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        "protein_names_refseq": "",
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        ],
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            {
                "id": "NP_001401842",
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        "gene_names_refseq": "Susd2",
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        "protein_names_refseq": "sushi domain-containing protein 2 precursor; sushi domain-containing protein 2",
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        "ec_number_list": [],
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            }
        ],
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        ],
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        "refseq_ac": [],
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        "protein_names_uniprotkb": "Zinc finger protein 945",
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        "tax_id": 10116,
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        "protein_names_refseq": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9",
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    },
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            {
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        ],
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        "protein_name": "A disintegrin and metalloproteinase with thrombospondin motifs 10",
        "gene_name": "Adamts10",
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            {
                "id": "NP_001258374",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001258374",
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            }
        ],
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        "protein_names_uniprotkb": "A disintegrin and metalloproteinase with thrombospondin motifs 10",
        "protein_names_refseq": "A disintegrin and metalloproteinase with thrombospondin motifs 10 precursor; A disintegrin and metalloproteinase with thrombospondin motifs 10; a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 10; a disintegrin-like and metalloprotease with thrombospondin type 1 motif, 10",
        "tax_id": 10116,
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            {
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            {
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        "pathway": " (rno:308444);  (R-RNO-4420097)",
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        "function": "AXL signaling in primary sensory neurons contributes to chronic compression of dorsal root ganglion-induced neuropathic pain in rats., [RefSeq, PubMed]; Axl expression pattern suggests a role in the early progression of LV remodeling in HF but not in the later systolic dysfunction. Publication Status: Online-Only, [RefSeq, PubMed]; Cilostazol-mediated protection against uremic toxin-related vascular smooth muscle cell dysfunction via Axl signaling pathway., [RefSeq, PubMed]; The Gas6/Axl interaction was inhibited by R428, which abolished the preventive effect of VK2 on CaCl2- and beta-GP-induced apoptosis and calcification. These results suggest that Gas6 is critical in VK2-mediated functions that attenuate CaCl2- and beta-GP-induced VSMC calcification by blocking apoptosis., [RefSeq, PubMed]; Tumor perivascular cell-derived extracellular vesicles promote angiogenesis via the Gas6/Axl pathway., [RefSeq, PubMed]",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.12.1",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.153",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.82",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.23",
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        "go_biological_process": "GO:0001779 natural killer cell differentiation;GO:0035457 cellular response to interferon-alpha;GO:0001961 positive regulation of cytokine-mediated signaling pathway;GO:2000669 negative regulation of dendritic cell apoptotic process;GO:0006954 inflammatory response",
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        "gene_name": "Sprr1b",
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    },
    {
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            {
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                "type": "external"
            }
        ],
        "mass": 71528.0,
        "length": 644,
        "protein_name": "Synaptotagmin 16",
        "gene_name": "Syt16",
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        "refseq_name": "synaptotagmin 16 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001415561",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001415561",
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            }
        ],
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        "protein_names_uniprotkb": "Synaptotagmin 16",
        "protein_names_refseq": "synaptotagmin 16 isoform 1; synaptotagmin XVI",
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        "function": "May be involved in the trafficking and exocytosis of secretory vesicles in non-neuronal tissues. Is Ca(2+)-independent., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005543 phospholipid binding;GO:0042802 identical protein binding",
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    },
    {
        "uniprot_canonical_ac": "A0A0G2K665-1",
        "uniprot_id": [
            {
                "id": "A0A0G2K665_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2K665",
                "type": "external"
            }
        ],
        "mass": 157602.0,
        "length": 1387,
        "protein_name": "GTPase activating protein testicular GAP1",
        "gene_name": "Tgap1",
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        "refseq_name": "GTPase activating protein testicular GAP1 isoform X1",
        "refseq_ac": [
            {
                "id": "XP_038957885",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_038957885",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tgap1; Tgap1l11; tGap1",
        "gene_names_refseq": "Tgap1",
        "protein_names_uniprotkb": "GTPase activating protein testicular GAP1",
        "protein_names_refseq": "GTPase activating protein testicular GAP1 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:294892)",
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        "go_molecular_function": "GO:0005096 GTPase activator activity",
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        "go_biological_process": "GO:0007165 signal transduction;GO:0035023 regulation of Rho protein signal transduction",
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    },
    {
        "uniprot_canonical_ac": "A0A0G2K6D5-1",
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            {
                "id": "A0A0G2K6D5_RAT",
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                "type": "external"
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        ],
        "mass": 117421.0,
        "length": 1035,
        "protein_name": "Presequence protease, mitochondrial",
        "gene_name": "Pitrm1",
        "organism": "Rat",
        "refseq_name": "presequence protease, mitochondrial isoform 2",
        "refseq_ac": [
            {
                "id": "NP_001402089",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001402089",
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        ],
        "gene_names_uniprotkb": "Pitrm1",
        "gene_names_refseq": "Pitrm1",
        "protein_names_uniprotkb": "Presequence protease, mitochondrial; Pitrilysin metalloproteinase 1",
        "protein_names_refseq": "pitrilysin metallepetidase 1; pitrilysin metalloprotease 1; presequence protease, mitochondrial isoform 2; presequence protease, mitochondrial",
        "tax_id": 10116,
        "disease": "hereditary ataxia (Disease Ontology:DOID:0050951); autosomal recessive spinocerebellar ataxia 30 (Disease Ontology:DOID:0070411); Alzheimer's disease (Disease Ontology:DOID:10652); primary cerebellar degeneration (Disease Ontology:DOID:9277)",
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        "function": "Metalloendopeptidase of the mitochondrial matrix that functions in peptide cleavage and degradation rather than in protein processing. Has an ATP-independent activity. Specifically cleaves peptides in the range of 5 to 65 residues. Shows a preference for cleavage after small polar residues and before basic residues, but without any positional preference. Degrades the transit peptides of mitochondrial proteins after their cleavage. Also degrades other unstructured peptides. It is also able to degrade amyloid-beta protein 40, one of the peptides produced by APP processing, when it accumulates in mitochondrion. It is a highly efficient protease, at least toward amyloid-beta protein 40. Cleaves that peptide at a specific position and is probably not processive, releasing digested peptides intermediates that can be further cleaved subsequently. It is also able to degrade amyloid-beta protein 42., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004222 metalloendopeptidase activity;GO:0008237 metallopeptidase activity;GO:0008270 zinc ion binding;GO:0046872 metal ion binding",
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    {
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        ],
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        "protein_name": "Olfactory receptor",
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                "id": "NP_001000575",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000575",
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        ],
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        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 741; olfactory receptor Olr741-like; olfactory receptor Olr741; olfactory receptor gene Olr741",
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        "disease": "oligoasthenoteratozoospermia (Disease Ontology:DOID:0070311)",
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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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        "secondary_ac_list": "A0A0G2K8F8",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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                "id": "A0A0G2K6V9_RAT",
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        ],
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        "protein_name": "non-specific serine/threonine protein kinase",
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        "gene_names_uniprotkb": "Smokwl2; Smokwl3; LOC134479633; LOC134479831; RGD1564409; RGD1565071; Smokwl3",
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        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
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        "function": "May play a role in sperm motility, especially in the regulation of flagellar function., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.23",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.38",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.21",
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                "id": "2.7.1.40",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.40",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.12",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.11",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "kg_view_protein": true
    },
    {
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            {
                "id": "A0A0G2K9L9_RAT",
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            }
        ],
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        "refseq_name": "midasin",
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            {
                "id": "NP_001413944",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001413944",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Mdn1",
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        "function": "Nuclear chaperone required for maturation and nuclear export of pre-60S ribosome subunits., [UniProtKB, UniProtKB]",
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        ],
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        "protein_name": "Suppressor of cytokine signaling 7",
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            {
                "id": "NP_001413938",
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                "type": "external"
            }
        ],
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        "function": "Substrate-recognition component of a cullin-5-RING E3 ubiquitin-protein ligase complex (ECS complex, also named CRL5 complex), which mediates the ubiquitination and subsequent proteasomal degradation of target proteins, such as DAB1 and IRS1. Specifically recognizes and binds phosphorylated proteins via its SH2 domain, promoting their ubiquitination. The ECS(SOCS7) complex acts as a key regulator of reelin signaling by mediating ubiquitination and degradation of phosphorylated DAB1 in the cortical plate of the developing cerebral cortex, thereby regulating neuron positioning during cortex development. Functions in insulin signaling and glucose homeostasis through IRS1 ubiquitination and subsequent proteasomal degradation. Also inhibits prolactin, growth hormone and leptin signaling by preventing STAT3 and STAT5 activation, sequestering them in the cytoplasm and reducing their binding to DNA., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0021799 cerebral cortex radially oriented cell migration;GO:0035556 intracellular signal transduction;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0016567 protein ubiquitination;GO:0045444 fat cell differentiation",
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    },
    {
        "uniprot_canonical_ac": "A0A0G2KAC6-1",
        "uniprot_id": [
            {
                "id": "A0A0G2KAC6_RAT",
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        ],
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        "length": 173,
        "protein_name": "Keratin associated protein 1-3",
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            {
                "id": "NP_001395601",
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            }
        ],
        "gene_names_uniprotkb": "Krtap1-3",
        "gene_names_refseq": "Krtap1-3",
        "protein_names_uniprotkb": "Keratin associated protein 1-3",
        "protein_names_refseq": "keratin associated protein 1-3; keratin-associated protein 1-3-like; keratin-associated protein 9-3-like",
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        "disease": "",
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        "function": "In the hair cortex, hair keratin intermediate filaments are embedded in an interfilamentous matrix, consisting of hair keratin-associated proteins (KRTAP), which are essential for the formation of a rigid and resistant hair shaft through their extensive disulfide bond cross-linking with abundant cysteine residues of hair keratins. The matrix proteins include the high-sulfur and high-glycine-tyrosine keratins., [UniProtKB, UniProtKB]",
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    },
    {
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            {
                "id": "A0A0G2KAH7_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2KAH7",
                "type": "external"
            }
        ],
        "mass": 90179.0,
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        "protein_name": "Exostosin-2",
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        "protein_names_uniprotkb": "Exostosin-2; 2.4.1.224; Exostosin glycosyltransferase 2; Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase",
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        "tax_id": 10116,
        "disease": "hereditary multiple exostoses (Disease Ontology:DOID:206)",
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        "function": "Glycosyltransferase forming with EXT1 the heterodimeric heparan sulfate polymerase which catalyzes the elongation of the heparan sulfate glycan backbone. Glycan backbone extension consists in the alternating transfer of (1->4)-beta-D-GlcA and (1->4)-alpha-D-GlcNAc residues from their respective UDP-sugar donors. Both EXT1 and EXT2 are required for the full activity of the polymerase since EXT1 bears the N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase activity within the complex while EXT2 carries the glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase activity. Heparan sulfate proteoglycans are ubiquitous components of the extracellular matrix and play an important role in tissue homeostasis and signaling., [UniProtKB, UniProtKB]",
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            {
                "id": "2.4.1.225",
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        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0043541 UDP-N-acetylglucosamine transferase complex;GO:1902494 catalytic complex;GO:0005789 endoplasmic reticulum membrane",
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        ],
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        "protein_name": "Developmentally regulated GTP binding protein 2",
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    },
    {
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            {
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        ],
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        "protein_name": "Vomeronasal 2 receptor 19 like 1",
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            {
                "id": "XP_003748781",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_003748781",
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            }
        ],
        "gene_names_uniprotkb": "Vom2r19l1; LOC682419",
        "gene_names_refseq": "Vom2r19l1",
        "protein_names_uniprotkb": "Vomeronasal 2 receptor 19 like 1",
        "protein_names_refseq": "vomeronasal type-2 receptor 116-like isoform X2",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity",
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    {
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        ],
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        "protein_name": "Colony stimulating factor 2 receptor subunit alpha",
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        "protein_names_refseq": "ATG4 autophagy related 4 homolog B; autophagy-related 4B; autophagy-related protein 4 homolog B; cysteine protease ATG4B",
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        "function": "Cysteine protease that plays a key role in autophagy by mediating both proteolytic activation and delipidation of ATG8 family proteins. Required for canonical autophagy (macroautophagy), non-canonical autophagy as well as for mitophagy. The protease activity is required for proteolytic activation of ATG8 family proteins: cleaves the C-terminal amino acid of ATG8 proteins MAP1LC3A, MAP1LC3B, MAP1LC3C, GABARAPL1, GABARAPL2 and GABARAP, to reveal a C-terminal glycine. Exposure of the glycine at the C-terminus is essential for ATG8 proteins conjugation to phosphatidylethanolamine (PE) and insertion to membranes, which is necessary for autophagy. Protease activity is also required to counteract formation of high-molecular weight conjugates of ATG8 proteins (ATG8ylation): acts as a deubiquitinating-like enzyme that removes ATG8 conjugated to other proteins, such as ATG3. In addition to the protease activity, also mediates delipidation of ATG8 family proteins. Catalyzes delipidation of PE-conjugated forms of ATG8 proteins during macroautophagy. Also involved in non-canonical autophagy, a parallel pathway involving conjugation of ATG8 proteins to single membranes at endolysosomal compartments, by catalyzing delipidation of ATG8 proteins conjugated to phosphatidylserine (PS). Compared to other members of the family (ATG4A, ATG4C or ATG4C), constitutes the major protein for proteolytic activation of ATG8 proteins, while it displays weaker delipidation activity than other ATG4 paralogs. Involved in phagophore growth during mitophagy independently of its protease activity and of ATG8 proteins: acts by regulating ATG9A trafficking to mitochondria and promoting phagophore-endoplasmic reticulum contacts during the lipid transfer phase of mitophagy., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "function": "Regulatory subunit of the condensin-2 complex, a complex which establishes mitotic chromosome architecture and is involved in physical rigidity of the chromatid axis. May promote the resolution of double-strand DNA catenanes (intertwines) between sister chromatids. Condensin-mediated compaction likely increases tension in catenated sister chromatids, providing directionality for type II topoisomerase-mediated strand exchanges toward chromatid decatenation. Specifically required for decatenation of centromeric ultrafine DNA bridges during anaphase. Early in neurogenesis, may play an essential role to ensure accurate mitotic chromosome condensation in neuron stem cells, ultimately affecting neuron pool and cortex size., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005506 iron ion binding;GO:0020037 heme binding;GO:0016712 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen",
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        ],
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            {
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                "id": "NP_001414327",
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        "protein_names_refseq": "SH2 domain-containing adapter protein B; Src homology 2 domain containing adaptor protein B",
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            {
                "id": "XP_006256515",
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        "protein_names_uniprotkb": "Ferroptosis suppressor protein 1; Apoptosis-inducing factor homologous mitochondrion-associated inducer of death; p53-responsive gene 3 protein",
        "protein_names_refseq": "ferroptosis suppressor protein 1 isoform X2",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005741 mitochondrial outer membrane;GO:0005811 lipid droplet",
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        "protein_name": "Mitogen-activated protein kinase kinase kinase 20",
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            {
                "id": "NP_001385922",
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        "gene_names_refseq": "MLTK; Map3k20; RGD1561394; Zak",
        "protein_names_uniprotkb": "Mitogen-activated protein kinase kinase kinase 20; 2.7.11.25; Leucine zipper- and sterile alpha motif-containing kinase; MLK-like mitogen-activated protein triple kinase; Mitogen-activated protein kinase kinase kinase MLT; Mixed lineage kinase-related kinase; Sterile alpha motif- and leucine zipper-containing kinase AZK",
        "protein_names_refseq": "mitogen-activated protein kinase kinase kinase 20 isoform 1; mitogen-activated protein kinase kinase kinase MLT; sterile alpha motif and leucine zipper containing kinase AZK",
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        "disease": "split hand-foot malformation (Disease Ontology:DOID:0090020); centronuclear myopathy 6 with fiber-type disproportion (Disease Ontology:DOID:0111221)",
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        "disease": "Fleck corneal dystrophy (Disease Ontology:DOID:0060448); cataract (Disease Ontology:DOID:83); Crohn's disease (Disease Ontology:DOID:8778)",
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
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        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 6,
        "glyco_site_count": 5,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0000922 spindle pole;GO:0005634 nucleus;GO:0005813 centrosome;GO:0034451 centriolar satellite",
        "go_biological_process": "GO:0021987 cerebral cortex development;GO:0045664 regulation of neuron differentiation;GO:0022008 neurogenesis;GO:0002052 positive regulation of neuroblast proliferation;GO:0046605 regulation of centrosome cycle",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "F1M5K2-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.010000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZYV3-1",
        "uniprot_id": [
            {
                "id": "D3ZYV3_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZYV3",
                "type": "external"
            }
        ],
        "mass": 38443.0,
        "length": 348,
        "protein_name": "Peptidoglycan recognition protein 3-like",
        "gene_name": "Pglyrp3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Pglyrp3; LOC134485743",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Peptidoglycan recognition protein 3-like",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-6803157)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Pattern receptor that binds to murein peptidoglycans (PGN) of Gram-positive bacteria. Has bactericidal activity towards Gram-positive bacteria. May kill Gram-positive bacteria by interfering with peptidoglycan biosynthesis. Also binds to Gram-negative bacteria, and has bacteriostatic activity towards Gram-negative bacteria. Plays a role in innate immunity., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_s_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "F1M4E6",
        "ec_number_list": [],
        "go_molecular_function": "GO:0008745 N-acetylmuramoyl-L-alanine amidase activity;GO:0008270 zinc ion binding;GO:0042834 peptidoglycan binding;GO:0046982 protein heterodimerization activity;GO:0016019 peptidoglycan immune receptor activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0002376 immune system process;GO:0009253 peptidoglycan catabolic process;GO:0051239 regulation of multicellular organismal process;GO:0032827 negative regulation of natural killer cell differentiation involved in immune response;GO:0006955 immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZYV3-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D4A0U9-1",
        "uniprot_id": [
            {
                "id": "D4A0U9_RAT",
                "url": "https://www.uniprot.org/uniprot/D4A0U9",
                "type": "external"
            }
        ],
        "mass": 159493.0,
        "length": 1441,
        "protein_name": "DNA mismatch repair protein",
        "gene_name": "Msh6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Msh6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "DNA mismatch repair protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "hereditary nonpolyposis colorectal cancer type 5 (Disease Ontology:DOID:0070272); colorectal carcinoma (Disease Ontology:DOID:0080199); mismatch repair cancer syndrome (Disease Ontology:DOID:0112182); urinary bladder cancer (Disease Ontology:DOID:11054); endometrial cancer (Disease Ontology:DOID:1380); breast cancer (Disease Ontology:DOID:1612); ovarian cancer (Disease Ontology:DOID:2394); osteosarcoma (Disease Ontology:DOID:3347); breast carcinoma (Disease Ontology:DOID:3459); Lynch syndrome (Disease Ontology:DOID:3883); primary ovarian insufficiency (Disease Ontology:DOID:5426)",
        "pathway": " (R-RNO-5358565)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Component of the post-replicative DNA mismatch repair system (MMR)., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "biomarker_type": "",
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0005524 ATP binding;GO:0030983 mismatched DNA binding;GO:0140664 ATP-dependent DNA damage sensor activity;GO:0032357 oxidized purine DNA binding;GO:0032142 single guanine insertion binding",
        "go_cellular_component": "GO:0032301 MutSalpha complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0000785 chromatin",
        "go_biological_process": "GO:0006298 mismatch repair;GO:0006281 DNA repair;GO:0007283 spermatogenesis;GO:0008630 intrinsic apoptotic signaling pathway in response to DNA damage;GO:0009411 response to UV",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A0U9-1",
        "record_type": "protein",
        "filter_code": "0000000.1000111.010000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZER4-1",
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            {
                "id": "D3ZER4_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZER4",
                "type": "external"
            }
        ],
        "mass": 84884.0,
        "length": 783,
        "protein_name": "Denticleless protein homolog",
        "gene_name": "Dtl",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Dtl",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Denticleless protein homolog; Lethal(2) denticleless protein homolog; Retinoic acid-regulated nuclear matrix-associated protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-110314);  (R-RNO-8951664)",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity;GO:0004842 ubiquitin-protein transferase activity",
        "go_cellular_component": "GO:0031464 Cul4A-RING E3 ubiquitin ligase complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005813 centrosome;GO:0031965 nuclear membrane",
        "go_biological_process": "GO:0010971 positive regulation of G2/M transition of mitotic cell cycle;GO:0006974 DNA damage response;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0009411 response to UV;GO:0048511 rhythmic process",
        "synthesized_glycan_count": 0,
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        "record_id": "D3ZER4-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZEX3-1",
        "uniprot_id": [
            {
                "id": "D3ZEX3_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZEX3",
                "type": "external"
            }
        ],
        "mass": 20739.0,
        "length": 181,
        "protein_name": "Trafficking protein particle complex subunit",
        "gene_name": "Trappc3l",
        "organism": "Rat",
        "refseq_name": "trafficking protein particle complex subunit 3L",
        "refseq_ac": [
            {
                "id": "NP_001419413",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001419413",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Trappc3l; Bet3l",
        "gene_names_refseq": "Bet3l; Trappc3l",
        "protein_names_uniprotkb": "Trafficking protein particle complex subunit",
        "protein_names_refseq": "BET3 like; trafficking protein particle complex 3-like; trafficking protein particle complex subunit 3L",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100362279)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May play a role in vesicular transport from endoplasmic reticulum to Golgi., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005829 cytosol;GO:0033106 cis-Golgi network membrane;GO:0030008 TRAPP complex;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport;GO:0006891 intra-Golgi vesicle-mediated transport;GO:0048193 Golgi vesicle transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZEX3-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZF32-1",
        "uniprot_id": [
            {
                "id": "D3ZF32_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZF32",
                "type": "external"
            }
        ],
        "mass": 37214.0,
        "length": 330,
        "protein_name": "Trem-like transcript 2 protein",
        "gene_name": "Treml2",
        "organism": "Rat",
        "refseq_name": "triggering receptor expressed on myeloid cells-like 2 precursor",
        "refseq_ac": [
            {
                "id": "NP_001420259",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001420259",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Treml2",
        "gene_names_refseq": "Treml2",
        "protein_names_uniprotkb": "Trem-like transcript 2 protein; Triggering receptor expressed on myeloid cells-like protein 2",
        "protein_names_refseq": "triggering receptor expressed on myeloid cells-like 2 precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:680844);  (R-RNO-198933)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Cell surface receptor that may play a role in the innate and adaptive immune response. Acts as a counter-receptor for CD276 and interaction with CD276 on T-cells enhances T-cell activation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface",
        "go_biological_process": "GO:0042110 T cell activation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZF32-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZFL6-1",
        "uniprot_id": [
            {
                "id": "D3ZFL6_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZFL6",
                "type": "external"
            }
        ],
        "mass": 59221.0,
        "length": 576,
        "protein_name": "Mex-3 RNA binding family member B",
        "gene_name": "Mex3b",
        "organism": "Rat",
        "refseq_name": "RNA-binding protein MEX3B",
        "refseq_ac": [
            {
                "id": "NP_001178555",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001178555",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Mex3b",
        "gene_names_refseq": "Mex3b; Rkhd3",
        "protein_names_uniprotkb": "Mex-3 RNA binding family member B",
        "protein_names_refseq": "RNA-binding protein MEX3B; mex3 homolog B; ring finger and KH domain containing 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308790)",
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        "predicted_glycosites": 3,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003723 RNA binding;GO:0008270 zinc ion binding;GO:0032794 GTPase activating protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000932 P-body",
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        "protein_name": "Dual endothelin-1/VEGF signal peptide receptor",
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        "refseq_name": "dual endothelin-1/VEGF signal peptide receptor",
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001004448",
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        "protein_name": "Nucleoside diphosphate kinase 5",
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414325",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0016787 hydrolase activity;GO:0004550 nucleoside diphosphate kinase activity;GO:0008296 3'-5'-DNA exonuclease activity",
        "go_cellular_component": "GO:0005929 cilium;GO:0001534 radial spoke;GO:0005576 extracellular region;GO:0036126 sperm flagellum;GO:0097729 9+2 motile cilium",
        "go_biological_process": "GO:0007286 spermatid development;GO:1902176 negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway;GO:0003341 cilium movement;GO:0006183 GTP biosynthetic process;GO:0006228 UTP biosynthetic process",
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            {
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            }
        ],
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        "protein_names_refseq": "ly6/PLAUR domain-containing protein 4 precursor; ly6/PLAUR domain-containing protein 4-like; ly6/PLAUR domain-containing protein 4",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger SWIM-type containing 9",
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            {
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        "function": "Catalyzes the conjugation of long-chain fatty acyl-CoA thioester and glycine to produce long-chain N-(fatty acyl)glycine, an intermediate in the primary fatty acid amide biosynthetic pathway., [UniProtKB, UniProtKB]",
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            {
                "id": "2.3.1.13",
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            {
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            }
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                "id": "NP_001000133",
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            }
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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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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
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            {
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        ],
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        "length": 1315,
        "protein_name": "Sal-like protein 1",
        "gene_name": "Sall1",
        "organism": "Rat",
        "refseq_name": "sal-like protein 1",
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            {
                "id": "NP_001100885",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100885",
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            }
        ],
        "gene_names_uniprotkb": "Sall1",
        "gene_names_refseq": "Sall1",
        "protein_names_uniprotkb": "Sal-like protein 1",
        "protein_names_refseq": "sal-like 1; sal-like protein 1",
        "tax_id": 10116,
        "disease": "Townes-Brocks syndrome (Disease Ontology:DOID:0050887); middle lobe syndrome (Disease Ontology:DOID:2810); carcinoma (Disease Ontology:DOID:305); renal Wilms' tumor (Disease Ontology:DOID:5176); hepatoblastoma (Disease Ontology:DOID:687); chronic kidney disease (Disease Ontology:DOID:784)",
        "pathway": " (rno:307740)",
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        "function": "Transcriptional repressor involved in organogenesis. Plays an essential role in ureteric bud invasion during kidney development., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0008270 zinc ion binding;GO:0044877 protein-containing complex binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0000792 heterochromatin;GO:0010369 chromocenter;GO:0016581 NuRD complex",
        "go_biological_process": "GO:0061034 olfactory bulb mitral cell layer development;GO:0003340 negative regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis;GO:0021553 olfactory nerve development;GO:0072092 ureteric bud invasion;GO:0000122 negative regulation of transcription by RNA polymerase II",
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        ],
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        "length": 1190,
        "protein_name": "F-box protein 38",
        "gene_name": "Fbxo38",
        "organism": "Rat",
        "refseq_name": "F-box only protein 38",
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            {
                "id": "NP_001358950",
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        "gene_names_refseq": "Fbxo38",
        "protein_names_uniprotkb": "F-box protein 38",
        "protein_names_refseq": "F-box only protein 38",
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        "disease": "autosomal dominant distal hereditary motor neuronopathy 6 (Disease Ontology:DOID:0111210)",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZJ86-1",
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            {
                "id": "SL9A6_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZJ86",
                "type": "external"
            }
        ],
        "mass": 79894.0,
        "length": 721,
        "protein_name": "Sodium/hydrogen exchanger 6",
        "gene_name": "Slc9a6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Slc9a6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Sodium/hydrogen exchanger 6; NHE-6; Na(+)/H(+) exchanger 6; Sodium/hydrogen exchanger; Solute carrier family 9 member 6",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); Christianson syndrome (Disease Ontology:DOID:0060825)",
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        "function": "Endosomal Na(+), K(+)/H(+) antiporter. Mediates the electroneutral exchange of endosomal luminal H(+) for a cytosolic Na(+) or K(+). By facilitating proton efflux, SLC9A6 counteracts the acidity generated by vacuolar (V)-ATPase, thereby limiting luminal acidification. Responsible for alkalizing and maintaining the endosomal pH, and consequently in, e.g., endosome maturation and trafficking of recycling endosomal cargo (By similarity). Plays a critical role during neurodevelopment by regulating synaptic development and plasticity (By similarity). Implicated in the maintenance of cell polarity in a manner that is dependent on its ability to modulate intravesicular pH (By similarity). Regulates intracellular pH in some specialized cells, osteoclasts and stereocilia where this transporter localizes to the plasma membrane (By similarity)., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0015385 sodium:proton antiporter activity;GO:0015386 potassium:proton antiporter activity;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005768 endosome;GO:0005769 early endosome;GO:0005886 plasma membrane;GO:0030425 dendrite",
        "go_biological_process": "GO:0050808 synapse organization;GO:0048812 neuron projection morphogenesis;GO:0060996 dendritic spine development;GO:0030010 establishment of cell polarity;GO:0048675 axon extension",
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    },
    {
        "uniprot_canonical_ac": "D3ZJE2-1",
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            {
                "id": "D3ZJE2_RAT",
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            }
        ],
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        "protein_name": "Large ribosomal subunit protein uL11",
        "gene_name": "Rpl12-ps1",
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        "gene_names_uniprotkb": "Rpl12-ps1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Large ribosomal subunit protein uL11; 60S ribosomal protein L12",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "systemic lupus erythematosus (Disease Ontology:DOID:9074)",
        "pathway": " (R-RNO-156827);  (R-RNO-1799339);  (R-RNO-6791226);  (R-RNO-72689);  (R-RNO-72706);  (R-RNO-975956);  (R-RNO-975957);  (R-RNO-9954709);  (R-RNO-9954714);  (R-RNO-9954716)",
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        "function": "Component of the large ribosomal subunit. The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell. Binds directly to 26S ribosomal RNA., [UniProtKB, UniProtKB]",
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            {
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        ],
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        "protein_name": "Serpin family B member 3A",
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            {
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        "gene_names_uniprotkb": "Serpinb3; Serpinb3a",
        "gene_names_refseq": "Serpinb3",
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        "protein_names_refseq": "serine protease inhibitor B3; serpin family B member 3; serpin peptidase inhibitor, clade B (ovalbumin), member 3",
        "tax_id": 10116,
        "disease": "alpha 1-antitrypsin deficiency (Disease Ontology:DOID:13372)",
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        "go_molecular_function": "GO:0002020 protease binding;GO:0004867 serine-type endopeptidase inhibitor activity;GO:0019899 enzyme binding;GO:0004869 cysteine-type endopeptidase inhibitor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0070062 extracellular exosome;GO:0031410 cytoplasmic vesicle",
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        ],
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        "protein_name": "Histone deacetylase complex subunit SAP30L",
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        "refseq_name": "histone deacetylase complex subunit SAP30L",
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            {
                "id": "NP_001385727",
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            }
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        "protein_names_uniprotkb": "Histone deacetylase complex subunit SAP30L; Sin3 corepressor complex subunit SAP30L; Sin3-associated protein p30-like",
        "protein_names_refseq": "histone deacetylase complex subunit SAP30L",
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        "pathway": " (rno:360531);  (R-RNO-3214815)",
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        "function": "Functions as a transcription repressor, probably via its interaction with histone deacetylase complexes. Involved in the functional recruitment of the class 1 Sin3-histone deacetylase complex (HDAC) to the nucleolus. Binds DNA, apparently without sequence-specificity, and bends bound double-stranded DNA. Binds phosphoinositol phosphates (phosphoinositol 3-phosphate, phosphoinositol 4-phosphate and phosphoinositol 5-phosphate) via the same basic sequence motif that mediates DNA binding and nuclear import., [UniProtKB, UniProtKB]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0010314 phosphatidylinositol-5-phosphate binding;GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0042393 histone binding;GO:0070273 phosphatidylinositol-4-phosphate binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0001650 fibrillar center;GO:0000118 histone deacetylase complex",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription",
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        ],
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        "length": 315,
        "protein_name": "60S acidic ribosomal protein P0",
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            {
                "id": "XP_227546",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_227546",
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        ],
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        "gene_names_refseq": "Rplp0l1",
        "protein_names_uniprotkb": "60S acidic ribosomal protein P0",
        "protein_names_refseq": "large ribosomal subunit protein uL10-like",
        "tax_id": 10116,
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        "pathway": " (rno:295340)",
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        "function": "Ribosomal protein P0 is the functional equivalent of E.coli protein L10., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003735 structural constituent of ribosome;GO:0070180 large ribosomal subunit rRNA binding",
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            {
                "id": "D3ZJU8_RAT",
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                "type": "external"
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        ],
        "mass": 33485.0,
        "length": 297,
        "protein_name": "Serine/threonine-protein phosphatase PP1-beta catalytic subunit",
        "gene_name": "ENSRNOG00000069573",
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        "gene_names_uniprotkb": "ENSRNOG00000069573",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Serine/threonine-protein phosphatase PP1-beta catalytic subunit; 3.1.3.53",
        "protein_names_refseq": "",
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        "ec_number_list": [
            {
                "id": "3.1.3.53",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.53",
                "type": "external"
            },
            {
                "id": "3.1.3.16",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.16",
                "type": "external"
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        ],
        "go_molecular_function": "GO:0050115 myosin-light-chain-phosphatase activity;GO:0004722 protein serine/threonine phosphatase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0042752 regulation of circadian rhythm;GO:0032922 circadian regulation of gene expression",
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    },
    {
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            {
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        ],
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        "length": 410,
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            {
                "id": "NP_001386660",
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        ],
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        ],
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        ],
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        ],
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        ],
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            {
                "id": "NP_001000819",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000819",
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        ],
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
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        ],
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        "length": 1141,
        "protein_name": "Collagen alpha-1(XXVIII) chain",
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            {
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001418648",
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        ],
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        "gene_names_refseq": "Col28a1; RGD1564680",
        "protein_names_uniprotkb": "Collagen alpha-1(XXVIII) chain",
        "protein_names_refseq": "collagen alpha-1(XXVIII) chain; collagen type XXVIII alpha 1 chain precursor; collagen, type XXVIII, alpha 1",
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        "pathway": " (R-RNO-1650814);  (R-RNO-8948216)",
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        "function": "May act as a cell-binding protein., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004867 serine-type endopeptidase inhibitor activity;GO:0030020 extracellular matrix structural constituent conferring tensile strength",
        "go_cellular_component": "GO:0031012 extracellular matrix;GO:0005604 basement membrane",
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        "function": "Component of a multiprotein complex required for the assembly of the RNA endonuclease module of the integrator complex. Associates with INTS9 and INTS11 in the cytoplasm and blocks the active site of INTS11 to inhibit the endonuclease activity of INTS11 before formation of the full integrator complex. Following dissociation of WDR73 of the complex, BRAT1 facilitates the nuclear import of the INTS9-INTS11 heterodimer. In the nucleus, INTS4 is integrated to the INTS9-INTS11 heterodimer and BRAT1 is released from the mature RNA endonuclease module by inositol hexakisphosphate (InsP6). BRAT1 is also involved in DNA damage response; activates kinases ATM, SMC1A and PRKDC by modulating their phosphorylation status following ionizing radiation (IR) stress. Plays a role in regulating mitochondrial function and cell proliferation. Required for protein stability of MTOR and MTOR-related proteins, and cell cycle progress by growth factors., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "IKAROS family zinc finger 3",
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            {
                "id": "NP_001100517",
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        ],
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        "disease": "small cell carcinoma (Disease Ontology:DOID:0050685); immunodeficiency 84 (Disease Ontology:DOID:0061054); childhood-onset asthma (Disease Ontology:DOID:0080815); atherosclerosis (Disease Ontology:DOID:1936); lung non-small cell carcinoma (Disease Ontology:DOID:3908); systemic lupus erythematosus (Disease Ontology:DOID:9074)",
        "pathway": " (rno:303511);  (R-RNO-9940951)",
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0046982 protein heterodimerization activity",
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        "go_biological_process": "GO:0045577 regulation of B cell differentiation;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0009617 response to bacterium",
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        "gene_names_refseq": "Armc4; Odad2; ddx5-ps1",
        "protein_names_uniprotkb": "Outer dynein arm-docking complex subunit 2; Armadillo repeat-containing protein 4",
        "protein_names_refseq": "outer dynein arm-docking complex subunit 2 isoform X1",
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        "disease": "Kartagener syndrome (Disease Ontology:DOID:0050144); visceral heterotaxy (Disease Ontology:DOID:0050545); primary ciliary dyskinesia 23 (Disease Ontology:DOID:0110609)",
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        "function": "Component of the outer dynein arm-docking complex (ODA-DC) that mediates outer dynein arms (ODA) binding onto the doublet microtubule. Involved in mediating assembly of both ODAs and their axonemal docking complex onto ciliary microtubules., [UniProtKB, UniProtKB]",
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            {
                "id": "D3ZXI3_RAT",
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        ],
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        "length": 503,
        "protein_name": "NOTUM, palmitoleoyl-protein carboxylesterase",
        "gene_name": "Notum",
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        "refseq_name": "palmitoleoyl-protein carboxylesterase NOTUM precursor",
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            {
                "id": "NP_001013997",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001013997",
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            }
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        "protein_names_uniprotkb": "NOTUM, palmitoleoyl-protein carboxylesterase",
        "protein_names_refseq": "palmitoleoyl-protein carboxylesterase NOTUM precursor; palmitoleoyl-protein carboxylesterase NOTUM",
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        "go_cellular_component": "GO:1990716 axonemal central apparatus;GO:0005576 extracellular region;GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0001669 acrosomal vesicle",
        "go_biological_process": "GO:1904158 axonemal central apparatus assembly;GO:0003351 epithelial cilium movement involved in extracellular fluid movement;GO:0007283 spermatogenesis;GO:0044458 motile cilium assembly;GO:1905198 manchette assembly",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0019904 protein domain specific binding;GO:0061630 ubiquitin protein ligase activity;GO:0004842 ubiquitin-protein transferase activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0032727 positive regulation of interferon-alpha production;GO:0001934 positive regulation of protein phosphorylation;GO:0050728 negative regulation of inflammatory response;GO:0060337 type I interferon-mediated signaling pathway;GO:0010508 positive regulation of autophagy",
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        ],
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        "protein_name": "Class A basic helix-loop-helix protein 9",
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        "refseq_name": "class A basic helix-loop-helix protein 9",
        "refseq_ac": [
            {
                "id": "NP_001385740",
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        "gene_names_refseq": "Bhlha9; RGD1311234",
        "protein_names_uniprotkb": "Class A basic helix-loop-helix protein 9",
        "protein_names_refseq": "class A basic helix-loop-helix protein 9",
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        "function": "Transcription factor, which play a role in limb development. Is an essential player in the regulatory network governing transcription of genes implicated in limb morphogenesis., [UniProtKB, UniProtKB]",
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            {
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        ],
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        "protein_names_refseq": "probable E3 ubiquitin-protein ligase makorin-3",
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        "function": "MKRN3 inhibits the reproductive axis through actions in kisspeptin-expressing neurons., [RefSeq, PubMed]",
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        ],
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            {
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        ],
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        ],
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        "protein_names_refseq": "probable E3 ubiquitin-protein ligase TRIML1; tripartite motif family-like 1 isoform 2",
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            {
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        "go_molecular_function": "GO:0005125 cytokine activity;GO:0005126 cytokine receptor binding",
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        "protein_name": "MAP7 domain-containing protein 2",
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        "gene_names_refseq": "Brelin; Map7d2; Mtap7d2; RGD1564852",
        "protein_names_uniprotkb": "MAP7 domain-containing protein 2; Brain-enriched E-MAP-115-like protein",
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        "function": "Microtubule-stabilizing protein involved in the control of cell motility and neurite outgrowth (By similarity). Acts as a critical cofactor for kinesin transport; in the proximal axon regulates kinesin-1 family members, KIF5A, KIF5B and KIF5C recruitment to microtubules and contributes to kinesin-1-mediated transport in the axons (PubMed:30784582)., [UniProtKB, UniProtKB, PubMed]",
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        "go_molecular_function": "GO:0008017 microtubule binding;GO:0019894 kinesin binding;GO:0140778 microtubule stabilizing activity",
        "go_cellular_component": "GO:0005813 centrosome;GO:0005874 microtubule;GO:0030424 axon;GO:0015630 microtubule cytoskeleton;GO:0043005 neuron projection",
        "go_biological_process": "GO:0000226 microtubule cytoskeleton organization;GO:0061564 axon development",
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        ],
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        "length": 490,
        "protein_name": "Bifunctional FAD diphosphatase/FAD synthase",
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        "refseq_name": "bifunctional FAD diphosphatase/FAD synthase",
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001103608",
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        "function": "This enzyme has two activities: FAD diphosphatase activity and FAD synthase activity (By similarity). FAD diphosphatase acts on FAD and NADH to produce FMN and NMNH(2-), respectively (By similarity). FAD synthase catalyzes the adenylation of flavin mononucleotide (FMN) to form flavin adenine dinucleotide (FAD) coenzyme (PubMed:9211336). In addition to its catalytic activities, the protein also facilitates the delivery of FAD to client apo-flavoproteins (By similarity). The balance between FAD synthesis and hydrolysis may be regulated by redox-sensing cysteine residues (By similarity). At a much lower rate, FAD synthase catalyzes the reverse pyrophosphorolytic reaction (By similarity)., [UniProtKB, PubMed, UniProtKB]",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.2",
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            {
                "id": "3.6.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.-",
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        ],
        "go_molecular_function": "GO:0003919 FMN adenylyltransferase activity;GO:0005524 ATP binding;GO:0042802 identical protein binding;GO:0046872 metal ion binding;GO:0035529 NADH pyrophosphatase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005759 mitochondrial matrix;GO:0005829 cytosol",
        "go_biological_process": "GO:0006747 FAD biosynthetic process;GO:0006771 riboflavin metabolic process",
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        ],
        "mass": 37405.0,
        "length": 326,
        "protein_name": "G protein-coupled receptor 171",
        "gene_name": "Gpr171",
        "organism": "Rat",
        "refseq_name": "G-protein coupled receptor 171",
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            {
                "id": "NP_001383757",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001383757",
                "type": "external"
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        ],
        "gene_names_uniprotkb": "Gpr171",
        "gene_names_refseq": "Gpr171",
        "protein_names_uniprotkb": "G protein-coupled receptor 171",
        "protein_names_refseq": "G-protein coupled receptor 171; probable G-protein coupled receptor 171",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:688737)",
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        "publication_id_list": "24043826;29393594",
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        "function": "G protein-coupled receptor for Big LEN, a 16-amino acid neuropeptide produced from the precursor protein, proSAAS (encoded by PCSK1N) (PubMed:24043826). Acts through a G(i)-alpha-mediated pathway in response to Big LEN. Big LEN-GPR171 system plays an important role in regulating feeding and metabolism. Also plays a role in modulating fear and anxiety-like behaviors in the basolateral amygdala. Big LEN-GPR171 modulates the mu-type opioid receptor signaling and antinociception. Acts as a negative regulator T cell function (By similarity)., [UniProtKB, UniProtKB, PubMed]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0009055 electron transfer activity;GO:0046872 metal ion binding;GO:0020037 heme binding",
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    },
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            {
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            }
        ],
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            {
                "id": "NP_001414349",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414349",
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            }
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        "disease": "brain glioma (Disease Ontology:DOID:0060108); hypertension (Disease Ontology:DOID:10763); breast cancer (Disease Ontology:DOID:1612); pancreatic cancer (Disease Ontology:DOID:1793); high grade glioma (Disease Ontology:DOID:3070); coronary artery disease (Disease Ontology:DOID:3393); meningioma (Disease Ontology:DOID:3565); central nervous system cancer (Disease Ontology:DOID:3620); myocardial infarction (Disease Ontology:DOID:5844); familial melanoma (Disease Ontology:DOID:6846); multiple myeloma (Disease Ontology:DOID:9538)",
        "pathway": " (rno:102551085);  (R-RNO-5685942);  (R-RNO-5693537);  (R-RNO-5693568);  (R-RNO-5693579)",
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        "function": "Involved in the homologous recombination repair (HRR) pathway of double-stranded DNA, thought to repair chromosomal fragmentation, translocations and deletions., [UniProtKB, UniProtKB, UniProtKB]",
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        ],
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        "protein_name": "Small ribosomal subunit protein eS10",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:1.14.13.32",
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        "protein_name": "Interleukin-17 receptor A",
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        "function": "(Microbial infection) Receptor for SARS coronavirus-2/SARS-CoV-2 virus protein ORF8, leading to IL17 pathway activation and an increased secretion of pro-inflammatory factors through activating NF-kappa-B signaling pathway., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005102 signaling receptor binding;GO:0030368 interleukin-17 receptor activity",
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            {
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        "go_biological_process": "GO:0090382 phagosome maturation;GO:0043473 pigmentation;GO:0032402 melanosome transport;GO:0048066 developmental pigmentation;GO:0032400 melanosome localization",
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        ],
        "mass": 35313.0,
        "length": 314,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or9r3c",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1069",
        "refseq_ac": [
            {
                "id": "NP_001000522",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000522",
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            }
        ],
        "gene_names_uniprotkb": "Or9r3c",
        "gene_names_refseq": "Olr1069; Or9r3c; ratchr7-8295412-8294468_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1069; olfactory receptor Olr1069; olfactory receptor gene Olr1069",
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        "pathway": " (rno:362821)",
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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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        "length": 879,
        "protein_name": "Holocarboxylase synthetase",
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        "refseq_name": "biotin--protein ligase isoform X1",
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            {
                "id": "XP_038944719",
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        ],
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        "tax_id": 10116,
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        "go_biological_process": "GO:0043687 post-translational protein modification;GO:0006768 biotin metabolic process;GO:0070781 response to biotin",
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        ],
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        "protein_name": "Kelch-like family member 40",
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            {
                "id": "NP_001101665",
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            }
        ],
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        "gene_names_refseq": "Kbtbd5; Klhl40",
        "protein_names_uniprotkb": "Kelch-like family member 40",
        "protein_names_refseq": "kelch repeat and BTB (POZ) domain containing 5; kelch repeat and BTB domain-containing protein 5; kelch-like 40; kelch-like protein 40",
        "tax_id": 10116,
        "disease": "nemaline myopathy 8 (Disease Ontology:DOID:0110930)",
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        "function": "Substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3 ubiquitin ligase complex that acts as a key regulator of skeletal muscle development. The BCR(KLHL40) complex acts by mediating ubiquitination and degradation of TFDP1, thereby regulating the activity of the E2F:DP transcription factor complex. Promotes stabilization of LMOD3 by acting as a negative regulator of LMOD3 ubiquitination; the molecular process by which it negatively regulates ubiquitination of LMOD3 is however unclear., [UniProtKB, UniProtKB]",
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                "id": "AT8B1_RAT",
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        ],
        "mass": 143834.0,
        "length": 1251,
        "protein_name": "Phospholipid-transporting ATPase IC",
        "gene_name": "Atp8b1",
        "organism": "Rat",
        "refseq_name": "phospholipid-transporting ATPase IC",
        "refseq_ac": [
            {
                "id": "NP_001424194",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001424194",
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        ],
        "gene_names_uniprotkb": "Atp8b1",
        "gene_names_refseq": "Atp8b1",
        "protein_names_uniprotkb": "Phospholipid-transporting ATPase IC; 7.6.2.1; ATPase class I type 8B member 1; P4-ATPase flippase complex alpha subunit ATP8B1",
        "protein_names_refseq": "ATPase, Class I, type 8B, member 1; ATPase, aminophospholipid transporter, class I, type 8B, member 1; P4-ATPase flippase complex alpha subunit ATP8B1; phospholipid-transporting ATPase IC; probable phospholipid-transporting ATPase IC",
        "tax_id": 10116,
        "disease": "progressive familial intrahepatic cholestasis 1 (Disease Ontology:DOID:0070226); intrahepatic cholestasis of pregnancy 1 (Disease Ontology:DOID:0070228); benign recurrent intrahepatic cholestasis 1 (Disease Ontology:DOID:0070231); intrahepatic cholestasis (Disease Ontology:DOID:1852)",
        "pathway": " (rno:291555);  (R-RNO-936837)",
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        "publication_id_list": "19027009;22673903;24643366;26240149",
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        "function": "ATP8B1, a P-type aminophospholipid translocase, is enriched in cerebral microvessels and may have a role in plasma membrane lipid transport, [RefSeq, PubMed]; Catalytic component of a P4-ATPase flippase complex which catalyzes the hydrolysis of ATP coupled to the transport of phospholipids, in particular phosphatidylcholines (PC), from the outer to the inner leaflet of the plasma membrane (By similarity) (PubMed:19027009). May participate in the establishment of the canalicular membrane integrity by ensuring asymmetric distribution of phospholipids in the canicular membrane. Thus may have a role in the regulation of bile acids transport into the canaliculus, uptake of bile acids from intestinal contents into intestinal mucosa or both and protect hepatocytes from bile salts (PubMed:19027009). Involved in the microvillus formation in polarized epithelial cells; the function seems to be independent from its flippase activity. Participates in correct apical membrane localization of CDC42, CFTR and SLC10A2 (By similarity). Enables CDC42 clustering at the apical membrane during enterocyte polarization through the interaction between CDC42 polybasic region and negatively charged membrane lipids provided by ATP8B1 (By similarity). Together with TMEM30A is involved in uptake of the synthetic drug alkylphospholipid perifosine (By similarity). Required for the preservation of cochlear hair cells in the inner ear. May act as cardiolipin transporter during inflammatory injury (By similarity)., [UniProtKB, PubMed, UniProtKB, UniProtKB]; The predominant P4 ATPases in pure pancreatic beta cells and human and rat pancreatic islets were ATP8B1, ATP8B2, and ATP9A. ATP8B1 and CDC50A were highly concentrated in ISG, [RefSeq, PubMed]",
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            {
                "id": "7.6.2.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.6.2.2",
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        ],
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        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0016324 apical plasma membrane;GO:0005802 trans-Golgi network",
        "go_biological_process": "GO:0015721 bile acid and bile salt transport;GO:0045892 negative regulation of DNA-templated transcription;GO:0045332 phospholipid translocation;GO:0015711 organic anion transport;GO:0007605 sensory perception of sound",
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        ],
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        "protein_name": "Zinc finger CCCH domain-containing protein 15",
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        "protein_names_refseq": "zinc finger CCCH domain-containing protein 15-like",
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        "length": 422,
        "protein_name": "Lipase",
        "gene_name": "Lipm",
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        "refseq_name": "lipase member M precursor",
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                "id": "NP_001419222",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001419222",
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        ],
        "gene_names_uniprotkb": "Lipm",
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        "protein_names_uniprotkb": "Lipase",
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                "id": "NP_001000870",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000870",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Or7e171d",
        "gene_names_refseq": "Olr1162; Or7e171d",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1162; olfactory receptor Olr1162; olfactory receptor gene Olr1162",
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        "disease": "",
        "pathway": " (rno:405167)",
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        "class_list": "",
        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "kg_view_protein": true
    },
    {
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            {
                "id": "D4AC36_RAT",
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            }
        ],
        "mass": 37997.0,
        "length": 361,
        "protein_name": "Eukaryotic translation initiation factor 3 subunit F",
        "gene_name": "Eif3f",
        "organism": "Rat",
        "refseq_name": "eukaryotic translation initiation factor 3 subunit F",
        "refseq_ac": [
            {
                "id": "NP_001264231",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001264231",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Eif3f; EIF3F; EIF3S5",
        "gene_names_refseq": "Eif3f; Eif3s5",
        "protein_names_uniprotkb": "Eukaryotic translation initiation factor 3 subunit F; Eukaryotic translation initiation factor 3 subunit 5; eIF-3-epsilon; eIF3 p47; eIF3f",
        "protein_names_refseq": "eukaryotic translation initiation factor 3 subunit F; eukaryotic translation initiation factor 3, subunit 5 (epsilon)",
        "tax_id": 10116,
        "disease": "autosomal recessive intellectual developmental disorder 67 (Disease Ontology:DOID:0081228); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": " (rno:293427);  (R-RNO-156827);  (R-RNO-72649);  (R-RNO-72689);  (R-RNO-72695);  (R-RNO-72702)",
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        "function": "Component of the eukaryotic translation initiation factor 3 (eIF-3) complex, which is required for several steps in the initiation of protein synthesis. The eIF-3 complex associates with the 40S ribosome and facilitates the recruitment of eIF-1, eIF-1A, eIF-2:GTP:methionyl-tRNAi and eIF-5 to form the 43S pre-initiation complex (43S PIC). The eIF-3 complex stimulates mRNA recruitment to the 43S PIC and scanning of the mRNA for AUG recognition. The eIF-3 complex is also required for disassembly and recycling of post-termination ribosomal complexes and subsequently prevents premature joining of the 40S and 60S ribosomal subunits prior to initiation. The eIF-3 complex specifically targets and initiates translation of a subset of mRNAs involved in cell proliferation, including cell cycling, differentiation and apoptosis, and uses different modes of RNA stem-loop binding to exert either translational activation or repression., [UniProtKB, HAMAP]; Deubiquitinates activated NOTCH1, promoting its nuclear import, thereby acting as a positive regulator of Notch signaling., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 4,
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0003743 translation initiation factor activity;GO:0004843 cysteine-type deubiquitinase activity;GO:0031369 translation initiation factor binding;GO:0140492 metal-dependent deubiquitinase activity",
        "go_cellular_component": "GO:0045202 synapse;GO:0016282 eukaryotic 43S preinitiation complex;GO:0033290 eukaryotic 48S preinitiation complex;GO:0071541 eukaryotic translation initiation factor 3 complex, eIF3m;GO:0005852 eukaryotic translation initiation factor 3 complex",
        "go_biological_process": "GO:0075522 IRES-dependent viral translational initiation;GO:0006413 translational initiation;GO:0001732 formation of cytoplasmic translation initiation complex",
        "synthesized_glycan_count": 0,
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        "filter_code": "0000000.0000011.100000.000000000000001000.0000000001001.001.00000",
        "kg_view_protein": true
    },
    {
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            {
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                "type": "external"
            }
        ],
        "mass": 22917.0,
        "length": 214,
        "protein_name": "Methyltransferase HEMK2",
        "gene_name": "Hemk2",
        "organism": "Rat",
        "refseq_name": "methyltransferase N6AMT1",
        "refseq_ac": [
            {
                "id": "NP_001178521",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001178521",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Hemk2; N6amt1",
        "gene_names_refseq": "Hemk2; N6amt1; RGD1311843",
        "protein_names_uniprotkb": "Methyltransferase HEMK2; HemK methyltransferase family member 2; Lysine N-methyltransferase 9; Methylarsonite methyltransferase N6AMT1; Methyltransferase N6AMT1; Protein N(5)-glutamine methyltransferase",
        "protein_names_refseq": "HemK methyltransferase family member 2; N(6)-adenine-specific DNA methyltransferase 1; N-6 adenine-specific DNA methyltransferase 1 (putative); methyltransferase N6AMT1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:288309)",
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        "function": "Methyltransferase that can methylate proteins and, to a lower extent, arsenic. Catalytic subunit of a heterodimer with TRMT112, which monomethylates 'Lys-12' of histone H4 (H4K12me1), a modification present at the promoters of numerous genes encoding cell cycle regulators. Catalytic subunit of a heterodimer with TRMT112, which catalyzes N5-methylation of Glu residue of proteins with a Gly-Gln-Xaa-Xaa-Xaa-Arg motif. Methylates ETF1 on 'Gln-185'; ETF1 needs to be complexed to ERF3 in its GTP-bound form to be efficiently methylated. May also play a role in the modulation of arsenic-induced toxicity by mediating the conversion of monomethylarsonous acid (3+) into the less toxic dimethylarsonic acid. It however only plays a limited role in arsenic metabolism compared with AS3MT., [UniProtKB, UniProtKB]",
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            }
        ],
        "go_molecular_function": "GO:0009007 site-specific DNA-methyltransferase (adenine-specific) activity;GO:0003676 nucleic acid binding;GO:0008276 protein methyltransferase activity;GO:0008757 S-adenosylmethionine-dependent methyltransferase activity;GO:0030791 arsenite methyltransferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0035097 histone methyltransferase complex;GO:0032991 protein-containing complex;GO:0035657 eRF1 methyltransferase complex",
        "go_biological_process": "GO:0030307 positive regulation of cell growth;GO:0045815 transcription initiation-coupled chromatin remodeling;GO:0009404 toxin metabolic process;GO:0045814 negative regulation of gene expression, epigenetic;GO:0018872 arsonoacetate metabolic process",
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    },
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            {
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            }
        ],
        "mass": 26546.0,
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        "protein_name": "RIKEN cDNA A630001G21 gene like",
        "gene_name": "A630001G21Rikl",
        "organism": "Rat",
        "refseq_name": "nuclear autoantigen Sp-100 isoform X1",
        "refseq_ac": [
            {
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                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_056840602",
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            }
        ],
        "gene_names_uniprotkb": "A630001G21Rikl; RGD1563917",
        "gene_names_refseq": "A630001G21Rikl",
        "protein_names_uniprotkb": "RIKEN cDNA A630001G21 gene like",
        "protein_names_refseq": "nuclear autoantigen Sp-100 isoform X1",
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    },
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            {
                "id": "D4ACK1_RAT",
                "url": "https://www.uniprot.org/uniprot/D4ACK1",
                "type": "external"
            }
        ],
        "mass": 219667.0,
        "length": 2143,
        "protein_name": "Nuclear pore complex protein Nup214",
        "gene_name": "Nup214",
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        "refseq_ac": [],
        "gene_names_uniprotkb": "Nup214",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Nuclear pore complex protein Nup214; 214 kDa nucleoporin; Nucleoporin Nup214",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "acute myeloid leukemia (Disease Ontology:DOID:9119); brain disease (Disease Ontology:DOID:936); acute lymphoblastic leukemia (Disease Ontology:DOID:9952)",
        "pathway": " (R-RNO-159227);  (R-RNO-159230);  (R-RNO-159231);  (R-RNO-159236);  (R-RNO-170822);  (R-RNO-1855170);  (R-RNO-1855196);  (R-RNO-1855229);  (R-RNO-191859);  (R-RNO-3108214);  (R-RNO-3232142);  (R-RNO-3301854);  (R-RNO-3371453);  (R-RNO-4085377);  (R-RNO-450520);  (R-RNO-4551638);  (R-RNO-4570464);  (R-RNO-4615885)",
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        "publication_id_list": "22673903;38843836",
        "class_list": "",
        "function": "Part of the nuclear pore complex. Has a critical role in nucleocytoplasmic transport. May serve as a docking site in the receptor-mediated import of substrates across the nuclear pore complex., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0017056 structural constituent of nuclear pore;GO:0008139 nuclear localization sequence binding;GO:0005049 nuclear export signal receptor activity",
        "go_cellular_component": "GO:0005635 nuclear envelope;GO:0005643 nuclear pore;GO:1990876 cytoplasmic side of nuclear pore;GO:0005634 nucleus",
        "go_biological_process": "GO:0006406 mRNA export from nucleus;GO:0046822 regulation of nucleocytoplasmic transport;GO:0006611 protein export from nucleus;GO:0051726 regulation of cell cycle;GO:0006405 RNA export from nucleus",
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                "type": "external"
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        ],
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        "length": 280,
        "protein_name": "Homeo box C12",
        "gene_name": "Hoxc12",
        "organism": "Rat",
        "refseq_name": "homeobox protein Hox-C12",
        "refseq_ac": [
            {
                "id": "NP_001100266",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100266",
                "type": "external"
            }
        ],
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        "gene_names_refseq": "Hoxc12",
        "protein_names_uniprotkb": "Homeo box C12",
        "protein_names_refseq": "homeobox protein Hox-C12",
        "tax_id": 10116,
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        "function": "Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding",
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        "gene_names_refseq": "Clec4a3; Dcir3",
        "protein_names_uniprotkb": "C-type lectin domain family 4, member A3",
        "protein_names_refseq": "C-type lectin domain family 4, member A3 isoform X1",
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        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0030246 carbohydrate binding;GO:0005537 D-mannose binding;GO:0038187 pattern recognition receptor activity",
        "go_cellular_component": "GO:0009897 external side of plasma membrane",
        "go_biological_process": "GO:0036037 CD8-positive, alpha-beta T cell activation;GO:0042590 antigen processing and presentation of exogenous peptide antigen via MHC class I;GO:0032720 negative regulation of tumor necrosis factor production;GO:0002250 adaptive immune response;GO:0001818 negative regulation of cytokine production",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "E9PT25-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "E9PTD9-1",
        "uniprot_id": [
            {
                "id": "E9PTD9_RAT",
                "url": "https://www.uniprot.org/uniprot/E9PTD9",
                "type": "external"
            }
        ],
        "mass": 89426.0,
        "length": 784,
        "protein_name": "Toll-like receptor 2",
        "gene_name": "Tlr2",
        "organism": "Rat",
        "refseq_name": "toll-like receptor 2 isoform X1",
        "refseq_ac": [
            {
                "id": "XP_008759324",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_008759324",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tlr2",
        "gene_names_refseq": "Tlr2",
        "protein_names_uniprotkb": "Toll-like receptor 2",
        "protein_names_refseq": "toll-like receptor 2 isoform X1",
        "tax_id": 10116,
        "disease": "sinusitis (Disease Ontology:DOID:0050127); alcohol dependence (Disease Ontology:DOID:0050741); renal fibrosis (Disease Ontology:DOID:0050855); ileitis (Disease Ontology:DOID:0060189); atrial fibrillation (Disease Ontology:DOID:0060224); mastoiditis (Disease Ontology:DOID:0060322); metabolic dysfunction and alcohol associated liver disease (Disease Ontology:DOID:0070508); meningococcal meningitis (Disease Ontology:DOID:0080176); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); urinary tract infection (Disease Ontology:DOID:0080784); acute necrotizing pancreatitis (Disease Ontology:DOID:0080998); hymenolepiasis (Disease Ontology:DOID:10074); dry eye syndrome (Disease Ontology:DOID:10140); dermatomyositis (Disease Ontology:DOID:10223); leprosy (Disease Ontology:DOID:1024); prostate cancer (Disease Ontology:DOID:10283); stomach cancer (Disease Ontology:DOID:10534); kidney failure (Disease Ontology:DOID:1074); otitis media (Disease Ontology:DOID:10754); Kuhnt-Junius degeneration (Disease Ontology:DOID:10873); cholesteatoma of middle ear (Disease Ontology:DOID:10964); urinary bladder cancer (Disease Ontology:DOID:11054); anogenital venereal wart (Disease Ontology:DOID:11168); suppurative otitis media (Disease Ontology:DOID:11506); alveolar echinococcosis (Disease Ontology:DOID:12148); vitiligo (Disease Ontology:DOID:12306); carotid stenosis (Disease Ontology:DOID:13001); Behcet's disease (Disease Ontology:DOID:13241); pulmonary sarcoidosis (Disease Ontology:DOID:13406); familial combined hyperlipidemia (Disease Ontology:DOID:13809); alcoholic liver cirrhosis (Disease Ontology:DOID:14018); anterior uveitis (Disease Ontology:DOID:1407); cystic echinococcosis (Disease Ontology:DOID:1495); alcohol use disorder (Disease Ontology:DOID:1574); diffuse scleroderma (Disease Ontology:DOID:1580); breast cancer (Disease Ontology:DOID:1612); transient cerebral ischemia (Disease Ontology:DOID:224); asthma (Disease Ontology:DOID:2841); severe acute respiratory syndrome (Disease Ontology:DOID:2945); pulmonary tuberculosis (Disease Ontology:DOID:2957); skin papilloma (Disease Ontology:DOID:3178); atopic dermatitis (Disease Ontology:DOID:3310); middle cerebral artery infarction (Disease Ontology:DOID:3525); tuberculosis (Disease Ontology:DOID:399); glucose metabolism disease (Disease Ontology:DOID:4194); allergic rhinitis (Disease Ontology:DOID:4481); rhinitis (Disease Ontology:DOID:4483); keratitis (Disease Ontology:DOID:4677); pancreatitis (Disease Ontology:DOID:4989); eye disease (Disease Ontology:DOID:5614); uric acid nephrolithiasis (Disease Ontology:DOID:580); primary immunodeficiency disease (Disease Ontology:DOID:612); acne (Disease Ontology:DOID:6543); hepatocellular carcinoma (Disease Ontology:DOID:684); end stage renal disease (Disease Ontology:DOID:783); peritonitis (Disease Ontology:DOID:8283); lung disease (Disease Ontology:DOID:850); gastroesophageal reflux disease (Disease Ontology:DOID:8534); collagen disease (Disease Ontology:DOID:854); perinatal necrotizing enterocolitis (Disease Ontology:DOID:8677); cholesteatoma (Disease Ontology:DOID:869); bacterial pneumonia (Disease Ontology:DOID:874); seborrheic dermatitis (Disease Ontology:DOID:8741); molluscum contagiosum (Disease Ontology:DOID:8867); psoriasis (Disease Ontology:DOID:8893); cutaneous leishmaniasis (Disease Ontology:DOID:9111); colorectal cancer (Disease Ontology:DOID:9256); type 2 diabetes mellitus (Disease Ontology:DOID:9352); keratoconjunctivitis (Disease Ontology:DOID:9368); type 1 diabetes mellitus (Disease Ontology:DOID:9744)",
        "pathway": " (R-RNO-1461957);  (R-RNO-5686938);  (R-RNO-6798695)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Cooperates with LY96 to mediate the innate immune response to bacterial lipoproteins and other microbial cell wall components. Cooperates with TLR1 or TLR6 to mediate the innate immune response to bacterial lipoproteins or lipopeptides. Acts via MYD88 and TRAF6, leading to NF-kappa-B activation, cytokine secretion and the inflammatory response., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0042497 triacyl lipopeptide binding;GO:0004888 transmembrane signaling receptor activity;GO:0038023 signaling receptor activity;GO:0042834 peptidoglycan binding;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0043235 receptor complex;GO:0045121 membrane raft;GO:0030670 phagocytic vesicle membrane;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006954 inflammatory response;GO:0045087 innate immune response;GO:0001819 positive regulation of cytokine production;GO:0002224 toll-like receptor signaling pathway;GO:0032680 regulation of tumor necrosis factor production",
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        "kg_view_protein": true
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            {
                "id": "E9PTF0_RAT",
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            }
        ],
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        "length": 480,
        "protein_name": "Probable ATP-dependent RNA helicase DDX49",
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        "refseq_name": "probable ATP-dependent RNA helicase DDX49 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001108495",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001108495",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ddx49",
        "gene_names_refseq": "Ddx49",
        "protein_names_uniprotkb": "Probable ATP-dependent RNA helicase DDX49; 3.6.4.13; DEAD box protein 49",
        "protein_names_refseq": "DEAD (Asp-Glu-Ala-Asp) box polypeptide 49; probable ATP-dependent RNA helicase DDX49 isoform 1; probable ATP-dependent RNA helicase DDX49",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:290660);  (R-RNO-6791226)",
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        "publication_id_list": "",
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        "function": "ATP-dependent RNA helicase that plays a role in various aspects of RNA metabolism including the regulation of mRNA export and the levels of pre-ribosomal RNA. Regulates the stability and synthesis of pre-ribosomal RNA and thereby regulates cell proliferation. Also possesses antiviral activity by recognizing gammaherpesvirus transcripts in the context of lytic reactivation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": [
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                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.3",
                "type": "external"
            },
            {
                "id": "3.6.4.13",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.13",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.12",
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            },
            {
                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
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                "id": "3.6.1.5",
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                "id": "3.6.4.10",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.10",
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            },
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                "id": "3.6.4.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.-",
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                "id": "2.3.2.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
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                "id": "3.6.5.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.-",
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            },
            {
                "id": "5.6.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.-",
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            },
            {
                "id": "3.1.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.-.-",
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            },
            {
                "id": "3.1.13.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.13.-",
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            {
                "id": "2.7.7.7",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.7",
                "type": "external"
            },
            {
                "id": "2.7.7.49",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.49",
                "type": "external"
            },
            {
                "id": "3.1.13.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.13.1",
                "type": "external"
            },
            {
                "id": "4.2.99.18",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.2.99.18",
                "type": "external"
            },
            {
                "id": "7.6.2.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.6.2.2",
                "type": "external"
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            {
                "id": "7.6.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.6.2.3",
                "type": "external"
            },
            {
                "id": "7.6.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.6.2.-",
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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": "7.2.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.2.2.-",
                "type": "external"
            },
            {
                "id": "3.6.1.15",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.15",
                "type": "external"
            },
            {
                "id": "3.6.4.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.6",
                "type": "external"
            },
            {
                "id": "3.1.3.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.1",
                "type": "external"
            },
            {
                "id": "3.9.1.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.9.1.1",
                "type": "external"
            },
            {
                "id": "6.1.1.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.1.1.12",
                "type": "external"
            },
            {
                "id": "2.1.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.-",
                "type": "external"
            },
            {
                "id": "3.6.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.-",
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            },
            {
                "id": "2.7.4.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.3",
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            },
            {
                "id": "3.1.4.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.4.-",
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            },
            {
                "id": "3.4.24.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.24.-",
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            },
            {
                "id": "3.6.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.-.-",
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            },
            {
                "id": "3.4.21.53",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.21.53",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.5",
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            }
        ],
        "go_molecular_function": "GO:0003723 RNA binding;GO:0005524 ATP binding;GO:0016787 hydrolase activity;GO:0003724 RNA helicase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus",
        "go_biological_process": "GO:0030307 positive regulation of cell growth;GO:0006364 rRNA processing;GO:0044357 regulation of rRNA stability",
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        "protein_name": "Uncharacterized protein",
        "gene_name": "AABR07008940.1",
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        "gene_names_refseq": "",
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        "reported_mutagensis": 0,
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        "missing_score": 10000,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "",
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        "go_biological_process": "",
        "synthesized_glycan_count": 0,
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        "record_id": "E9PTU6-1",
        "record_type": "protein",
        "filter_code": "0000000.0000000.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
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    {
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        "uniprot_id": [
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                "id": "F1LMB6_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LMB6",
                "type": "external"
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        ],
        "mass": 80909.0,
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        "uniprot_id": [
            {
                "id": "F1LSG7_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LSG7",
                "type": "external"
            }
        ],
        "mass": 94171.0,
        "length": 841,
        "protein_name": "Fibroblast growth factor receptor",
        "gene_name": "Fgfr2",
        "organism": "Rat",
        "refseq_name": "fibroblast growth factor receptor 2 isoform a precursor",
        "refseq_ac": [
            {
                "id": "NP_036844",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_036844",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Fgfr2",
        "gene_names_refseq": "Fgfr2; KGFR",
        "protein_names_uniprotkb": "Fibroblast growth factor receptor; 2.7.10.1",
        "protein_names_refseq": "fibroblast growth factor receptor 2 isoform a precursor",
        "tax_id": 10116,
        "disease": "idiopathic pulmonary fibrosis (Disease Ontology:DOID:0050156); lacrimoauriculodentodigital syndrome 1 (Disease Ontology:DOID:0050331); Beare-Stevenson cutis gyrata syndrome (Disease Ontology:DOID:0050660); colorectal adenocarcinoma (Disease Ontology:DOID:0050861); bent bone dysplasia syndrome 1 (Disease Ontology:DOID:0060992); bone disease (Disease Ontology:DOID:0080001); Antley-Bixler syndrome (Disease Ontology:DOID:0081289); Antley-Bixler syndrome without disordered steroidogenesis (Disease Ontology:DOID:0081290); Jackson-Weiss syndrome (Disease Ontology:DOID:0111337); prostate cancer (Disease Ontology:DOID:10283); intestinal atresia (Disease Ontology:DOID:10486); stomach cancer (Disease Ontology:DOID:10534); retinitis pigmentosa (Disease Ontology:DOID:10584); portal hypertension (Disease Ontology:DOID:10762); essential hypertension (Disease Ontology:DOID:10825); hypospadias (Disease Ontology:DOID:10892); urinary bladder cancer (Disease Ontology:DOID:11054); acrocephalosyndactylia (Disease Ontology:DOID:12960); primary pulmonary hypertension (Disease Ontology:DOID:14557); Pfeiffer syndrome (Disease Ontology:DOID:14705); Saethre-Chotzen syndrome (Disease Ontology:DOID:14768); breast cancer (Disease Ontology:DOID:1612); squamous cell carcinoma (Disease Ontology:DOID:1749); transient cerebral ischemia (Disease Ontology:DOID:224); Crouzon syndrome (Disease Ontology:DOID:2339); craniosynostosis (Disease Ontology:DOID:2340); transitional cell carcinoma (Disease Ontology:DOID:2671); endometriosis (Disease Ontology:DOID:289); high grade glioma (Disease Ontology:DOID:3070); dysgerminoma (Disease Ontology:DOID:4441); stomach carcinoma (Disease Ontology:DOID:5517); hepatocellular carcinoma (Disease Ontology:DOID:684); female breast carcinoma (Disease Ontology:DOID:7843); intestinal volvulus (Disease Ontology:DOID:8445); Kaposi's sarcoma (Disease Ontology:DOID:8632)",
        "pathway": " (rno:25022);  (R-RNO-109704);  (R-RNO-1257604);  (R-RNO-190375);  (R-RNO-190377);  (R-RNO-5654221);  (R-RNO-5654695);  (R-RNO-5654699);  (R-RNO-5654700);  (R-RNO-5654727);  (R-RNO-5673001);  (R-RNO-6811558)",
        "pathway_count": 12,
        "publication_count": 2,
        "publication_id_list": "32626929;35599572",
        "class_list": "",
        "function": "Knockdown of lncRNA TUG1 alleviates diabetic retinal vascular dysfunction through regulating miR-524-5p/FGFR2., [RefSeq, PubMed]; MiR2175p regulates myogenesis in skeletal muscle stem cells by targeting FGFR2., [RefSeq, PubMed]",
        "predicted_glycosites": 8,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 35,
        "glyco_site_count": 8,
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        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "2.7.12.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.12.1",
                "type": "external"
            },
            {
                "id": "2.7.10.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.10.1",
                "type": "external"
            },
            {
                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
            },
            {
                "id": "2.7.1.153",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.153",
                "type": "external"
            },
            {
                "id": "2.7.1.137",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.137",
                "type": "external"
            },
            {
                "id": "2.7.10.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.10.2",
                "type": "external"
            },
            {
                "id": "2.7.1.154",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.154",
                "type": "external"
            },
            {
                "id": "2.3.2.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
                "type": "external"
            },
            {
                "id": "2.7.12.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.12.2",
                "type": "external"
            },
            {
                "id": "2.7.1.40",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.40",
                "type": "external"
            },
            {
                "id": "3.6.5.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.2",
                "type": "external"
            },
            {
                "id": "2.7.11.17",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.17",
                "type": "external"
            },
            {
                "id": "2.7.11.13",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.13",
                "type": "external"
            },
            {
                "id": "3.1.4.11",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.4.11",
                "type": "external"
            },
            {
                "id": "2.7.11.24",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.24",
                "type": "external"
            },
            {
                "id": "2.7.10.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.10.4",
                "type": "external"
            },
            {
                "id": "3.1.3.48",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.48",
                "type": "external"
            },
            {
                "id": "2.7.1.32",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.32",
                "type": "external"
            },
            {
                "id": "2.7.1.82",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.82",
                "type": "external"
            },
            {
                "id": "3.2.2.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.2.2.6",
                "type": "external"
            },
            {
                "id": "2.7.11.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.23",
                "type": "external"
            },
            {
                "id": "3.2.1.31",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.2.1.31",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0005007 fibroblast growth factor receptor activity;GO:0005524 ATP binding;GO:0017134 fibroblast growth factor binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0031410 cytoplasmic vesicle;GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:1904888 cranial skeletal system development;GO:0008284 positive regulation of cell population proliferation;GO:0006915 apoptotic process;GO:0050680 negative regulation of epithelial cell proliferation;GO:0045595 regulation of cell differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "F1LSG7-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000010000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "F1LNY6-1",
        "uniprot_id": [
            {
                "id": "F1LNY6_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LNY6",
                "type": "external"
            }
        ],
        "mass": 137076.0,
        "length": 1200,
        "protein_name": "Transcription initiation factor TFIID subunit 2",
        "gene_name": "Taf2",
        "organism": "Rat",
        "refseq_name": "transcription initiation factor TFIID subunit 2",
        "refseq_ac": [
            {
                "id": "NP_579853",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_579853",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Taf2",
        "gene_names_refseq": "TAFIIB; Taf2",
        "protein_names_uniprotkb": "Transcription initiation factor TFIID subunit 2; TBP-associated factor 150 kDa; Transcription initiation factor TFIID 150 kDa subunit",
        "protein_names_refseq": "TAF2 RNA polymerase II, TATA box binding protein (TBP)-associated factor; TAF2 RNA polymerase II, TATA box binding protein-associated factor, 150 kD; transcription initiation factor TFIID subunit 2",
        "tax_id": 10116,
        "disease": "autosomal recessive intellectual developmental disorder 40 (Disease Ontology:DOID:0081205)",
        "pathway": " (rno:170844);  (R-RNO-674695);  (R-RNO-6804756);  (R-RNO-73776);  (R-RNO-73779);  (R-RNO-75953);  (R-RNO-76042)",
        "pathway_count": 7,
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "The TFIID basal transcription factor complex plays a major role in the initiation of RNA polymerase II (Pol II)-dependent transcription. TFIID recognizes and binds promoters with or without a TATA box via its subunit TBP, a TATA-box-binding protein, and promotes assembly of the pre-initiation complex (PIC). The TFIID complex consists of TBP and TBP-associated factors (TAFs), including TAF1, TAF2, TAF3, TAF4, TAF5, TAF6, TAF7, TAF8, TAF9, TAF10, TAF11, TAF12 and TAF13. TAF2 forms a promoter DNA binding subcomplex of TFIID, together with TAF7 and TAF1., [UniProtKB, UniProtKB]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0003682 chromatin binding;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0033276 transcription factor TFTC complex;GO:0005634 nucleus;GO:0005669 transcription factor TFIID complex",
        "go_biological_process": "GO:0060261 positive regulation of transcription initiation by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0000086 G2/M transition of mitotic cell cycle;GO:0006367 transcription initiation at RNA polymerase II promoter;GO:0042789 mRNA transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F1LNY6-1",
        "record_type": "protein",
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        "kg_view_protein": true
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    {
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        "uniprot_id": [
            {
                "id": "F1LP44_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LP44",
                "type": "external"
            }
        ],
        "mass": 127657.0,
        "length": 1161,
        "protein_name": "Integrin subunit alpha L",
        "gene_name": "Itgal",
        "organism": "Rat",
        "refseq_name": "integrin alpha-L isoform X1",
        "refseq_ac": [
            {
                "id": "XP_006230331",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006230331",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Itgal",
        "gene_names_refseq": "Itgal; LFA-1",
        "protein_names_uniprotkb": "Integrin subunit alpha L",
        "protein_names_refseq": "integrin alpha-L isoform X1",
        "tax_id": 10116,
        "disease": "nephritis (Disease Ontology:DOID:10952)",
        "pathway": " (R-RNO-198933);  (R-RNO-202733);  (R-RNO-216083);  (R-RNO-6798695)",
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        "publication_count": 0,
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        "class_list": "",
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        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0050839 cell adhesion molecule binding;GO:0044877 protein-containing complex binding;GO:0030369 ICAM-3 receptor activity;GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005911 cell-cell junction;GO:0009986 cell surface;GO:0009897 external side of plasma membrane;GO:0001772 immunological synapse",
        "go_biological_process": "GO:0022409 positive regulation of cell-cell adhesion;GO:0002291 T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell;GO:0007166 cell surface receptor signaling pathway;GO:0007229 integrin-mediated signaling pathway;GO:0007160 cell-matrix adhesion",
        "synthesized_glycan_count": 0,
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        ],
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        "gene_name": "",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Uncharacterized protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "filter_code": "0000000.0000000.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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        ],
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        "protein_name": "HECT and RLD domain containing E3 ubiquitin protein ligase family member 6",
        "gene_name": "Herc6",
        "organism": "Rat",
        "refseq_name": "probable E3 ubiquitin-protein ligase HERC6",
        "refseq_ac": [
            {
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                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Herc6",
        "gene_names_refseq": "Herc6",
        "protein_names_uniprotkb": "HECT and RLD domain containing E3 ubiquitin protein ligase family member 6",
        "protein_names_refseq": "hect domain and RLD 6; potential ubiquitin ligase; probable E3 ubiquitin-protein ligase HERC6",
        "tax_id": 10116,
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        "pathway": " (R-RNO-983168)",
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        "function": "Component of the large ribosomal subunit. The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell. Binds a specific region on the 26S rRNA. May promote p53/TP53 degradation possibly through the stimulation of MDM2-mediated TP53 polyubiquitination., [UniProtKB, UniProtKB]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0019843 rRNA binding;GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0005634 nucleus;GO:0022625 cytosolic large ribosomal subunit",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "F1LTE0-1",
        "uniprot_id": [
            {
                "id": "TANC2_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LTE0",
                "type": "external"
            }
        ],
        "mass": 219812.0,
        "length": 1992,
        "protein_name": "Protein TANC2",
        "gene_name": "Tanc2",
        "organism": "Rat",
        "refseq_name": "protein TANC2 isoform 2",
        "refseq_ac": [
            {
                "id": "NP_001178582",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001178582",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tanc2",
        "gene_names_refseq": "RGD1309285; Tanc2",
        "protein_names_uniprotkb": "Protein TANC2",
        "protein_names_refseq": "protein TANC2 isoform 2; protein TANC2",
        "tax_id": 10116,
        "disease": "intellectual developmental disorder with autistic features and language delay, with or without seizures (Disease Ontology:DOID:0081430)",
        "pathway": " (rno:303599)",
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        "function": "Liprin-alpha and TANC2 are not part of the KIF1A-cargo complex but capture dense core vesicles at dendritic spines., [RefSeq, PubMed]; Scaffolding protein in the dendritic spines which acts as immobile postsynaptic posts able to recruit KIF1A-driven dense core vesicles to dendritic spines., [UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0098919 structural constituent of postsynaptic density",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0014069 postsynaptic density;GO:0030424 axon;GO:0043197 dendritic spine;GO:0099092 postsynaptic density, intracellular component",
        "go_biological_process": "GO:0001701 in utero embryonic development;GO:0060998 regulation of dendritic spine development;GO:0061001 regulation of dendritic spine morphogenesis;GO:0099519 dense core granule cytoskeletal transport",
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        "kg_view_protein": true
    },
    {
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        ],
        "mass": 201525.0,
        "length": 1817,
        "protein_name": "Laminin subunit alpha-4",
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            {
                "id": "NP_001296376",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001296376",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Lama4",
        "gene_names_refseq": "Lama4; RGD1560062",
        "protein_names_uniprotkb": "Laminin subunit alpha-4; Laminin-14 subunit alpha; Laminin-8 subunit alpha; Laminin-9 subunit alpha",
        "protein_names_refseq": "laminin subunit alpha-4 precursor; laminin, alpha 4",
        "tax_id": 10116,
        "disease": "dilated cardiomyopathy 1JJ (Disease Ontology:DOID:0110438)",
        "pathway": " (rno:309816);  (R-RNO-3000157);  (R-RNO-8874081);  (R-RNO-9913351)",
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        "function": "Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components., [UniProtKB, UniProtKB]; Synthesized by mesangial cells (MC) and persists in the mature glomerulus; suggested that laminin alpha4 plays an important role in MC differentiation and in the maintenance of MC phenotype., [RefSeq, PubMed]",
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        ],
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        "protein_name": "Similar to human chromosome 2 open reading frame 78",
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            {
                "id": "XP_001073960",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_001073960",
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        ],
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        ],
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        "protein_name": "Protein argonaute-3",
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        "gene_names_uniprotkb": "Ago3; AGO3; EIF2C3",
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        "protein_names_uniprotkb": "Protein argonaute-3; Argonaute3; Eukaryotic translation initiation factor 2C 3; eIF-2C 3; eIF2C 3",
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        "function": "Required for RNA-mediated gene silencing (RNAi). Binds to short RNAs such as microRNAs (miRNAs) and represses the translation of mRNAs which are complementary to them. Lacks endonuclease activity and does not appear to cleave target mRNAs., [UniProtKB, HAMAP]",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0046872 metal ion binding;GO:0003725 double-stranded RNA binding;GO:0003727 single-stranded RNA binding;GO:0035198 miRNA binding",
        "go_cellular_component": "GO:0000794 condensed nuclear chromosome;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0000932 P-body;GO:0036464 cytoplasmic ribonucleoprotein granule",
        "go_biological_process": "GO:0070922 RISC complex assembly;GO:0010628 positive regulation of gene expression;GO:1901224 positive regulation of non-canonical NF-kappaB signal transduction;GO:0006402 mRNA catabolic process;GO:0031054 pre-miRNA processing",
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        ],
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        "protein_name": "Glyceraldehyde-3-phosphate dehydrogenase",
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        "gene_names_uniprotkb": "ENSRNOG00000066746",
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        "protein_names_uniprotkb": "Glyceraldehyde-3-phosphate dehydrogenase; 1.2.1.12",
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        "ec_number_list": [
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                "url": "https://www.rhea-db.org/rhea/?query=ec:1.2.1.12",
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            },
            {
                "id": "2.6.99.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.6.99.-",
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            }
        ],
        "go_molecular_function": "GO:0051287 NAD binding;GO:0016740 transferase activity;GO:0004365 glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity;GO:0050661 NADP binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol;GO:0005856 cytoskeleton",
        "go_biological_process": "GO:0006417 regulation of translation;GO:0045087 innate immune response;GO:0006915 apoptotic process;GO:0006094 gluconeogenesis;GO:0006096 glycolytic process",
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        ],
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        "protein_name": "Zinc finger protein 791",
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        "organism": "Rat",
        "refseq_name": "zinc finger protein 791-like",
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            {
                "id": "XP_008770655",
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        ],
        "gene_names_uniprotkb": "Zfp791",
        "gene_names_refseq": "Zfp791",
        "protein_names_uniprotkb": "Zinc finger protein 791",
        "protein_names_refseq": "zinc finger protein 791-like",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0044877 protein-containing complex binding;GO:0180000 histone methyltransferase inhibitor activity",
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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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        "protein_names_refseq": "calcium-binding mitochondrial carrier protein Aralar2; electrogenic aspartate/glutamate antiporter SLC25A13, mitochondrial isoform 1; electrogenic aspartate/glutamate antiporter SLC25A13, mitochondrial; solute carrier family 25 (aspartate/glutamate carrier), member 13; solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13; solute carrier family 25, member 13 (citrin)",
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        "pathway": " (rno:362322);  (R-RNO-8963693);  (R-RNO-9856872)",
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        "protein_name": "Sodium-independent sulfate anion transporter",
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        "protein_names_refseq": "sodium-independent sulfate anion transporter; solute carrier family 26 (anion exchanger), member 11",
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        "function": "Results demonstrate that prolonged Na+ entry via either of two independent pathways (either VGSCs or NMDARs) converge to activate a Cl- influx pathway via SLC26A11 that is ultimately required for neuronal swelling and subsequent cell death., [RefSeq, PubMed]; SLC26A11 Inhibition Reduces Oncotic Neuronal Death and Attenuates Stroke Reperfusion Injury., [RefSeq, PubMed]; Sodium-independent anion exchanger mediating bicarbonate, chloride, sulfate and oxalate transport. Exhibits sodium-independent sulfate anion transporter activity that may cooperate with SLC26A2 to mediate DIDS-sensitive sulfate uptake into high endothelial venules endothelial cells (HEVEC). In the kidney, mediates chloride-bicarbonate exchange, facilitating V-ATPase-mediated acid secretion. May function as a chloride channel, playing an important role in moderating chloride homeostasis and neuronal activity in the cerebellum., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0016020 membrane;GO:0016323 basolateral plasma membrane",
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        "protein_name": "Zinc finger protein 770",
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            {
                "id": "NP_001386575",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
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            {
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
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        "protein_names_refseq": "nuclear GTPase SLIP-GC",
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        "function": "Nuclear GTPase found in germinal center B-cells, where it may inhibit function of the activation-induced cytidine deaminase AICDA. Reduces somatic hypermutation in B-cells which may enhance genome stability., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding",
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001395986",
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        "protein_names_uniprotkb": "Zinc finger protein 239 like 1",
        "protein_names_refseq": "zinc finger protein 501; zinc finger protein 763; zinc finger protein 883-like; zinc finger protein 883",
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        "go_molecular_function": "GO:0004252 serine-type endopeptidase activity;GO:0042277 peptide binding",
        "go_cellular_component": "GO:0042629 mast cell granule",
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        "hit_score": 0.1,
        "record_id": "E9PTQ9-1",
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        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
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    },
    {
        "uniprot_canonical_ac": "F1LNR1-1",
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            {
                "id": "F1LNR1_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LNR1",
                "type": "external"
            }
        ],
        "mass": 163908.0,
        "length": 1488,
        "protein_name": "Cytoplasmic linker associated protein 1",
        "gene_name": "Clasp1",
        "organism": "Rat",
        "refseq_name": "CLIP-associating protein 1 isoform X21",
        "refseq_ac": [
            {
                "id": "XP_063128328",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_063128328",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Clasp1",
        "gene_names_refseq": "Clasp1",
        "protein_names_uniprotkb": "Cytoplasmic linker associated protein 1",
        "protein_names_refseq": "CLIP-associating protein 1 isoform X21",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-141430);  (R-RNO-141444);  (R-RNO-2467813);  (R-RNO-2500257);  (R-RNO-2565942);  (R-RNO-380259);  (R-RNO-380270);  (R-RNO-380284);  (R-RNO-380320);  (R-RNO-5620912);  (R-RNO-5663220);  (R-RNO-68877);  (R-RNO-8854518);  (R-RNO-9648025)",
        "pathway_count": 14,
        "publication_count": 2,
        "publication_id_list": "22673903;38843836",
        "class_list": "",
        "function": "Microtubule plus-end tracking protein that promotes the stabilization of dynamic microtubules. Involved in the nucleation of noncentrosomal microtubules originating from the trans-Golgi network (TGN). Required for the polarization of the cytoplasmic microtubule arrays in migrating cells towards the leading edge of the cell. May act at the cell cortex to enhance the frequency of rescue of depolymerizing microtubules by attaching their plus-ends to cortical platforms composed of ERC1 and PHLDB2. This cortical microtubule stabilizing activity is regulated at least in part by phosphatidylinositol 3-kinase signaling. Also performs a similar stabilizing function at the kinetochore which is essential for the bipolar alignment of chromosomes on the mitotic spindle., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0008017 microtubule binding;GO:0002162 dystroglycan binding;GO:0051010 microtubule plus-end binding;GO:0043515 kinetochore binding",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005813 centrosome;GO:0005819 spindle;GO:0005874 microtubule;GO:0000776 kinetochore",
        "go_biological_process": "GO:0031110 regulation of microtubule polymerization or depolymerization;GO:0051494 negative regulation of cytoskeleton organization;GO:1902904 negative regulation of supramolecular fiber organization;GO:0051301 cell division;GO:0007026 negative regulation of microtubule depolymerization",
        "synthesized_glycan_count": 0,
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        "filter_code": "0000000.0000101.010000.000000000000001000.0100000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZXT2-1",
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            {
                "id": "D3ZXT2_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZXT2",
                "type": "external"
            }
        ],
        "mass": 141307.0,
        "length": 1231,
        "protein_name": "Cohesin subunit SA",
        "gene_name": "Stag2",
        "organism": "Rat",
        "refseq_name": "cohesin subunit SA-2 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001166978",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001166978",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Stag2",
        "gene_names_refseq": "RGD1562042; Stag2",
        "protein_names_uniprotkb": "Cohesin subunit SA; SCC3 homolog; Stromal antigen",
        "protein_names_refseq": "cohesin subunit SA-2 isoform 1; cohesin subunit SA-2; stromal antigen 2",
        "tax_id": 10116,
        "disease": "Holoprosencephaly 13, X-linked (Disease Ontology:DOID:0060954); Mullegama-Klein-Martinez syndrome (Disease Ontology:DOID:0111845)",
        "pathway": " (rno:313304);  (R-RNO-2467813);  (R-RNO-2468052);  (R-RNO-2470946);  (R-RNO-2500257);  (R-RNO-3108214)",
        "pathway_count": 6,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Component of cohesin complex, a complex required for the cohesion of sister chromatids after DNA replication. The cohesin complex apparently forms a large proteinaceous ring within which sister chromatids can be trapped. At anaphase, the complex is cleaved and dissociates from chromatin, allowing sister chromatids to segregate., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003682 chromatin binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0001650 fibrillar center;GO:0000775 chromosome, centromeric region;GO:0016363 nuclear matrix;GO:0000785 chromatin",
        "go_biological_process": "GO:0051301 cell division;GO:0090307 mitotic spindle assembly;GO:0007062 sister chromatid cohesion;GO:0019827 stem cell population maintenance",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZXT2-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.010000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "F1MAP4-1",
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            {
                "id": "F1MAP4_RAT",
                "url": "https://www.uniprot.org/uniprot/F1MAP4",
                "type": "external"
            }
        ],
        "mass": 122806.0,
        "length": 1145,
        "protein_name": "Multiple epidermal growth factor-like domains protein 10",
        "gene_name": "Megf10",
        "organism": "Rat",
        "refseq_name": "multiple epidermal growth factor-like domains protein 10 precursor",
        "refseq_ac": [
            {
                "id": "NP_001094127",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001094127",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Megf10",
        "gene_names_refseq": "Megf10",
        "protein_names_uniprotkb": "Multiple epidermal growth factor-like domains protein 10",
        "protein_names_refseq": "multiple epidermal growth factor-like domains protein 10 precursor; multiple epidermal growth factor-like domains protein 10",
        "tax_id": 10116,
        "disease": "congenital myopathy 10B (Disease Ontology:DOID:0081345); congenital myopathy 10A (Disease Ontology:DOID:0111333); neurodegenerative disease (Disease Ontology:DOID:1289); myopathy (Disease Ontology:DOID:423)",
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        "go_molecular_function": "GO:0005044 scavenger receptor activity;GO:0005112 Notch binding;GO:0001849 complement component C1q complex binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0001891 phagocytic cup",
        "go_biological_process": "GO:0022409 positive regulation of cell-cell adhesion;GO:0014816 skeletal muscle satellite cell differentiation;GO:0034109 homotypic cell-cell adhesion;GO:0042552 myelination;GO:0043652 engulfment of apoptotic cell",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "M0RAI4-1",
        "uniprot_id": [
            {
                "id": "M0RAI4_RAT",
                "url": "https://www.uniprot.org/uniprot/M0RAI4",
                "type": "external"
            }
        ],
        "mass": 123871.0,
        "length": 1115,
        "protein_name": "Nondiscriminating glutamyl-tRNA synthetase EARS2, mitochondrial",
        "gene_name": "Ears2; Gga2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Ears2; Gga2; Gga2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Nondiscriminating glutamyl-tRNA synthetase EARS2, mitochondrial; 6.1.1.17; 6.1.1.24; Glutamate--tRNA(Gln) ligase EARS2, mitochondrial; Glutamyl-tRNA synthetase; Mitochondrial glutamyl-tRNA synthetase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "combined oxidative phosphorylation deficiency 12 (Disease Ontology:DOID:0111493); neurodegenerative disease (Disease Ontology:DOID:1289); lysosomal storage disease (Disease Ontology:DOID:3211)",
        "pathway": " (rno:293455);  (rno:361641)",
        "pathway_count": 2,
        "publication_count": 0,
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        "class_list": "",
        "function": "Non-discriminating glutamyl-tRNA synthetase that catalyzes aminoacylation of both mitochondrial tRNA(Glu) and tRNA(Gln) and participates in RNA aminoacylation for mitochondrial protein translation. Attachs glutamate to tRNA(Glu) or tRNA(Gln) in a two-step reaction: glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) or tRNA(Gln). In vitro, cytoplasmic tRNA(Gln) is slightly glutamylated, but with low activity., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "6.1.1.17",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.1.1.17",
                "type": "external"
            },
            {
                "id": "6.1.1.24",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.1.1.24",
                "type": "external"
            },
            {
                "id": "6.1.1.15",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.1.1.15",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0031267 small GTPase binding;GO:0035091 phosphatidylinositol binding;GO:0043130 ubiquitin binding;GO:0005524 ATP binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0031901 early endosome membrane;GO:0030136 clathrin-coated vesicle;GO:0005802 trans-Golgi network;GO:0005739 mitochondrion",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0043001 Golgi to plasma membrane protein transport;GO:0034394 protein localization to cell surface;GO:0016192 vesicle-mediated transport;GO:0006424 glutamyl-tRNA aminoacylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0RAI4-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.010000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "F1MAF1-1",
        "uniprot_id": [
            {
                "id": "F1MAF1_RAT",
                "url": "https://www.uniprot.org/uniprot/F1MAF1",
                "type": "external"
            }
        ],
        "mass": 57109.0,
        "length": 525,
        "protein_name": "Heat shock transcription factor 1",
        "gene_name": "Hsf1",
        "organism": "Rat",
        "refseq_name": "heat shock factor protein 1",
        "refseq_ac": [
            {
                "id": "NP_077369",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_077369",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Hsf1",
        "gene_names_refseq": "Hsf1",
        "protein_names_uniprotkb": "Heat shock transcription factor 1",
        "protein_names_refseq": "heat shock factor protein 1",
        "tax_id": 10116,
        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652); cryptorchidism (Disease Ontology:DOID:11383); Huntington's disease (Disease Ontology:DOID:12858); neurodegenerative disease (Disease Ontology:DOID:1289); Parkinson's disease (Disease Ontology:DOID:14330); transient cerebral ischemia (Disease Ontology:DOID:224); congestive heart failure (Disease Ontology:DOID:6000); muscular atrophy (Disease Ontology:DOID:767)",
        "pathway": " (rno:79245);  (R-RNO-3371453);  (R-RNO-3371511);  (R-RNO-3371568);  (R-RNO-3371571);  (R-RNO-9841251)",
        "pathway_count": 6,
        "publication_count": 6,
        "publication_id_list": "22673903;31522994;32457290;33989081;34530848;36741074",
        "class_list": "",
        "function": "BAG3 expression and sarcomere localization in the human heart are linked to HSF-1 and are differentially affected by sex and disease., [RefSeq, PubMed]; Decreased expression of FBXW7 by ERK1/2 activation in drug-resistant cancer cells confers transcriptional activation of MDR1 by suppression of ubiquitin degradation of HSF1. Publication Status: Online-Only, [RefSeq, PubMed]; HSF1 Alleviates Brain Injury by Inhibiting NLRP3-Induced Pyroptosis in a Sepsis Model. Publication Status: Online-Only, [RefSeq, PubMed]; HSF1 is involved in suppressing A1 phenotype conversion of astrocytes following spinal cord injury in rats. Publication Status: Online-Only, [RefSeq, PubMed]; Localized to both the cytoplasm and nuclei of myometrial cells in both muscle layers throughout gestation, [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "reported_c_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 1,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0019901 protein kinase binding;GO:0042802 identical protein binding;GO:0046982 protein heterodimerization activity;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0097165 nuclear stress granule;GO:0005813 centrosome;GO:0005829 cytosol;GO:0048471 perinuclear region of cytoplasm;GO:0016605 PML body",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0010628 positive regulation of gene expression;GO:0045931 positive regulation of mitotic cell cycle;GO:1900034 regulation of cellular response to heat;GO:0000165 MAPK cascade",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "F1MAF1-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
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        "protein_name": "Rho GTPase activating protein 4",
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            {
                "id": "NP_653341",
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            }
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        "pathway": " (rno:246249);  (R-RNO-8980692);  (R-RNO-9013148);  (R-RNO-9013149)",
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        "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]",
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            {
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        "function": "EXPRESSION OF DOUBLECORTIN AND NeuN IN THE DEVELOPING CEREBELLAR NEURONS IN RAT, [RefSeq, PubMed]; Pre-mRNA alternative splicing regulator. Regulates alternative splicing of RBFOX2 to enhance the production of mRNA species that are targeted for nonsense-mediated decay (NMD)., [UniProtKB, UniProtKB]; RNA-binding protein that regulates alternative splicing events., [UniProtKB, UniProtKB, UniProtKB]; Subcellular localization of neuronal nuclei (NeuN) antigen in size and calcitonin gene-related peptide (CGRP) populations of dorsal root ganglion (DRG) neurons during acute peripheral inflammation., [RefSeq, PubMed]; The presence of NeuN protein in the secretory epithelial cells of the exocrine part of this organ. The protein was located in the apical part of the cytoplasm slightly below the zone of zymogen granules., [RefSeq, PubMed]",
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        "protein_name": "Armadillo repeat-containing protein 8",
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            {
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        "function": "Component of the CTLH E3 ubiquitin-protein ligase complex that selectively accepts ubiquitin from UBE2H and mediates ubiquitination and subsequent proteasomal degradation of the transcription factor HBP1., [UniProtKB, UniProtKB, UniProtKB]",
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        "length": 1453,
        "protein_name": "Ribosome-binding protein 1",
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        "refseq_name": "ribosome-binding protein 1",
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            {
                "id": "NP_001414528",
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            }
        ],
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        "protein_names_refseq": "ribosome binding protein 1 homolog 180kDa (dog); ribosome-binding protein 1",
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        "pathway": " (rno:311483)",
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        "function": "Acts as a ribosome receptor and mediates interaction between the ribosome and the endoplasmic reticulum membrane., [UniProtKB, UniProtKB, UniProtKB]; Axonal endoplasmic reticulum tubules control local translation via P180/RRBP1-mediated ribosome interactions., [RefSeq, PubMed]",
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        "protein_name": "AT-rich interaction domain 5A",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:1901985 positive regulation of protein acetylation;GO:0032740 positive regulation of interleukin-17 production;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II",
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        "gene_name": "LOC134481322; Pilrb1l1; Pilrb1l3; Pilrb1l4; Pilrb2l3; Pilrb2",
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        "refseq_ac": [],
        "gene_names_uniprotkb": "LOC134481322; Pilrb1l1; Pilrb1l3; Pilrb1l4; Pilrb2l3; Pilrb2; LOC102554231; LOC120095902; LOC134481169; LOC134481322; Pilrb1l3; Pilrb2l3; Pilrb2l5; RGD1561143; RGD1561730",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Uncharacterized protein",
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        "pathway": " (rno:102554231);  (rno:304382);  (rno:498169);  (R-RNO-198933)",
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        "gene_name": "Tmtc4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Tmtc4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein O-mannosyl-transferase TMTC4; 2.4.1.109; Transmembrane O-mannosyltransferase targeting cadherins 4; Transmembrane and tetratricopeptide repeat-containing 4",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autosomal recessive nonsyndromic deafness (Disease Ontology:DOID:0050565)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Transfers mannosyl residues to the hydroxyl group of serine or threonine residues. The 4 members of the TMTC family are O-mannosyl-transferases dedicated primarily to the cadherin superfamily, each member seems to have a distinct role in decorating the cadherin domains with O-linked mannose glycans at specific regions. Also acts as O-mannosyl-transferase on other proteins such as PDIA3., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0004169 dolichyl-phosphate-mannose-protein mannosyltransferase activity;GO:0051117 ATPase binding;GO:0000030 mannosyltransferase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0016020 membrane",
        "go_biological_process": "GO:0007605 sensory perception of sound;GO:0030968 endoplasmic reticulum unfolded protein response;GO:0035269 protein O-linked glycosylation via mannose;GO:0032470 positive regulation of endoplasmic reticulum calcium ion concentration;GO:1905584 outer hair cell apoptotic process",
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    },
    {
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            {
                "id": "D3ZGN2_RAT",
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            }
        ],
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        "protein_name": "Copine-5",
        "gene_name": "Cpne5",
        "organism": "Rat",
        "refseq_name": "copine-5",
        "refseq_ac": [
            {
                "id": "NP_001101086",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001101086",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Cpne5",
        "gene_names_refseq": "Cpne5",
        "protein_names_uniprotkb": "Copine-5; Copine V",
        "protein_names_refseq": "copine 5 protein; copine V; copine-5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:309650)",
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        "publication_id_list": "16641100;22673903",
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        "function": "Probable calcium-dependent phospholipid-binding protein that may play a role in calcium-mediated intracellular processes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005544 calcium-dependent phospholipid binding;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0043025 neuronal cell body;GO:0043204 perikaryon;GO:0043005 neuron projection",
        "go_biological_process": "GO:1903861 positive regulation of dendrite extension;GO:0030154 cell differentiation;GO:0071277 cellular response to calcium ion",
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        "kg_view_protein": true
    },
    {
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            {
                "id": "F7F0U1_RAT",
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        ],
        "mass": 63096.0,
        "length": 554,
        "protein_name": "Cytochrome P450 3A",
        "gene_name": "Cyp3a62",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Cyp3a62; Cyp3a9",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Cytochrome P450 3A; 1.14.14.-",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "alcohol-associated liver disease (Disease Ontology:DOID:0070658); familial Mediterranean fever (Disease Ontology:DOID:2987)",
        "pathway": " (R-RNO-211945);  (R-RNO-211958);  (R-RNO-211981);  (R-RNO-5423646);  (R-RNO-9027307);  (R-RNO-9749641);  (R-RNO-9754706);  (R-RNO-9757110)",
        "pathway_count": 8,
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        "class_list": "",
        "function": "Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It oxidizes a variety of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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            {
                "id": "1.14.14.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.14.14.1",
                "type": "external"
            },
            {
                "id": "1.14.14.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.14.14.-",
                "type": "external"
            },
            {
                "id": "4.2.1.152",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.2.1.152",
                "type": "external"
            },
            {
                "id": "1.14.13.n7",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.14.13.n7",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0005506 iron ion binding;GO:0020037 heme binding;GO:0016712 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen;GO:0050649 testosterone 6-beta-hydroxylase activity",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0070989 oxidative demethylation;GO:0008202 steroid metabolic process",
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            {
                "id": "F1MAD3_RAT",
                "url": "https://www.uniprot.org/uniprot/F1MAD3",
                "type": "external"
            }
        ],
        "mass": 466168.0,
        "length": 4292,
        "protein_name": "Polycystin-1",
        "gene_name": "Pkd1",
        "organism": "Rat",
        "refseq_name": "polycystin-1 precursor",
        "refseq_ac": [
            {
                "id": "NP_001400942",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001400942",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Pkd1",
        "gene_names_refseq": "Pkd1",
        "protein_names_uniprotkb": "Polycystin-1",
        "protein_names_refseq": "polycystic kidney disease 1 homolog; polycystin-1 precursor",
        "tax_id": 10116,
        "disease": "polycystic liver disease (Disease Ontology:DOID:0050770); polycystic kidney disease (Disease Ontology:DOID:0080322); polycystic kidney disease 1 (Disease Ontology:DOID:0110858); autosomal recessive polycystic kidney disease (Disease Ontology:DOID:0110861); intracranial aneurysm (Disease Ontology:DOID:10941); hypertrophic cardiomyopathy (Disease Ontology:DOID:11984); autosomal dominant polycystic kidney disease (Disease Ontology:DOID:898)",
        "pathway": " (rno:24650);  (R-RNO-5620916)",
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        "publication_id_list": "29133434;29949809;33065236;34407229",
        "class_list": "",
        "function": "Component of a heteromeric calcium-permeable ion channel formed by PKD1 and PKD2 that is activated by interaction between PKD1 and a Wnt family member, such as WNT3A and WNT9B. Both PKD1 and PKD2 are required for channel activity. Involved in renal tubulogenesis. Involved in fluid-flow mechanosensation by the primary cilium in renal epithelium. Acts as a regulator of cilium length, together with PKD2. The dynamic control of cilium length is essential in the regulation of mechanotransductive signaling. The cilium length response creates a negative feedback loop whereby fluid shear-mediated deflection of the primary cilium, which decreases intracellular cAMP, leads to cilium shortening and thus decreases flow-induced signaling. May be an ion-channel regulator. Involved in adhesive protein-protein and protein-carbohydrate interactions. Likely to be involved with polycystin-1-interacting protein 1 in the detection, sequestration and exocytosis of senescent mitochondria., [UniProtKB, UniProtKB, UniProtKB]; PKD1 alleviates oxidative stress-inhibited osteogenesis of rat bone marrow-derived mesenchymal stem cells through TAZ activation., [RefSeq, PubMed]; PKD1 enhances the stability of N-cadherin on cell membrane and promotes synapse morphogenesis and synaptic plasticity in an activity-dependent manner, [RefSeq, PubMed]; PKD1 mediates the PKC effects on KV11.1 and we found that PKD targets S284 in the N-terminus of the channel., [RefSeq, PubMed]; Polycystin-1 mitigates damage and regulates CTGF expression through AKT activation during cardiac ischemia/reperfusion., [RefSeq, PubMed]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0030246 carbohydrate binding;GO:0005262 calcium channel activity;GO:0019901 protein kinase binding;GO:0019904 protein domain specific binding;GO:0044325 transmembrane transporter binding",
        "go_cellular_component": "GO:0002133 polycystin complex;GO:0005576 extracellular region;GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007507 heart development;GO:0001822 kidney development;GO:0006816 calcium ion transport;GO:0098609 cell-cell adhesion;GO:0009887 animal organ morphogenesis",
        "synthesized_glycan_count": 0,
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        "record_id": "F1MAD3-1",
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        "kg_view_protein": true
    },
    {
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            {
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                "url": "https://www.uniprot.org/uniprot/D3ZFD8",
                "type": "external"
            }
        ],
        "mass": 35688.0,
        "length": 325,
        "protein_name": "TNF superfamily member 13b",
        "gene_name": "Tnfsf13b",
        "organism": "Rat",
        "refseq_name": "tumor necrosis factor ligand superfamily member 13B isoform X1",
        "refseq_ac": [
            {
                "id": "XP_006253542",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006253542",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tnfsf13b",
        "gene_names_refseq": "BAFF; RGD1561519; Tnfsf13b; Tnlg7a",
        "protein_names_uniprotkb": "TNF superfamily member 13b",
        "protein_names_refseq": "tumor necrosis factor ligand superfamily member 13B isoform X1",
        "tax_id": 10116,
        "disease": "Sjogren's syndrome (Disease Ontology:DOID:12894); IgA glomerulonephritis (Disease Ontology:DOID:2986)",
        "pathway": " (R-RNO-5668541);  (R-RNO-5669034);  (R-RNO-5676594)",
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        "go_molecular_function": "GO:0005125 cytokine activity;GO:0005164 tumor necrosis factor receptor binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0016020 membrane;GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0048471 perinuclear region of cytoplasm",
        "go_biological_process": "GO:0006955 immune response;GO:0002260 lymphocyte homeostasis;GO:0031295 T cell costimulation;GO:0050776 regulation of immune response;GO:0002636 positive regulation of germinal center formation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZFD8-1",
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    {
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            {
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        ],
        "mass": 217336.0,
        "length": 1975,
        "protein_name": "Germinal-center associated nuclear protein",
        "gene_name": "Mcm3ap",
        "organism": "Rat",
        "refseq_name": "germinal-center associated nuclear protein",
        "refseq_ac": [
            {
                "id": "NP_001421547",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001421547",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Mcm3ap",
        "gene_names_refseq": "Mcm3ap",
        "protein_names_uniprotkb": "Germinal-center associated nuclear protein; 2.3.1.48",
        "protein_names_refseq": "80 kDa MCM3-associated protein; germinal-center associated nuclear protein; minichromosome maintenance deficient 3 associated protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:294339)",
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        "publication_id_list": "22673903;35113004",
        "class_list": "",
        "function": "As a component of the TREX-2 complex, involved in the export of mRNAs to the cytoplasm through the nuclear pores. Through the acetylation of histones, affects the assembly of nucleosomes at immunoglobulin variable region genes and promotes the recruitment and positioning of transcription complex to favor DNA cytosine deaminase AICDA/AID targeting, hence promoting somatic hypermutations., [UniProtKB, UniProtKB, UniProtKB]; Long non-coding RNA MCM3AP antisense RNA 1 silencing upregulates microRNA-24-3p to accelerate proliferation and migration of vascular endothelial cells in myocardial infarction rats by reducing EIF4G2., [RefSeq, PubMed]",
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            {
                "id": "2.7.11.1",
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                "id": "NP_001033684",
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        "function": "Changes in cellular TID1 are a factor in the pathogenesis of Parkinson's disease, [RefSeq, PubMed]; Modulates apoptotic signal transduction or effector structures within the mitochondrial matrix. Affect cytochrome C release from the mitochondria and caspase 3 activation, but not caspase 8 activation. Isoform 1 increases apoptosis triggered by both TNF and the DNA-damaging agent mytomycin C; in sharp contrast, isoform 2 suppresses apoptosis. Can modulate IFN-gamma-mediated transcriptional activity. Isoform 2 may play a role in neuromuscular junction development as an effector of the MUSK signaling pathway., [UniProtKB, UniProtKB, UniProtKB]; Tid1-S attenuates LPS-induced cardiac hypertrophy and apoptosis through ER-a mediated modulation of p-PI3K/p-Akt signaling cascade., [RefSeq, PubMed]",
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        "function": "Alterations in the immunoreactivities and expressions of beta-dystroglycan, utrophin, and laminin seem to correlate with angiogenesis rather than BBB disruption during cerebral hypoperfusion., [RefSeq, PubMed]; May play a role in anchoring the cytoskeleton to the plasma membrane., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; N-utro may be responsible for the anchoring of the cortical actin cytoskeleton to the membranes in muscle and other tissues., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003714 transcription corepressor activity;GO:0035091 phosphatidylinositol binding;GO:0001222 transcription corepressor binding",
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            {
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        "function": "Functions as a calcium- and diacylglycerol (DAG)-regulated nucleotide exchange factor specifically activating Ras through the exchange of bound GDP for GTP. Activates the Erk/MAP kinase cascade. Regulates T-cell/B-cell development, homeostasis and differentiation by coupling T-lymphocyte/B-lymphocyte antigen receptors to Ras. Regulates NK cell cytotoxicity and ITAM-dependent cytokine production by activation of Ras-mediated ERK and JNK pathways. Functions in mast cell degranulation and cytokine secretion, regulating FcERI-evoked allergic responses. May also function in differentiation of other cell types. Proto-oncogene, which promotes T-cell lymphomagenesis when its expression is deregulated., [UniProtKB, UniProtKB]; These results indicate that RasGRP3 is implicated in phorbol ester-induced, PKC-independent exocytosis., [RefSeq, PubMed]; Together these data demonstrate a novel mechanism in which the balance between stability and plasticity in dendritic spines depends on binding of drebrin to actin filaments in a manner that is regulated by Ras., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0008270 zinc ion binding;GO:0005509 calcium ion binding;GO:0019900 kinase binding;GO:0005085 guanyl-nucleotide exchange factor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0048471 perinuclear region of cytoplasm;GO:0032045 guanyl-nucleotide exchange factor complex",
        "go_biological_process": "GO:0007265 Ras protein signal transduction",
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        "protein_name": "Nucleolar and spindle associated protein 1",
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        "go_cellular_component": "GO:0005730 nucleolus;GO:0005874 microtubule;GO:0072686 mitotic spindle;GO:0005634 nucleus;GO:0005819 spindle",
        "go_biological_process": "GO:0007076 mitotic chromosome condensation;GO:0000281 mitotic cytokinesis;GO:0040001 establishment of mitotic spindle localization;GO:0045840 positive regulation of mitotic nuclear division;GO:0000070 mitotic sister chromatid segregation",
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    },
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            {
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            }
        ],
        "mass": 68638.0,
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        "protein_name": "Polypeptide N-acetylgalactosaminyltransferase",
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        "refseq_name": "polypeptide N-acetylgalactosaminyltransferase 9 isoform A",
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            {
                "id": "NP_001116116",
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            }
        ],
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        "protein_names_uniprotkb": "Polypeptide N-acetylgalactosaminyltransferase; 2.4.1.-; Protein-UDP acetylgalactosaminyltransferase",
        "protein_names_refseq": "UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 9; polypeptide N-acetylgalactosaminyltransferase 9 isoform A",
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        "pathway": " (R-RNO-913709)",
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        "function": "Catalyzes the initial reaction in O-linked oligosaccharide biosynthesis, the transfer of an N-acetyl-D-galactosamine residue to a serine or threonine residue on the protein receptor. Does not glycosylate apomucin or SDC3., [UniProtKB, UniProtKB, UniProtKB]",
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            },
            {
                "id": "2.4.1.41",
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                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0030246 carbohydrate binding;GO:0004653 polypeptide N-acetylgalactosaminyltransferase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus",
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            {
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            }
        ],
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        "protein_name": "43 kDa receptor-associated protein of the synapse",
        "gene_name": "Rapsn",
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        "refseq_name": "43 kDa receptor-associated protein of the synapse isoform 1",
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            {
                "id": "NP_001386657",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001386657",
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            }
        ],
        "gene_names_uniprotkb": "Rapsn",
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        "protein_names_uniprotkb": "43 kDa receptor-associated protein of the synapse; 43 kDa postsynaptic protein; Acetylcholine receptor-associated 43 kDa protein",
        "protein_names_refseq": "43 kDa receptor-associated protein of the synapse isoform 1; 43 kDa receptor-associated protein of the synapse; nicotinic acetylcholine receptor-associated 46K protein; receptor-associated protein of the synapse, 43 kDa",
        "tax_id": 10116,
        "disease": "congenital myasthenic syndrome 11 (Disease Ontology:DOID:0110675); fetal akinesia deformation sequence syndrome 2 (Disease Ontology:DOID:0111378)",
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        "function": "Postsynaptic protein required for clustering of nicotinic acetylcholine receptors (nAChRs) at the neuromuscular junction. It may link the receptor to the underlying postsynaptic cytoskeleton, possibly by direct association with actin or spectrin., [UniProtKB, UniProtKB]; Rapsyn binds to acetylcholine receptor at the cell surface, and its recruitment is induced by agrin GeneRIF: rapsyn binds to AChR at the cell surface, and its recruitment is induced by agrin., [RefSeq, PubMed]",
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            {
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        "go_molecular_function": "GO:0140693 molecular condensate scaffold activity;GO:0062072 histone H3K9me2/3 reader activity;GO:0106222 lncRNA binding;GO:0140038 histone H3K27cr reader activity;GO:0140017 histone H3K18cr reader activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0000785 chromatin;GO:0005634 nucleus",
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        "tax_id": 10116,
        "disease": "Williams-Beuren syndrome (Disease Ontology:DOID:1928)",
        "pathway": " (rno:304528);  (R-RNO-110312);  (R-RNO-110314);  (R-RNO-110320);  (R-RNO-174411);  (R-RNO-176187);  (R-RNO-5651801);  (R-RNO-5655862);  (R-RNO-5656121);  (R-RNO-5656169);  (R-RNO-5685938);  (R-RNO-5685942);  (R-RNO-5693537);  (R-RNO-5693607);  (R-RNO-5696397);  (R-RNO-5696400);  (R-RNO-6782135);  (R-RNO-6782210);  (R-RNO-6804756);  (R-RNO-69091);  (R-RNO-69473)",
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        "function": "Subunit of the replication factor C (RFC) complex which acts during elongation of primed DNA templates by DNA polymerases delta and epsilon, and is necessary for ATP-dependent loading of proliferating cell nuclear antigen (PCNA) onto primed DNA., [UniProtKB, UniProtKB]",
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        "protein_name": "AADACL2 family member 3 like 1",
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        ],
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        "disease": "Kufor-Rakeb syndrome (Disease Ontology:DOID:0060556); juvenile-onset Parkinson's disease (Disease Ontology:DOID:0060893); hereditary spastic paraplegia 78 (Disease Ontology:DOID:0112348); Parkinson's disease (Disease Ontology:DOID:14330); neuronal ceroid lipofuscinosis (Disease Ontology:DOID:14503); hereditary spastic paraplegia (Disease Ontology:DOID:2476); amyotrophic lateral sclerosis (Disease Ontology:DOID:332)",
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        "function": "ATPase which acts as a lysosomal polyamine exporter with high affinity for spermine. Also stimulates cellular uptake of polyamines and protects against polyamine toxicity. Plays a role in intracellular cation homeostasis and the maintenance of neuronal integrity. Contributes to cellular zinc homeostasis. Confers cellular protection against Mn(2+) and Zn(2+) toxicity and mitochondrial stress. Required for proper lysosomal and mitochondrial maintenance. Regulates the autophagy-lysosome pathway through the control of SYT11 expression at both transcriptional and post-translational levels. Facilitates recruitment of deacetylase HDAC6 to lysosomes to deacetylate CTTN, leading to actin polymerization, promotion of autophagosome-lysosome fusion and completion of autophagy. Promotes secretion of exosomes as well as secretion of SCNA via exosomes. Plays a role in lipid homeostasis., [UniProtKB, UniProtKB, UniProtKB]; Pink1 -/- rats show significantly decreased levels of Atp13a2, a transmembrane lysosomal P5-type ATPase suggesting a potential mechanism for the observed abnormal aggregation., [RefSeq, PubMed]; Regulation of intracellular manganese homeostasis by Kufor-Rakeb syndrome-associated ATP13A2 protein., [RefSeq, PubMed]",
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                "id": "NP_001094309",
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        "protein_name": "LIM homeobox transcription factor 1-beta",
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        "refseq_name": "LIM homeobox transcription factor 1-beta",
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            {
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        "function": "LMX1B may be considered to be a negative regulator of the renal fibrosis index., [RefSeq, PubMed]; Transcription factor involved in the regulation of podocyte-expressed genes. Essential for the specification of dorsal limb fate at both the zeugopodal and autopodal levels., [UniProtKB, UniProtKB]",
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        "protein_name": "RNA polymerase-associated protein CTR9 homolog",
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            {
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        "protein_name": "Ceramide synthase 2",
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            {
                "id": "NP_001028872",
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        "function": "Sciatic nerve injury promotes Schwann cell proliferation and migration through the regulation of miR-221/222 by targeting LASS2, [RefSeq, PubMed]",
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        "go_biological_process": "GO:0006688 glycosphingolipid biosynthetic process;GO:0046513 ceramide biosynthetic process;GO:0019216 regulation of lipid metabolic process;GO:0030148 sphingolipid biosynthetic process;GO:0009611 response to wounding",
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        "protein_name": "NHP2-like protein 1",
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            {
                "id": "XP_038956542",
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        "gene_names_uniprotkb": "Snu13l1; AABR07042323.1; RGD1566078",
        "gene_names_refseq": "Snu13l1",
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        "protein_names_refseq": "NHP2-like protein 1",
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        "function": "Common component of the spliceosome and rRNA processing machinery., [UniProtKB, UniProtKB]; Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome. Involved in pre-mRNA splicing as component of the spliceosome. Binds to the 5'-stem-loop of U4 snRNA and thereby contributes to spliceosome assembly. The protein undergoes a conformational change upon RNA-binding. Core component of box C/D small nucleolar ribonucleoprotein (snoRNP) complexes that function in methylation of multiple sites on ribosomal RNAs (rRNAs) and messenger RNAs (mRNAs)., [UniProtKB, UniProtKB]",
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        "protein_name": "L antigen family member 3",
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        "protein_name": "Choline/ethanolamine transporter FLVCR1",
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        "protein_names_uniprotkb": "Choline/ethanolamine transporter FLVCR1; Feline leukemia virus subgroup C receptor-related protein 1; Heme transporter FLVCR1",
        "protein_names_refseq": "FLVCR heme transporter 1; feline leukemia virus subgroup C cellular receptor 1; feline leukemia virus subgroup C receptor-related protein 1-like; feline leukemia virus subgroup C receptor-related protein 1; heme transporter FLVCR1",
        "tax_id": 10116,
        "disease": "neurodevelopmental disorder with microcephaly, absent speech, and hypotonia (Disease Ontology:DOID:0051030); retinopathy sensory neuropathy syndrome (Disease Ontology:DOID:0061157); Diamond-Blackfan anemia (Disease Ontology:DOID:1339)",
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            }
        ],
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        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 51F2-like; olfactory receptor 56; olfactory receptor Olr56; olfactory receptor family 51 subfamily F member 23C, pseudogene 1; olfactory receptor gene Olr56",
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            {
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        "function": "Amino acids H159 and E167 in the rbCLCA1 metalloprotease motif are important in rbCLCA1 processing for localization to the cell surface., [RefSeq, PubMed]; Dexamethasone substantially downregulates the expression of CLCA3 mRNA and Muc5ac protein in nasal mucosa in allergic rhinitis., [RefSeq, PubMed]",
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    {
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        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005829 cytosol;GO:0016020 membrane;GO:0031965 nuclear membrane;GO:0032541 cortical endoplasmic reticulum",
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        "protein_name": "Deleted in azoospermia-like",
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        "protein_name": "Probable ATP-dependent RNA helicase DDX56",
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        "tax_id": 10116,
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        "function": "Nucleolar RNA helicase that plays a role in various biological processes including innate immunity, ribosome biogenesis or nucleolus organization. Plays an essential role in maintaining nucleolar integrity in planarian stem cells. Maintains embryonic stem cells proliferation by conventional regulation of ribosome assembly and interaction with OCT4 and POU5F1 complex. Regulates antiviral innate immunity by inhibiting the virus-triggered signaling nuclear translocation of IRF3. Mechanistically, acts by disrupting the interaction between IRF3 and importin IPO5. May play a role in later stages of the processing of the pre-ribosomal particles leading to mature 60S ribosomal subunits. Has intrinsic ATPase activity., [UniProtKB, UniProtKB]",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0005520 insulin-like growth factor binding;GO:0048018 receptor ligand activity",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "GO:0071228 cellular response to tumor cell;GO:0001558 regulation of cell growth;GO:0009966 regulation of signal transduction",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B0BN16-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "B0BN63-1",
        "uniprot_id": [
            {
                "id": "B0BN63_RAT",
                "url": "https://www.uniprot.org/uniprot/B0BN63",
                "type": "external"
            }
        ],
        "mass": 38104.0,
        "length": 338,
        "protein_name": "Activator of 90 kDa heat shock protein ATPase homolog 1",
        "gene_name": "Ahsa1",
        "organism": "Rat",
        "refseq_name": "activator of 90 kDa heat shock protein ATPase homolog 1",
        "refseq_ac": [
            {
                "id": "NP_001108506",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001108506",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ahsa1; LOC681996",
        "gene_names_refseq": "Ahsa1",
        "protein_names_uniprotkb": "Activator of 90 kDa heat shock protein ATPase homolog 1",
        "protein_names_refseq": "AHA1, activator of heat shock 90kDa protein ATPase homolog 1; activator of 90 kDa heat shock protein ATPase homolog 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:681996)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Acts as a co-chaperone of HSP90AA1. Activates the ATPase activity of HSP90AA1 leading to increase in its chaperone activity. Competes with the inhibitory co-chaperone FNIP1 for binding to HSP90AA1, thereby providing a reciprocal regulatory mechanism for chaperoning of client proteins. Competes with the inhibitory co-chaperone TSC1 for binding to HSP90AA1, thereby providing a reciprocal regulatory mechanism for chaperoning of client proteins., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0051082 unfolded protein binding;GO:0051087 protein-folding chaperone binding;GO:0001671 ATPase activator activity;GO:0051879 Hsp90 protein binding;GO:0044183 protein folding chaperone",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005829 cytosol",
        "go_biological_process": "GO:0006457 protein folding;GO:0032781 positive regulation of ATP-dependent activity;GO:0036506 maintenance of unfolded protein",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B0BN63-1",
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        "kg_view_protein": true
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    {
        "uniprot_canonical_ac": "B0BN98-1",
        "uniprot_id": [
            {
                "id": "B0BN98_RAT",
                "url": "https://www.uniprot.org/uniprot/B0BN98",
                "type": "external"
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        ],
        "mass": 14933.0,
        "length": 126,
        "protein_name": "Protein LLP homolog",
        "gene_name": "Llph",
        "organism": "Rat",
        "refseq_name": "protein LLP homolog",
        "refseq_ac": [
            {
                "id": "NP_001127936",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001127936",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Llph; Llph-ps1",
        "gene_names_refseq": "Llph; RGD1308261",
        "protein_names_uniprotkb": "Protein LLP homolog; Protein LAPS18-like",
        "protein_names_refseq": "LLP homolog, long-term synaptic facilitation (Aplysia); protein LLP homolog",
        "tax_id": 10116,
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        "pathway": " (rno:299818)",
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        "go_molecular_function": "GO:0001099 basal RNA polymerase II transcription machinery binding",
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        "go_biological_process": "GO:0060999 positive regulation of dendritic spine development;GO:0097484 dendrite extension",
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            {
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        ],
        "mass": 40968.0,
        "length": 370,
        "protein_name": "2-Hydroxyacid oxidase 1",
        "gene_name": "Hao1",
        "organism": "Rat",
        "refseq_name": "2-Hydroxyacid oxidase 1",
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            {
                "id": "NP_001101250",
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        ],
        "gene_names_uniprotkb": "Hao1",
        "gene_names_refseq": "GOX; Gox1; HAOX1; Hao1; XDH1",
        "protein_names_uniprotkb": "2-Hydroxyacid oxidase 1; 1.1.3.15; 1.2.3.5; GOX; Glycolate oxidase; Glyoxylate oxidase; HAOX1",
        "protein_names_refseq": "2-Hydroxyacid oxidase 1; glycolate oxidase; glyoxylate oxidase; hydroxyacid oxidase (glycolate oxidase) 1; hydroxyacid oxidase 1, liver",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:311446);  (R-RNO-389661);  (R-RNO-9033241)",
        "pathway_count": 3,
        "publication_count": 5,
        "publication_id_list": "10777549;14578854;16396499;19758989;22673903",
        "class_list": "",
        "function": "Broad substrate specificity (S)-2-hydroxy-acid oxidase that preferentially oxidizes glycolate. The glyoxylate produced by the oxidation of glycolate can then be utilized by alanine-glyoxylate aminotransferase for the peroxisomal synthesis of glycine; this pathway appears to be an important step for the detoxification of glyoxylate which, if allowed to accumulate, may be metabolized to oxalate with formation of kidney stones. Can also catalyze the oxidation of glyoxylate, and long chain hydroxyacids such as 2-hydroxyhexadecanoate and 2-hydroxyoctanoate. Active in vitro with the artificial electron acceptor 2,6-dichlorophenolindophenol (DCIP), but O2 is believed to be the physiological electron acceptor, leading to the production of H2O2., [UniProtKB, UniProtKB]; Down-regulation of Hao1 during oxidative stress may provide mechanism to prevent excessive H2O2 formation in liver peroxisomes. May be prototype of response to oxidative injury involving down-regulation of reactive oxygen species-producing enzymes., [RefSeq, PubMed]; The turnover of the enzyme and the rate constant for flavin were pH-independent, suggesting the involvement of an unprotonated group acting as a base in the chemical step of glycolate oxidation., [RefSeq, PubMed]",
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                "id": "6.2.1.-",
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                "id": "3.6.1.-",
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        ],
        "go_molecular_function": "GO:0010181 FMN binding;GO:0003973 (S)-2-hydroxy-acid oxidase activity;GO:0047969 glyoxylate oxidase activity",
        "go_cellular_component": "GO:0005777 peroxisome;GO:0005782 peroxisomal matrix",
        "go_biological_process": "GO:0006545 glycine biosynthetic process;GO:0006979 response to oxidative stress;GO:0001561 fatty acid alpha-oxidation;GO:0046296 glycolate catabolic process",
        "synthesized_glycan_count": 0,
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        "kg_view_protein": true
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        "mass": 58986.0,
        "length": 567,
        "protein_name": "Peroxisomal leader peptide-processing protease",
        "gene_name": "Tysnd1",
        "organism": "Rat",
        "refseq_name": "peroxisomal leader peptide-processing protease",
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        "gene_names_uniprotkb": "Tysnd1",
        "gene_names_refseq": "Tysnd1",
        "protein_names_uniprotkb": "Peroxisomal leader peptide-processing protease; 3.4.21.-",
        "protein_names_refseq": "peroxisomal leader peptide-processing protease; trypsin domain containing 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:365571);  (R-RNO-9033241);  (R-RNO-9033500)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "17255948",
        "class_list": "",
        "function": "Peroxisomal protease that mediates both the removal of the leader peptide from proteins containing a PTS2 target sequence and processes several PTS1-containing proteins. Catalyzes the processing of PTS1-proteins involved in the peroxisomal beta-oxidation of fatty acids., [UniProtKB, UniProtKB, UniProtKB]; Tysnd1-mediated processing of the peroxisomal enzymes promotes their assembly into a supramolecular complex to enhance the rate of beta-oxidation., [RefSeq, PubMed]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 2,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
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        "reported_s_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_s_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [
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                "id": "1.1.3.15",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.1.3.15",
                "type": "external"
            },
            {
                "id": "1.2.3.5",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.2.3.5",
                "type": "external"
            },
            {
                "id": "3.4.21.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.21.-",
                "type": "external"
            },
            {
                "id": "2.3.2.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
                "type": "external"
            },
            {
                "id": "1.4.3.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.4.3.1",
                "type": "external"
            },
            {
                "id": "1.4.3.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.4.3.3",
                "type": "external"
            },
            {
                "id": "3.1.2.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.2.2",
                "type": "external"
            },
            {
                "id": "3.1.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.2.-",
                "type": "external"
            },
            {
                "id": "1.11.1.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.11.1.6",
                "type": "external"
            },
            {
                "id": "1.3.3.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.3.3.6",
                "type": "external"
            },
            {
                "id": "2.6.1.51",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.6.1.51",
                "type": "external"
            },
            {
                "id": "2.6.1.44",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.6.1.44",
                "type": "external"
            },
            {
                "id": "2.3.1.137",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.137",
                "type": "external"
            },
            {
                "id": "2.3.1.176",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.176",
                "type": "external"
            },
            {
                "id": "2.3.1.16",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.16",
                "type": "external"
            },
            {
                "id": "2.3.1.155",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.155",
                "type": "external"
            },
            {
                "id": "2.3.2.36",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.36",
                "type": "external"
            },
            {
                "id": "2.5.1.18",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.5.1.18",
                "type": "external"
            },
            {
                "id": "3.4.24.56",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.24.56",
                "type": "external"
            },
            {
                "id": "1.1.1.42",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.1.1.42",
                "type": "external"
            },
            {
                "id": "5.1.99.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.1.99.4",
                "type": "external"
            },
            {
                "id": "4.1.3.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.1.3.4",
                "type": "external"
            },
            {
                "id": "6.2.1.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.2.1.3",
                "type": "external"
            },
            {
                "id": "6.2.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.2.1.-",
                "type": "external"
            },
            {
                "id": "6.2.1.7",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.2.1.7",
                "type": "external"
            },
            {
                "id": "6.2.1.24",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.2.1.24",
                "type": "external"
            },
            {
                "id": "6.2.1.15",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.2.1.15",
                "type": "external"
            },
            {
                "id": "1.14.13.39",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.14.13.39",
                "type": "external"
            },
            {
                "id": "3.4.21.53",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.21.53",
                "type": "external"
            },
            {
                "id": "5.3.3.8",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.3.3.8",
                "type": "external"
            },
            {
                "id": "5.3.3.21",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.3.3.21",
                "type": "external"
            },
            {
                "id": "3.1.2.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.2.27",
                "type": "external"
            },
            {
                "id": "2.3.1.65",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.65",
                "type": "external"
            },
            {
                "id": "3.6.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.-",
                "type": "external"
            },
            {
                "id": "3.6.1.77",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.77",
                "type": "external"
            },
            {
                "id": "2.3.1.7",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.7",
                "type": "external"
            },
            {
                "id": "4.1.2.63",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.1.2.63",
                "type": "external"
            },
            {
                "id": "3.1.2.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.2.1",
                "type": "external"
            },
            {
                "id": "3.1.2.11",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.2.11",
                "type": "external"
            },
            {
                "id": "3.1.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.2.3",
                "type": "external"
            },
            {
                "id": "3.1.2.5",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.2.5",
                "type": "external"
            },
            {
                "id": "1.1.1.300",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.1.1.300",
                "type": "external"
            },
            {
                "id": "1.1.1.184",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.1.1.184",
                "type": "external"
            },
            {
                "id": "4.1.1.9",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.1.1.9",
                "type": "external"
            },
            {
                "id": "2.3.1.42",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.42",
                "type": "external"
            },
            {
                "id": "1.3.1.38",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.3.1.38",
                "type": "external"
            },
            {
                "id": "2.7.4.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.6",
                "type": "external"
            },
            {
                "id": "1.3.1.124",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.3.1.124",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0002020 protease binding;GO:0004252 serine-type endopeptidase activity;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005777 peroxisome;GO:0005782 peroxisomal matrix",
        "go_biological_process": "GO:0006508 proteolysis;GO:0016485 protein processing;GO:0031998 regulation of fatty acid beta-oxidation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "B1H261-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "B1WBS6-1",
        "uniprot_id": [
            {
                "id": "B1WBS6_RAT",
                "url": "https://www.uniprot.org/uniprot/B1WBS6",
                "type": "external"
            }
        ],
        "mass": 73262.0,
        "length": 646,
        "protein_name": "beta-galactosidase",
        "gene_name": "Glb1l",
        "organism": "Rat",
        "refseq_name": "beta-galactosidase-1-like protein precursor",
        "refseq_ac": [
            {
                "id": "NP_001121001",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001121001",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Glb1l",
        "gene_names_refseq": "Glb1l",
        "protein_names_uniprotkb": "beta-galactosidase; 3.2.1.23",
        "protein_names_refseq": "beta-galactosidase-1-like protein precursor; beta-galactosidase-1-like protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:301525);  (R-RNO-2022857);  (R-RNO-2024101);  (R-RNO-9840310)",
        "pathway_count": 4,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Cleaves beta-linked terminal galactosyl residues from gangliosides, glycoproteins, and glycosaminoglycans., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "3.2.1.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.2.1.23",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0004565 beta-galactosidase activity",
        "go_cellular_component": "GO:0005773 vacuole",
        "go_biological_process": "GO:0019388 galactose catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B1WBS6-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "B1WBV3-1",
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            {
                "id": "B1WBV3_RAT",
                "url": "https://www.uniprot.org/uniprot/B1WBV3",
                "type": "external"
            }
        ],
        "mass": 40636.0,
        "length": 369,
        "protein_name": "Glucose-fructose oxidoreductase domain-containing protein 2",
        "gene_name": "Gfod2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Gfod2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Glucose-fructose oxidoreductase domain-containing protein 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:307801)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Promotes matrix assembly., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "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:0016491 oxidoreductase activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0031012 extracellular matrix",
        "go_biological_process": "GO:0030198 extracellular matrix organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B1WBV3-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
                "id": "B1WBZ9_RAT",
                "url": "https://www.uniprot.org/uniprot/B1WBZ9",
                "type": "external"
            }
        ],
        "mass": 34022.0,
        "length": 299,
        "protein_name": "Katanin regulatory subunit B1 like 1",
        "gene_name": "Katnbl1",
        "organism": "Rat",
        "refseq_name": "KATNB1-like protein 1",
        "refseq_ac": [
            {
                "id": "NP_001103115",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001103115",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Katnbl1",
        "gene_names_refseq": "Katnbl1",
        "protein_names_uniprotkb": "Katanin regulatory subunit B1 like 1",
        "protein_names_refseq": "KATNB1-like protein 1; katanin p80 subunit B-like 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:691543)",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0008017 microtubule binding",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0005856 cytoskeleton;GO:0008352 katanin complex;GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0051495 positive regulation of cytoskeleton organization;GO:0031122 cytoplasmic microtubule organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B1WBZ9-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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            {
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                "type": "external"
            }
        ],
        "mass": 29294.0,
        "length": 261,
        "protein_name": "protein-serine/threonine phosphatase",
        "gene_name": "Ctdsp1",
        "organism": "Rat",
        "refseq_name": "carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1",
        "refseq_ac": [
            {
                "id": "NP_001121551",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001121551",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ctdsp1",
        "gene_names_refseq": "Ctdsp1",
        "protein_names_uniprotkb": "protein-serine/threonine phosphatase; 3.1.3.16",
        "protein_names_refseq": "CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 1; carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1",
        "tax_id": 10116,
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        "pathway": " (rno:363249)",
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        "go_molecular_function": "GO:0005507 copper ion binding;GO:0004500 dopamine beta-monooxygenase activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0030667 secretory granule membrane",
        "go_biological_process": "GO:0042420 dopamine catabolic process;GO:0006589 octopamine biosynthetic process;GO:0042421 norepinephrine biosynthetic process",
        "synthesized_glycan_count": 0,
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        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3Z8G7-1",
        "uniprot_id": [
            {
                "id": "D3Z8G7_RAT",
                "url": "https://www.uniprot.org/uniprot/D3Z8G7",
                "type": "external"
            }
        ],
        "mass": 100219.0,
        "length": 911,
        "protein_name": "Tight junction protein 3",
        "gene_name": "Tjp3",
        "organism": "Rat",
        "refseq_name": "tight junction protein ZO-3 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001424894",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001424894",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tjp3",
        "gene_names_refseq": "Tjp3",
        "protein_names_uniprotkb": "Tight junction protein 3",
        "protein_names_refseq": "tight junction protein ZO-3 isoform 1; tight junction protein ZO-3",
        "tax_id": 10116,
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        "publication_id_list": "16641100;22673903",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0005911 cell-cell junction",
        "go_biological_process": "GO:2000045 regulation of G1/S transition of mitotic cell cycle",
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        "hit_score": 0.3,
        "record_id": "D3Z8G7-1",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3Z922-1",
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            {
                "id": "D3Z922_RAT",
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            }
        ],
        "mass": 15451.0,
        "length": 136,
        "protein_name": "V-set pre-B cell surrogate light chain 1B",
        "gene_name": "Vpreb1a; Vpreb1b",
        "organism": "Rat",
        "refseq_name": "immunoglobulin iota chain precursor",
        "refseq_ac": [
            {
                "id": "NP_001102315",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102315",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Vpreb1a; Vpreb1b; Vpreb1a; Vpreb1b",
        "gene_names_refseq": "Vpreb1a; Vpreb1",
        "protein_names_uniprotkb": "V-set pre-B cell surrogate light chain 1B",
        "protein_names_refseq": "Immunoglobulin lambda Vpreb1 chain; V-set pre-B cell surrogate light chain 1; immunoglobulin iota chain precursor; immunoglobulin iota chain; immunoglobulin omega chain-like; pre-B lymphocyte 1; pre-B lymphocyte gene 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:303782);  (rno:363830)",
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        "function": "Associates with the Ig-mu chain to form a molecular complex that is expressed on the surface of pre-B-cells. This complex presumably regulates Ig gene rearrangements in the early steps of B-cell differentiation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0019814 immunoglobulin complex;GO:0005886 plasma membrane;GO:0009897 external side of plasma membrane",
        "go_biological_process": "GO:0006955 immune response;GO:0001782 B cell homeostasis;GO:0042100 B cell proliferation;GO:0000902 cell morphogenesis;GO:0030097 hemopoiesis",
        "synthesized_glycan_count": 0,
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    },
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        "uniprot_canonical_ac": "D3Z980-1",
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            {
                "id": "D3Z980_RAT",
                "url": "https://www.uniprot.org/uniprot/D3Z980",
                "type": "external"
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        ],
        "mass": 87051.0,
        "length": 767,
        "protein_name": "Cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2",
        "gene_name": "Cmtr2",
        "organism": "Rat",
        "refseq_name": "cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2",
        "refseq_ac": [
            {
                "id": "NP_001099656",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099656",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Cmtr2; Ftsjd1",
        "gene_names_refseq": "Cmtr2; Ftsjd1; RGD1309394",
        "protein_names_uniprotkb": "Cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2; 2.1.1.296; Cap methyltransferase 2; Cap2 2'O-ribose methyltransferase 2; FtsJ methyltransferase domain-containing protein 1",
        "protein_names_refseq": "FtsJ methyltransferase domain containing 1; cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2; ftsJ methyltransferase domain-containing protein 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:292016)",
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        "publication_id_list": "29393594",
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        "function": "S-adenosyl-L-methionine-dependent methyltransferase that mediates mRNA cap2 2'-O-ribose methylation to the 5'-cap structure of mRNAs. Methylates the ribose of the second nucleotide of a m(7)GpppG-capped mRNA and small nuclear RNA (snRNA) (cap0) to produce m(7)GpppRmpNm (cap2). Recognizes a guanosine cap on RNA independently of its N(7) methylation status. Display cap2 methylation on both cap0 and cap1. Displays a preference for cap1 RNAs., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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                "id": "2.1.1.296",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.296",
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            }
        ],
        "go_molecular_function": "GO:0004483 methyltransferase cap1 activity;GO:0120550 methyltransferase cap2 activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
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                "id": "D3ZA29_RAT",
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        ],
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        "length": 310,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5w12",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr578",
        "refseq_ac": [
            {
                "id": "NP_001000568",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000568",
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            }
        ],
        "gene_names_uniprotkb": "Or5w12",
        "gene_names_refseq": "Olr578; Or5w12",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 578; olfactory receptor Olr578; olfactory receptor gene Olr578",
        "tax_id": 10116,
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        "pathway": " (rno:366109)",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "record_id": "D3ZA29-1",
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        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
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            {
                "id": "D3ZA46_RAT",
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                "type": "external"
            }
        ],
        "mass": 107197.0,
        "length": 969,
        "protein_name": "Gem-interacting protein",
        "gene_name": "Gmip",
        "organism": "Rat",
        "refseq_name": "GEM-interacting protein",
        "refseq_ac": [
            {
                "id": "NP_001100778",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100778",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Gmip",
        "gene_names_refseq": "Gmip; RGD1565577",
        "protein_names_uniprotkb": "Gem-interacting protein",
        "protein_names_refseq": "GEM-interacting protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:306357);  (R-RNO-8980692);  (R-RNO-9013148);  (R-RNO-9013149)",
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        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0035556 intracellular signal transduction;GO:0051058 negative regulation of small GTPase mediated signal transduction;GO:0007264 small GTPase-mediated signal transduction",
        "synthesized_glycan_count": 0,
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        "record_id": "D3ZA46-1",
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        "filter_code": "0000000.0000101.010000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZA93-1",
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                "id": "D3ZA93_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZA93",
                "type": "external"
            }
        ],
        "mass": 13623.0,
        "length": 126,
        "protein_name": "Acyl-coenzyme A thioesterase 13",
        "gene_name": "Acot13",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Acot13",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Acyl-coenzyme A thioesterase 13; 3.1.2.2; Hotdog-fold thioesterase superfamily member 2; Palmitoyl-CoA hydrolase; Thioesterase superfamily member 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:291135);  (R-RNO-77289)",
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        "publication_count": 0,
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        "class_list": "",
        "function": "Catalyzes the hydrolysis of acyl-CoAs into free fatty acids and coenzyme A (CoASH), regulating their respective intracellular levels. Has acyl-CoA thioesterase activity towards medium (C12) and long-chain (C18) fatty acyl-CoA substrates. Can also hydrolyze 3-hydroxyphenylacetyl-CoA and 3,4-dihydroxyphenylacetyl-CoA (in vitro). May play a role in controlling adaptive thermogenesis., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "3.1.2.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.2.2",
                "type": "external"
            },
            {
                "id": "3.5.2.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.5.2.6",
                "type": "external"
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
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        "length": 504,
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            {
                "id": "NP_001102772",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102772",
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        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); hypertension (Disease Ontology:DOID:10763); dilated cardiomyopathy (Disease Ontology:DOID:12930); lymphangioleiomyomatosis (Disease Ontology:DOID:3319); congestive heart failure (Disease Ontology:DOID:6000); hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (rno:501099);  (R-RNO-5663220);  (R-RNO-9031628)",
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        "function": "Acidosis-Induced Regulation of Egr1 and Ccn1 In Vitro and in Experimental Tumours In Vivo., [RefSeq, PubMed]; Crucial role of serum response factor in renal tubular epithelial cell epithelial-mesenchymal transition in hyperuricemic nephropathy., [RefSeq, PubMed]; SRF and SRF Cofactor mRNA Expression Is Differentially Regulated by BDNF Stimulation in Cortical Neurons., [RefSeq, PubMed]; SRF is a transcription factor that binds to the serum response element (SRE), a short sequence of dyad symmetry located 300 bp to the 5' of the site of transcription initiation of some genes (such as FOS). Together with MRTFA transcription coactivator, controls expression of genes regulating the cytoskeleton during development, morphogenesis and cell migration. The SRF-MRTFA complex activity responds to Rho GTPase-induced changes in cellular globular actin (G-actin) concentration, thereby coupling cytoskeletal gene expression to cytoskeletal dynamics. Required for cardiac differentiation and maturation., [UniProtKB, UniProtKB]; Serum response factor promoting axonal regeneration by activating the Ras-Raf-Cofilin signaling pathway after the spinal cord injury., [RefSeq, PubMed]; Serum response factor, a novel early diagnostic biomarker of acute kidney injury., [RefSeq, PubMed]",
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            {
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        "tax_id": 10116,
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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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        "length": 92,
        "protein_name": "Dolichol-phosphate mannosyltransferase subunit 3",
        "gene_name": "Dpm3",
        "organism": "Rat",
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            {
                "id": "NP_001102801",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102801",
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        ],
        "gene_names_uniprotkb": "Dpm3; Dpm3-ps1; LOC100910177",
        "gene_names_refseq": "Dpm3; RGD1561807",
        "protein_names_uniprotkb": "Dolichol-phosphate mannosyltransferase subunit 3",
        "protein_names_refseq": "dolichol-phosphate mannosyltransferase subunit 3; dolichyl-phosphate mannosyltransferase polypeptide 3",
        "tax_id": 10116,
        "disease": "congenital disorder of glycosylation type I (Disease Ontology:DOID:0050570); muscular dystrophy-dystroglycanopathy type B15 (Disease Ontology:DOID:0112376)",
        "pathway": " (rno:502017);  (R-RNO-162699)",
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        "function": "Stabilizer subunit of the dolichol-phosphate mannose (DPM) synthase complex; tethers catalytic subunit to the ER., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008047 enzyme activator activity",
        "go_cellular_component": "GO:0033185 dolichol-phosphate-mannose synthase complex;GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0009101 glycoprotein biosynthetic process;GO:0043048 dolichyl monophosphate biosynthetic process;GO:0180047 dolichol phosphate mannose biosynthetic process",
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        ],
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        "length": 287,
        "protein_name": "Programmed cell death protein 1",
        "gene_name": "Pdcd1",
        "organism": "Rat",
        "refseq_name": "programmed cell death protein 1",
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            {
                "id": "NP_001100397",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100397",
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        "gene_names_refseq": "Pdcd1",
        "protein_names_uniprotkb": "Programmed cell death protein 1",
        "protein_names_refseq": "programmed cell death protein 1-like; programmed cell death protein 1",
        "tax_id": 10116,
        "disease": "infantile onset multisystem autoimmune disease 4 (Disease Ontology:DOID:0061163); Cryptococcal meningitis (Disease Ontology:DOID:0080159); lupus nephritis (Disease Ontology:DOID:0080162); stomach cancer (Disease Ontology:DOID:10534); pre-eclampsia (Disease Ontology:DOID:10591); anogenital venereal wart (Disease Ontology:DOID:11168); hepatitis A (Disease Ontology:DOID:12549); respiratory syncytial virus infectious disease (Disease Ontology:DOID:1273); dilated cardiomyopathy (Disease Ontology:DOID:12930); toxic shock syndrome (Disease Ontology:DOID:14115); hepatitis C (Disease Ontology:DOID:1883); hepatitis B (Disease Ontology:DOID:2043); autoimmune hepatitis (Disease Ontology:DOID:2048); hepatitis (Disease Ontology:DOID:2237); pulmonary tuberculosis (Disease Ontology:DOID:2957); lung adenocarcinoma (Disease Ontology:DOID:3910); tuberculosis (Disease Ontology:DOID:399); renal cell carcinoma (Disease Ontology:DOID:4450); anti-basement membrane glomerulonephritis (Disease Ontology:DOID:4780); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); hepatocellular carcinoma (Disease Ontology:DOID:684); periodontitis (Disease Ontology:DOID:824); cervix uteri carcinoma in situ (Disease Ontology:DOID:8991); systemic lupus erythematosus (Disease Ontology:DOID:9074)",
        "pathway": " (rno:301626);  (R-RNO-389948);  (R-RNO-9931295)",
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        "publication_id_list": "34170847;34847253",
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        "function": "A newly intervention strategy in preeclampsia: Targeting PD-1/Tim-3 signaling pathways to modulate the polarization of decidual macrophages., [RefSeq, PubMed]; Programmed death-1 mediates venous neointimal hyperplasia in humans and rats., [RefSeq, PubMed]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0005198 structural molecule activity;GO:0045296 cadherin binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0048471 perinuclear region of cytoplasm",
        "go_biological_process": "GO:0007165 signal transduction;GO:0043124 negative regulation of canonical NF-kappaB signal transduction;GO:1900026 positive regulation of substrate adhesion-dependent cell spreading;GO:0050777 negative regulation of immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZMI6-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZMU8-1",
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            {
                "id": "D3ZMU8_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZMU8",
                "type": "external"
            }
        ],
        "mass": 85532.0,
        "length": 765,
        "protein_name": "SIM bHLH transcription factor 1",
        "gene_name": "Sim1",
        "organism": "Rat",
        "refseq_name": "single-minded homolog 1",
        "refseq_ac": [
            {
                "id": "NP_001101111",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001101111",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Sim1",
        "gene_names_refseq": "Sim1",
        "protein_names_uniprotkb": "SIM bHLH transcription factor 1",
        "protein_names_refseq": "single-minded 1; single-minded family bHLH transcription factor 1; single-minded homolog 1",
        "tax_id": 10116,
        "disease": "obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:309888)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Transcriptional factor that may have pleiotropic effects during embryogenesis and in the adult., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "predicted_s_glycosites": 0,
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        "go_molecular_function": "GO:0046982 protein heterodimerization activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007399 nervous system development;GO:0030154 cell differentiation;GO:0006355 regulation of DNA-templated transcription",
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            {
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        ],
        "mass": 28779.0,
        "length": 263,
        "protein_name": "Src-like-adapter 2",
        "gene_name": "Sla2",
        "organism": "Rat",
        "refseq_name": "src-like-adapter 2",
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            {
                "id": "NP_001165589",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001165589",
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            }
        ],
        "gene_names_uniprotkb": "Sla2",
        "gene_names_refseq": "RGD1562071; Sla2",
        "protein_names_uniprotkb": "Src-like-adapter 2; Src-like adapter protein 2",
        "protein_names_refseq": "src-like-adapter 2",
        "tax_id": 10116,
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        "pathway": " (rno:499931)",
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        "publication_id_list": "",
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        "function": "Adapter protein, which negatively regulates T-cell receptor (TCR) signaling. Inhibits T-cell antigen-receptor induced activation of nuclear factor of activated T-cells. May act by linking signaling proteins such as ZAP70 with CBL, leading to a CBL dependent degradation of signaling proteins., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0035591 signaling adaptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0031410 cytoplasmic vesicle;GO:0005770 late endosome;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0050849 negative regulation of calcium-mediated signaling;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0042110 T cell activation;GO:0050860 negative regulation of T cell receptor signaling pathway",
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        "kg_view_protein": true
    },
    {
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            {
                "id": "D3ZN69_RAT",
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            }
        ],
        "mass": 86546.0,
        "length": 754,
        "protein_name": "Serine/threonine-protein phosphatase with EF-hands",
        "gene_name": "Ppef2",
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        "refseq_name": "serine/threonine-protein phosphatase with EF-hands 2",
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            {
                "id": "NP_001100680",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100680",
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        "gene_names_refseq": "Ppef2",
        "protein_names_uniprotkb": "Serine/threonine-protein phosphatase with EF-hands; 3.1.3.16",
        "protein_names_refseq": "protein phosphatase, EF hand calcium-binding domain 2; serine/threonine-protein phosphatase with EF-hands 2",
        "tax_id": 10116,
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        "pathway": " (rno:305246)",
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        "class_list": "",
        "function": "May play a role in phototransduction. May dephosphorylate photoactivated rhodopsin. May function as a calcium sensing regulator of ionic currents, energy production or synaptic transmission., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.53",
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                "id": "3.1.3.52",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.52",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.67",
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                "id": "3.1.3.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.-",
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                "id": "3.1.3.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.27",
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                "id": "2.7.11.22",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.22",
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                "id": "3.1.3.74",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.74",
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        ],
        "go_molecular_function": "GO:0005506 iron ion binding;GO:0030145 manganese ion binding;GO:0005509 calcium ion binding;GO:0004722 protein serine/threonine phosphatase activity;GO:0051879 Hsp90 protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol",
        "go_biological_process": "GO:0050906 detection of stimulus involved in sensory perception;GO:0007601 visual perception;GO:0070301 cellular response to hydrogen peroxide;GO:0043409 negative regulation of MAPK cascade;GO:2001234 negative regulation of apoptotic signaling pathway",
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                "url": "https://www.uniprot.org/uniprot/D3ZND9",
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        ],
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        "length": 529,
        "protein_name": "Serine/threonine-protein kinase RIO3",
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        "protein_names_uniprotkb": "Serine/threonine-protein kinase RIO3; 2.7.11.1",
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        "function": "Serine/threonine-protein kinase involved in a ribosome quality control that takes place when ribosomes have stalled, leading to 18S non-functional rRNA decay and degradation of the 40S ribosomal subunit. Acts downstream of RNF10: specifically recognizes and binds RPS2/us5 and RPS3/us3 monoubiquitinated by RNF10, promoting degradation of the 40S ribosomal subunit in a kinase-dependent manner. The RNF10-RIOK3 ribosome quality control takes place in response to ribosome subunit imbalance or downstream the EIF2AK4/GCN2-mediated integrated stress response (ISR). Also involved in regulation of type I interferon (IFN)-dependent immune response, possibly by acting as an adapter protein essential for the recruitment of TBK1 to IRF3. Phosphorylates IFIH1 on 'Ser-828' interfering with IFIH1 filament assembly on long dsRNA and resulting in attenuated IFIH1-signaling. Can inhibit CASP10 isoform 7-mediated activation of the NF-kappa-B signaling pathway., [UniProtKB, UniProtKB]",
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        "ec_number_list": [
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        "protein_names_refseq": "olfactory receptor 783; olfactory receptor Olr783; olfactory receptor gene Olr783",
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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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        "refseq_name": "olfactory receptor Olr1630",
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            {
                "id": "NP_001000092",
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            }
        ],
        "gene_names_uniprotkb": "Or4k5; Olr1630",
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        "protein_names_refseq": "ATP-dependent RNA helicase DHX33; DEAH (Asp-Glu-Ala-His) box polypeptide 33; putative ATP-dependent RNA helicase DHX33",
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        "function": "Implicated in nucleolar organization, ribosome biogenesis, protein synthesis and cytoplasmic dsRNA sensing. Stimulates RNA polymerase I transcription of the 47S precursor rRNA. Associates with ribosomal DNA (rDNA) loci where it is involved in POLR1A recruitment. In the cytoplasm, promotes elongation-competent 80S ribosome assembly at the late stage of mRNA translation initiation. Senses cytosolic dsRNA mediating NLRP3 inflammasome formation in macrophages and type I interferon production in myeloid dendritic cells. Required for NLRP3 activation induced by viral dsRNA and bacterial RNA. In dendritic cells, required for induction of type I interferon production induced by cytoplasmic dsRNA via the activation of MAPK and NF-kappa-B signaling pathways., [UniProtKB, UniProtKB, UniProtKB]",
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            {
                "id": "3.6.5.-",
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                "id": "3.1.-.-",
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            {
                "id": "3.6.1.-",
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            {
                "id": "2.7.4.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.3",
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            {
                "id": "3.1.4.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.4.-",
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            {
                "id": "3.4.24.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.24.-",
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            {
                "id": "3.6.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.-.-",
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                "id": "3.4.21.53",
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        ],
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0072559 NLRP3 inflammasome complex",
        "go_biological_process": "GO:0043410 positive regulation of MAPK cascade;GO:0006413 translational initiation;GO:0045943 positive regulation of transcription by RNA polymerase I;GO:0032481 positive regulation of type I interferon production;GO:1900227 positive regulation of NLRP3 inflammasome complex assembly",
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        ],
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        "protein_name": "Terminal nucleotidyltransferase 4A",
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            {
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        "protein_names_uniprotkb": "Terminal nucleotidyltransferase 4A; 2.7.7.19; DNA polymerase sigma; Non-canonical poly(A) RNA polymerase PAPD7; PAP-associated domain-containing protein 7; TRAMP-like complex polyadenylate polymerase; Terminal guanylyltransferase",
        "protein_names_refseq": "DNA polymerase sigma; PAP associated domain containing 7; non-canonical poly(A) RNA polymerase PAPD7; poly(A) RNA polymerase D7, non-canonical; polymerase (DNA directed) sigma; terminal nucleotidyltransferase 4A isoform 1",
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        "function": "Terminal nucleotidyltransferase that catalyzes preferentially the transfer of ATP and GTP on RNA 3' poly(A) tail creating a heterogeneous 3' poly(A) tail leading to mRNAs stabilization by protecting mRNAs from active deadenylation. Also functions as a catalytic subunit of a TRAMP-like complex which has a poly(A) RNA polymerase activity and is involved in a post-transcriptional quality control mechanism. Polyadenylation with short oligo(A) tails is required for the degradative activity of the exosome on several of its nuclear RNA substrates. Has no terminal uridylyltransferase activity, and does not play a role in replication-dependent histone mRNA degradation via uridylation., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0009410 response to xenobiotic stimulus;GO:0031123 RNA 3'-end processing;GO:1905870 positive regulation of 3'-UTR-mediated mRNA stabilization;GO:0060212 negative regulation of nuclear-transcribed mRNA poly(A) tail shortening;GO:0043634 polyadenylation-dependent ncRNA catabolic process",
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        "protein_name": "Vacuolar protein sorting-associated protein 11 homolog",
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        "gene_names_refseq": "Vps11",
        "protein_names_uniprotkb": "Vacuolar protein sorting-associated protein 11 homolog",
        "protein_names_refseq": "VPS11 CORVET/HOPS core subunit; vacuolar protein sorting 11 homolog; vacuolar protein sorting-associated protein 11 homolog",
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        "disease": "hypomyelinating leukoencephalopathy (Disease Ontology:DOID:0050987); hypomyelinating leukodystrophy 12 (Disease Ontology:DOID:0060796); dystonia 32 (Disease Ontology:DOID:0060939)",
        "pathway": " (rno:315600)",
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        "function": "Plays a role in vesicle-mediated protein trafficking to lysosomal compartments including the endocytic membrane transport and autophagic pathways. Believed to act as a core component of the putative HOPS and CORVET endosomal tethering complexes., [UniProtKB, UniProtKB]",
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        "pathway": " (rno:305420);  (R-RNO-141430);  (R-RNO-174048);  (R-RNO-174084);  (R-RNO-174154);  (R-RNO-174178);  (R-RNO-174184);  (R-RNO-176407);  (R-RNO-176408);  (R-RNO-176412);  (R-RNO-179409);  (R-RNO-2467813);  (R-RNO-2559582);  (R-RNO-68867);  (R-RNO-69017);  (R-RNO-983168)",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:7.2.2.-",
                "type": "external"
            },
            {
                "id": "3.6.1.15",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.15",
                "type": "external"
            },
            {
                "id": "3.6.4.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.6",
                "type": "external"
            },
            {
                "id": "3.1.3.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.1",
                "type": "external"
            },
            {
                "id": "3.9.1.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.9.1.1",
                "type": "external"
            },
            {
                "id": "6.1.1.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.1.1.12",
                "type": "external"
            },
            {
                "id": "3.6.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.-",
                "type": "external"
            },
            {
                "id": "2.7.4.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.3",
                "type": "external"
            },
            {
                "id": "3.1.4.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.4.-",
                "type": "external"
            },
            {
                "id": "3.4.24.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.24.-",
                "type": "external"
            },
            {
                "id": "3.6.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.-.-",
                "type": "external"
            },
            {
                "id": "3.4.21.53",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.21.53",
                "type": "external"
            },
            {
                "id": "5.6.2.5",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.5",
                "type": "external"
            },
            {
                "id": "3.1.26.n2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.26.n2",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0003723 RNA binding;GO:0005524 ATP binding;GO:0016787 hydrolase activity;GO:0032574 5'-3' RNA helicase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol;GO:0000932 P-body;GO:0036464 cytoplasmic ribonucleoprotein granule;GO:0043186 P granule",
        "go_biological_process": "GO:0051607 defense response to virus;GO:0035194 regulatory ncRNA-mediated post-transcriptional gene silencing;GO:0035279 miRNA-mediated gene silencing by mRNA destabilization;GO:0035195 miRNA-mediated post-transcriptional gene silencing;GO:0061014 positive regulation of mRNA catabolic process",
        "synthesized_glycan_count": 0,
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        "record_id": "D3ZUC2-1",
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        "kg_view_protein": true
    },
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            {
                "id": "D3ZUI1_RAT",
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            }
        ],
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        "protein_name": "Methylthioribulose-1-phosphate dehydratase",
        "gene_name": "Apip",
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        "refseq_name": "methylthioribulose-1-phosphate dehydratase",
        "refseq_ac": [
            {
                "id": "NP_001099962",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099962",
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            }
        ],
        "gene_names_uniprotkb": "Apip; APIP",
        "gene_names_refseq": "Apip; RGD1564562",
        "protein_names_uniprotkb": "Methylthioribulose-1-phosphate dehydratase; 4.2.1.109; APAF1-interacting protein; MTRu-1-P dehydratase",
        "protein_names_refseq": "methylthioribulose-1-phosphate dehydratase; probable methylthioribulose-1-phosphate dehydratase",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295961);  (R-RNO-111458);  (R-RNO-9627069)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the dehydration of methylthioribulose-1-phosphate (MTRu-1-P) into 2,3-diketo-5-methylthiopentyl-1-phosphate (DK-MTP-1-P). Functions in the methionine salvage pathway, which plays a key role in cancer, apoptosis, microbial proliferation and inflammation. May inhibit the CASP1-related inflammatory response (pyroptosis), the CASP9-dependent apoptotic pathway and the cytochrome c-dependent and APAF1-mediated cell death., [UniProtKB, HAMAP, UniProtKB]",
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        "biomarker_type": "",
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            {
                "id": "4.2.1.109",
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            },
            {
                "id": "3.4.22.62",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.22.62",
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            }
        ],
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0012505 endomembrane system",
        "go_biological_process": "GO:0043066 negative regulation of apoptotic process;GO:0051289 protein homotetramerization;GO:0006915 apoptotic process;GO:0070269 pyroptotic inflammatory response;GO:0070372 regulation of ERK1 and ERK2 cascade",
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        "kg_view_protein": true
    },
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        "uniprot_canonical_ac": "D3ZUL8-1",
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            {
                "id": "D3ZUL8_RAT",
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            }
        ],
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        "protein_name": "Zinc finger CCHC domain-containing protein 8",
        "gene_name": "Zcchc8",
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        "refseq_name": "zinc finger CCHC domain-containing protein 8",
        "refseq_ac": [
            {
                "id": "NP_001387897",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001387897",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Zcchc8",
        "gene_names_refseq": "Zcchc8",
        "protein_names_uniprotkb": "Zinc finger CCHC domain-containing protein 8; TRAMP-like complex RNA-binding factor ZCCHC8",
        "protein_names_refseq": "zinc finger CCHC domain-containing protein 8; zinc finger, CCHC domain containing 8",
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        "disease": "",
        "pathway": " (rno:288661);  (R-RNO-9930044)",
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        "function": "Scaffolding subunit of the trimeric nuclear exosome targeting (NEXT) complex that is involved in the surveillance and turnover of aberrant transcripts and non-coding RNAs. NEXT functions as an RNA exosome cofactor that directs a subset of non-coding short-lived RNAs for exosomal degradation. May be involved in pre-mRNA splicing. It is required for 3'-end maturation of telomerase RNA component (TERC), TERC 3'-end targeting to the nuclear RNA exosome, and for telomerase function., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0006396 RNA processing;GO:0031124 mRNA 3'-end processing;GO:0180034 co-transcriptional lncRNA 3' end processing, cleavage and polyadenylation pathway",
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    },
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        "uniprot_canonical_ac": "D3ZV49-1",
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            {
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            }
        ],
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        "length": 551,
        "protein_name": "Autoimmune regulator",
        "gene_name": "Aire",
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        "refseq_name": "autoimmune regulator isoform 1",
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            {
                "id": "NP_001421546",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001421546",
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            }
        ],
        "gene_names_uniprotkb": "Aire",
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        "protein_names_refseq": "autoimmune regulator (autoimmune polyendocrinopathy candidiasis ectodermal dystrophy); autoimmune regulator isoform 1",
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        "disease": "autoimmune polyendocrine syndrome type 1 (Disease Ontology:DOID:0050167); Guillain-Barre syndrome (Disease Ontology:DOID:12842); Sjogren's syndrome (Disease Ontology:DOID:12894); autoimmune polyendocrine syndrome (Disease Ontology:DOID:14040)",
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        "go_molecular_function": "GO:0003682 chromatin binding;GO:0008270 zinc ion binding;GO:0042802 identical protein binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0042393 histone binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0016604 nuclear body",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription;GO:0032722 positive regulation of chemokine production;GO:0045893 positive regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
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    },
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            {
                "id": "D3ZV76_RAT",
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            }
        ],
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        "length": 97,
        "protein_name": "Mitochondrial import inner membrane translocase subunit",
        "gene_name": "Timm8a2",
        "organism": "Rat",
        "refseq_name": "translocase of inner mitochondrial membrane 8A2",
        "refseq_ac": [
            {
                "id": "NP_001102899",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102899",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Timm8a2",
        "gene_names_refseq": "Timm8a2",
        "protein_names_uniprotkb": "Mitochondrial import inner membrane translocase subunit",
        "protein_names_refseq": "translocase of inner mitochondrial membrane 8 homolog a2; translocase of inner mitochondrial membrane 8A2",
        "tax_id": 10116,
        "disease": "deafness-dystonia-optic neuronopathy syndrome (Disease Ontology:DOID:0050757)",
        "pathway": " (rno:680794)",
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        "publication_id_list": "",
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        "function": "Mitochondrial intermembrane chaperone that participates in the import and insertion of some multi-pass transmembrane proteins into the mitochondrial inner membrane. Also required for the transfer of beta-barrel precursors from the TOM complex to the sorting and assembly machinery (SAM complex) of the outer membrane. Acts as a chaperone-like protein that protects the hydrophobic precursors from aggregation and guide them through the mitochondrial intermembrane space., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0046872 metal ion binding",
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            {
                "id": "D3ZVP6_RAT",
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            }
        ],
        "mass": 73495.0,
        "length": 646,
        "protein_name": "Peptidylprolyl isomerase domain and WD repeat-containing protein 1",
        "gene_name": "Ppwd1",
        "organism": "Rat",
        "refseq_name": "peptidylprolyl isomerase domain and WD repeat-containing protein 1",
        "refseq_ac": [
            {
                "id": "NP_001099876",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099876",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ppwd1",
        "gene_names_refseq": "Ppwd1; RGD1310204",
        "protein_names_uniprotkb": "Peptidylprolyl isomerase domain and WD repeat-containing protein 1; 5.2.1.8",
        "protein_names_refseq": "peptidylprolyl isomerase domain and WD repeat-containing protein 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:294711);  (R-RNO-72163)",
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        "class_list": "",
        "function": "PPIase that catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and may therefore assist protein folding. May be involved in pre-mRNA splicing., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "ec_number_list": [
            {
                "id": "3.6.4.13",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.13",
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            },
            {
                "id": "5.2.1.8",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.2.1.8",
                "type": "external"
            },
            {
                "id": "2.7.7.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.6",
                "type": "external"
            },
            {
                "id": "3.6.4.10",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.10",
                "type": "external"
            },
            {
                "id": "2.3.2.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
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        "go_biological_process": "GO:0033609 oxalate metabolic process;GO:0042866 pyruvate biosynthetic process;GO:0019470 trans-4-hydroxy-L-proline catabolic process;GO:0046487 glyoxylate metabolic process;GO:0009436 glyoxylate catabolic process",
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        ],
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        "protein_name": "Sperm microtubule inner protein 5",
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        "go_cellular_component": "GO:0036126 sperm flagellum;GO:0160111 axonemal A tubule inner sheath",
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        ],
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        "protein_name": "[histone H3]-lysine(4) N-trimethyltransferase",
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        "function": "Role of Muscle-Specific Histone Methyltransferase (Smyd1) in Exercise-Induced Cardioprotection against Pathological Remodeling after Myocardial Infarction. Publication Status: Online-Only, [RefSeq, PubMed]; Smyd1 is responsible for restricting growth in the adult heart, with its absence leading to cellular hypertrophy, organ remodeling, and fulminate heart failure. Molecular studies reveal Smyd1 to be a muscle-specific regulator of gene expression and indicate that Smyd1 modulates expression of gene isoforms whose expression is associated with cardiac pathology. Activation of Smyd1 can prevent pathological cell growth., [RefSeq, PubMed]",
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            {
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        "protein_names_uniprotkb": "Keratin associated protein 10-9",
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        "function": "In the hair cortex, hair keratin intermediate filaments are embedded in an interfilamentous matrix, consisting of hair keratin-associated proteins (KRTAP), which are essential for the formation of a rigid and resistant hair shaft through their extensive disulfide bond cross-linking with abundant cysteine residues of hair keratins. The matrix proteins include the high-sulfur and high-glycine-tyrosine keratins., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0016740 transferase activity;GO:1904047 S-adenosyl-L-methionine binding;GO:0106388 rRNA small subunit aminocarboxypropyltransferase activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0000455 enzyme-directed rRNA pseudouridine synthesis;GO:0030490 maturation of SSU-rRNA",
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    },
    {
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        ],
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        "refseq_name": "homeobox protein Nkx-2.8",
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            {
                "id": "NP_001100202",
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            }
        ],
        "gene_names_uniprotkb": "Nkx2-8",
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        "protein_names_refseq": "NK2 transcription factor related, locus 9; homeobox protein Nkx-2.8",
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0003690 double-stranded DNA binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0043565 sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
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            {
                "id": "NP_001100256",
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            {
                "id": "2.7.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.2.3",
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            {
                "id": "2.7.11.11",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.11",
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            {
                "id": "3.1.3.48",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.48",
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            {
                "id": "2.7.11.31",
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                "id": "3.1.11.-",
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                "id": "2.7.13.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.13.3",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.18",
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            {
                "id": "3.1.24.-",
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                "id": "3.4.19.12",
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        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
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    {
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        ],
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        "disease": "obstructive sleep apnea (Disease Ontology:DOID:0050848); oral squamous cell carcinoma (Disease Ontology:DOID:0050866); stroke (Disease Ontology:DOID:0051061); lupus nephritis (Disease Ontology:DOID:0080162); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); metabolic dysfunction-associated steatohepatitis (Disease Ontology:DOID:0080547); COVID-19 (Disease Ontology:DOID:0080600); Graves ophthalmopathy (Disease Ontology:DOID:0081120); portal hypertension (Disease Ontology:DOID:10762); Kuhnt-Junius degeneration (Disease Ontology:DOID:10873); nephritis (Disease Ontology:DOID:10952); IgA vasculitis (Disease Ontology:DOID:11123); allergic conjunctivitis (Disease Ontology:DOID:11204); pneumocystosis (Disease Ontology:DOID:11339); familial hyperlipidemia (Disease Ontology:DOID:1168); gestational diabetes (Disease Ontology:DOID:11714); alcoholic hepatitis (Disease Ontology:DOID:12351); Guillain-Barre syndrome (Disease Ontology:DOID:12842); autistic disorder (Disease Ontology:DOID:12849); cardiovascular system disease (Disease Ontology:DOID:1287); uveitis (Disease Ontology:DOID:13141); proliferative diabetic retinopathy (Disease Ontology:DOID:13207); Behcet's disease (Disease Ontology:DOID:13241); temporal arteritis (Disease Ontology:DOID:13375); anterior uveitis (Disease Ontology:DOID:1407); toxic shock syndrome (Disease Ontology:DOID:14115); aggressive periodontitis (Disease Ontology:DOID:1474); cystic fibrosis (Disease Ontology:DOID:1485); fungal infectious disease (Disease Ontology:DOID:1564); thrombocytopenia (Disease Ontology:DOID:1588); multiple sclerosis (Disease Ontology:DOID:2377); asthma (Disease Ontology:DOID:2841); endometriosis (Disease Ontology:DOID:289); severe acute respiratory syndrome (Disease Ontology:DOID:2945); pulmonary tuberculosis (Disease Ontology:DOID:2957); interstitial lung disease (Disease Ontology:DOID:3082); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); ischemia (Disease Ontology:DOID:326); bipolar disorder (Disease Ontology:DOID:3312); coronary artery disease (Disease Ontology:DOID:3393); systemic scleroderma (Disease Ontology:DOID:418); macular degeneration (Disease Ontology:DOID:4448); macular retinal edema (Disease Ontology:DOID:4449); rhinitis (Disease Ontology:DOID:4483); periapical granuloma (Disease Ontology:DOID:4617); pancreatitis (Disease Ontology:DOID:4989); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); retinal detachment (Disease Ontology:DOID:5327); pneumonia (Disease Ontology:DOID:552); myocardial infarction (Disease Ontology:DOID:5844); fibromyalgia (Disease Ontology:DOID:631); hepatocellular carcinoma (Disease Ontology:DOID:684); rheumatoid arthritis (Disease Ontology:DOID:7148); end stage renal disease (Disease Ontology:DOID:783); lipodystrophy (Disease Ontology:DOID:811); myocarditis (Disease Ontology:DOID:820); periapical periodontitis (Disease Ontology:DOID:823); ulcerative colitis (Disease Ontology:DOID:8577); skin melanoma (Disease Ontology:DOID:8923); systemic lupus erythematosus (Disease Ontology:DOID:9074); acute myeloid leukemia (Disease Ontology:DOID:9119); viral infectious disease (Disease Ontology:DOID:934); ethmoid sinusitis (Disease Ontology:DOID:9507); pulmonary emphysema (Disease Ontology:DOID:9675); type 1 diabetes mellitus (Disease Ontology:DOID:9744); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:287562);  (R-RNO-380108)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 66,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0004672 protein kinase activity;GO:0016004 phospholipase activator activity;GO:0008009 chemokine activity;GO:0048020 CCR chemokine receptor binding;GO:0031727 CCR2 chemokine receptor binding",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "GO:0001525 angiogenesis;GO:0006954 inflammatory response;GO:0007267 cell-cell signaling;GO:0030335 positive regulation of cell migration;GO:0061844 antimicrobial humoral immune response mediated by antimicrobial peptide",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4ABS1-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D4ABX3-1",
        "uniprot_id": [
            {
                "id": "D4ABX3_RAT",
                "url": "https://www.uniprot.org/uniprot/D4ABX3",
                "type": "external"
            }
        ],
        "mass": 36835.0,
        "length": 330,
        "protein_name": "Endonuclease 8-like 2",
        "gene_name": "Neil2",
        "organism": "Rat",
        "refseq_name": "endonuclease 8-like 2",
        "refseq_ac": [
            {
                "id": "NP_001100740",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100740",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Neil2",
        "gene_names_refseq": "Neil2",
        "protein_names_uniprotkb": "Endonuclease 8-like 2; 4.2.99.18; DNA glycosylase/AP lyase Neil2; DNA-(apurinic or apyrimidinic site) lyase Neil2; Endonuclease VIII-like 2; Nei-like protein 2",
        "protein_names_refseq": "endonuclease 8-like 2; endonuclease VIII-like 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:305957);  (R-RNO-110329);  (R-RNO-5649702)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "21145906",
        "class_list": "",
        "function": "In the spleen aniline-induced oxidative stress is associated with an induction of NEIL1/2., [RefSeq, PubMed]; Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Has DNA glycosylase activity towards 5-hydroxyuracil and other oxidized derivatives of cytosine with a preference for mismatched double-stranded DNA (DNA bubbles). Has low or no DNA glycosylase activity towards thymine glycol, 2-hydroxyadenine, hypoxanthine and 8-oxoguanine. Has AP (apurinic/apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "6.5.1.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.5.1.1",
                "type": "external"
            },
            {
                "id": "2.7.1.78",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.78",
                "type": "external"
            },
            {
                "id": "3.1.3.32",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.32",
                "type": "external"
            },
            {
                "id": "4.2.99.18",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.2.99.18",
                "type": "external"
            },
            {
                "id": "2.7.7.7",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.7",
                "type": "external"
            },
            {
                "id": "4.2.99.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.2.99.-",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0008017 microtubule binding;GO:0008270 zinc ion binding;GO:0003684 damaged DNA binding;GO:0019104 DNA N-glycosylase activity;GO:0140078 class I DNA-(apurinic or apyrimidinic site) endonuclease activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0015630 microtubule cytoskeleton;GO:0072686 mitotic spindle",
        "go_biological_process": "GO:0006284 base-excision repair",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4ABX3-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D4ACA6-1",
        "uniprot_id": [
            {
                "id": "D4ACA6_RAT",
                "url": "https://www.uniprot.org/uniprot/D4ACA6",
                "type": "external"
            }
        ],
        "mass": 119673.0,
        "length": 1089,
        "protein_name": "Mitotic deacetylase associated SANT domain protein",
        "gene_name": "Mideas",
        "organism": "Rat",
        "refseq_name": "mitotic deacetylase-associated SANT domain protein",
        "refseq_ac": [
            {
                "id": "NP_001162587",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001162587",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Mideas; Elmsan1",
        "gene_names_refseq": "Elmsan1; Mideas; RGD1306119",
        "protein_names_uniprotkb": "Mitotic deacetylase associated SANT domain protein",
        "protein_names_refseq": "ELM2 and Myb/SANT domain containing 1; ELM2 and Myb/SANT-like domain containing 1; ELM2 and SANT domain-containing protein 1; mitotic deacetylase-associated SANT domain protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:314306)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "22673903;29393594",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
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        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003714 transcription corepressor activity;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005667 transcription regulator complex;GO:0000118 histone deacetylase complex;GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045892 negative regulation of DNA-templated transcription;GO:0006325 chromatin organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D4ACA6-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.010000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D4ACC1-1",
        "uniprot_id": [
            {
                "id": "D4ACC1_RAT",
                "url": "https://www.uniprot.org/uniprot/D4ACC1",
                "type": "external"
            }
        ],
        "mass": 32111.0,
        "length": 279,
        "protein_name": "Dual adapter for phosphotyrosine and 3-phosphotyrosine and 3-phosphoinositide",
        "gene_name": "Dapp1",
        "organism": "Rat",
        "refseq_name": "dual adapter for phosphotyrosine and 3-phosphotyrosine and 3-phosphoinositide",
        "refseq_ac": [
            {
                "id": "NP_001102038",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102038",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Dapp1",
        "gene_names_refseq": "Dapp1",
        "protein_names_uniprotkb": "Dual adapter for phosphotyrosine and 3-phosphotyrosine and 3-phosphoinositide; B lymphocyte adapter protein Bam32; B-cell adapter molecule of 32 kDa",
        "protein_names_refseq": "dual adapter for phosphotyrosine and 3-phosphotyrosine and 3-phosphoinositide; dual adaptor for phosphotyrosine and 3-phosphoinositides 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362046);  (R-RNO-983695)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
        "function": "May act as a B-cell-associated adapter that regulates B-cell antigen receptor (BCR)-signaling downstream of PI3K., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "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:0005543 phospholipid binding;GO:0005547 phosphatidylinositol-3,4,5-trisphosphate binding;GO:0043325 phosphatidylinositol-3,4-bisphosphate binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4ACC1-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D4ACE1-1",
        "uniprot_id": [
            {
                "id": "D4ACE1_RAT",
                "url": "https://www.uniprot.org/uniprot/D4ACE1",
                "type": "external"
            }
        ],
        "mass": 27485.0,
        "length": 251,
        "protein_name": "Homeobox protein Hox-D4",
        "gene_name": "Hoxd4",
        "organism": "Rat",
        "refseq_name": "homeobox protein Hox-D4",
        "refseq_ac": [
            {
                "id": "NP_001099355",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099355",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Hoxd4",
        "gene_names_refseq": "Hoxd4",
        "protein_names_uniprotkb": "Homeobox protein Hox-D4",
        "protein_names_refseq": "homeobox protein Hox-D4",
        "tax_id": 10116,
        "disease": "leukemia (Disease Ontology:DOID:1240)",
        "pathway": " (rno:288153)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0048863 stem cell differentiation;GO:0009952 anterior/posterior pattern specification;GO:0048704 embryonic skeletal system morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4ACE1-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D4ACK0-1",
        "uniprot_id": [
            {
                "id": "D4ACK0_RAT",
                "url": "https://www.uniprot.org/uniprot/D4ACK0",
                "type": "external"
            }
        ],
        "mass": 43692.0,
        "length": 396,
        "protein_name": "G protein-coupled receptor 84",
        "gene_name": "Gpr84",
        "organism": "Rat",
        "refseq_name": "G-protein coupled receptor 84",
        "refseq_ac": [
            {
                "id": "NP_001102979",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102979",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Gpr84",
        "gene_names_refseq": "Gpr84",
        "protein_names_uniprotkb": "G protein-coupled receptor 84",
        "protein_names_refseq": "G-protein coupled receptor 84",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:688730);  (R-RNO-6798695)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "23449982",
        "class_list": "",
        "function": "Medium-chain fatty acid-sensing receptor, GPR84, is a proinflammatory receptor., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "protein_name": "Olfactory receptor",
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        "refseq_name": "olfactory receptor Olr1404",
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            {
                "id": "NP_001000787",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000787",
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        "gene_names_refseq": "Olr1404; Or1ad6; tpcr10",
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        "protein_names_refseq": "olfactory receptor 1404; olfactory receptor Olr1404; olfactory receptor gene Olr1404",
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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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            {
                "id": "NP_001124008",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001124008",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Fzd6",
        "gene_names_refseq": "Fzd6",
        "protein_names_uniprotkb": "Frizzled-6",
        "protein_names_refseq": "frizzled family receptor 6; frizzled-6 precursor; frizzled-6",
        "tax_id": 10116,
        "disease": "nonsyndromic congenital nail disorder 1 (Disease Ontology:DOID:0080079)",
        "pathway": " (rno:282581);  (R-RNO-4086398);  (R-RNO-4086400);  (R-RNO-4641263)",
        "pathway_count": 4,
        "publication_count": 1,
        "publication_id_list": "38710294",
        "class_list": "",
        "function": "Fengshi Liuhe Decoction treatment for rheumatoid arthritis via the Fzd6/NF-kappaB signaling axis., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0031625 ubiquitin protein ligase binding;GO:0017147 Wnt-protein binding;GO:0042813 Wnt receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0045177 apical part of cell;GO:0005789 endoplasmic reticulum membrane;GO:0016324 apical plasma membrane",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0042472 inner ear morphogenesis;GO:0090090 negative regulation of canonical Wnt signaling pathway;GO:0030168 platelet activation;GO:0001843 neural tube closure",
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    },
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            {
                "id": "G3V6M8_RAT",
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            }
        ],
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        "protein_name": "Nucleoporin Nup37",
        "gene_name": "Nup37",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Nup37",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Nucleoporin Nup37; Nup107-160 subcomplex subunit Nup37",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "primary autosomal recessive microcephaly 24 (Disease Ontology:DOID:0051035)",
        "pathway": " (rno:299706);  (R-RNO-141430);  (R-RNO-141444);  (R-RNO-159227);  (R-RNO-159230);  (R-RNO-159231);  (R-RNO-159236);  (R-RNO-170822);  (R-RNO-1855170);  (R-RNO-1855196);  (R-RNO-1855229);  (R-RNO-191859);  (R-RNO-2467813);  (R-RNO-2500257);  (R-RNO-3108214);  (R-RNO-3232142);  (R-RNO-3301854);  (R-RNO-3371453);  (R-RNO-4085377);  (R-RNO-4551638);  (R-RNO-4570464);  (R-RNO-4615885);  (R-RNO-5663220);  (R-RNO-68877);  (R-RNO-9615933);  (R-RNO-9648025)",
        "pathway_count": 26,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Component of the Nup107-160 subcomplex of the nuclear pore complex (NPC). The Nup107-160 subcomplex is required for the assembly of a functional NPC. The Nup107-160 subcomplex is also required for normal kinetochore microtubule attachment, mitotic progression and chromosome segregation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": [],
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        "go_cellular_component": "GO:0031080 nuclear pore outer ring;GO:0005635 nuclear envelope;GO:0000776 kinetochore;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0007059 chromosome segregation;GO:0015031 protein transport;GO:0051301 cell division;GO:0051028 mRNA transport",
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        "kg_view_protein": true
    },
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            {
                "id": "G3V6U3_RAT",
                "url": "https://www.uniprot.org/uniprot/G3V6U3",
                "type": "external"
            }
        ],
        "mass": 47319.0,
        "length": 415,
        "protein_name": "Alpha-1,3/1,6-mannosyltransferase ALG2",
        "gene_name": "Alg2",
        "organism": "Rat",
        "refseq_name": "alpha-1,3/1,6-mannosyltransferase ALG2",
        "refseq_ac": [
            {
                "id": "NP_001094180",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001094180",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Alg2",
        "gene_names_refseq": "Alg2",
        "protein_names_uniprotkb": "Alpha-1,3/1,6-mannosyltransferase ALG2; 2.4.1.132; 2.4.1.257; GDP-Man:Man(1)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase",
        "protein_names_refseq": "alpha-1,3-mannosyltransferase ALG2; alpha-1,3/1,6-mannosyltransferase ALG2; asparagine-linked glycosylation 2 homolog (S. cerevisiae, alpha-1,3-mannosyltransferase); asparagine-linked glycosylation 2, alpha-1,3-mannosyltransferase homolog",
        "tax_id": 10116,
        "disease": "congenital disorder of glycosylation Ii (Disease Ontology:DOID:0080561); congenital myasthenic syndrome 14 (Disease Ontology:DOID:0110669)",
        "pathway": " (rno:313231);  (R-RNO-446193)",
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        "publication_id_list": "38843836",
        "class_list": "",
        "function": "Mannosylates Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.4.1.132",
                "type": "external"
            },
            {
                "id": "2.4.1.257",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.4.1.257",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0000033 alpha-1,3-mannosyltransferase activity;GO:0004378 GDP-Man:Man(1)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase activity;GO:0102704 GDP-Man:Man(2)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase activity",
        "go_cellular_component": "GO:0098554 cytoplasmic side of endoplasmic reticulum membrane;GO:0012505 endomembrane system",
        "go_biological_process": "GO:0009101 glycoprotein biosynthetic process;GO:0006488 dolichol-linked oligosaccharide biosynthetic process;GO:0006487 protein N-linked glycosylation",
        "synthesized_glycan_count": 13365,
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        "kg_view_protein": true
    },
    {
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            {
                "id": "G3V6W6_RAT",
                "url": "https://www.uniprot.org/uniprot/G3V6W6",
                "type": "external"
            }
        ],
        "mass": 45797.0,
        "length": 403,
        "protein_name": "26S proteasome regulatory subunit 10B",
        "gene_name": "Psmc6",
        "organism": "Rat",
        "refseq_name": "26S proteasome regulatory subunit 10B",
        "refseq_ac": [
            {
                "id": "NP_001093979",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001093979",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Psmc6; LOC100365869",
        "gene_names_refseq": "Psmc6",
        "protein_names_uniprotkb": "26S proteasome regulatory subunit 10B; 26S proteasome AAA-ATPase subunit RPT4; Proteasome 26S subunit ATPase 6; Proteasome subunit p42",
        "protein_names_refseq": "26S protease regulatory subunit 10B; 26S proteasome regulatory subunit 10B; proteasome (prosome, macropain) 26S subunit, ATPase, 6-like",
        "tax_id": 10116,
        "disease": "fetal alcohol spectrum disorder (Disease Ontology:DOID:0050696)",
        "pathway": " (rno:289990)",
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        "go_cellular_component": "GO:0031597 cytosolic proteasome complex;GO:0022624 proteasome accessory complex;GO:0005634 nucleus;GO:0008021 synaptic vesicle;GO:0000502 proteasome complex",
        "go_biological_process": "GO:0010498 proteasomal protein catabolic process;GO:0090261 positive regulation of inclusion body assembly;GO:2000311 regulation of AMPA receptor activity",
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    },
    {
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        "uniprot_id": [
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                "type": "external"
            }
        ],
        "mass": 86334.0,
        "length": 749,
        "protein_name": "Phosphate regulating endopeptidase X-linked",
        "gene_name": "Phex",
        "organism": "Rat",
        "refseq_name": "phosphate-regulating neutral endopeptidase PHEX",
        "refseq_ac": [
            {
                "id": "NP_037136",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_037136",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Phex",
        "gene_names_refseq": "PEX; Phex",
        "protein_names_uniprotkb": "Phosphate regulating endopeptidase X-linked",
        "protein_names_refseq": "Phosphate regulating neutral endopeptidase on the X chromosome (X-linked hypophosphatemia XLH); metalloendopeptidase homolog PEX-like; metalloendopeptidase homolog PEX; phosphate regulating endopeptidase homolog, X-linked; phosphate regulating gene with homologies to endopeptidases on the X chromosome (hypophosphatemia, vitamin D resistant rickets); phosphate-regulating neutral endopeptidase PHEX; phosphate-regulating neutral endopeptidase",
        "tax_id": 10116,
        "disease": "X-linked hypophosphatemic rickets (Disease Ontology:DOID:0050445); heart conduction disease (Disease Ontology:DOID:10273); kidney failure (Disease Ontology:DOID:1074); otitis media (Disease Ontology:DOID:10754)",
        "pathway": " (rno:25512)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "38116308",
        "class_list": "",
        "function": "The contribution of a novel PHEX gene mutation to X-linked hypophosphatemic rickets: a case report and an analysis of the gene mutation dosage effect in a rat model. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0004222 metalloendopeptidase activity;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0048471 perinuclear region of cytoplasm",
        "go_biological_process": "GO:1904383 response to sodium phosphate;GO:0006508 proteolysis;GO:0016485 protein processing;GO:0030324 lung development;GO:0042476 odontogenesis",
        "synthesized_glycan_count": 0,
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        "kg_view_protein": true
    },
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                "url": "https://www.uniprot.org/uniprot/G3V7L4",
                "type": "external"
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        ],
        "mass": 90091.0,
        "length": 830,
        "protein_name": "Cadherin-16",
        "gene_name": "Cdh16",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Cdh16",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Cadherin-16; Kidney-specific cadherin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "thyroid cancer (Disease Ontology:DOID:1781)",
        "pathway": "",
        "pathway_count": 0,
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0050839 cell adhesion molecule binding",
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        "go_biological_process": "GO:0098609 cell-cell adhesion;GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules;GO:0016339 calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules",
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            {
                "id": "F1M9D6_RAT",
                "url": "https://www.uniprot.org/uniprot/F1M9D6",
                "type": "external"
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        ],
        "mass": 88008.0,
        "length": 755,
        "protein_name": "Signal transducer and activator of transcription",
        "gene_name": "Stat1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Stat1; Stat4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Signal transducer and activator of transcription",
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        "tax_id": 10116,
        "disease": "chromosome 1q21.1 deletion syndrome (Disease Ontology:DOID:0060411); metabolic dysfunction and alcohol associated liver disease (Disease Ontology:DOID:0070508); trimethylaminuria (Disease Ontology:DOID:0080361); polymyositis (Disease Ontology:DOID:0080745); disabling pansclerotic morphea (Disease Ontology:DOID:0081373); immunodeficiency 31B (Disease Ontology:DOID:0111944); immunodeficiency 31A (Disease Ontology:DOID:0111945); immunodeficiency 31C (Disease Ontology:DOID:0111946); dermatomyositis (Disease Ontology:DOID:10223); hypertension (Disease Ontology:DOID:10763); primary biliary cholangitis (Disease Ontology:DOID:12236); Vogt-Koyanagi-Harada disease (Disease Ontology:DOID:12297); Sjogren's syndrome (Disease Ontology:DOID:12894); Behcet's disease (Disease Ontology:DOID:13241); limited scleroderma (Disease Ontology:DOID:1577); diffuse scleroderma (Disease Ontology:DOID:1580); breast cancer (Disease Ontology:DOID:1612); hepatitis C (Disease Ontology:DOID:1883); viral hepatitis (Disease Ontology:DOID:1884); rectum adenocarcinoma (Disease Ontology:DOID:1996); autoimmune hepatitis (Disease Ontology:DOID:2048); nephroblastoma (Disease Ontology:DOID:2154); colon adenocarcinoma (Disease Ontology:DOID:234); prostate adenocarcinoma (Disease Ontology:DOID:2526); asthma (Disease Ontology:DOID:2841); severe acute respiratory syndrome (Disease Ontology:DOID:2945); IgA glomerulonephritis (Disease Ontology:DOID:2986); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); angiomyolipoma (Disease Ontology:DOID:3314); lymphangioleiomyomatosis (Disease Ontology:DOID:3319); breast carcinoma (Disease Ontology:DOID:3459); gastric adenocarcinoma (Disease Ontology:DOID:3717); pulmonary fibrosis (Disease Ontology:DOID:3770); tuberculosis (Disease Ontology:DOID:399); systemic scleroderma (Disease Ontology:DOID:418); inherited metabolic disorder (Disease Ontology:DOID:655); hepatocellular carcinoma (Disease Ontology:DOID:684); Sezary's disease (Disease Ontology:DOID:8541); cholesteatoma (Disease Ontology:DOID:869); genital herpes (Disease Ontology:DOID:8704); psoriasis (Disease Ontology:DOID:8893); psoriatic arthritis (Disease Ontology:DOID:9008); systemic lupus erythematosus (Disease Ontology:DOID:9074); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (R-RNO-1059683);  (R-RNO-1169408);  (R-RNO-1433557);  (R-RNO-186763);  (R-RNO-6785807);  (R-RNO-877300);  (R-RNO-877312);  (R-RNO-8854691);  (R-RNO-8984722);  (R-RNO-8985947);  (R-RNO-9020956);  (R-RNO-9020958);  (R-RNO-909733);  (R-RNO-912694);  (R-RNO-9833482);  (R-RNO-9860927)",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0030424 axon",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0071345 cellular response to cytokine stimulus;GO:0019221 cytokine-mediated signaling pathway;GO:0045063 T-helper 1 cell differentiation;GO:0070106 interleukin-27-mediated signaling pathway",
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        "mass": 410017.0,
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        "protein_name": "Msx2-interacting protein",
        "gene_name": "Spen",
        "organism": "Rat",
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        "refseq_ac": [],
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Msx2-interacting protein; SMART/HDAC1-associated repressor protein; SPEN homolog",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); nasopharynx carcinoma (Disease Ontology:DOID:9261)",
        "pathway": " (rno:690911);  (R-RNO-9013422)",
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        "go_molecular_function": "GO:0047325 inositol-3,4,5,6-tetrakisphosphate 1-kinase activity;GO:0052725 inositol-1,3,4-trisphosphate 6-kinase activity;GO:0052726 inositol-1,3,4-trisphosphate 5-kinase activity;GO:0000287 magnesium ion binding;GO:0005524 ATP binding",
        "go_cellular_component": "GO:0016324 apical plasma membrane",
        "go_biological_process": "GO:0021915 neural tube development;GO:0070266 necroptotic process;GO:0032957 inositol trisphosphate metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0G2K7L4-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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            {
                "id": "A0A0G2K1L0_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2K1L0",
                "type": "external"
            }
        ],
        "mass": 231674.0,
        "length": 2110,
        "protein_name": "Tenascin",
        "gene_name": "Tnc",
        "organism": "Rat",
        "refseq_name": "tenascin isoform X3",
        "refseq_ac": [
            {
                "id": "XP_008761978",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_008761978",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tnc",
        "gene_names_refseq": "Tnc",
        "protein_names_uniprotkb": "Tenascin; Hexabrachion; Tenascin-C",
        "protein_names_refseq": "tenascin isoform X3",
        "tax_id": 10116,
        "disease": "polycystic kidney disease (Disease Ontology:DOID:0080322); autosomal dominant nonsyndromic deafness 56 (Disease Ontology:DOID:0110581); asbestosis (Disease Ontology:DOID:10320); pleural tuberculosis (Disease Ontology:DOID:106); allergic conjunctivitis (Disease Ontology:DOID:11204); intracranial vasospasm (Disease Ontology:DOID:13100); lung cancer (Disease Ontology:DOID:1324); pulmonary sarcoidosis (Disease Ontology:DOID:13406); asthma (Disease Ontology:DOID:2841); glioblastoma (Disease Ontology:DOID:3068); high grade glioma (Disease Ontology:DOID:3070); pleural empyema (Disease Ontology:DOID:3798); cholangiocarcinoma (Disease Ontology:DOID:4947); pneumonia (Disease Ontology:DOID:552); myocardial infarction (Disease Ontology:DOID:5844); pulmonary hypertension (Disease Ontology:DOID:6432); extrinsic allergic alveolitis (Disease Ontology:DOID:841)",
        "pathway": " (rno:116640);  (R-RNO-216083);  (R-RNO-3000178);  (R-RNO-381426);  (R-RNO-8957275)",
        "pathway_count": 5,
        "publication_count": 1,
        "publication_id_list": "28657654",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 2,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 1,
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        "missing_score": 0,
        "biomarker_type": "",
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        "disease_count": 17,
        "glyco_site_count": 3,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0005178 integrin binding;GO:0045545 syndecan binding",
        "go_cellular_component": "GO:0098966 perisynaptic extracellular matrix;GO:0005615 extracellular space;GO:0005604 basement membrane;GO:0005614 interstitial matrix;GO:0098978 glutamatergic synapse",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0009611 response to wounding;GO:0030155 regulation of cell adhesion;GO:0001558 regulation of cell growth;GO:0050727 regulation of inflammatory response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0A0G2K1L0-1",
        "record_type": "protein",
        "filter_code": "0000000.1000111.010000.000000000000001000.0100000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "G3V6T1-1",
        "uniprot_id": [
            {
                "id": "G3V6T1_RAT",
                "url": "https://www.uniprot.org/uniprot/G3V6T1",
                "type": "external"
            }
        ],
        "mass": 138656.0,
        "length": 1227,
        "protein_name": "Coatomer subunit alpha",
        "gene_name": "Copa",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Copa",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Coatomer subunit alpha",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autoimmune interstitial lung, joint, and kidney disease (Disease Ontology:DOID:0081242)",
        "pathway": " (rno:304978);  (R-RNO-6807878);  (R-RNO-6811434)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin-coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. In mammals, the coatomer can only be recruited by membranes associated to ADP-ribosylation factors (ARFs), which are small GTP-binding proteins; the complex also influences the Golgi structural integrity, as well as the processing, activity, and endocytic recycling of LDL receptors., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Xenin stimulates exocrine pancreatic secretion. It inhibits pentagastrin-stimulated secretion of acid, to induce exocrine pancreatic secretion and to affect small and large intestinal motility. In the gut, xenin interacts with the neurotensin receptor., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0005198 structural molecule activity;GO:0003729 mRNA binding",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0030126 COPI vesicle coat;GO:0005615 extracellular space;GO:0005737 cytoplasm;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport;GO:0006890 retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum;GO:0006891 intra-Golgi vesicle-mediated transport;GO:0099612 protein localization to axon",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "G3V6T1-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.010000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A0G2JUH4-1",
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            {
                "id": "A0A0G2JUH4_RAT",
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                "type": "external"
            }
        ],
        "mass": 57448.0,
        "length": 525,
        "protein_name": "Bifunctional polynucleotide phosphatase/kinase",
        "gene_name": "Pnkp",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Pnkp",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Bifunctional polynucleotide phosphatase/kinase; 2.7.1.78; 3.1.3.32; DNA 5'-kinase/3'-phosphatase; Polynucleotide kinase-3'-phosphatase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "microcephaly, seizures, and developmental delay (Disease Ontology:DOID:0080457); ataxia-oculomotor apraxia 4 (Disease Ontology:DOID:0081383); Charcot-Marie-Tooth disease type 2B2 (Disease Ontology:DOID:0110179)",
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Plays a key role in the repair of DNA damage, functioning as part of both the non-homologous end-joining (NHEJ) and base excision repair (BER) pathways. Through its two catalytic activities, PNK ensures that DNA termini are compatible with extension and ligation by either removing 3'-phosphates from, or by phosphorylating 5'-hydroxyl groups on, the ribose sugar of the DNA backbone., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "ec_number_list": [
            {
                "id": "6.5.1.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.5.1.1",
                "type": "external"
            },
            {
                "id": "2.7.1.78",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.78",
                "type": "external"
            },
            {
                "id": "3.1.3.32",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.32",
                "type": "external"
            },
            {
                "id": "4.2.99.18",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.2.99.18",
                "type": "external"
            },
            {
                "id": "2.7.7.7",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.7",
                "type": "external"
            },
            {
                "id": "4.2.99.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.2.99.-",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0046404 ATP-dependent polydeoxyribonucleotide 5'-hydroxyl-kinase activity;GO:0046403 polynucleotide 3'-phosphatase activity;GO:1990756 ubiquitin-like ligase-substrate adaptor activity;GO:0016787 hydrolase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0019005 SCF ubiquitin ligase complex;GO:0035861 site of double-strand break",
        "go_biological_process": "GO:0006281 DNA repair;GO:2001034 positive regulation of double-strand break repair via nonhomologous end joining;GO:0006979 response to oxidative stress;GO:0006974 DNA damage response;GO:0006303 double-strand break repair via nonhomologous end joining",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A0G2JUH4-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q66HB1-1",
        "uniprot_id": [
            {
                "id": "Q66HB1_RAT",
                "url": "https://www.uniprot.org/uniprot/Q66HB1",
                "type": "external"
            }
        ],
        "mass": 34951.0,
        "length": 318,
        "protein_name": "TATA box binding protein",
        "gene_name": "Tbp",
        "organism": "Rat",
        "refseq_name": "TATA-box-binding protein isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001004198",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001004198",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tbp",
        "gene_names_refseq": "TFIID; Tbp",
        "protein_names_uniprotkb": "TATA box binding protein",
        "protein_names_refseq": "TATA-box-binding protein isoform 1",
        "tax_id": 10116,
        "disease": "sleep apnea (Disease Ontology:DOID:0050847); spinocerebellar ataxia 17 (Disease Ontology:DOID:0050967); late onset Parkinson's disease (Disease Ontology:DOID:0060892); Alzheimer's disease (Disease Ontology:DOID:10652); Huntington's disease (Disease Ontology:DOID:12858); neurodegenerative disease (Disease Ontology:DOID:1289); schizophrenia (Disease Ontology:DOID:5419); type 1 diabetes mellitus (Disease Ontology:DOID:9744)",
        "pathway": " (rno:117526);  (R-RNO-5250924);  (R-RNO-674695);  (R-RNO-6804756);  (R-RNO-6807505);  (R-RNO-73762);  (R-RNO-73772);  (R-RNO-73776);  (R-RNO-73779);  (R-RNO-73863);  (R-RNO-75953);  (R-RNO-76042);  (R-RNO-76061);  (R-RNO-76066);  (R-RNO-76071);  (R-RNO-9018519)",
        "pathway_count": 16,
        "publication_count": 1,
        "publication_id_list": "28134789",
        "class_list": "",
        "function": "Mrpl10 and Tbp might be used as suitable reference genes for sciatic nerve stump and dorsal root ganglions, respectively. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0001093 TFIIB-class transcription factor binding;GO:0019899 enzyme binding;GO:0017162 aryl hydrocarbon receptor binding;GO:0000979 RNA polymerase II core promoter sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005668 RNA polymerase transcription factor SL1 complex;GO:0000791 euchromatin;GO:0005672 transcription factor TFIIA complex;GO:0005669 transcription factor TFIID complex",
        "go_biological_process": "GO:0006352 DNA-templated transcription initiation;GO:0060261 positive regulation of transcription initiation by RNA polymerase II;GO:0045945 positive regulation of transcription by RNA polymerase III;GO:0042789 mRNA transcription by RNA polymerase II;GO:0051123 RNA polymerase II preinitiation complex assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "Q66HB1-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A0G2JW29-1",
        "uniprot_id": [
            {
                "id": "A0A0G2JW29_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2JW29",
                "type": "external"
            }
        ],
        "mass": 82331.0,
        "length": 747,
        "protein_name": "alpha-1,2-Mannosidase",
        "gene_name": "Man1a1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Man1a1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "alpha-1,2-Mannosidase; 3.2.1.-",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:294410);  (R-RNO-964827)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in the maturation of Asn-linked oligosaccharides. Progressively trim alpha-1,2-linked mannose residues from Man(9)GlcNAc(2) to produce Man(5)GlcNAc(2)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "3.2.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.2.1.-",
                "type": "external"
            },
            {
                "id": "3.2.1.113",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.2.1.113",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0004571 mannosyl-oligosaccharide 1,2-alpha-mannosidase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005783 endoplasmic reticulum;GO:0031410 cytoplasmic vesicle;GO:0005793 endoplasmic reticulum-Golgi intermediate compartment;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0005975 carbohydrate metabolic process;GO:0036503 ERAD pathway;GO:0045047 protein targeting to ER;GO:1904382 mannose trimming involved in glycoprotein ERAD pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0G2JW29-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A0G2K6R0-1",
        "uniprot_id": [
            {
                "id": "A0A0G2K6R0_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2K6R0",
                "type": "external"
            }
        ],
        "mass": 198655.0,
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        ],
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        "protein_name": "Complement C2",
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        "refseq_ac": [],
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Complement C2; C3/C5 convertase",
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        "tax_id": 10116,
        "disease": "sinusitis (Disease Ontology:DOID:0050127); complement component 2 deficiency (Disease Ontology:DOID:0060295); lupus nephritis (Disease Ontology:DOID:0080162); atypical hemolytic-uremic syndrome (Disease Ontology:DOID:0080301); polycystic kidney disease (Disease Ontology:DOID:0080322); erythema nodosum (Disease Ontology:DOID:0080750); age related macular degeneration 14 (Disease Ontology:DOID:0110026); Alport syndrome 3A (Disease Ontology:DOID:0110032); Alport syndrome 2 (Disease Ontology:DOID:0110033); benign familial hematuria (Disease Ontology:DOID:0111365); Alzheimer's disease (Disease Ontology:DOID:10652); lepromatous leprosy (Disease Ontology:DOID:10887); sickle cell anemia (Disease Ontology:DOID:10923); membranous glomerulonephritis (Disease Ontology:DOID:10976); Alport syndrome (Disease Ontology:DOID:10983); pyelonephritis (Disease Ontology:DOID:11400); factor VIII deficiency (Disease Ontology:DOID:12134); beta thalassemia (Disease Ontology:DOID:12241); paracoccidioidomycosis (Disease Ontology:DOID:12662); Behcet's disease (Disease Ontology:DOID:13241); anterior uveitis (Disease Ontology:DOID:1407); boutonneuse fever (Disease Ontology:DOID:14095); breast cancer (Disease Ontology:DOID:1612); membranoproliferative glomerulonephritis (Disease Ontology:DOID:2920); glomerulonephritis (Disease Ontology:DOID:2921); IgA glomerulonephritis (Disease Ontology:DOID:2986); systemic scleroderma (Disease Ontology:DOID:418); macular degeneration (Disease Ontology:DOID:4448); conjunctivitis (Disease Ontology:DOID:6195); end stage renal disease (Disease Ontology:DOID:783); retinal degeneration (Disease Ontology:DOID:8466); psoriasis (Disease Ontology:DOID:8893); diabetic retinopathy (Disease Ontology:DOID:8947); autosomal dominant polycystic kidney disease (Disease Ontology:DOID:898); systemic lupus erythematosus (Disease Ontology:DOID:9074); type 1 diabetes mellitus (Disease Ontology:DOID:9744); acute lymphoblastic leukemia (Disease Ontology:DOID:9952)",
        "pathway": " (rno:294257);  (R-RNO-166663);  (R-RNO-174577);  (R-RNO-977606)",
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        "function": "Catalytic component of the complement C3 and C5 convertase complexes. Following complement activation, recruited to the surface of pathogens by complement C4b opsonin to form the C3 convertase, or C3b and C4b opsonins to form the C5 convertase. As part of the C3 convertase, cleaves and activate C3 into C3a anaphylatoxin and C3b opsonin, the next components of the complement pathways. As part of the C5 convertase, cleaves and activate C5 into C5a anaphylatoxin and C5b component of the membrane attack complex., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Involved in proliferation and differentiation of preactivated B-lymphocytes, rapid spreading of peripheral blood monocytes, stimulation of lymphocyte blastogenesis and lysis of erythrocytes., [UniProtKB, UniProtKB]; Precursor of the catalytic component of the C3 and C5 convertase complexes of the alternative pathway of the complement system, a cascade of proteins that leads to phagocytosis and breakdown of pathogens and signaling that strengthens the adaptive immune system. The alternative complement pathway acts as an amplification loop that enhances other complement pathways (classical, lectin and GZMK) by promoting formation of additional C3 and C5 convertases. CFB is cleaved and activated by CFD to generate Ba and Bb chains; Bb chain constituting the catalytic component of the C3 and C5 convertases., [UniProtKB, UniProtKB]; Precursor of the catalytic component of the C3 and C5 convertase complexes, which are part of the complement pathway, a cascade of proteins that leads to phagocytosis and breakdown of pathogens and signaling that strengthens the adaptive immune system. Component C2 is part of the classical, lectin and GZMK complement systems., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Serine protease component of the complement C3 and C5 convertase complexes of the alternative complement pathway. Following cleavage and activation by factor D (CFD), forms the C3 convertase together with complement C3b. As part of the C3 convertase, cleaves and activates C3 into C3a anaphylatoxin and C3b opsonin, the next components of the complement pathways. When an additional complement C3b molecule binds to the C3 convertase, forms the C5 convertase, which cleaves and activates C5 into C5a anaphylatoxin and C5b component of the membrane attack complex., [UniProtKB, UniProtKB]",
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            {
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        "protein_name": "Inhibitor of nuclear factor kappa-B kinase subunit alpha",
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        "pathway": " (rno:309361);  (R-RNO-1169091);  (R-RNO-1810476);  (R-RNO-198323);  (R-RNO-202424);  (R-RNO-2871837);  (R-RNO-445989);  (R-RNO-5357905);  (R-RNO-5357956);  (R-RNO-5607761);  (R-RNO-5607764);  (R-RNO-5676590);  (R-RNO-5684264);  (R-RNO-9020702);  (R-RNO-933542);  (R-RNO-937039);  (R-RNO-937041);  (R-RNO-975144);  (R-RNO-9758274);  (R-RNO-9833482);  (R-RNO-9860276);  (R-RNO-9860927);  (R-RNO-9909505)",
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        "function": "The potential function of IKKalpha in gastric precancerous lesion via mediating Maspin., [RefSeq, PubMed]",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.34",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.10",
                "type": "external"
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.10.2",
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                "id": "3.6.5.-",
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                "id": "6.2.1.64",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.2.1.64",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.13",
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        ],
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        "go_biological_process": "GO:0030316 osteoclast differentiation;GO:0032727 positive regulation of interferon-alpha production;GO:0061847 response to cholecystokinin;GO:0003009 skeletal muscle contraction;GO:0007229 integrin-mediated signaling pathway",
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        "protein_name": "Kallikrein related-peptidase 9",
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        ],
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        ],
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        "gene_names_refseq": "Cdmp1; Gdf5",
        "protein_names_uniprotkb": "Growth/differentiation factor 5; Bone morphogenetic protein 14",
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        "tax_id": 10116,
        "disease": "fibular hypoplasia and complex brachydactyly (Disease Ontology:DOID:0050790); multiple synostoses syndrome (Disease Ontology:DOID:0050794); developmental dysplasia of the hip 1 (Disease Ontology:DOID:0060931); acromesomelic dysplasia, Hunter-Thompson type (Disease Ontology:DOID:0080051); acromesomelic dysplasia, Grebe type (Disease Ontology:DOID:0080052); proximal symphalangism 2 (Disease Ontology:DOID:0080788); multiple synostoses syndrome 1 (Disease Ontology:DOID:0081317); multiple synostoses syndrome 2 (Disease Ontology:DOID:0081318); brachydactyly type A1 (Disease Ontology:DOID:0110964); brachydactyly type A2 (Disease Ontology:DOID:0110965); brachydactyly type C (Disease Ontology:DOID:0110970); brachydactyly type A1C (Disease Ontology:DOID:0110977); Parkinson's disease (Disease Ontology:DOID:14330); osteoarthritis (Disease Ontology:DOID:8398)",
        "pathway": " (rno:252835);  (R-RNO-2129379)",
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        "publication_id_list": "26010756;37310547",
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        "function": "Gdf-5 induced the expression of the alpha5 sub-unit, while Bmp-7 induced the expression of the alphaV sub-unit. Publication Status: Online-Only, [RefSeq, PubMed]; Growth differentiation factor 5 inhibits lipopolysaccharide-mediated pyroptosis of nucleus pulposus mesenchymal stem cells via RhoA signaling pathway., [RefSeq, PubMed]; Growth factor involved in bone and cartilage formation. During cartilage development regulates differentiation of chondrogenic tissue through two pathways. Firstly, positively regulates differentiation of chondrogenic tissue through its binding of high affinity with BMPR1B and of less affinity with BMPR1A, leading to induction of SMAD1-SMAD5-SMAD8 complex phosphorylation and then SMAD protein signaling transduction. Secondly, negatively regulates chondrogenic differentiation through its interaction with NOG. Required to prevent excessive muscle loss upon denervation. This function requires SMAD4 and is mediated by phosphorylated SMAD1/5/8. Binds bacterial lipopolysaccharide (LPS) and mediates LPS-induced inflammatory response, including TNF secretion by monocytes., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005615 extracellular space;GO:0005886 plasma membrane",
        "go_biological_process": "GO:2001054 negative regulation of mesenchymal cell apoptotic process;GO:0040014 regulation of multicellular organism growth;GO:0045666 positive regulation of neuron differentiation;GO:0050680 negative regulation of epithelial cell proliferation;GO:0043524 negative regulation of neuron apoptotic process",
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            {
                "id": "NP_001104836",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001104836",
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            }
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        "gene_names_refseq": "Afmid",
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        "function": "Catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes (in vitro). Binds calcium ions., [UniProtKB, UniProtKB, UniProtKB]",
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        ],
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        "protein_names_uniprotkb": "DNA methyltransferase 1-associated protein 1",
        "protein_names_refseq": "DNA methyltransferase 1-associated protein 1",
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        "disease": "",
        "pathway": " (rno:298447)",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0003714 transcription corepressor activity;GO:0061629 RNA polymerase II-specific DNA-binding transcription factor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0035267 NuA4 histone acetyltransferase complex",
        "go_biological_process": "GO:0042307 positive regulation of protein import into nucleus;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006281 DNA repair;GO:0006338 chromatin remodeling;GO:0006351 DNA-templated transcription",
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        "kg_view_protein": true
    },
    {
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            {
                "id": "Q569A7_RAT",
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            }
        ],
        "mass": 31190.0,
        "length": 281,
        "protein_name": "diphthine methyl ester synthase",
        "gene_name": "Dph5",
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        "refseq_name": "diphthine methyl ester synthase",
        "refseq_ac": [
            {
                "id": "NP_001017449",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001017449",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Dph5",
        "gene_names_refseq": "CGI-30; Dph5; RGD1307867",
        "protein_names_uniprotkb": "diphthine methyl ester synthase; 2.1.1.314",
        "protein_names_refseq": "DPH5 homolog; diphthine methyl ester synthase; diphthine synthase",
        "tax_id": 10116,
        "disease": "neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties (Disease Ontology:DOID:0070479)",
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        "function": "S-adenosyl-L-methionine-dependent methyltransferase that catalyzes four methylations of the modified target histidine residue in translation elongation factor 2 (EF-2), to form an intermediate called diphthine methyl ester. The four successive methylation reactions represent the second step of diphthamide biosynthesis., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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            {
                "id": "3.6.5.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.-",
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            },
            {
                "id": "2.1.1.314",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.314",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0004164 diphthine synthase activity;GO:0141133 diphthine methyl ester synthase activity",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0032259 methylation;GO:0017183 protein histidyl modification to diphthamide",
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    },
    {
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            {
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            }
        ],
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        "length": 239,
        "protein_name": "Claudin",
        "gene_name": "Cldn14",
        "organism": "Rat",
        "refseq_name": "claudin-14",
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            {
                "id": "NP_001013447",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001013447",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Cldn14",
        "gene_names_refseq": "Cldn14",
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        "tax_id": 10116,
        "disease": "autosomal recessive nonsyndromic deafness 29 (Disease Ontology:DOID:0110487)",
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        "publication_id_list": "33283646;33903003",
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        "function": "Claudin 14/15 play important roles in early wallerian degeneration after rat sciatic nerve injury., [RefSeq, PubMed]; Claudins function as major constituents of the tight junction complexes that regulate the permeability of epithelia., [UniProtKB, UniProtKB]; Localization and regulation of claudin-14 in experimental models of hypercalcemia., [RefSeq, PubMed]",
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        ],
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        "length": 362,
        "protein_name": "Talin rod domain-containing protein 1",
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        "refseq_name": "talin rod domain-containing protein 1",
        "refseq_ac": [
            {
                "id": "NP_001013167",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001013167",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tlnrd1; Mesdc1",
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        "protein_names_uniprotkb": "Talin rod domain-containing protein 1; Mesoderm development candidate 1",
        "protein_names_refseq": "mesoderm development candidate 1; talin rod domain-containing protein 1",
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        "function": "Actin-binding protein which may have an oncogenic function and regulates cell proliferation, migration and invasion in cancer cells., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003779 actin binding;GO:0042802 identical protein binding",
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        ],
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        "length": 293,
        "protein_name": "GTPase, IMAP family member 7",
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            {
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        "gene_names_uniprotkb": "Gimap7",
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        "protein_names_refseq": "GTPase, IMAP family member 7",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005811 lipid droplet",
        "go_biological_process": "GO:0046039 GTP metabolic process",
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    {
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        ],
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        "length": 507,
        "protein_name": "Tyrosine-protein kinase",
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            {
                "id": "NP_001011961",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001011961",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Srms",
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        "protein_names_refseq": "tyrosine-protein kinase Srms",
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        "function": "Non-receptor tyrosine-protein kinase which phosphorylates DOK1 on tyrosine residues. Also phosphorylates KHDRBS1/SAM68 and VIM on tyrosine residues. Phosphorylation of KHDRBS1 is EGF-dependent. Phosphorylates OTUB1, promoting deubiquitination of RPTOR., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": [
            {
                "id": "2.7.12.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.12.1",
                "type": "external"
            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.10.1",
                "type": "external"
            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.10.2",
                "type": "external"
            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.12.2",
                "type": "external"
            },
            {
                "id": "2.7.1.40",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.40",
                "type": "external"
            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.13",
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            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.10.4",
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            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.32",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.82",
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        ],
        "go_molecular_function": "GO:0004713 protein tyrosine kinase activity;GO:0004715 non-membrane spanning protein tyrosine kinase activity;GO:0005102 signaling receptor binding;GO:0005524 ATP binding",
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        "go_biological_process": "GO:1904263 positive regulation of TORC1 signaling;GO:0007169 cell surface receptor protein tyrosine kinase signaling pathway;GO:0018108 peptidyl-tyrosine phosphorylation;GO:0030154 cell differentiation;GO:0038083 peptidyl-tyrosine autophosphorylation",
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        "mass": 17055.0,
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            {
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        "protein_names_refseq": "vomernasal 1 receptor Vom1r108; vomeronasal 1 receptor 108; vomeronasal 1 receptor, G6; vomeronasal V1r-type receptor V1rg6; vomeronasal type-1 receptor 3",
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                "id": "NP_001014039",
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        ],
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        "protein_name": "Zinc finger and BTB domain containing 16",
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        "organism": "Rat",
        "refseq_name": "zinc finger and BTB domain-containing protein 16",
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            {
                "id": "NP_001013199",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001013199",
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        "protein_names_uniprotkb": "Zinc finger and BTB domain containing 16",
        "protein_names_refseq": "Polydactyly-luxate syndrome; promyelocytic leukemia zinc finger; zinc finger and BTB domain containing 16 protein; zinc finger and BTB domain-containing protein 16; zinc finger protein 145",
        "tax_id": 10116,
        "disease": "acute promyelocytic leukemia (Disease Ontology:DOID:0060318); caudal regression syndrome (Disease Ontology:DOID:0080700); polydactyly (Disease Ontology:DOID:1148)",
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        "function": "All homozygous PLZF gene mutated animals exhibited manifestations of a caudal regression syndrome including tail anomalies and serious size reduction and deformities of long bones, and oligo- or polydactyly on the hindlimbs. Erratum:[PLoS One. 2020 Jan 16;15(1):e0228139. PMID: 31945126] Publication Status: Online-Only, [RefSeq, PubMed]; GCN5 regulates ZBTB16 through acetylation, mediates osteogenic differentiation, and affects orthodontic tooth movement., [RefSeq, PubMed]; This study idnetifed that the ZBTB16 as inhibitors of neurite outgrowth., [RefSeq, PubMed]",
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        "protein_name": "NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0051539 4 iron, 4 sulfur cluster binding;GO:0051287 NAD binding;GO:0008137 NADH dehydrogenase (ubiquinone) activity;GO:0010181 FMN binding",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane;GO:0045271 respiratory chain complex I",
        "go_biological_process": "GO:0006120 mitochondrial electron transport, NADH to ubiquinone;GO:0042775 mitochondrial ATP synthesis coupled electron transport",
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            {
                "id": "NP_542953",
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            {
                "id": "NP_001007608",
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        "protein_name": "Intercellular adhesion molecule 2",
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            {
                "id": "NP_001007726",
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        "pathway": " (rno:360647);  (R-RNO-198933);  (R-RNO-216083);  (R-RNO-5621575)",
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        "function": "Data suggest that ICAM2 plays important role in apical dynamics/sperm head during spermatogenesis; ICAM2 surrounds heads of elongating/elongated spermatids in all stages of seminiferous epithelial cycle. Publication Status: Online-Only, [RefSeq, PubMed]; Flotillin-2 is involved with adhesion between UECs and the implanting blastocyst, whereas ICAM-2 is associated with the ability for UECs to be removed at the time of implantation., [RefSeq, PubMed]",
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            {
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001014121",
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        "function": "Expression patterns of Paqr8 is low and homogeneous in the hypothalamus and more abundant in thalamic nuclei, and is likely to regulate sensory and cognitive functions in forebrain tissues of female rats., [RefSeq, PubMed]; PAQR8 and PAQR9 expression is altered in the ventral tegmental area of aged rats infected with varicella zoster virus., [RefSeq, PubMed]",
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        "protein_name": "Ectodermal-neural cortex 1",
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            {
                "id": "NP_001003401",
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        "gene_names_uniprotkb": "Enc1",
        "gene_names_refseq": "Enc1; Nrpb",
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        "protein_names_refseq": "ectoderm-neural cortex protein 1; nuclear restrict protein in brain",
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        "function": "Knockdown of Enc1 protects neurons from apoptosis induced by oxygen-glucose deprivation associated with Nrf2 and HO-1., [RefSeq, PubMed]; Show that overexpression of the Nrp/b cDNA in C6/ST1 cells suppresses anchorage independence in vitro and tumorigenicity in vivo, altering their malignant nature towards a more benign phenotype., [RefSeq, PubMed]; The study further shows the physical association of ENC1 and F-actin, implicating the role of ENC1 in cytoskeletal reorganization during the differentiation of granulosa cells., [RefSeq, PubMed]",
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        "go_biological_process": "GO:0010976 positive regulation of neuron projection development;GO:0016567 protein ubiquitination;GO:0017148 negative regulation of translation;GO:0006511 ubiquitin-dependent protein catabolic process;GO:0010499 proteasomal ubiquitin-independent protein catabolic process",
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        "protein_name": "Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16",
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        "refseq_name": "pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16",
        "refseq_ac": [
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_997661",
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        "gene_names_refseq": "Dbp2; Ddx16; Dhx16",
        "protein_names_uniprotkb": "Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16; 3.6.4.13; DEAH-box protein 16",
        "protein_names_refseq": "DEAH (Asp-Glu-Ala-His) box polypeptide 16; pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16; putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16",
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        "pathway": " (rno:294232);  (R-RNO-72163)",
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        "function": "Required for pre-mRNA splicing as a component of the spliceosome. Contributes to pre-mRNA splicing after spliceosome formation and prior to the first transesterification reaction. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs. Also plays a role in innate antiviral response by acting as a pattern recognition receptor sensing splicing signals in viral RNA. Mechanistically, TRIM6 promotes the interaction between unanchored 'Lys-48'-polyubiquitin chains and DHX16, leading to DHX16 interaction with RIGI and ssRNA to amplify RIGI-dependent innate antiviral immune responses., [UniProtKB, UniProtKB, UniProtKB]",
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                "id": "5.6.2.3",
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        "function": "Cdx2 expression levels, elevated by IPTG treatment, are not affected by Slfn3-specific siRNA, suggesting that Cdx2 lies upstream of Slfn3 in IEC-Cdx1-L1 enterocytes., [RefSeq, PubMed]; Cdx2-regulated genes were elucidated,which suggested the functions of Cdx2 in cell fate decision and maintenance of intestinal epithelium, [RefSeq, PubMed]; Data indicate HB-EGF gene expression can be regulated by Cdx2 in intestinal epithelial (IEC-6) cells, [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0000794 condensed nuclear chromosome;GO:0005634 nucleus;GO:0017053 transcription repressor complex;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0008284 positive regulation of cell population proliferation;GO:0030154 cell differentiation;GO:0045944 positive regulation of transcription by RNA polymerase II",
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        ],
        "mass": 17273.0,
        "length": 153,
        "protein_name": "Prostaglandin E synthase",
        "gene_name": "Ptges",
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                "id": "NP_067594",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_067594",
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        "gene_names_uniprotkb": "Ptges; Pges; Pig12",
        "gene_names_refseq": "Pges; Ptges; mPGES-1",
        "protein_names_uniprotkb": "Prostaglandin E synthase; 1.11.1.-; 2.5.1.18; 5.3.99.3; Glutathione peroxidase PTGES; Glutathione transferase PTGES; Inducible prostaglandin E synthase; Microsomal prostaglandin E synthase 1; mPGES-1",
        "protein_names_refseq": "glutathione peroxidase PTGES; glutathione transferase PTGES; inducible prostaglandin E synthase; microsomal prostaglandin E synthase 1; prostaglandin E synthase",
        "tax_id": 10116,
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        "function": "In conclusion, microsomal PGES-1 plays a critical role in the continuous suppression of motor function in the post-bowel obstruction state. Publication Status: Online-Only, [RefSeq, PubMed]; PTGES is involved in myofibroblast differentiation via HIF-1alpha-dependent glycolysis pathway., [RefSeq, PubMed]; Suggest pivotal role of COX-2-mPGES-1-PGE2 axis in vascular calcification. Inhibition of COX-2 or mPGES-1 may increase the risk of calcification and subsequent adverse cardiovascular events during chronic renal failure., [RefSeq, PubMed]; Terminal enzyme of the cyclooxygenase (COX)-2-mediated prostaglandin E2 (PGE2) biosynthetic pathway. Catalyzes the glutathione-dependent oxidoreduction of prostaglandin endoperoxide H2 (PGH2) to prostaglandin E2 (PGE2) in response to inflammatory stimuli (PubMed:10869354, PubMed:11067848). Plays a key role in inflammation response, fever and pain (By similarity). Also catalyzes the oxidoreduction of endocannabinoids into prostaglandin glycerol esters and PGG2 into 15-hydroperoxy-PGE2. In addition, displays low glutathione transferase and glutathione-dependent peroxidase activities, toward 1-chloro-2,4-dinitrobenzene and 5-hydroperoxyicosatetraenoic acid (5-HPETE), respectively (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed, UniProtKB]; Using metabolic profiling and exploratory rat toxicity studies, a new and active mPGES-1 inhibitor with improved margins to chemically induced kidney toxicity in rats has been identified., [RefSeq, PubMed]",
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        "ec_number_list": [
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                "id": "1.11.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.11.1.-",
                "type": "external"
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            {
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                "type": "external"
            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:5.3.99.3",
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            },
            {
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        ],
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        "go_biological_process": "GO:0031620 regulation of fever generation;GO:0008285 negative regulation of cell population proliferation;GO:0032496 response to lipopolysaccharide;GO:0051592 response to calcium ion;GO:0019233 sensory perception of pain",
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099764",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ndufab1",
        "gene_names_refseq": "Ndufab1",
        "protein_names_uniprotkb": "Acyl carrier protein",
        "protein_names_refseq": "NADH dehydrogenase (ubiquinone) 1, alpha/beta subcomplex, 1; acyl carrier protein, mitochondrial",
        "tax_id": 10116,
        "disease": "neurodegeneration with brain iron accumulation (Disease Ontology:DOID:0110734)",
        "pathway": " (rno:293453);  (R-RNO-611105);  (R-RNO-6799198);  (R-RNO-77289);  (R-RNO-9857492);  (R-RNO-9937383)",
        "pathway_count": 6,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Carrier of the growing fatty acid chain in fatty acid biosynthesis., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0000035 acyl binding;GO:0000036 acyl carrier activity;GO:0005198 structural molecule activity;GO:0140978 mitochondrial large ribosomal subunit binding",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0031966 mitochondrial membrane;GO:0045271 respiratory chain complex I;GO:0005743 mitochondrial inner membrane;GO:0099128 mitochondrial [2Fe-2S] assembly complex",
        "go_biological_process": "GO:0022904 respiratory electron transport chain;GO:0009249 protein lipoylation;GO:1902775 mitochondrial large ribosomal subunit assembly;GO:0044571 [2Fe-2S] cluster assembly;GO:0006633 fatty acid biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZF13-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZF53-1",
        "uniprot_id": [
            {
                "id": "D3ZF53_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZF53",
                "type": "external"
            }
        ],
        "mass": 25038.0,
        "length": 235,
        "protein_name": "BPI fold containing family B, member 9A",
        "gene_name": "Bpifb9a",
        "organism": "Rat",
        "refseq_name": "Protein RoBo-1-like precursor",
        "refseq_ac": [
            {
                "id": "NP_001103103",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001103103",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Bpifb9a; LOC691277",
        "gene_names_refseq": "Bpifb9a",
        "protein_names_uniprotkb": "BPI fold containing family B, member 9A",
        "protein_names_refseq": "Protein RoBo-1-like precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:691277)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005576 extracellular region",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZF53-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZG87-1",
        "uniprot_id": [
            {
                "id": "D3ZG87_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZG87",
                "type": "external"
            }
        ],
        "mass": 32191.0,
        "length": 291,
        "protein_name": "RPE-retinal G protein-coupled receptor",
        "gene_name": "Rgr",
        "organism": "Rat",
        "refseq_name": "RPE-retinal G protein-coupled receptor",
        "refseq_ac": [
            {
                "id": "NP_001100769",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100769",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Rgr",
        "gene_names_refseq": "Rgr",
        "protein_names_uniprotkb": "RPE-retinal G protein-coupled receptor",
        "protein_names_refseq": "RPE-retinal G protein-coupled receptor",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa 44 (Disease Ontology:DOID:0110394); retinitis pigmentosa (Disease Ontology:DOID:10584)",
        "pathway": " (rno:306307);  (R-RNO-418594);  (R-RNO-419771)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Receptor for all-trans- and 11-cis-retinal. Binds preferentially to the former and may catalyze the isomerization of the chromophore by a retinochrome-like mechanism., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0008020 G protein-coupled photoreceptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007601 visual perception;GO:0007602 phototransduction;GO:0071482 cellular response to light stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZG87-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    }
]
