot_id": "IRF1_MOUSE", "mass": 37319.0, "length": 329, "protein_name": "Interferon regulatory factor 1", "gene_name": "Irf1", "organism": "Mouse", "refseq_name": "interferon regulatory factor 1 isoform a", "refseq_ac": "NP_001152868", "gene_names_uniprotkb": "Irf1", "gene_names_refseq": "Irf-1; Irf1", "protein_names_uniprotkb": "Interferon regulatory factor 1; IRF-1", "protein_names_refseq": "interferon regulatory factor 1 isoform a", "tax_id": 10090, "disease": "immunodeficiency 117 (Disease Ontology:DOID:0061083); stomach cancer (Disease Ontology:DOID:10534); allergic conjunctivitis (Disease Ontology:DOID:11204); respiratory syncytial virus infectious disease (Disease Ontology:DOID:1273); lung cancer (Disease Ontology:DOID:1324); asthma (Disease Ontology:DOID:2841); endometrial adenocarcinoma (Disease Ontology:DOID:2870); gastric adenocarcinoma (Disease Ontology:DOID:3717); lung non-small cell carcinoma (Disease Ontology:DOID:3908); ureteral obstruction (Disease Ontology:DOID:5199); lung disease (Disease Ontology:DOID:850); smallpox (Disease Ontology:DOID:8736)", "pathway": " (mmu:16362)", "pathway_count": 1, "publication_count": 23, "publication_id_list": "10712599;11244049;11846971;11846974;12387893;16932750;17018642;18641303;18955028;20049431;20308629;21750661;21909274;2208287;25774715;27693356;29321274;30635240;3409321;34428180;39026271;8402903;9422515", "class_list": "", "function": "IRF1 regulation of ZBP1 links mitochondrial DNA and chondrocyte damage in osteoarthritis. Publication Status: Online-Only, [RefSeq, PubMed]; Transcriptional regulator which displays a remarkable functional diversity in the regulation of cellular responses (PubMed:11244049, PubMed:11846971, PubMed:11846974, PubMed:16932750, PubMed:20049431, PubMed:25774715). Regulates transcription of IFN and IFN-inducible genes, host response to viral and bacterial infections, regulation of many genes expressed during hematopoiesis, inflammation, immune responses and cell proliferation and differentiation, regulation of the cell cycle and induction of growth arrest and programmed cell death following DNA damage (PubMed:11244049, PubMed:11846971, PubMed:11846974, PubMed:16932750, PubMed:20049431, PubMed:2208287, PubMed:3409321, PubMed:8402903). Stimulates both innate and acquired immune responses through the activation of specific target genes and can act as a transcriptional activator and repressor regulating target genes by binding to an interferon-stimulated response element (ISRE) in their promoters (PubMed:11244049, PubMed:11846971, PubMed:11846974, PubMed:16932750, PubMed:20049431). Has an essential role in IFNG-dependent immunity to mycobacteria (By similarity). Binds to a consensus sequence in gene promoters (By similarity). Its target genes for transcriptional activation activity are: genes involved in anti-viral response, such as IFN-alpha/beta, RIGI, TNFSF10/TRAIL, ZBP1, OAS1/2, PIAS1/GBP, EIF2AK2/PKR and RSAD2/viperin; antibacterial response, such as GBP2, GBP5, IRGB10 and NOS2/INOS; anti-proliferative response, such as p53/TP53, LOX and CDKN1A; apoptosis, such as BBC3/PUMA, CASP1, CASP7 and CASP8; immune response, such as IL7, IL12A/B and IL15, PTGS2/COX2 and CYBB; DNA damage responses and DNA repair, such as POLQ/POLH; MHC class I expression, such as TAP1, PSMB9/LMP2, PSME1/PA28A, PSME2/PA28B and B2M and MHC class II expression, such as CIITA; metabolic enzymes, such as ACOD1/IRG1 (PubMed:12387893, PubMed:17018642, PubMed:18955028, PubMed:20308629, PubMed:21909274, PubMed:25774715, PubMed:27693356, PubMed:29321274, PubMed:30635240). Represses genes involved in anti-proliferative response, such as BIRC5/survivin, CCNB1, CCNE1, CDK1, CDK2 and CDK4 and in immune response, such as FOXP3, IL4, ANXA2 and TLR4 (PubMed:18641303). Stimulates p53/TP53-dependent transcription through enhanced recruitment of EP300 leading to increased acetylation of p53/TP53 (By similarity). Plays an important role in immune response directly affecting NK maturation and activity, macrophage production of IL12, Th1 development and maturation of CD8+ T-cells (PubMed:11244049, PubMed:11846971, PubMed:11846974, PubMed:16932750, PubMed:20049431). Also implicated in the differentiation and maturation of dendritic cells and in the suppression of regulatory T (Treg) cells development (PubMed:11244049, PubMed:11846971, PubMed:11846974, PubMed:16932750, PubMed:20049431). Acts as a tumor suppressor and plays a role not only in antagonism of tumor cell growth but also in stimulating an immune response against tumor cells (PubMed:11244049, PubMed:11846971, PubMed:11846974, PubMed:16932750, PubMed:20049431)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 12, "glyco_site_count": 0, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000976 transcription cis-regulatory region binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0000785 chromatin", "go_biological_process": "GO:0043374 CD8-positive, alpha-beta T cell differentiation;GO:2000564 regulation of CD8-positive, alpha-beta T cell proliferation;GO:0034124 regulation of MyD88-dependent toll-like receptor signaling pathway;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II", "synthesized_glycan_count": 0, "hit_score": 2.4, "record_id": "P15314-1", "record_type": "protein" }, { "uniprot_canonical_ac": "O70570-1", "uniprot_id": "PIGR_MOUSE", "mass": 84999.0, "length": 771, "protein_name": "Polymeric immunoglobulin receptor", "gene_name": "Pigr", "organism": "Mouse", "refseq_name": "polymeric immunoglobulin receptor precursor", "refseq_ac": "NP_035212", "gene_names_uniprotkb": "Pigr", "gene_names_refseq": "Pigr", "protein_names_uniprotkb": "Polymeric immunoglobulin receptor; PIgR; Poly-Ig receptor", "protein_names_refseq": "phosphatidylinositol glycan, class R; poly-Ig receptor; polymeric immunoglobulin receptor precursor", "tax_id": 10090, "disease": "", "pathway": " (mmu:18703); (R-MMU-6798695)", "pathway_count": 2, "publication_count": 10, "publication_id_list": "10.1101/2023.09.13.557529;10481312;17242355;21750661;25428506;30084848;34428180;35820727;7836758;9409786", "class_list": "", "function": "Mediates selective transcytosis of polymeric IgA and IgM across mucosal epithelial cells. Binds polymeric IgA and IgM at the basolateral surface of epithelial cells. The complex is then transported across the cell to be secreted at the apical surface. During this process, a cleavage occurs that separates the extracellular (known as the secretory component) from the transmembrane segment., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Through its N-linked glycans ensures anchoring of secretory IgA (sIgA) molecules to mucus lining the epithelial surface to neutralize extracellular pathogens. On its own (free form) may act as a non-specific microbial scavenger to prevent pathogen interaction with epithelial cells., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]", "predicted_glycosites": 4, "predicted_n_glycosites": 4, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 2, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 4, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 2, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 2, "disease_count": 0, "glyco_site_count": 6, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0001792 polymeric immunoglobulin receptor activity;GO:0004888 transmembrane signaling receptor activity;GO:0005154 epidermal growth factor receptor binding;GO:0001790 polymeric immunoglobulin binding", "go_cellular_component": "GO:0005615 extracellular space;GO:0005886 plasma membrane;GO:0043235 receptor complex;GO:0055038 recycling endosome membrane;GO:0071751 secretory IgA immunoglobulin complex", "go_biological_process": "GO:0002415 immunoglobulin transcytosis in epithelial cells mediated by polymeric immunoglobulin receptor;GO:0038093 Fc receptor signaling pathway;GO:0007165 signal transduction;GO:0007173 epidermal growth factor receptor signaling pathway;GO:0043113 receptor clustering", "synthesized_glycan_count": 0, "hit_score": 1.5, "record_id": "O70570-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q9ES81-1", "uniprot_id": "POPD3_MOUSE", "mass": 33612.0, "length": 291, "protein_name": "Popeye domain-containing protein 3", "gene_name": "Popdc3", "organism": "Mouse", "refseq_name": "popeye domain-containing protein 3", "refseq_ac": "NP_077248", "gene_names_uniprotkb": "Popdc3; Pop3", "gene_names_refseq": "Pop3; Popdc3", "protein_names_uniprotkb": "Popeye domain-containing protein 3; Popeye protein 3", "protein_names_refseq": "popeye 3; popeye domain-containing protein 3; popeye protein 3", "tax_id": 10090, "disease": "autosomal recessive limb-girdle muscular dystrophy type 26 (Disease Ontology:DOID:0061131); muscular dystrophy (Disease Ontology:DOID:9884)", "pathway": " (mmu:78977)", "pathway_count": 1, "publication_count": 3, "publication_id_list": "10882522;21750661;22354168", "class_list": "", "function": "May play a role in the maintenance of heart function mediated, at least in part, through cAMP-binding. May play a role in the regulation of KCNK2-mediated current amplitude (By similarity)., [UniProtKB, PubMed, PubMed, UniProtKB]", "predicted_glycosites": 1, "predicted_n_glycosites": 1, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 0, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 0, "disease_count": 2, "glyco_site_count": 1, "binding_glycan_count": 0, "secondary_ac_list": "Q1RME0", "ec_number_list": "", "go_molecular_function": "GO:0030552 cAMP binding", "go_cellular_component": "GO:0016020 membrane;GO:0042383 sarcolemma", "go_biological_process": "GO:0007507 heart development;GO:0042391 regulation of membrane potential;GO:0051146 striated muscle cell differentiation;GO:0007519 skeletal muscle tissue development", "synthesized_glycan_count": 0, "hit_score": 0.4, "record_id": "Q9ES81-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q7TPM1-1", "uniprot_id": "PRC2B_MOUSE", "mass": 160913.0, "length": 1486, "protein_name": "Protein PRRC2B", "gene_name": "Prrc2b", "organism": "Mouse", "refseq_name": "protein PRRC2B isoform 1", "refseq_ac": "NP_001153106", "gene_names_uniprotkb": "Prrc2b; Bat2l1; Bat2l; Kiaa0515", "gene_names_refseq": "5830434P21Rik; Bat2l1; Bat2l; D430039P21; Prrc2b; mKIAA0515", "protein_names_uniprotkb": "Protein PRRC2B; HLA-B-associated transcript 2-like 1; Proline-rich coiled-coil protein 2B", "protein_names_refseq": "HLA-B-associated transcript 2-like 1; proline-rich coiled-coil protein 2B; protein BAT2-like 1; protein PRRC2B isoform 1; protein PRRC2B", "tax_id": 10090, "disease": "", "pathway": " (mmu:227723)", "pathway_count": 1, "publication_count": 19, "publication_id_list": "16452087;17242355;19144319;21183079;21750661;22517741;24129315;29237092;30059200;32782141;32848054;34203471;34428180;35820727;35822049;36852467;37395402;40021952;40885482", "class_list": "", "function": "The Role of PRRC2B in Cerebral Vascular Remodeling Under Acute Hypoxia in Mice., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 0, "reported_o_glycosites_with_glycan": 9, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 0, "total_reported_o_glycosites": 9, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 0, "total_o_glycosites": 9, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 1, "reported_phosphosites": 15, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 5, "reported_interactions": 0, "missing_score": 0, "biomarker_type": "", "glycan_count": 1, "disease_count": 0, "glyco_site_count": 9, "binding_glycan_count": 0, "secondary_ac_list": "A2AN31;Q8C755", "ec_number_list": "", "go_molecular_function": "", "go_cellular_component": "", "go_biological_process": "GO:0001701 in utero embryonic development", "synthesized_glycan_count": 0, "hit_score": 3.0, "record_id": "Q7TPM1-1", "record_type": "protein" }, { "uniprot_canonical_ac": "Q8VI24-1", "uniprot_id": "SATB2_MOUSE", "mass": 82559.0, "length": 733, "protein_name": "DNA-binding protein SATB2", "gene_name": "Satb2", "organism": "Mouse", "refseq_name": "DNA-binding protein SATB2 isoform 1", "refseq_ac": "NP_631885", "gene_names_uniprotkb": "Satb2; Kiaa1034", "gene_names_refseq": "BAP002; Satb2; mKIAA1034", "protein_names_uniprotkb": "DNA-binding protein SATB2; Special AT-rich sequence-binding protein 2", "protein_names_refseq": "DNA-binding protein SATB2 isoform 1; DNA-binding protein SATB2; KIAA1034-like DNA binding protein; two cut domains-containing homeodomain protein", "tax_id": 10090, "disease": "SATB2-associated syndrome (Disease Ontology:DOID:0060428); isolated cleft palate (Disease Ontology:DOID:0110213)", "pathway": " (mmu:212712); (R-MMU-4551638)", "pathway_count": 2, "publication_count": 12, "publication_id_list": "10.1101/2023.09.13.557529;12915443;15733084;16751105;18255030;18255031;21750661;25428506;30084848;31219806;34428180;36210013", "class_list": "", "function": "Binds to DNA, at nuclear matrix- or scaffold-associated regions. Thought to recognize the sugar-phosphate structure of double-stranded DNA. Transcription factor controlling nuclear gene expression, by binding to matrix attachment regions (MARs) of DNA and inducing a local chromatin-loop remodeling. Acts as a docking site for several chromatin remodeling enzymes and also by recruiting corepressors (HDACs) or coactivators (HATs) directly to promoters and enhancers. Required for the initiation of the upper-layer neurons (UL1) specific genetic program and for the inactivation of deep-layer neurons (DL) and UL2 specific genes, probably by modulating Bcl11b expression. Repressor of Ctip2 and regulatory determinant of corticocortical connections in the developing cerebral cortex. May play an important role in palate formation. Acts as a molecular node in a transcriptional network regulating skeletal development and osteoblast differentiation., [UniProtKB, PubMed, PubMed, PubMed]; SATB2 acts as a molecular node in a transcriptional network regulating skeletal development and osteoblast differentiation., [RefSeq, PubMed]; Satb2 may regulate differentiation of subsets of neurons at the level of higher order chromatin structure via binding to matrix attachment region DNA elements (MARs)., [RefSeq, PubMed]", "predicted_glycosites": 0, "predicted_n_glycosites": 0, "predicted_o_glycosites": 0, "predicted_c_glycosites": 0, "predicted_s_glycosites": 0, "mined_glycosites": 0, "mined_n_glycosites": 0, "mined_o_glycosites": 0, "mined_c_glycosites": 0, "mined_s_glycosites": 0, "reported_n_glycosites": 0, "reported_o_glycosites": 0, "reported_c_glycosites": 0, "reported_s_glycosites": 0, "reported_n_glycosites_with_glycan": 2, "reported_o_glycosites_with_glycan": 0, "reported_c_glycosites_with_glycan": 0, "reported_s_glycosites_with_glycan": 0, "total_reported_n_glycosites": 2, "total_reported_o_glycosites": 0, "total_reported_c_glycosites": 0, "total_reported_s_glycosites": 0, "total_n_glycosites": 2, "total_o_glycosites": 0, "total_c_glycosites": 0, "total_s_glycosites": 0, "reported_fully_resolved_glycans": 0, "reported_phosphosites": 5, "reported_mutagensis": 0, "reported_glycation": 0, "reported_snv": 0, "reported_interactions": 0, "missing_score": 10000, "biomarker_type": "", "glycan_count": 2, "disease_count": 2, "glyco_site_count": 2, "binding_glycan_count": 0, "secondary_ac_list": "", "ec_number_list": "", "go_molecular_function": "GO:0003682 chromatin binding;GO:0042826 histone deacetylase binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding", "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016363 nuclear matrix;GO:0005667 transcription regulator complex;GO:0000785 chromatin", "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006338 chromatin remodeling;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II", "synthesized_glycan_count": 0, "hit_score": 1.7, "record_id": "Q8VI24-1", "record_type": "protein" } ]