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        ],
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        "gene_names_refseq": "CG12269; Dmel\\CG12269; euc",
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                "type": "external"
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        ],
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        "protein_name": "Uncharacterized protein",
        "gene_name": "noncoding_17732",
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        "refseq_name": "uncharacterized protein",
        "refseq_ac": [
            {
                "id": "NP_001247194",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001247194",
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            }
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        "protein_names_uniprotkb": "Uncharacterized protein",
        "protein_names_refseq": "CG43203-PA; uncharacterized protein",
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                "id": "A0A0B4K7I2_DROME",
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        ],
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        "length": 552,
        "protein_name": "Smooth, isoform T",
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        "organism": "Fruit fly",
        "refseq_name": "smooth, isoform T",
        "refseq_ac": [
            {
                "id": "NP_001246428",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001246428",
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            }
        ],
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        "protein_names_uniprotkb": "Smooth, isoform T",
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        "organism": "Fruit fly",
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        "gene_names_refseq": "CG11856; Dmel\\CG11856; NUP358; Nup358; Q9VBU7_DROME; RanBP2; dmRanBP; nup358; ranbp2",
        "protein_names_uniprotkb": "E3 SUMO-protein ligase RanBP2; 2.3.2.-; 358 kDa nucleoporin; Nuclear pore complex protein Nup358",
        "protein_names_refseq": "CG11856-PB; Nup358-PB; nucleoporin 358kD, isoform B; nucleoporin 358",
        "tax_id": 7227,
        "disease": "inflammatory myofibroblastic tumor (Disease Ontology:DOID:0050905); brain disease (Disease Ontology:DOID:936); multiple myeloma (Disease Ontology:DOID:9538)",
        "pathway": " (dme:Dmel_CG11856);  (R-DME-159227);  (R-DME-159230);  (R-DME-159231);  (R-DME-159236);  (R-DME-3108214);  (R-DME-3301854);  (R-DME-3371453);  (R-DME-4085377);  (R-DME-4551638);  (R-DME-4615885)",
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                "id": "2.3.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.-",
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                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
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                "id": "3.6.4.13",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.13",
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                "id": "3.1.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.-.-",
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            }
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        ],
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            {
                "id": "NP_001246193",
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        "protein_names_uniprotkb": "Myoblast city, isoform B",
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        "tax_id": 7227,
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            {
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        ],
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            {
                "id": "NP_001261166",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001261166",
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            }
        ],
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        ],
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            {
                "id": "NP_001261072",
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        "protein_names_uniprotkb": "Valine--tRNA ligase; 6.1.1.9; Valyl-tRNA synthetase",
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        "disease": "myoclonic-atonic epilepsy (Disease Ontology:DOID:0060475); combined oxidative phosphorylation deficiency 20 (Disease Ontology:DOID:0111478); mitochondrial metabolism disease (Disease Ontology:DOID:700); mitochondrial encephalomyopathy (Disease Ontology:DOID:890)",
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        "protein_name": "Diuretic hormone 31 receptor, isoform C",
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        "organism": "Fruit fly",
        "refseq_name": "diuretic hormone 31 receptor, isoform C",
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                "id": "NP_001260951",
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        "gene_names_refseq": "CG17043; CG17415; CG32843; DH31-R1; DH31-R; DH31R; DH31; Dh31-R1; Dh31-R; Dh31R; Dh31r; DmeCG32843; Dmel\\CG32843; anon-WO0170980.136; anon-WO0170980.137; dh31-R1",
        "protein_names_uniprotkb": "Diuretic hormone 31 receptor, isoform C",
        "protein_names_refseq": "CG32843-PC; Calcitonin-like diuretic hormone receptor; DH31 receptor; DH31-receptor; DH[[31]] receptor; Dh31-R-PC; diuretic hormone 31 receptor 1; diuretic hormone 31 receptor, isoform C",
        "tax_id": 7227,
        "disease": "hereditary lymphedema (Disease Ontology:DOID:0050580); osteoporosis (Disease Ontology:DOID:11476); brain infarction (Disease Ontology:DOID:3454)",
        "pathway": " (dme:Dmel_CG32843);  (R-DME-419812)",
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        "protein_name": "Mangetout, isoform G",
        "gene_name": "mtt",
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        ],
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        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0016020 membrane",
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        ],
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            {
                "id": "NP_001261023",
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            }
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        "protein_names_refseq": "Atg9-PB; Autophagy-related 9, isoform B; Autophagy-specific gene 9; CG3615-PB",
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        "disease": "Parkinson's disease (Disease Ontology:DOID:14330)",
        "pathway": " (dme:Dmel_CG3615);  (R-DME-1632852);  (R-DME-5205685)",
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        "function": "Phospholipid scramblase involved in autophagy. Cycles between the preautophagosomal structure/phagophore assembly site (PAS) and the cytoplasmic vesicle pool and supplies membrane for the growing autophagosome. Lipid scramblase activity plays a key role in preautophagosomal structure/phagophore assembly by distributing the phospholipids that arrive through ATG2 from the cytoplasmic to the luminal leaflet of the bilayer, thereby driving autophagosomal membrane expansion., [UniProtKB, UniProtKB, UniProtKB]",
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            {
                "id": "NP_001260785",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001260785",
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            }
        ],
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            }
        ],
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        ],
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            {
                "id": "NP_001189184",
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        ],
        "gene_names_uniprotkb": "CG31367; CG33097; CG15187; CG31367; CG33097; CG42724; Dmel\\CG42724; Dmel_CG42724",
        "gene_names_refseq": "CG15187; CG31367; CG33097; CG42724; Dmel\\CG42724",
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        ],
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        "protein_names_refseq": "CG7734-PF; quo vadis; schnurri, isoform F; schnurri; shn-PF; umnitza",
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        "disease": "juvenile polyposis syndrome (Disease Ontology:DOID:0050787); autosomal dominant intellectual developmental disorder 43 (Disease Ontology:DOID:0070073); intellectual disability (Disease Ontology:DOID:1059); Alzheimer's disease (Disease Ontology:DOID:10652); asthma (Disease Ontology:DOID:2841); schizophrenia (Disease Ontology:DOID:5419)",
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        ],
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        "protein_names_uniprotkb": "Ribbon, isoform C",
        "protein_names_refseq": "CG7230-PC; SGP cluster fusion defects 1; rib-PC; ribbon, isoform C",
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        "disease": "non-syndromic X-linked intellectual disability (Disease Ontology:DOID:0050776); non-syndromic X-linked intellectual disability 63 (Disease Ontology:DOID:0112050); prostate cancer (Disease Ontology:DOID:10283); intellectual disability (Disease Ontology:DOID:1059); lung cancer (Disease Ontology:DOID:1324); Sjogren-Larsson syndrome (Disease Ontology:DOID:14501); breast cancer (Disease Ontology:DOID:1612); asthma (Disease Ontology:DOID:2841)",
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        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); myelodysplastic syndrome (Disease Ontology:DOID:0050908); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); systemic primary carnitine deficiency disease (Disease Ontology:DOID:14365); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); congestive heart failure (Disease Ontology:DOID:6000); inherited metabolic disorder (Disease Ontology:DOID:655); rheumatoid arthritis (Disease Ontology:DOID:7148); Crohn's disease (Disease Ontology:DOID:8778)",
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        "protein_names_uniprotkb": "Entomoglyceroporin 4, isoform F",
        "protein_names_refseq": "CG4019-PF; Eglp4-PF; entomoglyceroporin 4, isoform F",
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        "disease": "Alpers-Huttenlocher syndrome (Disease Ontology:DOID:0080122); megalencephalic leukoencephalopathy with subcortical cysts (Disease Ontology:DOID:0080315); transverse myelitis (Disease Ontology:DOID:0080743); nephrogenic diabetes insipidus type 2 (Disease Ontology:DOID:0081061); cataract 15 multiple types (Disease Ontology:DOID:0110251); autosomal recessive polycystic kidney disease (Disease Ontology:DOID:0110861); Bothnian type palmoplantar keratoderma (Disease Ontology:DOID:0111707); dry eye syndrome (Disease Ontology:DOID:10140); Alzheimer's disease (Disease Ontology:DOID:10652); hypertension (Disease Ontology:DOID:10763); hydrocephalus (Disease Ontology:DOID:10908); optic neuritis (Disease Ontology:DOID:1210); primary biliary cholangitis (Disease Ontology:DOID:12236); malaria (Disease Ontology:DOID:12365); nephrogenic diabetes insipidus (Disease Ontology:DOID:12387); uveitis (Disease Ontology:DOID:13141); blindness (Disease Ontology:DOID:1432); retinal vein occlusion (Disease Ontology:DOID:1727); status epilepticus (Disease Ontology:DOID:1824); diabetic ketoacidosis (Disease Ontology:DOID:1837); transient cerebral ischemia (Disease Ontology:DOID:224); brain ischemia (Disease Ontology:DOID:2316); thymoma (Disease Ontology:DOID:3275); amyotrophic lateral sclerosis (Disease Ontology:DOID:332); temporal lobe epilepsy (Disease Ontology:DOID:3328); middle cerebral artery infarction (Disease Ontology:DOID:3525); brain edema (Disease Ontology:DOID:4724); retinal disease (Disease Ontology:DOID:5679); central pontine myelinolysis (Disease Ontology:DOID:636); cataract (Disease Ontology:DOID:83); neuromyelitis optica (Disease Ontology:DOID:8869); diabetic retinopathy (Disease Ontology:DOID:8947); cerebral amyloid angiopathy (Disease Ontology:DOID:9246); diabetes mellitus (Disease Ontology:DOID:9351); diabetes insipidus (Disease Ontology:DOID:9409); intracranial hypertension (Disease Ontology:DOID:9428); Meniere's disease (Disease Ontology:DOID:9849)",
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        ],
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            {
                "id": "NP_001262575",
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        ],
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        "protein_names_uniprotkb": "Serine/threonine-protein kinase receptor; 2.7.11.30",
        "protein_names_refseq": "Activin-A-receptor-88CD; CG7904-PB; DPP receptor; TGF-beta-type-receptor-like; activin receptor type II; activin receptor; dorsal holes C; punt, isoform B; punt; put-PB",
        "tax_id": 7227,
        "disease": "visceral heterotaxy (Disease Ontology:DOID:0050545); juvenile polyposis syndrome (Disease Ontology:DOID:0050787); visceral heterotaxy 4 (Disease Ontology:DOID:0051019); right atrial isomerism (Disease Ontology:DOID:0060856); pre-eclampsia (Disease Ontology:DOID:10591); Marfan syndrome (Disease Ontology:DOID:14323); pancreatic cancer (Disease Ontology:DOID:1793); colon cancer (Disease Ontology:DOID:219); Lynch syndrome (Disease Ontology:DOID:3883); Weissenbacher-Zweymuller syndrome (Disease Ontology:DOID:4258); cocaine dependence (Disease Ontology:DOID:9975)",
        "pathway": " (dme:Dmel_CG7904);  (R-DME-1502540);  (R-DME-201451)",
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            }
        ],
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    },
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        ],
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            {
                "id": "NP_001262677",
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            }
        ],
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        "protein_names_uniprotkb": "2.7.11.1; 2.7.12.1; Monopolar spindle 1, isoform B",
        "protein_names_refseq": "CG7643-PB; Mps1-PB; altered disjunction; monopolar spindle 1, isoform B; monopolar spindles 1",
        "tax_id": 7227,
        "disease": "cancer (Disease Ontology:DOID:162); bipolar disorder (Disease Ontology:DOID:3312); hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (dme:Dmel_CG7643)",
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        "go_biological_process": "GO:0048133 male germ-line stem cell asymmetric division;GO:0016321 female meiosis chromosome segregation;GO:0033316 meiotic spindle assembly checkpoint signaling;GO:0007059 chromosome segregation;GO:0001666 response to hypoxia",
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    },
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        ],
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        "protein_name": "ENL/AF9-related, isoform B",
        "gene_name": "ear",
        "organism": "Fruit fly",
        "refseq_name": "ENL/AF9-related, isoform B",
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            {
                "id": "NP_001262595",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262595",
                "type": "external"
            }
        ],
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        "protein_names_uniprotkb": "ENL/AF9-related, isoform B",
        "protein_names_refseq": "CG4913-PB; ENL/AF9-related, isoform B; ear-PB",
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    },
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            {
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        ],
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        "protein_name": "Metastasis-associated protein MTA3",
        "gene_name": "MTA1-like",
        "organism": "Fruit fly",
        "refseq_name": "metastasis associated 1-like, isoform D",
        "refseq_ac": [
            {
                "id": "NP_001262293",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262293",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "MTA1-like; CG2244; Dmel\\CG2244; Dmel_CG2244; MTA-1like; MTA-like; MTA1; MTA; dMTA-1; dMTA1-like; dMTA; p120",
        "gene_names_refseq": "CG2244; Dmel\\CG2244; MTA-1like; MTA-like; MTA1-like; MTA1; MTA; dMTA-1; dMTA1-like; dMTA; p120",
        "protein_names_uniprotkb": "Metastasis-associated protein MTA3",
        "protein_names_refseq": "CG2244-PD; MTA-like; MTA1-like-PD; metastasis associated 1-like, isoform D; metastasis-associated-1-like-protein",
        "tax_id": 7227,
        "disease": "systemic lupus erythematosus (Disease Ontology:DOID:9074)",
        "pathway": " (dme:Dmel_CG2244);  (R-DME-3214815);  (R-DME-3232118);  (R-DME-6804758);  (R-DME-8943724)",
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        "function": "Acts as a component of the histone deacetylase NuRD complex which participates in the remodeling of chromatin. Plays a role in maintenance of the normal epithelial architecture through the repression of SNAI1 transcription in a histone deacetylase-dependent manner, and thus the regulation of E-cadherin levels. Contributes to transcriptional repression by BCL6., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0000118 histone deacetylase complex;GO:0016581 NuRD complex",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0030261 chromosome condensation;GO:0006355 regulation of DNA-templated transcription",
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    },
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        ],
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        "protein_name": "Uncharacterized protein, isoform B; Uncharacterized protein, isoform C",
        "gene_name": "Dmel\\CG44013",
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        "refseq_name": "uncharacterized protein, isoform C",
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            {
                "id": "NP_001262606",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262606",
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            }
        ],
        "gene_names_uniprotkb": "Dmel\\CG44013; CG14872; CG44013; Dmel_CG44013",
        "gene_names_refseq": "CG14872; CG44013; Dmel\\CG44013",
        "protein_names_uniprotkb": "Uncharacterized protein, isoform B; Uncharacterized protein, isoform C",
        "protein_names_refseq": "CG44013-PC; uncharacterized protein, isoform C",
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            {
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                "url": "https://www.uniprot.org/uniprot/A0A0B4KG96",
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        ],
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        "length": 827,
        "protein_name": "polynucleotide adenylyltransferase",
        "gene_name": "hrg",
        "organism": "Fruit fly",
        "refseq_name": "hiiragi, isoform D",
        "refseq_ac": [
            {
                "id": "NP_001261097",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001261097",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "hrg; CG9854; Dmel\\CG9854; Dmel_CG9854; PAP; Pap; dHrg; hrg-RA; l(2)07619; l(2)k07619",
        "gene_names_refseq": "CG9854; Dmel\\CG9854; Hiiragi; PAP; Pap; dHrg; hrg; l(2)07619; l(2)k07619",
        "protein_names_uniprotkb": "polynucleotide adenylyltransferase; 2.7.7.19",
        "protein_names_refseq": "CG9854-PD; Poly(A) polymerase; hiiragi, isoform D; hrg-PD; poly (A) polymerase",
        "tax_id": 7227,
        "disease": "",
        "pathway": " (dme:Dmel_CG9854);  (R-DME-73856);  (R-DME-77595);  (R-DME-9770562);  (R-DME-9930044)",
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        "class_list": "",
        "function": "Polymerase that creates the 3'-poly(A) tail of mRNA's., [UniProtKB, UniProtKB]",
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        "protein_names_refseq": "CG44159-PF; Irk1-PF; drosophila inward rectifier; inwardly rectifying potassium channel 1, isoform F; inwardly rectifying potassium channel",
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        "disease": "Andersen-Tawil syndrome (Disease Ontology:DOID:0050434); familial atrial fibrillation (Disease Ontology:DOID:0050650); metabolic acidosis (Disease Ontology:DOID:0050758); short QT syndrome (Disease Ontology:DOID:0050793); atrial fibrillation (Disease Ontology:DOID:0060224); hypertrichotic osteochondrodysplasia Cantu type (Disease Ontology:DOID:0060569); permanent neonatal diabetes mellitus (Disease Ontology:DOID:0060639); familial hyperinsulinemic hypoglycemia 2 (Disease Ontology:DOID:0070218); Parkinsonism (Disease Ontology:DOID:0080855); long QT syndrome 13 (Disease Ontology:DOID:0110654); maturity-onset diabetes of the young type 13 (Disease Ontology:DOID:0111110); familial periodic paralysis (Disease Ontology:DOID:1029); hypertension (Disease Ontology:DOID:10763); sciatic neuropathy (Disease Ontology:DOID:11446); prediabetes syndrome (Disease Ontology:DOID:11716); Leber congenital amaurosis (Disease Ontology:DOID:14791); alcohol use disorder (Disease Ontology:DOID:1574); status epilepticus (Disease Ontology:DOID:1824); epilepsy (Disease Ontology:DOID:1826); hyperinsulinism (Disease Ontology:DOID:2018); coronary artery disease (Disease Ontology:DOID:3393); primary hyperaldosteronism (Disease Ontology:DOID:446); hypokalemia (Disease Ontology:DOID:4500); diabetes mellitus (Disease Ontology:DOID:9351); type 2 diabetes mellitus (Disease Ontology:DOID:9352); heroin dependence (Disease Ontology:DOID:9976)",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane;GO:0005829 cytosol",
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        "protein_names_refseq": "CG5669-PB; Sp1-like factor for pairing Sensitive-silencing; Sp1-like factor for pairing sensitive-silencing, isoform B; Spps-PB",
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        "disease": "dilated cardiomyopathy (Disease Ontology:DOID:12930); congenital heart disease (Disease Ontology:DOID:1682); schizophrenia (Disease Ontology:DOID:5419)",
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        "protein_names_refseq": "CG18208-PB; Octalpha2R-PB; alpha2-adrenergic-like octopamine receptor, isoform B; octopamine receptor",
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        "disease": "familial partial lipodystrophy (Disease Ontology:DOID:0050440); alcohol dependence (Disease Ontology:DOID:0050741); nicotine dependence (Disease Ontology:DOID:0050742); metabolic dysfunction and alcohol associated liver disease (Disease Ontology:DOID:0070508); metabolic dysfunction-associated steatohepatitis (Disease Ontology:DOID:0080547); hypertension (Disease Ontology:DOID:10763); attention deficit hyperactivity disorder (Disease Ontology:DOID:1094); depressive disorder (Disease Ontology:DOID:1596); anxiety disorder (Disease Ontology:DOID:2030); morphine dependence (Disease Ontology:DOID:2560); substance abuse (Disease Ontology:DOID:302); myocardial infarction (Disease Ontology:DOID:5844); congestive heart failure (Disease Ontology:DOID:6000); type 2 diabetes mellitus (Disease Ontology:DOID:9352); diabetic neuropathy (Disease Ontology:DOID:9743); obesity (Disease Ontology:DOID:9970)",
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        "gene_names_refseq": "AI945337; CG17838; Dmel\\CG17838; Syp; anon-WO0118547.613; cg17838; l(3)03806; syp",
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        "gene_name": "Grik",
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        "gene_names_refseq": "CG5621; CT17756; DKaiRIC; DmelCG5621; Dmel\\CG5621; Grik; KaiR1C; anon-WO0138359.5",
        "protein_names_uniprotkb": "Grik, isoform C",
        "protein_names_refseq": "CG5621-PC; Grik-PC; grik, isoform C",
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        "disease": "autosomal recessive intellectual developmental disorder 6 (Disease Ontology:DOID:0081182); Huntington's disease (Disease Ontology:DOID:12858); childhood absence epilepsy (Disease Ontology:DOID:1825); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); temporal lobe epilepsy (Disease Ontology:DOID:3328)",
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        "protein_name": "Dynein heavy chain at 93AB, isoform C",
        "gene_name": "Dhc93AB",
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        "refseq_name": "dynein heavy chain at 93AB, isoform C",
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        "gene_names_refseq": "CG3723; DHC4C; DHC; Dhc 93AB; Dhc93AB; Dhc; Dmel\\CG3723; dhc93AB; dhc",
        "protein_names_uniprotkb": "Dynein heavy chain at 93AB, isoform C",
        "protein_names_refseq": "CG3723-PC; Dhc93AB-PC; dynein heavy chain at 93AB, isoform C; dynein-related heavy chain polypeptide",
        "tax_id": 7227,
        "disease": "Kartagener syndrome (Disease Ontology:DOID:0050144); visceral heterotaxy (Disease Ontology:DOID:0050545); atrioventricular septal defect (Disease Ontology:DOID:0050651); primary ciliary dyskinesia 7 (Disease Ontology:DOID:0110605); primary ciliary dyskinesia 40 (Disease Ontology:DOID:0111853); spermatogenic failure 39 (Disease Ontology:DOID:0111926); sensorineural hearing loss (Disease Ontology:DOID:10003)",
        "pathway": " (dme:Dmel_CG3723)",
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        "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_cellular_component": "GO:0005874 microtubule;GO:0005930 axoneme;GO:0030286 dynein complex;GO:0036157 outer dynein arm;GO:0097729 9+2 motile cilium",
        "go_biological_process": "GO:0060294 cilium movement involved in cell motility;GO:0007605 sensory perception of sound;GO:0003341 cilium movement;GO:0007018 microtubule-based movement",
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        ],
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        "refseq_name": "glyceronephosphate O-acyltransferase, isoform C",
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            {
                "id": "NP_001262957",
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        "protein_names_uniprotkb": "Dihydroxyacetone phosphate acyltransferase; 2.3.1.42; Glycerone-phosphate O-acyltransferase",
        "protein_names_refseq": "CG4625-PC; Gnpat-PC; dihydroxyacetone phosphate acyltansferase; dihydroxyacetone phosphate acyltransferase; glycerol 3-phosphate acyltransferase; glycerol-3-phosphate acyltransferase; glycerol-3-phosphate-acyltransferase; glyceronephosphate O-acyltransferase, isoform C",
        "tax_id": 7227,
        "disease": "rhizomelic chondrodysplasia punctata type 2 (Disease Ontology:DOID:0110852); disease of mental health (Disease Ontology:DOID:150)",
        "pathway": " (dme:Dmel_CG4625);  (R-DME-1483166);  (R-DME-75896);  (R-DME-9033241)",
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        "publication_id_list": "10731132;12537568;12537572;12537573;12537574;16110336;17569856;17569867;25589440;26109356;26109357",
        "class_list": "",
        "function": "Dihydroxyacetonephosphate acyltransferase catalyzing the first step in the biosynthesis of plasmalogens, a subset of phospholipids that differ from other glycerolipids by having an alkyl chain attached through a vinyl ether linkage at the sn-1 position of the glycerol backbone, and which unique physical properties have an impact on various aspects of cell signaling and membrane biology., [UniProtKB, UniProtKB, UniProtKB]",
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        "biomarker_type": "",
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                "id": "1.11.1.6",
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                "id": "1.14.13.39",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.14.13.39",
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                "id": "4.1.2.63",
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                "id": "2.3.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.-.-",
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            },
            {
                "id": "2.3.1.137",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.137",
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            },
            {
                "id": "1.-.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.-.-.-",
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                "id": "2.3.1.7",
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                "id": "5.1.99.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.1.99.4",
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                "id": "2.3.1.176",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.176",
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                "id": "2.3.1.16",
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                "id": "4.1.3.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.1.3.4",
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            },
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                "id": "1.4.3.3",
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                "id": "1.1.1.270",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.1.1.270",
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                "id": "1.1.1.184",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.1.1.184",
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                "id": "2.3.2.27",
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                "id": "5.3.3.8",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.3.3.8",
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            },
            {
                "id": "3.4.21.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.21.-",
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                "id": "2.6.1.44",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.6.1.44",
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            }
        ],
        "go_molecular_function": "GO:0016287 glycerone-phosphate O-acyltransferase activity",
        "go_cellular_component": "GO:0005777 peroxisome;GO:0005778 peroxisomal membrane",
        "go_biological_process": "GO:0008611 ether lipid biosynthetic process",
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    },
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        ],
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        "protein_name": "Supernumerary limbs, isoform B",
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        "refseq_name": "supernumerary limbs, isoform B",
        "refseq_ac": [
            {
                "id": "NP_001262802",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262802",
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            }
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        "protein_names_uniprotkb": "Supernumerary limbs, isoform B",
        "protein_names_refseq": "CG3412-PB; SCF-betaTrCP complex; SLIMB; centrosome replication defective; icare; pingiel; shiva; slmb-PB; supernumerary limbs, isoform B; supernumerary limbs; wellman",
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        "disease": "Menkes disease (Disease Ontology:DOID:1838)",
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        "go_cellular_component": "GO:0019005 SCF ubiquitin ligase complex;GO:0005634 nucleus;GO:0005737 cytoplasm",
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                "id": "NP_001263139",
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        "protein_names_uniprotkb": "Uncharacterized protein, isoform C; Uncharacterized protein, isoform D",
        "protein_names_refseq": "CG1607-PC; uncharacterized protein, isoform C",
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            {
                "id": "NP_001262624",
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        ],
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        "gene_names_refseq": "CG6963; CK1-gamma; CK1[[gamma]]; CK1gamma; CK1; CKI-related; CKIgamma; Dmel\\CG6963; Gish; Hrr25; NEST:bs27c08; Spider; anon-WO0118547.425; gish; ms(3)89B; spider",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "CG6963-PL; CKIg-like; NEST:bs27c08; casein kinase 1gamma; gilgamesh, isoform L; gilgamesh; gish-PL; spider",
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        "pathway": " (dme:Dmel_CG6963);  (R-DME-1660661);  (R-DME-209387);  (R-DME-209440);  (R-DME-209472)",
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                "id": "2.7.11.21",
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                "id": "2.7.11.23",
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        "protein_names_uniprotkb": "BRCA1-associated protein; 2.3.2.27; BRAP2; Impedes mitogenic signal propagation; RING-type E3 ubiquitin transferase BRAP2",
        "protein_names_refseq": "CG5555-PB; uncharacterized protein, isoform B",
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        "function": "Negatively regulates MAP kinase activation by limiting the formation of Raf/MEK complexes probably by inactivation of the KSR1 scaffold protein. Also acts as a Ras responsive E3 ubiquitin ligase that, on activation of Ras, is modified by auto-polyubiquitination resulting in the release of inhibition of Raf/MEK complex formation. May also act as a cytoplasmic retention protein with a role in regulating nuclear transport., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Ecdysone-induced protein 93F, isoform C",
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            {
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        "disease": "colorectal adenocarcinoma (Disease Ontology:DOID:0050861); cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome (Disease Ontology:DOID:0050997); colorectal carcinoma (Disease Ontology:DOID:0080199); isolated hyperchlorhidrosis (Disease Ontology:DOID:0111371); lung cancer (Disease Ontology:DOID:1324); colon adenocarcinoma (Disease Ontology:DOID:234); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); Lynch syndrome (Disease Ontology:DOID:3883); lung non-small cell carcinoma (Disease Ontology:DOID:3908); fibrolamellar carcinoma (Disease Ontology:DOID:5015); hepatocellular carcinoma (Disease Ontology:DOID:684)",
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        ],
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        "function": "Capsid protein (CA) is the structural component of the virus-like particle (VLP), forming the shell that encapsulates the retrotransposons dimeric RNA genome., [UniProtKB]; Integrase (IN) targets the VLP to the nucleus, where a subparticle preintegration complex (PIC) containing at least integrase and the newly synthesized dsDNA copy of the retrotransposon must transit the nuclear membrane. Once in the nucleus, integrase performs the integration of the dsDNA into the host genome., [UniProtKB]; Reverse transcriptase/ribonuclease H (RT) is a multifunctional enzyme that catalyzes the conversion of the retro-elements RNA genome into dsDNA within the VLP. The enzyme displays a DNA polymerase activity that can copy either DNA or RNA templates, and a ribonuclease H (RNase H) activity that cleaves the RNA strand of RNA-DNA heteroduplexes during plus-strand synthesis and hydrolyzes RNA primers. The conversion leads to a linear dsDNA copy of the retrotransposon that includes long terminal repeats (LTRs) at both ends., [UniProtKB]; The aspartyl protease (PR) mediates the proteolytic cleavages of the Gag and Gag-Pol polyproteins after assembly of the VLP., [UniProtKB]",
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001104390",
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        "gene_names_refseq": "41Ad; CG40084; CG42595; CR41594; Dmel\\CG42595; EMS45-73; GroupIII; IR3; l(2)41Ad; l(2)EMS34-7; l(2)IR3; l(2R)A'; l(2R)EMS45-73; l(2Rh)IR3; uex",
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        "protein_names_refseq": "CG42595-PF; lethal (2) IR3; uex-PF; unextended, isoform F",
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        "disease": "renal hypomagnesemia 6 (Disease Ontology:DOID:0060884); Jalili syndrome (Disease Ontology:DOID:0111404); schizophrenia (Disease Ontology:DOID:5419)",
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        "go_cellular_component": "GO:0005576 extracellular region;GO:0005886 plasma membrane;GO:0019814 immunoglobulin complex",
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        ],
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            {
                "id": "NP_611765",
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        "gene_names_refseq": "34371; CG13546; CG13547; CG13548; CG30188; CG34371; CT32921; CT32922; Dmel\\CG34371; side-V",
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            {
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_730894",
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        "gene_names_refseq": "CG1116; Dmel\\CG1116; Rgp1; anon-WO0118547.337; cg1116",
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        "protein_names_refseq": "CG1116-PD; uncharacterized protein, isoform D",
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        "protein_name": "Aldehyde dehydrogenase type III, isoform Q",
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        "refseq_name": "aldehyde dehydrogenase type III, isoform Q",
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            {
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        "protein_names_uniprotkb": "Aldehyde dehydrogenase type III, isoform Q",
        "protein_names_refseq": "Aldh-III-PQ; CG11140-PQ; aldehyde dehydrogenase type III, isoform Q; fatty aldehyde dehydrogenase",
        "tax_id": 7227,
        "disease": "Sjogren-Larsson syndrome (Disease Ontology:DOID:14501); arteriosclerosis (Disease Ontology:DOID:2349)",
        "pathway": " (dme:Dmel_CG11140);  (R-DME-211945);  (R-DME-389599);  (R-DME-6798695);  (R-DME-9603798);  (R-DME-9609523);  (R-DME-9845614)",
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        "protein_name": "Alpha-catenin related, isoform C",
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        "refseq_name": "alpha-catenin related, isoform C",
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            {
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        "protein_names_refseq": "CG2987-PC; alpha-Catr-PC; alpha-catenin related, isoform C; alpha-catenin-related",
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        "protein_name": "Mind the gap, isoform E",
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                "id": "NP_731221",
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        "gene_names_refseq": "0849/10; CG7549; Dmel\\CG7549; MTG; Mtg; l(3)S084910b; l(3)S084910; mtg",
        "protein_names_uniprotkb": "Mind the gap, isoform E",
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        "go_molecular_function": "GO:0008061 chitin binding;GO:0097367 carbohydrate derivative binding",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0043195 terminal bouton;GO:0043083 synaptic cleft",
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        ],
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        "length": 1262,
        "protein_name": "Dystroglycan 1",
        "gene_name": "Dg",
        "organism": "Fruit fly",
        "refseq_name": "dystroglycan, isoform D",
        "refseq_ac": [
            {
                "id": "NP_788363",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_788363",
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        ],
        "gene_names_uniprotkb": "Dg; CG18250; CT41273; DG; DmDG; Dmel\\CG18250; Dmel_CG18250; alpha-DG; atu; dgn; dg; dys",
        "gene_names_refseq": "CG18250; CT41273; DG; Dg; DmDG; Dmel\\CG18250; alpha-DG; atu; dgn; dg; dys",
        "protein_names_uniprotkb": "Dystroglycan 1; Dystroglycan; Dystrophin-associated glycoprotein 1",
        "protein_names_refseq": "CG18250-PD; Dg-PD; alphaDystroglycan; atsugari; dystroglican; dystroglycan, isoform D; dystroglycan-like; dystroglycan",
        "tax_id": 7227,
        "disease": "lissencephaly (Disease Ontology:DOID:0050453); Fukuyama congenital muscular dystrophy (Disease Ontology:DOID:0050559); muscular dystrophy-dystroglycanopathy type B1 (Disease Ontology:DOID:0050588); autosomal recessive limb-girdle muscular dystrophy type 2D (Disease Ontology:DOID:0110278); autosomal recessive limb-girdle muscular dystrophy type 2P (Disease Ontology:DOID:0110293); congenital muscular dystrophy-dystroglycanopathy type A9 (Disease Ontology:DOID:0111232); muscular dystrophy-dystroglycanopathy (Disease Ontology:DOID:0112374); bronchopulmonary dysplasia (Disease Ontology:DOID:11650); Duchenne muscular dystrophy (Disease Ontology:DOID:11723); primary biliary cholangitis (Disease Ontology:DOID:12236); dilated cardiomyopathy (Disease Ontology:DOID:12930); inclusion body myositis (Disease Ontology:DOID:3429); myocardial infarction (Disease Ontology:DOID:5844); muscular atrophy (Disease Ontology:DOID:767); type 2 diabetes mellitus (Disease Ontology:DOID:9352); muscular dystrophy (Disease Ontology:DOID:9884)",
        "pathway": " (dme:Dmel_CG18250);  (R-DME-3000178);  (R-DME-8932504);  (R-DME-8932505);  (R-DME-8932506);  (R-DME-9010553);  (R-DME-9913351);  (R-DME-9939291)",
        "pathway_count": 8,
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        "class_list": "",
        "function": "The dystroglycan complex is involved in a number of processes including laminin and basement membrane assembly, sarcolemmal stability, cell survival, peripheral nerve myelination, nodal structure, cell migration, and epithelial polarization., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Transmembrane protein that plays important roles in connecting the extracellular matrix to the cytoskeleton. Acts as a cell adhesion receptor in both muscle and non-muscle tissues. Receptor for both DMD and UTRN and, through these interactions, scaffolds axin to the cytoskeleton. Also functions in cell adhesion-mediated signaling and implicated in cell polarity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "mass": 113199.0,
        "length": 997,
        "protein_name": "RNA helicase",
        "gene_name": "ifih1",
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        "gene_names_uniprotkb": "ifih1; MDA5a; MDA5b; si:dkey-81j5.2",
        "gene_names_refseq": "MDA5a; MDA5b; ifih1; si:dkey-81j5.2",
        "protein_names_uniprotkb": "RNA helicase; 3.6.4.13",
        "protein_names_refseq": "interferon-induced helicase C domain-containing protein 1; mda5; melanoma differentiation-associated protein 5a; melanoma differentiation-associated protein 5b",
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        "disease": "Aicardi-Goutieres syndrome (Disease Ontology:DOID:0050629); immunodeficiency 95 (Disease Ontology:DOID:0061065); Fanconi anemia (Disease Ontology:DOID:13636); systemic lupus erythematosus (Disease Ontology:DOID:9074)",
        "pathway": " (dre:565759);  (R-DRE-5689880)",
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        "publication_id_list": "19474100;20728541;23594743;24116956;24683187;25100833;25445907;35764162;35982787;36314827;36577070;38077314",
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        "function": "##Evidence-Data-START## Transcript exon combination :: JX462556.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA4476756, SAMEA4476806 [ECO:0000348] ##Evidence-Data-END## PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from JX462556.1. On May 13, 2015 this sequence version replaced XP_694124.4. Publication Note:  This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications., [RefSeq]; A zebrafish model of Ifih1-driven Aicardi-Goutieres syndrome reproduces the interferon signature and the exacerbated inflammation of patients. Erratum:[Front Immunol. 2025 Jan 06;15:1544703. doi: 10.3389/fimmu.2024.1544703. PMID: 39835125] Publication Status: Online-Only, [RefSeq, PubMed]; Shorter spliced form, MDA5b when co-transfected with MDA5a or mitochondrial antiviral signalling protein (MAVS), induced a significantly higher level of interferon promoter activity, [RefSeq, PubMed]",
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        "biomarker_type": "",
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                "id": "3.6.4.13",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.13",
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            },
            {
                "id": "2.3.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.-",
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            },
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                "id": "2.3.2.27",
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            },
            {
                "id": "3.6.4.-",
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            },
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                "id": "3.6.4.12",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:7.6.2.2",
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            },
            {
                "id": "5.6.1.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.1.6",
                "type": "external"
            },
            {
                "id": "7.6.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.6.2.3",
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            },
            {
                "id": "3.6.4.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.6",
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            },
            {
                "id": "5.6.2.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.4",
                "type": "external"
            },
            {
                "id": "3.6.1.15",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.15",
                "type": "external"
            },
            {
                "id": "3.1.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.-.-",
                "type": "external"
            },
            {
                "id": "3.6.4.10",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.10",
                "type": "external"
            },
            {
                "id": "5.6.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.-",
                "type": "external"
            },
            {
                "id": "3.6.5.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.-",
                "type": "external"
            },
            {
                "id": "3.1.3.48",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.48",
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            },
            {
                "id": "3.4.26.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.26.1",
                "type": "external"
            },
            {
                "id": "3.4.19.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.19.12",
                "type": "external"
            },
            {
                "id": "3.6.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.-",
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            },
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                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0005524 ATP binding;GO:0008270 zinc ion binding;GO:0016787 hydrolase activity;GO:0046982 protein heterodimerization activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0039530 MDA-5 signaling pathway;GO:0140374 antiviral innate immune response",
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        "hit_score": 1.3,
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        "kg_view_protein": true
    },
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                "id": "A0A0E3KLW5_PIG",
                "url": "https://www.uniprot.org/uniprot/A0A0E3KLW5",
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        ],
        "mass": 19451.0,
        "length": 172,
        "protein_name": "diphosphoinositol-polyphosphate diphosphatase",
        "gene_name": "NUDT3",
        "organism": "Pig",
        "refseq_name": "diphosphoinositol polyphosphate phosphohydrolase 1",
        "refseq_ac": [
            {
                "id": "NP_001295339",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001295339",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "NUDT3",
        "gene_names_refseq": "NUDT3; nudix",
        "protein_names_uniprotkb": "diphosphoinositol-polyphosphate diphosphatase; 3.6.1.52",
        "protein_names_refseq": "diphosphoinositol polyphosphate phosphohydrolase 1; nucleoside diphosphate linked moiety X-type motif 3; nudix-type motif 3",
        "tax_id": 9823,
        "disease": "",
        "pathway": " (ssc:100737442);  (R-SSC-1855167)",
        "pathway_count": 2,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0000298 endopolyphosphatase activity;GO:0008486 diphosphoinositol-polyphosphate diphosphatase activity;GO:0034431 bis(5'-adenosyl)-hexaphosphatase activity;GO:0034432 bis(5'-adenosyl)-pentaphosphatase activity;GO:0052840 inositol diphosphate tetrakisphosphate diphosphatase activity",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0071543 diphosphoinositol polyphosphate metabolic process;GO:0071544 diphosphoinositol polyphosphate catabolic process;GO:1901907 diadenosine pentaphosphate catabolic process;GO:1901909 diadenosine hexaphosphate catabolic process;GO:1901911 adenosine 5'-(hexahydrogen pentaphosphate) catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0E3KLW5-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.0000000000010000.0000000000000.000.000",
        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
                "id": "A0A0E4G213_DANRE",
                "url": "https://www.uniprot.org/uniprot/A0A0E4G213",
                "type": "external"
            }
        ],
        "mass": 60174.0,
        "length": 546,
        "protein_name": "ETT ergothioneine transporter; Uncharacterized protein LOC799908",
        "gene_name": "slc22a21",
        "organism": "Zebrafish",
        "refseq_name": "uncharacterized protein LOC799908",
        "refseq_ac": [
            {
                "id": "NP_001295487",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001295487",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "slc22a21; SLC22A4; si:ch1073-409b12.4",
        "gene_names_refseq": "SLC22A4; si:ch1073-409b12.4; slc22a21",
        "protein_names_uniprotkb": "ETT ergothioneine transporter; Uncharacterized protein LOC799908",
        "protein_names_refseq": "C2; ETT ergothioneine transporter; ETTzf; solute carrier family 22 (organic cation transporter), member 21; uncharacterized protein LOC799908",
        "tax_id": 7955,
        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); myelodysplastic syndrome (Disease Ontology:DOID:0050908); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); systemic primary carnitine deficiency disease (Disease Ontology:DOID:14365); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); congestive heart failure (Disease Ontology:DOID:6000); inherited metabolic disorder (Disease Ontology:DOID:655); rheumatoid arthritis (Disease Ontology:DOID:7148); Crohn's disease (Disease Ontology:DOID:8778)",
        "pathway": " (dre:799908);  (R-DRE-200425);  (R-DRE-549127)",
        "pathway_count": 3,
        "publication_count": 4,
        "publication_id_list": "23594743;25746775;26469318;35295584",
        "class_list": "",
        "function": "##Evidence-Data-START## Transcript exon combination :: HG917106.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA3505370, SAMEA3505371 [ECO:0000348] ##Evidence-Data-END## PREDICTED REFSEQ: This record has not been reviewed and the function is unknown. The reference sequence was derived from HG917106.1. On May 12, 2015 this sequence version replaced XP_009294018.1., [RefSeq]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0015651 quaternary ammonium group transmembrane transporter activity;GO:0015199 amino-acid betaine transmembrane transporter activity;GO:0005524 ATP binding",
        "go_cellular_component": "GO:0016020 membrane;GO:0012505 endomembrane system",
        "go_biological_process": "GO:0015697 quaternary ammonium group transport;GO:0006811 monoatomic ion transport;GO:0015838 amino-acid betaine transport",
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        "hit_score": 0.5,
        "record_id": "A0A0E4G213-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.0000000000000001.0000000000000.000.000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A0F6YFH3-1",
        "uniprot_id": [
            {
                "id": "A0A0F6YFH3_CHICK",
                "url": "https://www.uniprot.org/uniprot/A0A0F6YFH3",
                "type": "external"
            }
        ],
        "mass": 24934.0,
        "length": 224,
        "protein_name": "Peroxiredoxin-like 2A",
        "gene_name": "PRXL2A",
        "organism": "Chicken",
        "refseq_name": "selenoprotein U",
        "refseq_ac": [
            {
                "id": "NP_001180448",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001180448",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "PRXL2A",
        "gene_names_refseq": "C10ORF58; C6H10orf58; FAM213A; PAMM; PRXL2A; SELENOU",
        "protein_names_uniprotkb": "Peroxiredoxin-like 2A; Peroxiredoxin-like 2 activated in M-CSF stimulated monocytes; Redox-regulatory protein FAM213A",
        "protein_names_refseq": "Protein PAMM; UPF0765 protein C10orf58 homolog; family with sequence similarity 213 member A; peroxiredoxin (PRX)-like 2 activated in M-CSF stimulated monocytes; peroxiredoxin-like 2 activated in M-CSF stimulated monocytes; redox-regulatory protein FAM213A; redox-regulatory protein PAMM; selenoprotein U",
        "tax_id": 9031,
        "disease": "",
        "pathway": " (gga:423625)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "##Evidence-Data-START## Transcript exon combination :: AJ720950.1, HAEK01129750.1 [ECO:0000332] RNAseq introns :: mixed sample support SAMEA103992290, SAMEA103992323 [ECO:0006172] ##Evidence-Data-END## ##RefSeq-Attributes-START## protein contains selenocysteine :: inferred from conservation ##RefSeq-Attributes-END## REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from JAENSK010000227.1. The protein encoded by this gene belongs to a subfamily of FAM213A/selenoprotein U (SelU), within a peroxiredoxin-like FAM213 superfamily. SelU is unusual in that it has restricted phylogenetic distribution in vertebrates, such as in chicken and fish. Other vertebrate members of this family, including mammals, contain cysteine-containing homologues. SelU proteins contain UxxC (U for selenocysteine and C for cysteine) motif in place of the catalytic CxxC motif found in cysteine-containing homologues. The latter function as redox regulatory proteins, suggesting a similar role for SelU proteins. Like majority of selenoproteins, SelU contains a single selenocysteine (Sec) residue encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs in vertebrates contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2017]. Transcript Variant: This variant (2) contains an alternate 5' non-coding exon derived from a downstream promoter, compared to variant 1. Variants 1 and 2 encode the same selenoprotein., [RefSeq]",
        "predicted_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
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        "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,
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0016209 antioxidant activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0F6YFH3-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.0001000000000000.0000000000000.000.000",
        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
                "id": "A0A0F7C9F3_DANRE",
                "url": "https://www.uniprot.org/uniprot/A0A0F7C9F3",
                "type": "external"
            }
        ],
        "mass": 188531.0,
        "length": 1655,
        "protein_name": "IQGAP1 protein; Ras GTPase-activating-like protein IQGAP1",
        "gene_name": "iqgap1",
        "organism": "Zebrafish",
        "refseq_name": "ras GTPase-activating-like protein IQGAP1",
        "refseq_ac": [
            {
                "id": "NP_001295895",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001295895",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "iqgap1; IQGAP1; im:7152854; im:7156663",
        "gene_names_refseq": "im:7152854; im:7156663; iqgap1",
        "protein_names_uniprotkb": "IQGAP1 protein; Ras GTPase-activating-like protein IQGAP1",
        "protein_names_refseq": "ras GTPase-activating-like protein IQGAP1",
        "tax_id": 7955,
        "disease": "",
        "pathway": " (R-DRE-373753);  (R-DRE-5626467);  (R-DRE-5674135);  (R-DRE-6798695);  (R-DRE-8980692);  (R-DRE-9013106);  (R-DRE-9013148);  (R-DRE-9013149);  (R-DRE-9013404);  (R-DRE-9013406);  (R-DRE-9013420);  (R-DRE-9013424)",
        "pathway_count": 12,
        "publication_count": 7,
        "publication_id_list": "16466575;19619483;23594743;25504979;26286209;26469318;27935819",
        "class_list": "",
        "function": "##Evidence-Data-START## Transcript exon combination :: KP862587.1 [ECO:0000332] RNAseq introns :: mixed sample support SAMEA3505370, SAMEA3505371 [ECO:0006172] ##Evidence-Data-END## PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from KP862587.1. On May 19, 2015 this sequence version replaced XP_009301707.1., [RefSeq]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0005516 calmodulin binding;GO:0051015 actin filament binding;GO:0031267 small GTPase binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005886 plasma membrane;GO:0005938 cell cortex;GO:0015629 actin cytoskeleton;GO:0031252 cell leading edge",
        "go_biological_process": "GO:0007173 epidermal growth factor receptor signaling pathway;GO:0010761 fibroblast migration;GO:1903479 mitotic actomyosin contractile ring assembly actin filament organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.8,
        "record_id": "A0A0F7C9F3-1",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0061436 establishment of skin barrier;GO:0006355 regulation of DNA-templated transcription;GO:0008544 epidermis development",
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        "record_id": "A0A0G2JTY1-1",
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        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
                "id": "NFAC3_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY4",
                "type": "external"
            }
        ],
        "mass": 115656.0,
        "length": 1076,
        "protein_name": "Nuclear factor of activated T-cells, cytoplasmic 3",
        "gene_name": "Nfatc3",
        "organism": "Rat",
        "refseq_name": "nuclear factor of activated T-cells, cytoplasmic 3 isoform 2",
        "refseq_ac": [
            {
                "id": "NP_001421511",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001421511",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Nfatc3; Nfat4",
        "gene_names_refseq": "NFAT4; NFATx; Nfatc3",
        "protein_names_uniprotkb": "Nuclear factor of activated T-cells, cytoplasmic 3; NFATc3; NFATx; T-cell transcription factor NFAT4",
        "protein_names_refseq": "T cell transcription factor NFAT4; nuclear factor of activated T-cells, cytoplasmic 3 isoform 2; nuclear factor of activated T-cells, cytoplasmic 3; nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:361400);  (R-RNO-2025928);  (R-RNO-2871809);  (R-RNO-5607763)",
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        "publication_id_list": "19538478;22673903;30980393;33495839;34845564;36373478;36825443;38242872",
        "class_list": "",
        "function": "Acts as a regulator of transcriptional activation. Binds to the TNFSF11/RANKL promoter region and promotes TNFSF11 transcription (By similarity). Binding to the TNFSF11 promoter region is increased by high levels of Ca(2+) which induce NFATC3 expression and may lead to regulation of TNFSF11 expression in osteoblasts (By similarity). Plays a role in promoting mesenteric arterial wall remodeling in response to the intermittent hypoxia-induced increase in EDN1 and ROCK signaling (By similarity). As a result NFATC3 colocalizes with F-actin filaments, translocates to the nucleus and promotes transcription of the smooth muscle hypertrophy and differentiation marker ACTA2 (By similarity). Promotes lipopolysaccharide-induced apoptosis and hypertrophy in cardiomyocytes (PubMed:30980393). Following JAK/STAT signaling activation and as part of a complex with NFATC4 and STAT3, binds to the alpha-beta E4 promoter region of CRYAB and activates transcription in cardiomyocytes (PubMed:19538478). In conjunction with NFATC4, involved in embryonic heart development via maintenance of cardiomyocyte survival, proliferation and differentiation (By similarity). Plays a role in the inducible expression of cytokine genes in T-cells, especially in the induction of the IL-2 (By similarity). Required for thymocyte maturation during DN3 to DN4 transition and during positive selection (By similarity). Positively regulates macrophage-derived polymicrobial clearance, via binding to the promoter region and promoting transcription of NOS2 resulting in subsequent generation of nitric oxide (By similarity). Involved in Ca(2+)-mediated transcriptional responses upon Ca(2+) influx via ORAI1 CRAC channels., [UniProtKB, UniProtKB, PubMed, UniProtKB, PubMed]; Induction of cardiomyocyte calcification is dependent on FoxO1/NFATc3/Runx2 signaling., [RefSeq, PubMed]; MiR-339-3p promotes AT1-AA-induced vascular inflammation by upregulating NFATc3 protein expression in vascular smooth muscle cells., [RefSeq, PubMed]; MicroRNA153 attenuates hypoxiainduced excessive proliferation and migration of pulmonary arterial smooth muscle cells by targeting ROCK1 and NFATc3. Erratum:[Mol Med Rep. 2022 Nov;26(5):332. doi: 10.3892/mmr.2022.12848. PMID: 36082819], [RefSeq, PubMed]; MicroRNA153 induces apoptosis by targeting NFATc3 to improve vascular remodeling in pulmonary hypertension., [RefSeq, PubMed]; The transplant rejection response involves neutrophil and macrophage adhesion-mediated trogocytosis and is regulated by NFATc3. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0003700 DNA-binding transcription factor activity;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005667 transcription regulator complex;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0014904 myotube cell development;GO:0035886 vascular associated smooth muscle cell differentiation;GO:1905064 negative regulation of vascular associated smooth muscle cell differentiation;GO:0007507 heart development;GO:0043065 positive regulation of apoptotic process",
        "synthesized_glycan_count": 0,
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        "record_type": "protein",
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    {
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        "uniprot_id": [
            {
                "id": "A0A0G2JTZ0_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2JTZ0",
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        ],
        "mass": 21050.0,
        "length": 183,
        "protein_name": "Family with sequence similarity 237 member A; Neurosecretory protein GL",
        "gene_name": "Fam237a",
        "organism": "Rat",
        "refseq_name": "protein FAM237A precursor",
        "refseq_ac": [
            {
                "id": "NP_001388875",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001388875",
                "type": "external"
            }
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        "gene_names_uniprotkb": "Fam237a; LOC103690541",
        "gene_names_refseq": "Fam237a; NPGL",
        "protein_names_uniprotkb": "Family with sequence similarity 237 member A; Neurosecretory protein GL",
        "protein_names_refseq": "neurosecretory protein GL; protein FAM237A precursor",
        "tax_id": 10116,
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        "publication_id_list": "25708449;28323972;28799896",
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        "function": "Distribution of NPGL in the mammalian brain and point to an important role for this neuropeptide in energy homeostasis., [RefSeq, PubMed]; The synthesis of the entire 80-amino acid peptide sequence of rat NPGL was optimized by microwave-assisted solid-phase peptide synthesis., [RefSeq, PubMed]; These results point to NPGL as a novel neuronal regulator that drives food intake and fat deposition through de novo lipogenesis and acts to maintain steady-state fat level in concert with insulin. Dysregulation of NPGL may be a root cause of obesity. Publication Status: Online-Only, [RefSeq, PubMed]",
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    {
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        "uniprot_id": [
            {
                "id": "SOX6_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2JTZ2",
                "type": "external"
            }
        ],
        "mass": 91816.0,
        "length": 827,
        "protein_name": "Transcription factor SOX-6",
        "gene_name": "Sox6",
        "organism": "Rat",
        "refseq_name": "transcription factor SOX-6",
        "refseq_ac": [
            {
                "id": "NP_001019922",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001019922",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Sox6; Sox-6",
        "gene_names_refseq": "Sox6",
        "protein_names_uniprotkb": "Transcription factor SOX-6",
        "protein_names_refseq": "SRY (sex determining region Y)-box 6; SRY box 6; SRY-box containing gene 6; transcription factor SOX-6",
        "tax_id": 10116,
        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652); heart disease (Disease Ontology:DOID:114); high grade glioma (Disease Ontology:DOID:3070)",
        "pathway": " (rno:293165);  (R-RNO-3769402)",
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        "publication_count": 5,
        "publication_id_list": "12081133;26150426;26659076;31076992;32114773",
        "class_list": "",
        "function": "LncRNA Gm4419 induces cell apoptosis in hepatic ischemia-reperfusion injury via regulating the miR-455-SOX6 axis., [RefSeq, PubMed]; Sox6 was specifically expressed in the neonatal brain and adult testis with Northern blotting., [RefSeq, PubMed]; The apoptosis process enhanced by overexpression of SOX6 or PDCD4, was rescued by the cardiac-abundant miR-499 in rat cardiomyocytes., [RefSeq, PubMed]; The authors proved that miR-499-5p inhibited hypoxia/reoxygenation-induced cardiomyocytes injury by targeting SOX6., [RefSeq, PubMed]; Transcription factor that plays a key role in several developmental processes, including neurogenesis, chondrocytes differentiation and cartilage formation (By similarity). Specifically binds the 5'-AACAAT-3' DNA motif present in enhancers and super-enhancers and promotes expression of genes important for chondrogenesis (By similarity). Required for overt chondrogenesis when condensed prechondrocytes differentiate into early stage chondrocytes: SOX5 and SOX6 cooperatively bind with SOX9 on active enhancers and super-enhancers associated with cartilage-specific genes, and thereby potentiate SOX9's ability to transactivate (PubMed:26150426). Not involved in precartilaginous condensation, the first step in chondrogenesis, during which skeletal progenitors differentiate into prechondrocytes (By similarity). Together with SOX5, required to form and maintain a pool of highly proliferating chondroblasts between epiphyses and metaphyses, to form columnar chondroblasts, delay chondrocyte prehypertrophy but promote hypertrophy, and to delay terminal differentiation of chondrocytes on contact with ossification fronts (By similarity). Binds to the proximal promoter region of the myelin protein MPZ gene, and is thereby involved in the differentiation of oligodendroglia in the developing spinal tube (By similarity). Binds to the gene promoter of MBP and acts as a transcriptional repressor (By similarity)., [UniProtKB, PubMed, UniProtKB]",
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        "secondary_ac_list": "F1MAJ5;Q4V8G3",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0042803 protein homodimerization activity;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0048708 astrocyte differentiation;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001701 in utero embryonic development;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": 0.6,
        "record_id": "A0A0G2JTZ2-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.0000000000001000.0000000000001.000.000",
        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
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                "url": "https://www.uniprot.org/uniprot/A0A0G2JTZ6",
                "type": "external"
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        ],
        "mass": 98818.0,
        "length": 902,
        "protein_name": "Synphilin-1",
        "gene_name": "Sncaip",
        "organism": "Rat",
        "refseq_name": "synphilin-1 isoform 2",
        "refseq_ac": [
            {
                "id": "NP_001424404",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001424404",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Sncaip",
        "gene_names_refseq": "Sncaip; Syph1",
        "protein_names_uniprotkb": "Synphilin-1; Alpha-synuclein-interacting protein",
        "protein_names_refseq": "synphilin-1 isoform 2; synphilin-1; synuclein, alpha interacting protein (synphilin)",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:307309)",
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        "publication_id_list": "11956199;19224863",
        "class_list": "",
        "function": "Our data indicated that synphilin-1 is a synaptic partner of alpha-synuclein, and it may mediate synaptic roles attributed to alpha-synuclein. Erratum:[J Biol Chem 2002 Sep 13;277(37):34651-4], [RefSeq, PubMed]; Synphilin-1A has a novel role as a regulator of SIAH activity, modulating alpha-synuclein, and formation of Lewy body-like inclusions, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0031625 ubiquitin protein ligase binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0036464 cytoplasmic ribonucleoprotein granule",
        "go_biological_process": "GO:0046928 regulation of neurotransmitter secretion;GO:0042417 dopamine metabolic process;GO:0090083 regulation of inclusion body assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "A0A0G2JTZ6-1",
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    },
    {
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                "url": "https://www.uniprot.org/uniprot/A0A0G2JTZ7",
                "type": "external"
            }
        ],
        "mass": 41547.0,
        "length": 375,
        "protein_name": "Solute carrier family 35, member F2",
        "gene_name": "Slc35f2",
        "organism": "Rat",
        "refseq_name": "solute carrier family 35 member F2 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001382663",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001382663",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Slc35f2",
        "gene_names_refseq": "Slc35f2",
        "protein_names_uniprotkb": "Solute carrier family 35, member F2",
        "protein_names_refseq": "solute carrier family 35 member F2 isoform 1",
        "tax_id": 10116,
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        "pathway_count": 0,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Putative solute transporter., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_refseq": "80 kDa MCM3-associated protein; germinal-center associated nuclear protein; minichromosome maintenance deficient 3 associated protein",
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            },
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        "gene_names_refseq": "Slc25a23",
        "protein_names_uniprotkb": "Mitochondrial adenyl nucleotide antiporter SLC25A23; Short calcium-binding mitochondrial carrier protein 3; Solute carrier family 25 member 23",
        "protein_names_refseq": "calcium-binding mitochondrial carrier protein SCaMC-3; mitochondrial adenyl nucleotide antiporter SLC25A23; phosphate carrier), member 23; solute carrier family 25 (mitochondrial carrier",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:301113)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Electroneutral antiporter that mediates the transport of adenine 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 adenine nucleotide pool could adapt to changing cellular energetic demands and indirectly regulate adenine nucleotide-dependent metabolic pathways. Also acts as a regulator of mitochondrial calcium uptake and can probably transport trace amounts of other divalent metal cations in complex with ATP. In vitro, a low activity is also observed with guanyl and pyrimidine nucleotides., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
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        "reported_s_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0000295 adenine nucleotide transmembrane transporter activity;GO:0005347 ATP transmembrane transporter activity;GO:0140987 ATP:phosphate antiporter activity;GO:0140988 ADP:phosphate antiporter activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane",
        "go_biological_process": "GO:0043457 regulation of cellular respiration;GO:0071277 cellular response to calcium ion;GO:0006851 mitochondrial calcium ion transmembrane transport;GO:0015866 ADP transport;GO:0036444 calcium import into the mitochondrion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0G2JVD2-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.0000000000001000.0000000000000.000.000",
        "kg_view_protein": true
    },
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            {
                "id": "A0A0G2JVD5_RAT",
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                "type": "external"
            }
        ],
        "mass": 207428.0,
        "length": 1859,
        "protein_name": "Zinc finger protein 142",
        "gene_name": "Zfp142",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 142 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001418925",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001418925",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Zfp142",
        "gene_names_refseq": "Zfp142; Znf142",
        "protein_names_uniprotkb": "Zinc finger protein 142",
        "protein_names_refseq": "zinc finger protein 142 (clone pHZ-49); zinc finger protein 142 isoform 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:316524)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
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        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0010468 regulation of gene expression",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0G2JVD5-1",
        "record_type": "protein",
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    },
    {
        "uniprot_canonical_ac": "A0A0G2JVD6-1",
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            {
                "id": "A0A0G2JVD6_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2JVD6",
                "type": "external"
            }
        ],
        "mass": 595654.0,
        "length": 5544,
        "protein_name": "Histone-lysine N-methyltransferase 2D",
        "gene_name": "Kmt2d",
        "organism": "Rat",
        "refseq_name": "histone-lysine N-methyltransferase 2D isoform X11",
        "refseq_ac": [
            {
                "id": "XP_017450810",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_017450810",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Kmt2d",
        "gene_names_refseq": "Kmt2d; Mll2",
        "protein_names_uniprotkb": "Histone-lysine N-methyltransferase 2D; 2.1.1.364; ALL1-related protein; Myeloid/lymphoid or mixed-lineage leukemia protein 2",
        "protein_names_refseq": "histone-lysine N-methyltransferase 2D isoform X11",
        "tax_id": 10116,
        "disease": "oral squamous cell carcinoma (Disease Ontology:DOID:0050866); Kabuki syndrome (Disease Ontology:DOID:0060473); 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); 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); gastrointestinal lymphoma (Disease Ontology:DOID:903)",
        "pathway": " (R-RNO-3214841);  (R-RNO-8936459);  (R-RNO-9772755)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "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]",
        "predicted_glycosites": 13,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 16,
        "glyco_site_count": 13,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "2.1.1.364",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.364",
                "type": "external"
            },
            {
                "id": "2.1.1.370",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.370",
                "type": "external"
            },
            {
                "id": "2.1.1.371",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.371",
                "type": "external"
            },
            {
                "id": "2.3.1.48",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.48",
                "type": "external"
            },
            {
                "id": "2.1.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.-",
                "type": "external"
            },
            {
                "id": "2.1.1.85",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.85",
                "type": "external"
            },
            {
                "id": "2.1.1.359",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.359",
                "type": "external"
            },
            {
                "id": "2.1.1.355",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.355",
                "type": "external"
            },
            {
                "id": "2.1.1.354",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.354",
                "type": "external"
            },
            {
                "id": "2.1.1.362",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.362",
                "type": "external"
            },
            {
                "id": "2.1.1.361",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.361",
                "type": "external"
            },
            {
                "id": "2.1.1.319",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.319",
                "type": "external"
            }
        ],
        "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:0044666 MLL3/4 complex",
        "go_biological_process": "GO:0001701 in utero embryonic development;GO:0008284 positive regulation of cell population proliferation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0043627 response to estrogen;GO:0033148 positive regulation of intracellular estrogen receptor signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A0G2JVD6-1",
        "record_type": "protein",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A0G2JVD9-1",
        "uniprot_id": [
            {
                "id": "A0A0G2JVD9_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2JVD9",
                "type": "external"
            }
        ],
        "mass": 62051.0,
        "length": 562,
        "protein_name": "IKAROS family zinc finger 1",
        "gene_name": "Ikzf1",
        "organism": "Rat",
        "refseq_name": "DNA-binding protein Ikaros isoform X1",
        "refseq_ac": [
            {
                "id": "XP_006251556",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006251556",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ikzf1",
        "gene_names_refseq": "Ikzf1; RGD1562979",
        "protein_names_uniprotkb": "IKAROS family zinc finger 1",
        "protein_names_refseq": "DNA-binding protein Ikaros isoform X1",
        "tax_id": 10116,
        "disease": "B-lymphoblastic leukemia/lymphoma (Disease Ontology:DOID:0080630); common variable immunodeficiency 13 (Disease Ontology:DOID:0081155); lung adenocarcinoma (Disease Ontology:DOID:3910); hepatocellular carcinoma (Disease Ontology:DOID:684); colorectal cancer (Disease Ontology:DOID:9256); acute lymphoblastic leukemia (Disease Ontology:DOID:9952)",
        "pathway": "",
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        "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:0019904 protein domain specific binding;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0032993 protein-DNA complex;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0001779 natural killer cell differentiation;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;GO:0030900 forebrain development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A0G2JVD9-1",
        "record_type": "protein",
        "filter_code": "0000000.0000110.100000.0000000000001000.0000000000000.000.000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A0G2JVF0-1",
        "uniprot_id": [
            {
                "id": "A0A0G2JVF0_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2JVF0",
                "type": "external"
            }
        ],
        "mass": 107336.0,
        "length": 965,
        "protein_name": "Rho GTPase activating protein 4",
        "gene_name": "Arhgap4",
        "organism": "Rat",
        "refseq_name": "rho GTPase-activating protein 4",
        "refseq_ac": [
            {
                "id": "NP_653341",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_653341",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Arhgap4",
        "gene_names_refseq": "Arhgap4",
        "protein_names_uniprotkb": "Rho GTPase activating protein 4",
        "protein_names_refseq": "rho GTPase-activating protein 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:246249);  (R-RNO-8980692);  (R-RNO-9013148);  (R-RNO-9013149)",
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        "publication_id_list": "12414125;17804252;22673903",
        "class_list": "",
        "function": "ARHGAP4 occured in the hippocampus, ventral region of the brainstem and striatum, and in cerebellar granule cells. Subcellularly, ARHGAP4 localized to the Golgi complex and could redistribute to the microtubules, for example during mitosis., [RefSeq, PubMed]; These observations suggest that ARHGAP4 can act as a potent inhibitor of cell and axon motility when it is localized to the leading edge of motile cells and axons., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005096 GTPase activator activity",
        "go_cellular_component": "GO:0005874 microtubule;GO:0030426 growth cone;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0010764 negative regulation of fibroblast migration;GO:0007165 signal transduction;GO:0007399 nervous system development;GO:0035023 regulation of Rho protein signal transduction;GO:0030517 negative regulation of axon extension",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0A0G2JVF0-1",
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        "filter_code": "0000000.0000101.010000.0000000000001000.0000000000000.000.000",
        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
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                "url": "https://www.uniprot.org/uniprot/A0A0G2JVF5",
                "type": "external"
            }
        ],
        "mass": 42535.0,
        "length": 384,
        "protein_name": "High mobility group protein B3",
        "gene_name": "Hmgb3l1; Hmgb3",
        "organism": "Rat",
        "refseq_name": "high mobility group protein B3 isoform 3",
        "refseq_ac": [
            {
                "id": "NP_001385706",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001385706",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Hmgb3l1; Hmgb3; Hmgb3l1; LOC108348204",
        "gene_names_refseq": "Hmgb3; RGD1564407",
        "protein_names_uniprotkb": "High mobility group protein B3; High mobility group protein 2a; High mobility group protein 4",
        "protein_names_refseq": "high mobility group protein B3 isoform 3; high mobility group protein B3",
        "tax_id": 10116,
        "disease": "syndromic microphthalmia 13 (Disease Ontology:DOID:0111811)",
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        "protein_names_refseq": "FL cytokine receptor; FMS-like tyrosine kinase 3; fms-related tyrosine kinase 3; receptor-type tyrosine-protein kinase FLT3 precursor; receptor-type tyrosine-protein kinase FLT3",
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        "protein_name": "Retinoic acid receptor, alpha",
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        "protein_names_refseq": "PE responsive protein c64; melanoma-associated antigen MG50; peroxidasin homolog precursor; peroxidasin homolog",
        "tax_id": 10116,
        "disease": "anterior segment dysgenesis 7 (Disease Ontology:DOID:0080612)",
        "pathway": " (rno:554172);  (R-RNO-2243919)",
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        "publication_count": 6,
        "publication_id_list": "21292788;24021280;27651140;29186367;31216444;36029851",
        "class_list": "",
        "function": "NOX/VPO1 pathway-derived reactive oxygen species promote the oxidative injury and dysfunctions of EPCs in PH, which may contribute to endothelial dysfunctions in PH, [RefSeq, PubMed]; The over-expression of VPO1 during the development of hypertension, accompanied by the endothelial dysfunction, the decreased NO levels, the elevated NOX and ROS activities, indicates a clear connection between VPO1 gene and hypertension.(VPO1), [RefSeq, PubMed]; VPO1 promotes cardiac remodeling by accelerating the Ang II-induced hypertrophy of H9c2 cell via the NOX2/VPO1/HOCl/ERK1/2 signaling pathways., [RefSeq, PubMed]; VPO1 promotes hypoxia-induced proliferation, apoptosis resistance, and migration in pulmonary artery smooth muscle cells via the NOX4/VPO1/HOCl/NF-kappaB signalling pathway., [RefSeq, PubMed]; Vascular peroxidase 1 promotes phenotypic transformation of pulmonary artery smooth muscle cells via ERK pathway in hypoxia-induced pulmonary hypertensive rats., [RefSeq, PubMed]; Vascular peroxidase 1/peroxidasin is a novel regulator of angiotensin II-induced vascular smooth muscle cell proliferation via NADPH oxidase-hydrogen peroxide pathways., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005615 extracellular space;GO:0005783 endoplasmic reticulum;GO:0009986 cell surface;GO:0016020 membrane;GO:0031012 extracellular matrix",
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        "disease": "retinal macular dystrophy 2 (Disease Ontology:DOID:0070517); retinitis pigmentosa 41 (Disease Ontology:DOID:0110376); cone-rod dystrophy 12 (Disease Ontology:DOID:0111019); diabetes mellitus (Disease Ontology:DOID:9351)",
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            {
                "id": "NP_001413968",
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        "function": "Gamma-secretase activating protein (GSAP) and imatinib have roles in the regulation of gamma-secretase activity and amyloid-beta generation, [RefSeq, PubMed]",
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        ],
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        "protein_name": "Olfactory receptor",
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        "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]",
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    },
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        ],
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        ],
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        "protein_names_uniprotkb": "Loricrin cornified envelope precursor protein",
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        "go_molecular_function": "GO:0005200 structural constituent of cytoskeleton;GO:0030280 structural constituent of skin epidermis",
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        "go_biological_process": "GO:0030216 keratinocyte differentiation",
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            {
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        ],
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        "protein_name": "Polymerase delta-interacting protein 3",
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        "gene_names_uniprotkb": "Poldip3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Polymerase delta-interacting protein 3; S6K1 Aly/REF-like target",
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        "pathway": " (R-RNO-159236);  (R-RNO-73856)",
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        "function": "Is involved in regulation of translation. Is preferentially associated with CBC-bound spliced mRNA-protein complexes during the pioneer round of mRNA translation. Contributes to enhanced translational efficiency of spliced over nonspliced mRNAs. Recruits activated ribosomal protein S6 kinase beta-1 I/RPS6KB1 to newly synthesized mRNA. Involved in nuclear mRNA export; probably mediated by association with the TREX complex., [UniProtKB, UniProtKB, UniProtKB]",
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        ],
        "mass": 45188.0,
        "length": 410,
        "protein_name": "Transcription factor",
        "gene_name": "Tfdp1",
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        "refseq_name": "transcription factor Dp-1 isoform 1",
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            {
                "id": "NP_001423505",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001423505",
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            }
        ],
        "gene_names_uniprotkb": "Tfdp1; MGC112830",
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        "disease": "mismatch repair cancer syndrome (Disease Ontology:DOID:0112182)",
        "pathway": " (R-RNO-1538133);  (R-RNO-2173796);  (R-RNO-69231);  (R-RNO-8953750)",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005667 transcription regulator complex;GO:0090575 RNA polymerase II transcription regulator complex;GO:0035189 Rb-E2F complex",
        "go_biological_process": "GO:2000278 regulation of DNA biosynthetic process;GO:0070345 negative regulation of fat cell proliferation;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription",
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        ],
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        "protein_name": "Tripartite motif-containing protein 46",
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        "protein_names_uniprotkb": "Tripartite motif-containing protein 46",
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    {
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        ],
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            {
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        ],
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        ],
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        ],
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        "function": "F-box-like protein involved in the recruitment of the ubiquitin/19S proteasome complex to nuclear receptor-regulated transcription units. Plays an essential role in transcription activation mediated by nuclear receptors. Probably acts as integral component of corepressor complexes that mediates the recruitment of the 19S proteasome complex, leading to the subsequent proteasomal degradation of transcription repressor complexes, thereby allowing cofactor exchange., [UniProtKB, UniProtKB]",
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        ],
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        "protein_name": "Protein boule-like",
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        "go_biological_process": "GO:0060261 positive regulation of transcription initiation by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006367 transcription initiation at RNA polymerase II promoter;GO:0042789 mRNA transcription by RNA polymerase II",
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        "kg_view_protein": true
    },
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        "uniprot_id": [
            {
                "id": "SIR1_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2JZ79",
                "type": "external"
            }
        ],
        "mass": 62059.0,
        "length": 555,
        "protein_name": "NAD-dependent protein deacetylase sirtuin-1",
        "gene_name": "Sirt1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Sirt1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "NAD-dependent protein deacetylase sirtuin-1; 2.3.1.-; 2.3.1.286; NAD-dependent protein deacylase sirtuin-1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); prostate cancer (Disease Ontology:DOID:10283); Alzheimer's disease (Disease Ontology:DOID:10652); osteoporosis (Disease Ontology:DOID:11476); nephrogenic diabetes insipidus (Disease Ontology:DOID:12387); Huntington's disease (Disease Ontology:DOID:12858); Parkinson's disease (Disease Ontology:DOID:14330); alcohol use disorder (Disease Ontology:DOID:1574); epilepsy (Disease Ontology:DOID:1826); impotence (Disease Ontology:DOID:1875); atherosclerosis (Disease Ontology:DOID:1936); acute kidney failure (Disease Ontology:DOID:3021); middle cerebral artery infarction (Disease Ontology:DOID:3525); macular degeneration (Disease Ontology:DOID:4448); myocardial infarction (Disease Ontology:DOID:5844); diabetes mellitus (Disease Ontology:DOID:9351); type 2 diabetes mellitus (Disease Ontology:DOID:9352); steatotic liver disease (Disease Ontology:DOID:9452); senile cataract (Disease Ontology:DOID:9669); obesity (Disease Ontology:DOID:9970); cocaine dependence (Disease Ontology:DOID:9975)",
        "pathway": " (R-RNO-3371453);  (R-RNO-427359);  (R-RNO-9617629);  (R-RNO-9764725);  (R-RNO-9841922);  (R-RNO-9856649)",
        "pathway_count": 6,
        "publication_count": 1,
        "publication_id_list": "38300636",
        "class_list": "",
        "function": "NAD-dependent protein deacetylase that links transcriptional regulation directly to intracellular energetics and participates in the coordination of several separated cellular functions such as cell cycle, response to DNA damage, metabolism, apoptosis and autophagy. Can modulate chromatin function through deacetylation of histones and can promote alterations in the methylation of histones and DNA, leading to transcriptional repression. Deacetylates a broad range of transcription factors and coregulators, thereby regulating target gene expression positively and negatively. Serves as a sensor of the cytosolic ratio of NAD(+)/NADH which is altered by glucose deprivation and metabolic changes associated with caloric restriction. Is essential in skeletal muscle cell differentiation and in response to low nutrients mediates the inhibitory effect on skeletal myoblast differentiation which also involves 5'-AMP-activated protein kinase (AMPK) and nicotinamide phosphoribosyltransferase (NAMPT). Component of the eNoSC (energy-dependent nucleolar silencing) complex, a complex that mediates silencing of rDNA in response to intracellular energy status and acts by recruiting histone-modifying enzymes. The eNoSC complex is able to sense the energy status of cell: upon glucose starvation, elevation of NAD(+)/NADP(+) ratio activates SIRT1, leading to histone H3 deacetylation followed by dimethylation of H3 at 'Lys-9' (H3K9me2) by SUV39H1 and the formation of silent chromatin in the rDNA locus. Deacetylates 'Lys-266' of SUV39H1, leading to its activation. Inhibits skeletal muscle differentiation by deacetylating PCAF and MYOD1. Deacetylates H2A and 'Lys-26' of H1-4. Deacetylates 'Lys-16' of histone H4 (in vitro). Involved in NR0B2/SHP corepression function through chromatin remodeling: Recruited to LRH1 target gene promoters by NR0B2/SHP thereby stimulating histone H3 and H4 deacetylation leading to transcriptional repression. Proposed to contribute to genomic integrity via positive regulation of telomere length; however, reports on localization to pericentromeric heterochromatin are conflicting. Proposed to play a role in constitutive heterochromatin (CH) formation and/or maintenance through regulation of the available pool of nuclear SUV39H1. Upon oxidative/metabolic stress decreases SUV39H1 degradation by inhibiting SUV39H1 polyubiquitination by MDM2. This increase in SUV39H1 levels enhances SUV39H1 turnover in CH, which in turn seems to accelerate renewal of the heterochromatin which correlates with greater genomic integrity during stress response. Deacetylates 'Lys-382' of p53/TP53 and impairs its ability to induce transcription-dependent proapoptotic program and modulate cell senescence. Deacetylates TAF1B and thereby represses rDNA transcription by the RNA polymerase I. Deacetylates MYC, promotes the association of MYC with MAX and decreases MYC stability leading to compromised transformational capability. Deacetylates FOXO3 in response to oxidative stress thereby increasing its ability to induce cell cycle arrest and resistance to oxidative stress but inhibiting FOXO3-mediated induction of apoptosis transcriptional activity; also leading to FOXO3 ubiquitination and protesomal degradation. Appears to have a similar effect on MLLT7/FOXO4 in regulation of transcriptional activity and apoptosis. Deacetylates DNMT1; thereby impairs DNMT1 methyltransferase-independent transcription repressor activity, modulates DNMT1 cell cycle regulatory function and DNMT1-mediated gene silencing. Deacetylates RELA/NF-kappa-B p65 thereby inhibiting its transactivating potential and augments apoptosis in response to TNF-alpha. Deacetylates HIF1A, KAT5/TIP60, RB1 and HIC1. Deacetylates FOXO1 resulting in its nuclear retention and enhancement of its transcriptional activity leading to increased gluconeogenesis in liver. Inhibits E2F1 transcriptional activity and apoptotic function, possibly by deacetylation. Involved in HES1- and HEY2-mediated transcriptional repression. In cooperation with MYCN seems to be involved in transcriptional repression of DUSP6/MAPK3 leading to MYCN stabilization by phosphorylation at 'Ser-62'. Deacetylates MEF2D. Required for antagonist-mediated transcription suppression of AR-dependent genes which may be linked to local deacetylation of histone H3. Represses HNF1A-mediated transcription. Required for the repression of ESRRG by CREBZF. Deacetylates NR1H3 AND NR1H2 and deacetylation of NR1H3 at 'Lys-434' positively regulates transcription of NR1H3:RXR target genes, promotes NR1H3 proteasomal degradation and results in cholesterol efflux; a promoter clearing mechanism after reach round of transcription is proposed. Involved in lipid metabolism: deacetylates LPIN1, thereby inhibiting diacylglycerol synthesis. Implicated in regulation of adipogenesis and fat mobilization in white adipocytes by repression of PPARG which probably involves association with NCOR1 and SMRT/NCOR2. Deacetylates p300/EP300 and PRMT1. Deacetylates ACSS2 leading to its activation, and HMGCS1 deacetylation. Involved in liver and muscle metabolism. Through deacetylation and activation of PPARGC1A is required to activate fatty acid oxidation in skeletal muscle under low-glucose conditions and is involved in glucose homeostasis. Involved in regulation of PPARA and fatty acid beta-oxidation in liver. Involved in positive regulation of insulin secretion in pancreatic beta cells in response to glucose; the function seems to imply transcriptional repression of UCP2. Proposed to deacetylate IRS2 thereby facilitating its insulin-induced tyrosine phosphorylation. Deacetylates SREBF1 isoform SREBP-1C thereby decreasing its stability and transactivation in lipogenic gene expression. Involved in DNA damage response by repressing genes which are involved in DNA repair, such as XPC and TP73, deacetylating XRCC6/Ku70, and facilitating recruitment of additional factors to sites of damaged DNA, such as SIRT1-deacetylated NBN can recruit ATM to initiate DNA repair and SIRT1-deacetylated XPA interacts with RPA2. Also involved in DNA repair of DNA double-strand breaks by homologous recombination and specifically single-strand annealing independently of XRCC6/Ku70 and NBN. Promotes DNA double-strand breaks by mediating deacetylation of SIRT6. Transcriptional suppression of XPC probably involves an E2F4:RBL2 suppressor complex and protein kinase B (AKT) signaling. Transcriptional suppression of TP73 probably involves E2F4 and PCAF. Deacetylates WRN thereby regulating its helicase and exonuclease activities and regulates WRN nuclear translocation in response to DNA damage. Deacetylates APEX1 at 'Lys-6' and 'Lys-7' and stimulates cellular AP endonuclease activity by promoting the association of APEX1 to XRCC1. Catalyzes deacetylation of ERCC4/XPF, thereby impairing interaction with ERCC1 and nucleotide excision repair (NER). Increases p53/TP53-mediated transcription-independent apoptosis by blocking nuclear translocation of cytoplasmic p53/TP53 and probably redirecting it to mitochondria. Deacetylates XRCC6/Ku70 at 'Lys-539' and 'Lys-542' causing it to sequester BAX away from mitochondria thereby inhibiting stress-induced apoptosis. Is involved in autophagy, presumably by deacetylating ATG5, ATG7 and MAP1LC3B/ATG8. Deacetylates AKT1 which leads to enhanced binding of AKT1 and PDK1 to PIP3 and promotes their activation. Proposed to play role in regulation of STK11/LBK1-dependent AMPK signaling pathways implicated in cellular senescence which seems to involve the regulation of the acetylation status of STK11/LBK1. Can deacetylate STK11/LBK1 and thereby increase its activity, cytoplasmic localization and association with STRAD; however, the relevance of such activity in normal cells is unclear. In endothelial cells is shown to inhibit STK11/LBK1 activity and to promote its degradation. Deacetylates SMAD7 at 'Lys-64' and 'Lys-70' thereby promoting its degradation. Deacetylates CIITA and augments its MHC class II transactivation and contributes to its stability. Deacetylates MECOM/EVI1. Deacetylates PML at 'Lys-487' and this deacetylation promotes PML control of PER2 nuclear localization. During the neurogenic transition, represses selective NOTCH1-target genes through histone deacetylation in a BCL6-dependent manner and leading to neuronal differentiation. Regulates the circadian expression of several core clock genes, including BMAL1, RORC, PER2 and CRY1 and plays a critical role in maintaining a controlled rhythmicity in histone acetylation, thereby contributing to circadian chromatin remodeling. Deacetylates BMAL1 and histones at the circadian gene promoters in order to facilitate repression by inhibitory components of the circadian oscillator. Deacetylates PER2, facilitating its ubiquitination and degradation by the proteasome. Protects cardiomyocytes against palmitate-induced apoptosis. Deacetylates XBP1 isoform 2; deacetylation decreases protein stability of XBP1 isoform 2 and inhibits its transcriptional activity. Deacetylates PCK1 and directs its activity toward phosphoenolpyruvate production promoting gluconeogenesis. Involved in the CCAR2-mediated regulation of PCK1 and NR1D1. Deacetylates CTNB1 at 'Lys-49'. In POMC (pro-opiomelanocortin) neurons, required for leptin-induced activation of PI3K signaling. In addition to protein deacetylase activity, also acts as a protein-lysine deacylase by mediating protein depropionylation and decrotonylation. Mediates depropionylation of Osterix (SP7). Catalyzes decrotonylation of histones; it however does not represent a major histone decrotonylase. Deacetylates SOX9; promoting SOX9 nuclear localization and transactivation activity. Involved in the regulation of centrosome duplication. Deacetylates CENATAC in G1 phase, allowing for SASS6 accumulation on the centrosome and subsequent procentriole assembly (By similarity). Deacetylates NDC80/HEC1 (By similarity)., [UniProtKB, UniProtKB, UniProtKB]",
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        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 21,
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        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "2.3.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.-",
                "type": "external"
            },
            {
                "id": "2.3.1.286",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.286",
                "type": "external"
            },
            {
                "id": "2.4.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.4.2.-",
                "type": "external"
            },
            {
                "id": "2.1.1.355",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.355",
                "type": "external"
            },
            {
                "id": "3.4.22.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.22.-",
                "type": "external"
            },
            {
                "id": "3.9.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.9.1.-",
                "type": "external"
            },
            {
                "id": "3.6.4.10",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.10",
                "type": "external"
            },
            {
                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
            },
            {
                "id": "2.1.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.-",
                "type": "external"
            },
            {
                "id": "2.3.1.48",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.48",
                "type": "external"
            },
            {
                "id": "3.5.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.5.1.-",
                "type": "external"
            },
            {
                "id": "3.5.1.98",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.5.1.98",
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            }
        ],
        "go_molecular_function": "GO:0019904 protein domain specific binding;GO:0042802 identical protein binding;GO:0051019 mitogen-activated protein kinase binding;GO:0019213 deacetylase activity;GO:0042393 histone binding",
        "go_cellular_component": "GO:0005635 nuclear envelope;GO:0005730 nucleolus;GO:0005739 mitochondrion;GO:0000785 chromatin;GO:0005677 chromatin silencing complex",
        "go_biological_process": "GO:0070857 regulation of bile acid biosynthetic process;GO:0090400 stress-induced premature senescence;GO:0000720 pyrimidine dimer repair by nucleotide-excision repair;GO:0031393 negative regulation of prostaglandin biosynthetic process;GO:0042595 behavioral response to starvation",
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    },
    {
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        "uniprot_id": [
            {
                "id": "A0A0G2JZ84_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2JZ84",
                "type": "external"
            }
        ],
        "mass": 291350.0,
        "length": 2575,
        "protein_name": "Ectopic P-granules 5 autophagy tethering factor",
        "gene_name": "Epg5",
        "organism": "Rat",
        "refseq_name": "ectopic P granules protein 5 homolog",
        "refseq_ac": [
            {
                "id": "NP_001414542",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414542",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Epg5",
        "gene_names_refseq": "Epg5; RGD1306286",
        "protein_names_uniprotkb": "Ectopic P-granules 5 autophagy tethering factor",
        "protein_names_refseq": "ectopic P granules protein 5 homolog; ectopic P-granules autophagy protein 5 homolog",
        "tax_id": 10116,
        "disease": "Vici syndrome (Disease Ontology:DOID:0060356); retinitis pigmentosa (Disease Ontology:DOID:10584); amyotrophic lateral sclerosis (Disease Ontology:DOID:332)",
        "pathway": "",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0048471 perinuclear region of cytoplasm;GO:0005764 lysosome",
        "go_biological_process": "GO:0097352 autophagosome maturation;GO:0048877 homeostasis of number of retina cells;GO:0006954 inflammatory response;GO:0045087 innate immune response;GO:0051402 neuron apoptotic process",
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    },
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        ],
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        "gene_names_refseq": "Kiaa1671; RGD1306556; RGD1560125",
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        "protein_names_refseq": "uncharacterized protein KIAA1671 homolog",
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        "go_cellular_component": "GO:0005929 cilium;GO:0015630 microtubule cytoskeleton;GO:0045171 intercellular bridge",
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            {
                "id": "A0A0G2JZA1_RAT",
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                "type": "external"
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        ],
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        "length": 1386,
        "protein_name": "Roundabout guidance receptor 2",
        "gene_name": "Robo2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Robo2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Roundabout guidance receptor 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "myoclonic-atonic epilepsy (Disease Ontology:DOID:0060475); transient cerebral ischemia (Disease Ontology:DOID:224); vesicoureteral reflux (Disease Ontology:DOID:9620)",
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        "function": "Component of the sarcomere that tethers together nebulin (skeletal muscle) and nebulette (cardiac muscle) to alpha-actinin, at the Z lines., [UniProtKB, UniProtKB, UniProtKB]",
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        "function": "E3 ubiquitin-protein ligase which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. Ubiquitinates BCKDK and targets it for degradation, thereby regulating various metabolic processes. Involved in the positive regulation of neurite branching in hippocampal neurons and the control of neuronal spine number and morphology, through the ubiquitination of PPP3CC., [UniProtKB, UniProtKB]",
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        "function": "Changes of LRP6/beta-catenin pathway in adipose tissue of rats with intrauterine growth restriction with catch-up growth., [RefSeq, PubMed]; Component of the Wnt-Fzd-LRP5-LRP6 complex that triggers beta-catenin signaling through inducing aggregation of receptor-ligand complexes into ribosome-sized signalosomes. Cell-surface coreceptor of Wnt/beta-catenin signaling, which plays a pivotal role in bone formation. The Wnt-induced Fzd/LRP6 coreceptor complex recruits DVL1 polymers to the plasma membrane which, in turn, recruits the AXIN1/GSK3B-complex to the cell surface promoting the formation of signalosomes and inhibiting AXIN1/GSK3-mediated phosphorylation and destruction of beta-catenin. Required for posterior patterning of the epiblast during gastrulation., [UniProtKB, UniProtKB]; Knockdown of LRP6 inhibited the cell viability by activation of Drp1 in glucose deprived-cardiomyocytes., [RefSeq, PubMed]; LRP6 Bidirectionally Regulates Insulin Sensitivity through Insulin Receptor and S6K Signaling in Rats with CG-IUGR., [RefSeq, PubMed]; LRP6 acts as a scaffold protein in cardiac gap junction assembly and intracellular protein trafficking. Publication Status: Online-Only, [RefSeq, PubMed]; LRP6 regulates alternative pre-mRNA splicing., [RefSeq, PubMed]",
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        "go_biological_process": "GO:0060603 mammary gland duct morphogenesis;GO:0060059 embryonic retina morphogenesis in camera-type eye;GO:2000648 positive regulation of stem cell proliferation;GO:0050678 regulation of epithelial cell proliferation;GO:0060042 retina morphogenesis in camera-type eye",
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        "function": "Proposed core component of the chromatin remodeling Ino80 complex which exhibits DNA- and nucleosome-activated ATPase activity and catalyzes ATP-dependent nucleosome sliding., [UniProtKB, UniProtKB]",
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        "protein_name": "RNA polymerase II subunit A C-terminal domain phosphatase",
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        "protein_names_refseq": "cilia and flagella associated protein 221; primary ciliary dyskinesia protein 1",
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        "pathway": " (R-RNO-68911);  (R-RNO-69231)",
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        "function": "2-Acetylaminofluorene could possibly block G1/S-transition smf slter lelvels of E2f3., [RefSeq, PubMed]; Critical functions of microRNA-30a-5p-E2F3 in cardiomyocyte apoptosis induced by hypoxia/reoxygenation., [RefSeq, PubMed]; Long noncoding RNA MAPKAPK5-AS1 promoted lipopolysaccharide-induced inflammatory damage in the myocardium by sponging microRNA-124-3p/E2F3. Publication Status: Online-Only, [RefSeq, PubMed]; MicroRNA141 inhibits the differentiation of bone marrowderived mesenchymal stem cells in steroidinduced osteonecrosis via E2F3., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0090575 RNA polymerase II transcription regulator complex",
        "go_biological_process": "GO:0070345 negative regulation of fat cell proliferation;GO:0008284 positive regulation of cell population proliferation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription;GO:0045893 positive regulation of DNA-templated transcription",
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