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        "uniprot_canonical_ac": "D3ZGU3-1",
        "uniprot_id": [
            {
                "id": "D3ZGU3_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZGU3",
                "type": "external"
            }
        ],
        "mass": 30983.0,
        "length": 269,
        "protein_name": "C-type lectin domain family 1, member A",
        "gene_name": "Clec1a",
        "organism": "Rat",
        "refseq_name": "C-type lectin domain family 1 member A",
        "refseq_ac": [
            {
                "id": "NP_001102723",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102723",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Clec1a",
        "gene_names_refseq": "Clec1a; RGD1566110",
        "protein_names_uniprotkb": "C-type lectin domain family 1, member A",
        "protein_names_refseq": "C-type lectin domain family 1 member A",
        "tax_id": 10116,
        "disease": "aspergillosis (Disease Ontology:DOID:13564)",
        "pathway": " (rno:500337)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0004888 transmembrane signaling receptor activity;GO:0030246 carbohydrate binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0006955 immune response;GO:0007165 signal transduction;GO:0050832 defense response to fungus;GO:0008037 cell recognition",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZGU3-1",
        "record_type": "protein",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZHM5-1",
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            {
                "id": "D3ZHM5_RAT",
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                "type": "external"
            }
        ],
        "mass": 42991.0,
        "length": 413,
        "protein_name": "Homeobox A10",
        "gene_name": "Hoxa10",
        "organism": "Rat",
        "refseq_name": "homeobox protein Hox-A10 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001389216",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001389216",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Hoxa10",
        "gene_names_refseq": "Hoxa10",
        "protein_names_uniprotkb": "Homeobox A10",
        "protein_names_refseq": "homeobox protein Hox-A10 isoform 1; homeobox protein Hox-A10-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100911668)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "37062956",
        "class_list": "",
        "function": "Reduced expression of Il10, Stat3, Hoxa10, and Itgb3 in the embryo implantation site of rat model with prenatal androgen-induced polycystic ovary syndrome., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0042826 histone deacetylase 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:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0016604 nuclear body;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007283 spermatogenesis;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0007338 single fertilization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
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        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000000.000.00000",
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    {
        "uniprot_canonical_ac": "D3ZIA4-1",
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            {
                "id": "D3ZIA4_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZIA4",
                "type": "external"
            }
        ],
        "mass": 26287.0,
        "length": 232,
        "protein_name": "BTB/POZ domain-containing protein KCTD11",
        "gene_name": "Kctd11",
        "organism": "Rat",
        "refseq_name": "BTB/POZ domain-containing protein KCTD11 isoform 2",
        "refseq_ac": [
            {
                "id": "NP_001102301",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102301",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Kctd11",
        "gene_names_refseq": "Kctd11",
        "protein_names_uniprotkb": "BTB/POZ domain-containing protein KCTD11; KCASH1 protein; Potassium channel tetramerization domain-containing protein 11; RING-type E3 ubiquitin transferase subunit KCTD11",
        "protein_names_refseq": "BTB/POZ domain-containing protein KCTD11 isoform 2; BTB/POZ domain-containing protein KCTD11; potassium channel tetramerisation domain containing 11",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363634)",
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        "function": "Plays a role as a marker and a regulator of neuronal differentiation; Up-regulated by a variety of neurogenic signals, such as retinoic acid, epidermal growth factor/EGF and NGFB/nerve growth factor. Induces apoptosis, growth arrest and the expression of cyclin-dependent kinase inhibitor CDKN1B. Plays a role as a tumor repressor and inhibits cell growth and tumorigenicity of medulloblastoma (MDB). Acts as a probable substrate-specific adapter for a BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complex towards HDAC1. Functions as antagonist of the Hedgehog pathway on cell proliferation and differentiation by affecting the nuclear transfer of transcription factor GLI1, thus maintaining cerebellar granule cells in undifferentiated state, this effect probably occurs via HDAC1 down-regulation, keeping GLI1 acetylated and inactive. When knock-down, Hedgehog antagonism is impaired and proliferation of granule cells is sustained. Activates the caspase cascade., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0016740 transferase activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
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        "synthesized_glycan_count": 0,
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                "type": "external"
            }
        ],
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        "length": 296,
        "protein_name": "Enoyl CoA hydratase domain containing 2",
        "gene_name": "Echdc2",
        "organism": "Rat",
        "refseq_name": "enoyl-CoA hydratase domain-containing protein 2, mitochondrial",
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            {
                "id": "NP_001100145",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100145",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Echdc2",
        "gene_names_refseq": "Echdc2; RGD1308525",
        "protein_names_uniprotkb": "Enoyl CoA hydratase domain containing 2",
        "protein_names_refseq": "enoyl Coenzyme A hydratase domain containing 2; enoyl-CoA hydratase domain-containing protein 2, mitochondrial",
        "tax_id": 10116,
        "disease": "3-methylglutaconic aciduria type 1 (Disease Ontology:DOID:0110002)",
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        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "3.1.2.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.2.4",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0003723 RNA binding;GO:0004300 enoyl-CoA hydratase activity;GO:0016829 lyase activity;GO:0003824 catalytic activity;GO:0003860 3-hydroxyisobutyryl-CoA hydrolase activity",
        "go_cellular_component": "GO:0005739 mitochondrion",
        "go_biological_process": "GO:0006635 fatty acid beta-oxidation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZIL6-1",
        "record_type": "protein",
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        "kg_view_protein": true
    },
    {
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            {
                "id": "D3ZIM8_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZIM8",
                "type": "external"
            }
        ],
        "mass": 26374.0,
        "length": 231,
        "protein_name": "LKAAEAR motif containing 1",
        "gene_name": "Lkaaear1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Lkaaear1; RGD1306208",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "LKAAEAR motif containing 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:296483)",
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        ],
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        "length": 592,
        "protein_name": "Zinc finger protein 68",
        "gene_name": "Zfp68",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 68 isoform 1",
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        "protein_names_refseq": "zinc finger protein 68 isoform 1",
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        "missing_score": 10000,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZIP9-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
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    {
        "uniprot_canonical_ac": "D3ZJG5-1",
        "uniprot_id": [
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                "id": "D3ZJG5_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZJG5",
                "type": "external"
            }
        ],
        "mass": 35025.0,
        "length": 313,
        "protein_name": "Olfactory receptor family 10 subfamily G member 3C",
        "gene_name": "Or10g3c",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1639",
        "refseq_ac": [
            {
                "id": "NP_001000833",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000833",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Or10g3c",
        "gene_names_refseq": "Olr1639; Or10g3c",
        "protein_names_uniprotkb": "Olfactory receptor family 10 subfamily G member 3C",
        "protein_names_refseq": "olfactory receptor 1639; olfactory receptor Olr1639; olfactory receptor gene Olr1639",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:405122)",
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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]",
        "predicted_glycosites": 0,
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        ],
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        ],
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            {
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        "protein_names_refseq": "GTPase ERas",
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        "publication_id_list": "26884329",
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        "function": "Findings indicate that ERAS is important to maintain quiescence in HSCs., [RefSeq, PubMed]",
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            },
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            },
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            {
                "id": "3.6.1.-",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.4",
                "type": "external"
            }
        ],
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        ],
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        "length": 309,
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        "refseq_name": "olfactory receptor Olr1238",
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            {
                "id": "NP_001001013",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001001013",
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            }
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        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1238; olfactory receptor 8B3-like; olfactory receptor Olr1238; olfactory receptor gene Olr1238",
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        "go_cellular_component": "GO:0005886 plasma membrane",
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        ],
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        "protein_name": "Mitochondrial adenyl nucleotide antiporter SLC25A24",
        "gene_name": "Slc25a54",
        "organism": "Rat",
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            {
                "id": "NP_001103110",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001103110",
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            }
        ],
        "gene_names_uniprotkb": "Slc25a54; LOC691448",
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        "protein_names_uniprotkb": "Mitochondrial adenyl nucleotide antiporter SLC25A24; Small calcium-binding mitochondrial carrier protein 1; Solute carrier family 25 member 24",
        "protein_names_refseq": "solute carrier family 25, member 54",
        "tax_id": 10116,
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        "function": "Electroneutral antiporter that mediates the transport of adenyl nucleotides through the inner mitochondrial membrane. Originally identified as an ATP-magnesium/inorganic phosphate antiporter, it also acts as a broad specificity adenyl nucleotide antiporter. By regulating the mitochondrial matrix adenyl nucleotide pool, could adapt to changing cellular energetic demands and indirectly regulate adenyl nucleotide-dependent metabolic pathways. In vitro, a low activity is also observed with guanyl and pyrimidine nucleotides. May play a role in protecting cells against oxidative stress-induced cell death, by buffering calcium levels in the mitochondrial matrix through the formation of calcium-phosphate precipitates., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0015297 antiporter activity;GO:0005347 ATP transmembrane transporter activity",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane;GO:0005829 cytosol;GO:0005815 microtubule organizing center;GO:0033391 chromatoid body",
        "go_biological_process": "GO:0015866 ADP transport;GO:0015867 ATP transport",
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                "id": "D3ZTW9_RAT",
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        ],
        "mass": 41327.0,
        "length": 368,
        "protein_name": "Nuclease EXOG, mitochondrial",
        "gene_name": "Exog",
        "organism": "Rat",
        "refseq_name": "nuclease EXOG, mitochondrial precursor",
        "refseq_ac": [
            {
                "id": "NP_001100336",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100336",
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            }
        ],
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        "gene_names_refseq": "Endogl1; Exog",
        "protein_names_uniprotkb": "Nuclease EXOG, mitochondrial; Endonuclease G-like 1",
        "protein_names_refseq": "endo/exonuclease (5'-3'), endonuclease G-like; endonuclease G-like 1; nuclease EXOG, mitochondrial precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:301062)",
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        "publication_id_list": "27417117;33515431",
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        "function": "Endo/exonuclease G-like plays an essential role in cardiomyocyte physiology. Loss of endo/exonuclease G-like results in diminished adaptation to pathological stress. The decline in maximal respiration and reserve capacity is the first sign of mitochondrial dysfunction that determines subsequent cell death., [RefSeq, PubMed]; Endo/exonuclease with nicking activity towards supercoiled DNA, a preference for single-stranded DNA and 5'-3' exonuclease activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; PGC-1a Mediated-EXOG, a Specific Repair Enzyme for Mitochondrial DNA, Plays an Essential Role in the Rotenone-Induced Neurotoxicity of PC12 Cells., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005743 mitochondrial inner membrane;GO:0005739 mitochondrion;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0006309 apoptotic DNA fragmentation",
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        "protein_name": "Olfactory receptor",
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            {
                "id": "NP_001000554",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000554",
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            }
        ],
        "gene_names_uniprotkb": "Or6ae1",
        "gene_names_refseq": "Olr286; Or6ae1",
        "protein_names_uniprotkb": "Olfactory receptor",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "go_biological_process": "GO:0050911 detection of chemical stimulus involved in sensory perception of smell",
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        ],
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        "length": 75,
        "protein_name": "Protein BRICK1",
        "gene_name": "Brk1",
        "organism": "Rat",
        "refseq_name": "protein BRICK1",
        "refseq_ac": [
            {
                "id": "NP_001182405",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001182405",
                "type": "external"
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        ],
        "gene_names_uniprotkb": "Brk1",
        "gene_names_refseq": "Brk1",
        "protein_names_uniprotkb": "Protein BRICK1",
        "protein_names_refseq": "BRICK1, SCAR/WAVE actin-nucleating complex subunit; probable protein BRICK1; protein BRICK1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:679934);  (R-RNO-2029482);  (R-RNO-4420097);  (R-RNO-5663213);  (R-RNO-9013149);  (R-RNO-9013404);  (R-RNO-9013423)",
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        "function": "Involved in regulation of actin and microtubule organization. Part of a WAVE complex that activates the Arp2/3 complex. As component of the WAVE1 complex, required for BDNF-NTRK2 endocytic trafficking and signaling from early endosomes., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_cellular_component": "GO:0000785 chromatin",
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        "protein_name": "Iron-sulfur cluster assembly factor IBA57, mitochondrial",
        "gene_name": "Iba57",
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            {
                "id": "NP_001102297",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102297",
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            }
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        "protein_names_uniprotkb": "Iron-sulfur cluster assembly factor IBA57, mitochondrial; Iron-sulfur cluster assembly factor homolog",
        "protein_names_refseq": "IBA57 homolog, iron-sulfur cluster assembly; IBA57 iron-sulfur cluster assembly; IBA57, iron-sulfur cluster assembly homolog; putative transferase CAF17 homolog, mitochondrial; putative transferase CAF17, mitochondrial",
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        "disease": "multiple mitochondrial dysfunctions syndrome 3 (Disease Ontology:DOID:0080135); hereditary spastic paraplegia 74 (Disease Ontology:DOID:0110819)",
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        "function": "Mitochondrial protein involved in the maturation of mitochondrial [4Fe-4S]-proteins in the late stage of the iron-sulfur cluster assembly pathway. Operates in cooperation with ISCA2 in the maturation of [4Fe-4S] proteins., [UniProtKB, UniProtKB]",
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            {
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        "protein_name": "Protein-lysine N-methyltransferase SMYD4",
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            {
                "id": "NP_001099280",
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        "function": "Protein-lysine N-methyltransferase. Monomethylates PRMT5, modulating its transcriptional activity. May also act as a histone methyltransferase. Plays a critical role in cardiac development. Acts as a key epigenetic regulator of gene expression during cardiac development via its dual activities as a methyltransferase and negative regulator of HDAC1., [UniProtKB, UniProtKB, UniProtKB]",
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            {
                "id": "2.1.1.359",
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            {
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            },
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.362",
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        ],
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            {
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        "protein_names_refseq": "receptor transporter protein 1; receptor-transporting protein 1",
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        "protein_name": "Kinesin family member 4A",
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            {
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001387859",
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        ],
        "gene_names_uniprotkb": "Kif4a",
        "gene_names_refseq": "Kif4a; Kif4",
        "protein_names_uniprotkb": "Kinesin family member 4A",
        "protein_names_refseq": "chromosome-associated kinesin KIF4A; kinesin family member 4; kinesin heavy chain member 4",
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        "disease": "non-syndromic X-linked intellectual disability 100 (Disease Ontology:DOID:0112040); epilepsy (Disease Ontology:DOID:1826)",
        "pathway": " (rno:84393);  (R-RNO-2132295);  (R-RNO-437239);  (R-RNO-6811434);  (R-RNO-983189)",
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        "class_list": "",
        "function": "KIF4 is involved in the anterograde trafficking of ribosomal constituents to axons, [RefSeq, PubMed]; Knockdown of KIF4A expression with shRNA reduced the level of integrin beta1 in axons of developing neurons., [RefSeq, PubMed]",
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        "go_biological_process": "GO:0000281 mitotic cytokinesis;GO:0007018 microtubule-based movement;GO:0007052 mitotic spindle organization;GO:0051256 mitotic spindle midzone assembly;GO:0051231 spindle elongation",
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        "mass": 127584.0,
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        "protein_name": "Sentrin-specific protease 6",
        "gene_name": "Senp6",
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        "refseq_name": "sentrin-specific protease 6",
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                "id": "NP_001100312",
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        ],
        "gene_names_uniprotkb": "Senp6",
        "gene_names_refseq": "Senp6",
        "protein_names_uniprotkb": "Sentrin-specific protease 6; SUMO-1-specific protease 1; Sentrin/SUMO-specific protease SENP6",
        "protein_names_refseq": "SUMO/sentrin specific peptidase 6; SUMO/sentrin specific protease 6; SUMO1/sentrin specific peptidase 6; Sumo1/sentrin/SMT3 specific peptidase 6; sentrin-specific protease 6",
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        "function": "Our data suggest that ethanol exposure during adolescence induces the microglia-mediated neuroinflammation via TLR4 activation, and SENP6 plays an essential role in dampening NF-kappaB activation and neuroinflammation. Publication Status: Online-Only, [RefSeq, PubMed]; Protease that deconjugates SUMO1, SUMO2 and SUMO3 from targeted proteins. Processes preferentially poly-SUMO2 and poly-SUMO3 chains, but does not efficiently process SUMO1, SUMO2 and SUMO3 precursors. Deconjugates SUMO1 from RXRA, leading to transcriptional activation. Involved in chromosome alignment and spindle assembly, by regulating the kinetochore CENPH-CENPI-CENPK complex. Desumoylates PML and CENPI, protecting them from degradation by the ubiquitin ligase RNF4, which targets polysumoylated proteins for proteasomal degradation. Also desumoylates RPA1, thus preventing recruitment of RAD51 to the DNA damage foci to initiate DNA repair through homologous recombination., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0070139 SUMO-specific endopeptidase activity;GO:0008234 cysteine-type peptidase activity",
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        "go_biological_process": "GO:0070646 protein modification by small protein removal;GO:0006508 proteolysis;GO:0090169 regulation of spindle assembly;GO:0090234 regulation of kinetochore assembly;GO:0016926 protein desumoylation",
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            {
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                "id": "G3V6X6_RAT",
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        "length": 179,
        "protein_name": "Interleukin 22",
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        "refseq_name": "interleukin-22 precursor",
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            {
                "id": "NP_001178917",
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        "protein_names_uniprotkb": "Interleukin 22",
        "protein_names_refseq": "interferon 2b1; interleukin-22 precursor",
        "tax_id": 10116,
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        "pathway": " (rno:500836);  (R-RNO-8854691)",
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        "function": "Conclude that IL-22 expression level was increased and correlated with disease severity, which indicated that IL-22 may play an important role in development of PIA, and was helpful to explorer the pathogenesis of rheumatoid arthritis Publication Status: Online-Only, [RefSeq, PubMed]; IL22 may serve an important role in the pathological process of pristaneinduced arthritis, particularly in the chronic fluctuation phase., [RefSeq, PubMed]; The results suggest that the transplantation of mesenchymal stem cells can reduce the expression of RANKL in vivo by downregulating the levels of IL-22, thereby ameliorating the degree of rheumatoid arthritis. Publication Status: Online-Only, [RefSeq, PubMed]; The that IL-22 plays a protective role in this process via the down-regulation of uncoupling protein-2 (UCP-2)., [RefSeq, PubMed]",
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        "protein_name": "DNA repair protein Ku80",
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            {
                "id": "NP_803154",
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        ],
        "gene_names_uniprotkb": "Xrcc5",
        "gene_names_refseq": "Ku80; Kup80; Xrcc5",
        "protein_names_uniprotkb": "DNA repair protein Ku80; 4.2.99.18; 5.6.2.4",
        "protein_names_refseq": "Ku autoantigen, 80kD); X-ray repair complementing defective repair in Chinese hamster cells 5; X-ray repair cross complementation (double-strand-break rejoining; X-ray repair cross-complementing protein 5",
        "tax_id": 10116,
        "disease": "COVID-19 (Disease Ontology:DOID:0080600); neurodegeneration with brain iron accumulation (Disease Ontology:DOID:0110734); hemochromatosis type 5 (Disease Ontology:DOID:0111031); candidiasis (Disease Ontology:DOID:1508); alcohol use disorder (Disease Ontology:DOID:1574); squamous cell carcinoma (Disease Ontology:DOID:1749); rectum cancer (Disease Ontology:DOID:1993); basal cell carcinoma (Disease Ontology:DOID:2513); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); congestive heart failure (Disease Ontology:DOID:6000); hepatocellular carcinoma (Disease Ontology:DOID:684); multiple myeloma (Disease Ontology:DOID:9538)",
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        "go_cellular_component": "GO:0014069 postsynaptic density;GO:0030425 dendrite;GO:0045202 synapse;GO:0044297 cell body;GO:0005834 heterotrimeric G-protein complex",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007204 positive regulation of cytosolic calcium ion concentration",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
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        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000000.000.00000",
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    },
    {
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            {
                "id": "G3V8M6_RAT",
                "url": "https://www.uniprot.org/uniprot/G3V8M6",
                "type": "external"
            }
        ],
        "mass": 29571.0,
        "length": 255,
        "protein_name": "Folate receptor alpha",
        "gene_name": "Folr1",
        "organism": "Rat",
        "refseq_name": "folate receptor alpha precursor",
        "refseq_ac": [
            {
                "id": "NP_598211",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_598211",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Folr1",
        "gene_names_refseq": "Fbp1; Folr1",
        "protein_names_uniprotkb": "Folate receptor alpha",
        "protein_names_refseq": "folate binding protein 1; folate receptor 1 (adult); folate receptor alpha precursor",
        "tax_id": 10116,
        "disease": "cerebral folate receptor alpha deficiency (Disease Ontology:DOID:0050719)",
        "pathway": " (rno:171049);  (R-RNO-204005);  (R-RNO-5694530);  (R-RNO-6807878)",
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        "publication_id_list": "26667416;27011008;30113208;36675153",
        "class_list": "",
        "function": "A Paternal Methylation Error in the Congenital Hydrocephalic Texas (H-Tx) Rat Is Partially Rescued with Natural Folate Supplements. Publication Status: Online-Only, [RefSeq, PubMed]; Folr1 plays an important role in folate and sulfur amino acid levels and affects glucose and lipid metabolism in the rat., [RefSeq, PubMed]; Inherited variation in the expression of Folr1 in the kidney influences the development of the metabolic syndrome, [RefSeq, PubMed]; These observations have implications in the pathology of FRa-autoantibodies associated with neural tube defect pregnancy, preterm birth and neurodevelopmental disorders including autism Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0005542 folic acid binding;GO:0061714 folic acid receptor activity;GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane;GO:0009897 external side of plasma membrane;GO:0016324 apical plasma membrane",
        "go_biological_process": "GO:0017015 regulation of transforming growth factor beta receptor signaling pathway;GO:0046654 tetrahydrofolate biosynthetic process;GO:0035036 sperm-egg recognition;GO:0007155 cell adhesion;GO:0007342 fusion of sperm to egg plasma membrane involved in single fertilization",
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        "hit_score": 0.5,
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    },
    {
        "uniprot_canonical_ac": "G3V8N8-1",
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            {
                "id": "G3V8N8_RAT",
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            }
        ],
        "mass": 34903.0,
        "length": 304,
        "protein_name": "Probable RNA polymerase II nuclear localization protein SLC7A6OS",
        "gene_name": "Slc7a6os",
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        "refseq_name": "",
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        "protein_names_uniprotkb": "Probable RNA polymerase II nuclear localization protein SLC7A6OS",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "progressive myoclonus epilepsy (Disease Ontology:DOID:891)",
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        "publication_id_list": "22673903",
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        "function": "Directs RNA polymerase II nuclear import., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0015031 protein transport;GO:0032502 developmental process;GO:0002244 hematopoietic progenitor cell differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "G3V8N8-1",
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        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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            {
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                "type": "external"
            }
        ],
        "mass": 16078.0,
        "length": 142,
        "protein_name": "Hemoglobin subunit zeta",
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            {
                "id": "NP_001166316",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001166316",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Hbz",
        "gene_names_refseq": "Glne1; Hbz; RGD1307486",
        "protein_names_uniprotkb": "Hemoglobin subunit zeta; Hemoglobin zeta chain; Zeta-globin",
        "protein_names_refseq": "globin e1; hemoglobin subunit zeta; hemoglobin, zeta; zeta-globin",
        "tax_id": 10116,
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        "class_list": "",
        "function": "The zeta chain is an alpha-type chain of mammalian embryonic hemoglobin., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005506 iron ion binding;GO:0020037 heme binding;GO:0019825 oxygen binding;GO:0005344 oxygen carrier activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005833 hemoglobin complex;GO:0031838 haptoglobin-hemoglobin complex",
        "go_biological_process": "GO:0048821 erythrocyte development;GO:0015671 oxygen transport",
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        "kg_view_protein": true
    },
    {
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            {
                "id": "G3V8Z6_RAT",
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                "type": "external"
            }
        ],
        "mass": 84006.0,
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        "protein_name": "Krev interaction trapped protein 1",
        "gene_name": "Krit1",
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            {
                "id": "NP_001102088",
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                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Krit1",
        "gene_names_refseq": "Krit1; RGD1305929",
        "protein_names_uniprotkb": "Krev interaction trapped protein 1",
        "protein_names_refseq": "krev interaction trapped protein 1",
        "tax_id": 10116,
        "disease": "cerebral cavernous malformation (Disease Ontology:DOID:0060669); cerebral cavernous malformation 1 (Disease Ontology:DOID:0080491)",
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        "go_molecular_function": "GO:0005546 phosphatidylinositol-4,5-bisphosphate binding;GO:0008017 microtubule binding;GO:0030695 GTPase regulator activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005856 cytoskeleton;GO:0005886 plasma membrane;GO:0005911 cell-cell junction;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0001525 angiogenesis;GO:0001937 negative regulation of endothelial cell proliferation;GO:2000352 negative regulation of endothelial cell apoptotic process;GO:0016525 negative regulation of angiogenesis;GO:0010596 negative regulation of endothelial cell migration",
        "synthesized_glycan_count": 0,
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        "uniprot_id": [
            {
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                "url": "https://www.uniprot.org/uniprot/A0A0G2K779",
                "type": "external"
            }
        ],
        "mass": 73890.0,
        "length": 657,
        "protein_name": "Centrosomal protein of 76 kDa",
        "gene_name": "Cep76",
        "organism": "Rat",
        "refseq_name": "centrosomal protein of 76 kDa isoform X1",
        "refseq_ac": [
            {
                "id": "XP_038952592",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_038952592",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Cep76",
        "gene_names_refseq": "CSG11; Cep76; RGD1305183",
        "protein_names_uniprotkb": "Centrosomal protein of 76 kDa",
        "protein_names_refseq": "centrosomal protein of 76 kDa isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:291540);  (R-RNO-2565942);  (R-RNO-380259);  (R-RNO-380270);  (R-RNO-380284);  (R-RNO-380320);  (R-RNO-5620912);  (R-RNO-8854518)",
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        "function": "Centrosomal protein involved in regulation of centriole duplication. Required to limit centriole duplication to once per cell cycle by preventing centriole reduplication., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005814 centriole;GO:0005813 centrosome;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0046599 regulation of centriole replication",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A0G2K779-1",
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    },
    {
        "uniprot_canonical_ac": "G3V978-1",
        "uniprot_id": [
            {
                "id": "G3V978_RAT",
                "url": "https://www.uniprot.org/uniprot/G3V978",
                "type": "external"
            }
        ],
        "mass": 35755.0,
        "length": 330,
        "protein_name": "Dehydrogenase/reductase SDR family member 11",
        "gene_name": "Dhrs11",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Dhrs11",
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        "protein_names_uniprotkb": "Dehydrogenase/reductase SDR family member 11; 1.1.1.270; 1.1.1.62; 17-beta-hydroxysteroid dehydrogenase; 3-beta-hydroxysteroid 3-dehydrogenase; Estradiol 17-beta-dehydrogenase; Short-chain dehydrogenase/reductase family 24C member 1",
        "protein_names_refseq": "",
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        "predicted_glycosites": 0,
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        "ec_number_list": [
            {
                "id": "1.1.1.270",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.1.1.270",
                "type": "external"
            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:1.1.1.62",
                "type": "external"
            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:1.1.1.239",
                "type": "external"
            },
            {
                "id": "1.1.1.105",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.1.1.105",
                "type": "external"
            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:1.1.1.209",
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            },
            {
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    },
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            {
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        ],
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        "protein_name": "Olfactory receptor",
        "gene_name": "Or7g32",
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        "refseq_name": "olfactory receptor Olr1148",
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            {
                "id": "NP_001000875",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000875",
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            }
        ],
        "gene_names_uniprotkb": "Or7g32",
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        "protein_names_uniprotkb": "Olfactory receptor",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "protein_names_uniprotkb": "N-lysine methyltransferase KMT5A; 2.1.1.361; H4-K20-HMTase KMT5A; Histone-lysine N-methyltransferase KMT5A; Lysine-specific methylase 5A; PR/SET domain-containing protein 07; SET domain-containing protein 8",
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        "function": "Protein-lysine N-methyltransferase that monomethylates both histones and non-histone proteins. Specifically monomethylates 'Lys-20' of histone H4 (H4K20me1). H4K20me1 is enriched during mitosis and represents a specific tag for epigenetic transcriptional repression. Mainly functions in euchromatin regions, thereby playing a central role in the silencing of euchromatic genes. Required for cell proliferation, probably by contributing to the maintenance of proper higher-order structure of DNA during mitosis. Involved in chromosome condensation and proper cytokinesis. Nucleosomes are preferred as substrate compared to free histones. Mediates monomethylation of p53/TP53 at 'Lys-382', leading to repress p53/TP53-target genes. Plays a negative role in TGF-beta response regulation and a positive role in cell migration., [UniProtKB, UniProtKB]",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.361",
                "type": "external"
            },
            {
                "id": "2.1.1.359",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.359",
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            },
            {
                "id": "2.1.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.-",
                "type": "external"
            },
            {
                "id": "2.1.1.362",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.362",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.354",
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            }
        ],
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        ],
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        "protein_name": "Keratin associated protein 20-22",
        "gene_name": "LOC134481131",
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            {
                "id": "XP_063127032",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_063127032",
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            {
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                "type": "external"
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        ],
        "mass": 13670.0,
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        "protein_name": "Gamma-aminobutyric acid receptor-associated protein-like 2",
        "gene_name": "Gabarapl4",
        "organism": "Rat",
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        "refseq_ac": [],
        "gene_names_uniprotkb": "Gabarapl4; LOC120098596",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Gamma-aminobutyric acid receptor-associated protein-like 2; GABA(A) receptor-associated protein-like 2; Golgi-associated ATPase enhancer of 16 kDa",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:120098596)",
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        "function": "Ubiquitin-like modifier involved in intra-Golgi traffic. Modulates intra-Golgi transport through coupling between NSF activity and SNAREs activation. It first stimulates the ATPase activity of NSF which in turn stimulates the association with GOSR1. Involved in autophagy. Plays a role in mitophagy which contributes to regulate mitochondrial quantity and quality by eliminating the mitochondria to a basal level to fulfill cellular energy requirements and preventing excess ROS production. Whereas LC3s are involved in elongation of the phagophore membrane, the GABARAP/GATE-16 subfamily is essential for a later stage in autophagosome maturation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0031625 ubiquitin protein ligase binding;GO:0008429 phosphatidylethanolamine binding",
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    {
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        "uniprot_id": [
            {
                "id": "IQEC1_RAT",
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        ],
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        "protein_name": "IQ motif and SEC7 domain-containing protein 1",
        "gene_name": "Iqsec1",
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        "gene_names_uniprotkb": "Iqsec1; Brag2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "IQ motif and SEC7 domain-containing protein 1",
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        "tax_id": 10116,
        "disease": "intellectual developmental disorder with short stature and behavioral abnormalities (Disease Ontology:DOID:0111674); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung adenocarcinoma (Disease Ontology:DOID:3910)",
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        "function": "Guanine nucleotide exchange factor for ARF1 and ARF6. Guanine nucleotide exchange factor activity is enhanced by lipid binding. Accelerates GTP binding by ARFs of all three classes. Guanine nucleotide exchange protein for ARF6, mediating internalization of beta-1 integrin. Involved in neuronal development (By similarity). In neurons, plays a role in the control of vesicle formation by endocytoc cargo. Upon long term depression, interacts with GRIA2 and mediates the activation of ARF6 to internalize synaptic AMPAR receptors (PubMed:20547133)., [UniProtKB, UniProtKB, PubMed, UniProtKB]",
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        "go_molecular_function": "GO:0019901 protein kinase binding;GO:0008289 lipid binding;GO:0005085 guanyl-nucleotide exchange factor activity",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0008021 synaptic vesicle;GO:0099092 postsynaptic density, intracellular component",
        "go_biological_process": "GO:0051549 positive regulation of keratinocyte migration;GO:0060996 dendritic spine development;GO:0051965 positive regulation of synapse assembly;GO:0016192 vesicle-mediated transport;GO:0032012 regulation of ARF protein signal transduction",
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                "type": "external"
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        ],
        "mass": 129806.0,
        "length": 1171,
        "protein_name": "Thrombospondin-1",
        "gene_name": "Thbs1",
        "organism": "Rat",
        "refseq_name": "thrombospondin-1 isoform 2 precursor",
        "refseq_ac": [
            {
                "id": "NP_001385869",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001385869",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Thbs1",
        "gene_names_refseq": "TSP-1; Thbs1; Tsp1",
        "protein_names_uniprotkb": "Thrombospondin-1; Glycoprotein G",
        "protein_names_refseq": "thrombospondin-1 isoform 2 precursor",
        "tax_id": 10116,
        "disease": "COVID-19 (Disease Ontology:DOID:0080600); prostate cancer (Disease Ontology:DOID:10283); primary open angle glaucoma (Disease Ontology:DOID:1070); urinary bladder cancer (Disease Ontology:DOID:11054); heart disease (Disease Ontology:DOID:114); Sjogren's syndrome (Disease Ontology:DOID:12894); pancreatic cancer (Disease Ontology:DOID:1793); pancreatic ductal carcinoma (Disease Ontology:DOID:3587); cholangiocarcinoma (Disease Ontology:DOID:4947); myocardial infarction (Disease Ontology:DOID:5844); diabetic retinopathy (Disease Ontology:DOID:8947); colorectal cancer (Disease Ontology:DOID:9256); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (R-RNO-114608);  (R-RNO-186797);  (R-RNO-216083);  (R-RNO-5173214)",
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        "publication_id_list": "36920202;37573658;38108523;38237742;38439091",
        "class_list": "",
        "function": "Exosomes derived from menstrual blood stromal cells ameliorated premature ovarian insufficiency and granulosa cell apoptosis by regulating SMAD3/AKT/MDM2/P53 pathway via delivery of thrombospondin-1., [RefSeq, PubMed]; RNF7 Induces Skeletal Muscle Cell Apoptosis and Arrests Cell Autophagy via Upregulation of THBS1 and Inactivation of the PI3K/Akt Signaling Pathway in a Rat Sepsis Model., [RefSeq, PubMed]; Targeting Thbs1 reduces bladder remodeling caused by partial bladder outlet obstruction via the FGFR3/p-FGFR3 pathway., [RefSeq, PubMed]; Thrombospondin 1 enhances systemic inflammation and disease severity in acute-on-chronic liver failure. Publication Status: Online-Only, [RefSeq, PubMed]; Thrombospondin-1-mediated crosstalk between autophagy and oxidative stress orchestrates repair of blast lung injury., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0016491 oxidoreductase activity;GO:0070728 L-leucine binding;GO:0016684 oxidoreductase activity, acting on peroxide as acceptor",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0001650 fibrillar center;GO:0061700 GATOR2 complex;GO:0005634 nucleus",
        "go_biological_process": "GO:0051896 regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0030308 negative regulation of cell growth;GO:0042149 cellular response to glucose starvation;GO:0072593 reactive oxygen species metabolic process;GO:0034198 cellular response to amino acid starvation",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.7",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.-.-",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.17",
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        "go_biological_process": "GO:0006310 DNA recombination;GO:0002455 humoral immune response mediated by circulating immunoglobulin;GO:0006298 mismatch repair;GO:0016446 somatic hypermutation of immunoglobulin genes;GO:0045190 isotype switching",
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            {
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        "disease": "mantle cell lymphoma (Disease Ontology:DOID:0050746); isolated growth hormone deficiency type III (Disease Ontology:DOID:0060875); COVID-19 (Disease Ontology:DOID:0080600); X-linked agammaglobulinemia (Disease Ontology:DOID:14179); arthus reaction (Disease Ontology:DOID:1556); agammaglobulinemia (Disease Ontology:DOID:2583); central nervous system lymphoma (Disease Ontology:DOID:3234); lung adenocarcinoma (Disease Ontology:DOID:3910); B-cell lymphoma (Disease Ontology:DOID:707); Burkitt lymphoma (Disease Ontology:DOID:8584); colorectal cancer (Disease Ontology:DOID:9256)",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.-",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0045121 membrane raft",
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        "gene_names_refseq": "Mail; Nfkbiz; RGD1310834",
        "protein_names_uniprotkb": "NF-kappa-B inhibitor zeta; I-kappa-B-zeta; IL-1 inducible nuclear ankyrin-repeat protein; Molecule possessing ankyrin repeats induced by lipopolysaccharide",
        "protein_names_refseq": "IkappaB-zeta; NF-kappa-B inhibitor zeta; molecule possessing ankyrin-repeats induced by lipopolysaccharide; nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, zeta",
        "tax_id": 10116,
        "disease": "Stevens-Johnson syndrome (Disease Ontology:DOID:0050426); atopic dermatitis (Disease Ontology:DOID:3310)",
        "pathway": " (rno:304005)",
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        "publication_count": 1,
        "publication_id_list": "28099916",
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        "function": "Involved in regulation of NF-kappa-B transcription factor complexes. Inhibits NF-kappa-B activity without affecting its nuclear translocation upon stimulation. Inhibits DNA-binding of RELA and NFKB1/p50, and of the NF-kappa-B p65-p50 heterodimer and the NF-kappa-B p50-p50 homodimer. Also seems to activate NF-kappa-B-mediated transcription. In vitro, upon association with NFKB1/p50 has transcriptional activation activity and, together with NFKB1/p50 and RELA, is recruited to LCN2 promoters. Promotes transcription of LCN2 and DEFB4. Is recruited to IL-6 promoters and activates IL-6 but decreases TNF production in response to LPS. Seems to be involved in the induction of inflammatory genes activated through TLR/IL-1 receptor signaling. Involved in the induction of T helper 17 cells (Th17) differentiation upon recognition of antigen by T cell antigen receptor (TCR)., [UniProtKB, UniProtKB]; Suggest role for NF-kappaBIZ in age-associated progressive renal fibrosis via cytokine signaling., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000987 cis-regulatory region sequence-specific DNA binding;GO:0070974 POU domain binding;GO:0003712 transcription coregulator activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0016607 nuclear speck",
        "go_biological_process": "GO:0045063 T-helper 1 cell differentiation;GO:0098773 skin epidermis development;GO:0032980 keratinocyte activation;GO:2000321 positive regulation of T-helper 17 cell differentiation;GO:0006338 chromatin remodeling",
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    },
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        ],
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        "protein_name": "Sosondowah ankyrin repeat domain family member A",
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        "refseq_name": "",
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        ],
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        "protein_name": "Collagen type X alpha 1 chain",
        "gene_name": "Col10a1",
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            {
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        "protein_names_refseq": "collagen alpha-1(X) chain precursor; collagen alpha-1(X) chain; collagen, type X, alpha 1; procollagen, type X, alpha 1",
        "tax_id": 10116,
        "disease": "Schmid metaphyseal chondrodysplasia (Disease Ontology:DOID:0080021); osteochondrodysplasia (Disease Ontology:DOID:2256); lung adenocarcinoma (Disease Ontology:DOID:3910); degenerative disc disease (Disease Ontology:DOID:90)",
        "pathway": " (rno:25681);  (R-RNO-1442490);  (R-RNO-1650814);  (R-RNO-2022090);  (R-RNO-3000171);  (R-RNO-8948216)",
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        "function": "Atypical mitochondrial nucleoside-triphosphatase (NTPase) involved in mitochondrial trafficking. Probably involved in control of anterograde transport of mitochondria and their subcellular distribution. Promotes mitochondrial fission during high calcium conditions. Can hydrolyze GTP, ATP and UTP., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Miro proteins serve as a [Ca(2+)](c)-sensitive switch and bifunctional regulator for both the motility and fusion-fission dynamics of the mitochondria., [RefSeq, PubMed]; The data point to HDAC6-dependent deacetylation of Miro1 as a mediator of axon growth inhibition through decreased mitochondrial transport., [RefSeq, PubMed]; These data suggest that Miro1 and the kinesin adaptor Grif-1 play an important role in regulating mitochondrial transport in neurons., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005741 mitochondrial outer membrane;GO:0010494 cytoplasmic stress granule;GO:1990904 ribonucleoprotein complex",
        "go_biological_process": "GO:0047497 mitochondrion transport along microtubule;GO:0019725 cellular homeostasis;GO:0051260 protein homooligomerization;GO:0046928 regulation of neurotransmitter secretion;GO:0016567 protein ubiquitination",
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                "id": "2.7.4.6",
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                "id": "2.7.11.12",
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                "id": "2.7.11.26",
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                "id": "2.7.11.34",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.34",
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                "id": "2.7.1.150",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.150",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.13",
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                "id": "4.1.1.32",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.1.1.32",
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                "id": "2.7.11.19",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.19",
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                "id": "2.7.2.3",
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                "id": "2.7.11.31",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.31",
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                "id": "3.1.3.16",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.16",
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                "id": "2.7.11.4",
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                "id": "2.3.1.48",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.48",
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                "id": "3.1.11.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.11.-",
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                "id": "2.7.13.3",
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                "id": "2.7.4.18",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.18",
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            {
                "id": "3.1.24.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.24.-",
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                "id": "3.4.19.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.19.12",
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                "id": "2.7.11.39",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.39",
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                "id": "2.4.99.18",
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        ],
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                "id": "1.8.-.-",
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        "protein_names_uniprotkb": "tRNA wybutosine-synthesizing protein 3 homolog; 2.1.1.282; tRNA(Phe) 7-((3-amino-3-carboxypropyl)-4-demethylwyosine(37)-N(4))-methyltransferase",
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        "function": "Probable S-adenosyl-L-methionine-dependent methyltransferase that acts as a component of the wybutosine biosynthesis pathway. Wybutosine is a hyper modified guanosine with a tricyclic base found at the 3'-position adjacent to the anticodon of eukaryotic phenylalanine tRNA., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "mass": 63342.0,
        "length": 574,
        "protein_name": "Transmembrane protein 259",
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        "refseq_name": "membralin",
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            {
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        "go_cellular_component": "GO:0005783 endoplasmic reticulum",
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        "refseq_name": "serine-rich coiled-coil domain-containing protein 2 isoform 1",
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        "protein_names_uniprotkb": "Coiled-coil serine-rich protein 2",
        "protein_names_refseq": "family with sequence similarity 190, member B; granule cell antiserum positive 14; protein FAM190B; serine-rich coiled-coil domain-containing protein 2 isoform 1; serine-rich coiled-coil domain-containing protein 2",
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        "protein_names_uniprotkb": "Solute carrier family 35 member D2",
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            {
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        "function": "Correlation between relative mRNA levels of WSB-1 and USP-33 in numerous tissues that do not express type 2 deiodinase(D2) suggests that these ubiquitin-related enzymes share additional substrates besides D2., [RefSeq, PubMed]; Deubiquitinating enzyme that removes conjugated ubiquitin from specific proteins to regulate different cellular processes., [UniProtKB, UniProtKB]; High iodine intake had no discernible effects on USP20. Temporary increases in USP33 and USP19 mRNA levels were observed. The enzymes related to D2 ubiquitination change with prolonged high iodine intake. Increased D2 ubiquitination suppresses the activity of D2, causing a decrease in negative feedback of the hypothalamic-pituitary-thyroid axis., [RefSeq, PubMed]",
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        "function": "Both phosphacan and receptor protein tyrosine phosphatase beta splice variants participate in both the acute degenerative and long-term regenerative phases of reactive synaptogenesis, [RefSeq, PubMed]; Possesses tyrosine phosphatase activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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            {
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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.-",
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        "length": 1001,
        "protein_name": "Zinc finger protein, multitype 1",
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            {
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        "function": "Transcription regulator that plays an essential role in erythroid and megakaryocytic cell differentiation. Essential cofactor that acts via the formation of a heterodimer with transcription factors of the GATA family GATA1, GATA2 and GATA3. Such heterodimer can both activate or repress transcriptional activity, depending on the cell and promoter context. The heterodimer formed with GATA proteins is essential to activate expression of genes such as NFE2, ITGA2B, alpha- and beta-globin, while it represses expression of KLF1. May be involved in regulation of some genes in gonads. May also be involved in cardiac development, in a non-redundant way with ZFPM2/FOG2., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0003192 mitral valve formation;GO:0003195 tricuspid valve formation;GO:0010557 positive regulation of macromolecule biosynthetic process;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription",
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            {
                "id": "A0A0G2K8D1_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2K8D1",
                "type": "external"
            }
        ],
        "mass": 59743.0,
        "length": 518,
        "protein_name": "Motile sperm domain-containing protein 2",
        "gene_name": "Mospd2",
        "organism": "Rat",
        "refseq_name": "motile sperm domain-containing protein 2",
        "refseq_ac": [
            {
                "id": "NP_001385656",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001385656",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Mospd2",
        "gene_names_refseq": "Mospd2; RGD1563952",
        "protein_names_uniprotkb": "Motile sperm domain-containing protein 2",
        "protein_names_refseq": "motile sperm domain-containing protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363463);  (R-RNO-6798695)",
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        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Endoplasmic reticulum-anchored protein that mediates the formation of contact sites between the endoplasmic (ER) and endosomes, mitochondria or Golgi through interaction with conventional- and phosphorylated-FFAT-containing organelle-bound proteins. In addition, forms endoplasmic reticulum (ER)-lipid droplets (LDs) contacts through a direct protein-membrane interaction and participates in LDs homeostasis. The attachment mechanism involves an amphipathic helix that has an affinity for lipid packing defects present at the surface of LDs. Promotes migration of primary monocytes and neutrophils, in response to various chemokines., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0033149 FFAT motif binding",
        "go_cellular_component": "GO:0044232 organelle membrane contact site;GO:0005783 endoplasmic reticulum;GO:0005886 plasma membrane;GO:0005789 endoplasmic reticulum membrane;GO:0012505 endomembrane system",
        "go_biological_process": "GO:0006935 chemotaxis;GO:0051260 protein homooligomerization;GO:0090026 positive regulation of monocyte chemotaxis;GO:0140042 lipid droplet formation;GO:0090023 positive regulation of neutrophil chemotaxis",
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        "kg_view_protein": true
    },
    {
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            {
                "id": "D3ZQQ1_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZQQ1",
                "type": "external"
            }
        ],
        "mass": 98144.0,
        "length": 905,
        "protein_name": "Aftiphilin",
        "gene_name": "Aftph",
        "organism": "Rat",
        "refseq_name": "aftiphilin",
        "refseq_ac": [
            {
                "id": "NP_001292056",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001292056",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Aftph",
        "gene_names_refseq": "Aftph; RGD1311920",
        "protein_names_uniprotkb": "Aftiphilin",
        "protein_names_refseq": "aftiphilin",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:305544)",
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        "go_molecular_function": "GO:0030276 clathrin binding",
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    },
    {
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            {
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                "url": "https://www.uniprot.org/uniprot/D3ZD11",
                "type": "external"
            }
        ],
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        "length": 226,
        "protein_name": "Signal peptidase complex subunit 2",
        "gene_name": "Spcs2",
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            {
                "id": "NP_001178530",
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        "protein_names_uniprotkb": "Signal peptidase complex subunit 2",
        "protein_names_refseq": "signal peptidase complex subunit 2",
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        "disease": "Parkinson's disease (Disease Ontology:DOID:14330)",
        "pathway": " (rno:293142);  (R-RNO-422085);  (R-RNO-9768727)",
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        "function": "Component of the signal peptidase complex (SPC) which catalyzes the cleavage of N-terminal signal sequences from nascent proteins as they are translocated into the lumen of the endoplasmic reticulum. Enhances the enzymatic activity of SPC and facilitates the interactions between different components of the translocation site., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008233 peptidase activity",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0005787 signal peptidase complex",
        "go_biological_process": "GO:0045047 protein targeting to ER;GO:0006465 signal peptide processing",
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    {
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            }
        ],
        "mass": 24811.0,
        "length": 226,
        "protein_name": "Triggering receptor expressed on myeloid cells 1",
        "gene_name": "Trem1",
        "organism": "Rat",
        "refseq_name": "triggering receptor expressed on myeloid cells 1 precursor",
        "refseq_ac": [
            {
                "id": "NP_001100355",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100355",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Trem1",
        "gene_names_refseq": "Trem1",
        "protein_names_uniprotkb": "Triggering receptor expressed on myeloid cells 1",
        "protein_names_refseq": "triggering receptor expressed on myeloid cells 1 precursor",
        "tax_id": 10116,
        "disease": "pterygium (Disease Ontology:DOID:0002116); bacterial sepsis (Disease Ontology:DOID:0040085); Stevens-Johnson syndrome (Disease Ontology:DOID:0050426); inflammatory bowel disease (Disease Ontology:DOID:0050589); chorioamnionitis (Disease Ontology:DOID:0050697); diffuse large B-cell lymphoma (Disease Ontology:DOID:0050745); colorectal adenoma (Disease Ontology:DOID:0050860); colorectal adenocarcinoma (Disease Ontology:DOID:0050861); oral squamous cell carcinoma (Disease Ontology:DOID:0050866); medulloblastoma (Disease Ontology:DOID:0050902); myelodysplastic syndrome (Disease Ontology:DOID:0050908); stroke (Disease Ontology:DOID:0051061); pre-malignant neoplasm (Disease Ontology:DOID:0060071); drug allergy (Disease Ontology:DOID:0060500); alcohol-associated liver disease (Disease Ontology:DOID:0070658); hepatic veno-occlusive disease (Disease Ontology:DOID:0080177); colorectal carcinoma (Disease Ontology:DOID:0080199); erythema nodosum (Disease Ontology:DOID:0080750); graft-versus-host disease (Disease Ontology:DOID:0081267); osteonecrosis (Disease Ontology:DOID:10159); thalassemia (Disease Ontology:DOID:10241); prostate cancer (Disease Ontology:DOID:10283); asbestosis (Disease Ontology:DOID:10320); lymphoid leukemia (Disease Ontology:DOID:1037); esophageal atresia (Disease Ontology:DOID:10485); Hirschsprung's disease (Disease Ontology:DOID:10487); stomach cancer (Disease Ontology:DOID:10534); primary open angle glaucoma (Disease Ontology:DOID:1070); Kuhnt-Junius degeneration (Disease Ontology:DOID:10873); hypospadias (Disease Ontology:DOID:10892); urinary bladder cancer (Disease Ontology:DOID:11054); asphyxia neonatorum (Disease Ontology:DOID:11088); Human papillomavirus infectious disease (Disease Ontology:DOID:11166); bronchopulmonary dysplasia (Disease Ontology:DOID:11650); head and neck cancer (Disease Ontology:DOID:11934); allergic disease (Disease Ontology:DOID:1205); optic neuritis (Disease Ontology:DOID:1210); malaria (Disease Ontology:DOID:12365); aplastic anemia (Disease Ontology:DOID:12449); autistic disorder (Disease Ontology:DOID:12849); uterine fibroid (Disease Ontology:DOID:13223); lung cancer (Disease Ontology:DOID:1324); mesenteric vascular occlusion (Disease Ontology:DOID:13252); angle-closure glaucoma (Disease Ontology:DOID:13550); Fanconi anemia (Disease Ontology:DOID:13636); exfoliation syndrome (Disease Ontology:DOID:13641); toxic shock syndrome (Disease Ontology:DOID:14115); Parkinson's disease (Disease Ontology:DOID:14330); aggressive periodontitis (Disease Ontology:DOID:1474); cystic fibrosis (Disease Ontology:DOID:1485); urticaria (Disease Ontology:DOID:1555); acute chest syndrome (Disease Ontology:DOID:1584); depressive disorder (Disease Ontology:DOID:1596); keratosis (Disease Ontology:DOID:161); breast cancer (Disease Ontology:DOID:1612); congenital heart disease (Disease Ontology:DOID:1682); malignant mesothelioma (Disease Ontology:DOID:1790); hepatitis C (Disease Ontology:DOID:1883); hepatitis B (Disease Ontology:DOID:2043); ovary epithelial cancer (Disease Ontology:DOID:2152); multiple sclerosis (Disease Ontology:DOID:2377); larynx cancer (Disease Ontology:DOID:2596); transitional cell carcinoma (Disease Ontology:DOID:2671); asthma (Disease Ontology:DOID:2841); cervix carcinoma (Disease Ontology:DOID:2893); acute pancreatitis (Disease Ontology:DOID:2913); pulmonary tuberculosis (Disease Ontology:DOID:2957); adenocarcinoma (Disease Ontology:DOID:299); malignant astrocytoma (Disease Ontology:DOID:3069); high grade glioma (Disease Ontology:DOID:3070); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); gallbladder cancer (Disease Ontology:DOID:3121); porphyria cutanea tarda (Disease Ontology:DOID:3132); atopic dermatitis (Disease Ontology:DOID:3310); coronary artery disease (Disease Ontology:DOID:3393); middle cerebral artery infarction (Disease Ontology:DOID:3525); toxic encephalopathy (Disease Ontology:DOID:3602); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); pleural empyema (Disease Ontology:DOID:3798); Lynch syndrome (Disease Ontology:DOID:3883); gastritis (Disease Ontology:DOID:4029); bacterial gastritis (Disease Ontology:DOID:4033); systemic scleroderma (Disease Ontology:DOID:418); cervical cancer (Disease Ontology:DOID:4362); macular degeneration (Disease Ontology:DOID:4448); renal cell carcinoma (Disease Ontology:DOID:4450); movement disease (Disease Ontology:DOID:480); small intestine adenocarcinoma (Disease Ontology:DOID:4906); esophagus adenocarcinoma (Disease Ontology:DOID:4914); cholangiocarcinoma (Disease Ontology:DOID:4947); esophageal cancer (Disease Ontology:DOID:5041); melioidosis (Disease Ontology:DOID:5052); liver cirrhosis (Disease Ontology:DOID:5082); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); schizophrenia (Disease Ontology:DOID:5419); oral submucous fibrosis (Disease Ontology:DOID:5773); myocardial infarction (Disease Ontology:DOID:5844); congestive heart failure (Disease Ontology:DOID:6000); leukopenia (Disease Ontology:DOID:615); hepatocellular carcinoma (Disease Ontology:DOID:684); rheumatoid arthritis (Disease Ontology:DOID:7148); end stage renal disease (Disease Ontology:DOID:783); periodontitis (Disease Ontology:DOID:824); cataract (Disease Ontology:DOID:83); lung disease (Disease Ontology:DOID:850); Hodgkin's lymphoma (Disease Ontology:DOID:8567); infectious mononucleosis (Disease Ontology:DOID:8568); ulcerative colitis (Disease Ontology:DOID:8577); oral cavity cancer (Disease Ontology:DOID:8618); myeloid leukemia (Disease Ontology:DOID:8692); bacterial pneumonia (Disease Ontology:DOID:874); Crohn's disease (Disease Ontology:DOID:8778); skin melanoma (Disease Ontology:DOID:8923); diabetic retinopathy (Disease Ontology:DOID:8947); polycythemia vera (Disease Ontology:DOID:8997); systemic lupus erythematosus (Disease Ontology:DOID:9074); acute myeloid leukemia (Disease Ontology:DOID:9119); amyloidosis (Disease Ontology:DOID:9120); colorectal cancer (Disease Ontology:DOID:9256); nasopharynx carcinoma (Disease Ontology:DOID:9261); diabetes mellitus (Disease Ontology:DOID:9351); type 2 diabetes mellitus (Disease Ontology:DOID:9352); bacterial meningitis (Disease Ontology:DOID:9470); multiple myeloma (Disease Ontology:DOID:9538); oral mucosa leukoplakia (Disease Ontology:DOID:9655); senile cataract (Disease Ontology:DOID:9669); pulmonary emphysema (Disease Ontology:DOID:9675); type 1 diabetes mellitus (Disease Ontology:DOID:9744); acute lymphoblastic leukemia (Disease Ontology:DOID:9952)",
        "pathway": " (rno:301229);  (R-RNO-198933);  (R-RNO-202733);  (R-RNO-2172127)",
        "pathway_count": 4,
        "publication_count": 1,
        "publication_id_list": "33727099",
        "class_list": "",
        "function": "Cell surface receptor that plays important roles in innate and adaptive immunity by amplifying inflammatory responses. Upon activation by various ligands such as PGLYRP1, HMGB1 or HSP70, multimerizes and forms a complex with transmembrane adapter TYROBP/DAP12. In turn, initiates a SYK-mediated cascade of tyrosine phosphorylation, activating multiple downstream mediators such as BTK, MAPK1, MAPK3 or phospholipase C-gamma. This cascade promotes the neutrophil- and macrophage-mediated release of pro-inflammatory cytokines and/or chemokines, as well as their migration and thereby amplifies inflammatory responses that are triggered by bacterial and fungal infections. By also promoting the amplification of inflammatory signals that are initially triggered by Toll-like receptor (TLR) and NOD-like receptor engagement, plays a major role in the pathophysiology of acute and chronic inflammatory diseases of different etiologies including septic shock and atherosclerosis., [UniProtKB, UniProtKB, UniProtKB]; Role of TREM-1 in the development of early brain injury after subarachnoid hemorrhage., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "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_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 129,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0004888 transmembrane signaling receptor activity;GO:0097110 scaffold protein binding;GO:0140319 receptor decoy activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005615 extracellular space;GO:0009986 cell surface",
        "go_biological_process": "GO:0002250 adaptive immune response;GO:0070945 neutrophil-mediated killing of gram-negative bacterium;GO:0016477 cell migration;GO:0045087 innate immune response;GO:0071222 cellular response to lipopolysaccharide",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4ABU7-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZWL1-1",
        "uniprot_id": [
            {
                "id": "D3ZWL1_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZWL1",
                "type": "external"
            }
        ],
        "mass": 76364.0,
        "length": 677,
        "protein_name": "SKI-like proto-oncogene",
        "gene_name": "Skil",
        "organism": "Rat",
        "refseq_name": "ski-like protein isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001385519",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001385519",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Skil",
        "gene_names_refseq": "Skil; Skir; Sno",
        "protein_names_uniprotkb": "SKI-like proto-oncogene",
        "protein_names_refseq": "SKI-like oncogene; ski-like protein isoform 1; ski-like protein; ski/sno related",
        "tax_id": 10116,
        "disease": "ureteral obstruction (Disease Ontology:DOID:5199)",
        "pathway": " (rno:114208);  (R-RNO-2173795)",
        "pathway_count": 2,
        "publication_count": 5,
        "publication_id_list": "28765970;29402324;30847937;31028803;37389959",
        "class_list": "",
        "function": "BMP7 may ameliorate diabetic nephropathy and renal fibrosis via increasing the expression of SnoN mRNA and protein in renal tubular epithelial cells, rather than directly inhibiting the degradation of SnoN by E3 ubiquitin ligase., [RefSeq, PubMed]; SKIL/SnoN attenuates TGF-beta1/SMAD signaling-dependent collagen synthesis in hepatic fibrosis. Publication Status: Online-Only, [RefSeq, PubMed]; Ski-related novel protein suppresses the development of diabetic nephropathy by modulating kidney transforming growth factor-beta signaling and microRNA-21 expression., [RefSeq, PubMed]; Studied the effects of herbal compound 861 on transforming growth factor beta1 (TGF-beta1)/Sma and Mad-related proteins (Smad)/Ski-related novel protein N (SnoN) signal pathway in a rat hepatic fibrosis disease model. Publication Status: Online-Only, [RefSeq, PubMed]; TAK1 mediated the phosphorylation of Ski-related novel protein N (SnoN), resulting in SnoN ubiquitination and eventual degradation, which enhanced EMT and extracellular matrix deposition to promote renal fibrosis during diabetic nephropathy., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
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        "protein_names_refseq": "latent-transforming growth factor beta-binding protein 4 precursor",
        "tax_id": 10116,
        "disease": "autosomal recessive cutis laxa type IC (Disease Ontology:DOID:0070139); cutis laxa (Disease Ontology:DOID:3144)",
        "pathway": " (rno:292734);  (R-RNO-2129379);  (R-RNO-2173789)",
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        "class_list": "",
        "function": "Key regulator of transforming growth factor beta (TGFB1, TGFB2 and TGFB3) that controls TGF-beta activation by maintaining it in a latent state during storage in extracellular space. Associates specifically via disulfide bonds with the Latency-associated peptide (LAP), which is the regulatory chain of TGF-beta, and regulates integrin-dependent activation of TGF-beta., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "biomarker_type": "",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0019838 growth factor binding;GO:0005509 calcium ion binding;GO:0050431 transforming growth factor beta binding",
        "go_cellular_component": "GO:0031012 extracellular matrix;GO:0005615 extracellular space;GO:0001527 microfibril",
        "go_biological_process": "GO:0007179 transforming growth factor beta receptor signaling pathway;GO:0046879 hormone secretion;GO:0048251 elastic fiber assembly",
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        "kg_view_protein": true
    },
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            {
                "id": "F1LVK0_RAT",
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            }
        ],
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        "refseq_ac": [],
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Bridge-like lipid transfer protein family member 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Alkuraya-Kucinskas syndrome (Disease Ontology:DOID:0111555)",
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        "ec_number_list": [],
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        "go_cellular_component": "GO:0098793 presynapse",
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    },
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            }
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            {
                "id": "XP_038963383",
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            }
        ],
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        "kg_view_protein": true
    },
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        "uniprot_canonical_ac": "F1LSH0-1",
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                "type": "external"
            }
        ],
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        "protein_name": "Symplekin",
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        "refseq_name": "",
        "refseq_ac": [],
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        "gene_names_refseq": "",
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        "tax_id": 10116,
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        "pathway": " (rno:292683);  (R-RNO-159231);  (R-RNO-73856);  (R-RNO-77595);  (R-RNO-9770562)",
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        "function": "Scaffold protein that functions as a component of a multimolecular complex involved in histone mRNA 3'-end processing. Specific component of the tight junction (TJ) plaque, but might not be an exclusively junctional component. May have a house-keeping rule. Is involved in pre-mRNA polyadenylation. Enhances SSU72 phosphatase activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "predicted_o_glycosites": 1,
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0097165 nuclear stress granule;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0016604 nuclear body",
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        "kg_view_protein": true
    },
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            {
                "id": "A0A1B0GWP1_RAT",
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            }
        ],
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        "protein_name": "Elongation of very long chain fatty acids protein 1",
        "gene_name": "Elovl1",
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        "protein_names_uniprotkb": "Elongation of very long chain fatty acids protein 1; 2.3.1.199; 3-keto acyl-CoA synthase ELOVL1; ELOVL FA elongase 1; ELOVL fatty acid elongase 1; Very long chain 3-ketoacyl-CoA synthase 1; Very long chain 3-oxoacyl-CoA synthase 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "adrenoleukodystrophy (Disease Ontology:DOID:10588)",
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        "function": "Catalyzes the first and rate-limiting reaction of the four reactions that constitute the long-chain fatty acids elongation cycle. This endoplasmic reticulum-bound enzymatic process allows the addition of 2 carbons to the chain of long- and very long-chain fatty acids (VLCFAs) per cycle. Condensing enzyme that exhibits activity toward saturated C18 to C26 acyl-CoA substrates, with the highest activity towards C22:0 acyl-CoA. May participate to the production of both saturated and monounsaturated VLCFAs of different chain lengths that are involved in multiple biological processes as precursors of membrane lipids and lipid mediators. Important for saturated C24:0 and monounsaturated C24:1 sphingolipid synthesis. Indirectly inhibits RPE65 via production of VLCFAs., [UniProtKB, HAMAP, UniProtKB]",
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            {
                "id": "2.3.1.199",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.199",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0009922 fatty acid elongase activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006633 fatty acid biosynthetic process;GO:0046513 ceramide biosynthetic process;GO:0061436 establishment of skin barrier;GO:0030148 sphingolipid biosynthetic process;GO:0035338 long-chain fatty-acyl-CoA biosynthetic process",
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    },
    {
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            }
        ],
        "mass": 128021.0,
        "length": 1188,
        "protein_name": "Calpain-15",
        "gene_name": "Capn15",
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        "refseq_name": "calpain-15 isoform 2",
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            {
                "id": "NP_001426651",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001426651",
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            }
        ],
        "gene_names_uniprotkb": "Capn15; Solh",
        "gene_names_refseq": "Capn15; Solh",
        "protein_names_uniprotkb": "Calpain-15; Small optic lobes homolog",
        "protein_names_refseq": "calpain-15 isoform 2; small optic lobes homolog",
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        "go_molecular_function": "GO:0004198 calcium-dependent cysteine-type endopeptidase activity;GO:0008270 zinc ion binding",
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        "protein_name": "Neutral amino acid transporter B(0)",
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        "organism": "Rat",
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        "refseq_ac": [],
        "gene_names_uniprotkb": "Slc1a5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Neutral amino acid transporter B(0); ASC-like Na(+)-dependent neutral amino acid transporter ASCT2; ATB(0); Insulin-activated amino acid transporter; Sodium-dependent neutral amino acid transporter type 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "tongue squamous cell carcinoma (Disease Ontology:DOID:0050865); episodic ataxia type 6 (Disease Ontology:DOID:0050994); neurodegenerative disease (Disease Ontology:DOID:1289); epilepsy (Disease Ontology:DOID:1826); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); lung adenocarcinoma (Disease Ontology:DOID:3910); pulmonary hypertension (Disease Ontology:DOID:6432)",
        "pathway": " (rno:292657);  (R-RNO-352230);  (R-RNO-9013149);  (R-RNO-9013406);  (R-RNO-9013407);  (R-RNO-9013423)",
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        "publication_id_list": "10698697;22673903",
        "class_list": "",
        "function": "Sodium-coupled antiporter of neutral amino acids. In a tri-substrate transport cycle, exchanges neutral amino acids between the extracellular and intracellular compartments, coupled to the inward cotransport of at least one sodium ion (By similarity) (PubMed:10698697). The preferred substrate is the essential amino acid L-glutamine, a precursor for biosynthesis of proteins, nucleotides and amine sugars as well as an alternative fuel for mitochondrial oxidative phosphorylation. Exchanges L-glutamine with other neutral amino acids such as L-serine, L-threonine and L-asparagine in a bidirectional way. Provides L-glutamine to proliferating stem and activated cells driving the metabolic switch toward cell differentiation (By similarity). The transport cycle is usually pH-independent, with the exception of L-glutamate. Transports extracellular L-glutamate coupled to the cotransport of one proton and one sodium ion in exchange for intracellular L-glutamine counter-ion. May provide for L-glutamate uptake in glial cells regulating glutamine/glutamate cycle in the nervous system (By similarity). Part of transport systems for D-amino acids. Mediates D-serine release from the retinal glia potentially affecting NMDA receptor function in retinal neurons. May contribute to D-serine reabsorption at the brush border of renal proximal tubules thus modulating the dynamics of urinary versus blood D-serine levels (By similarity). Displays sodium- and amino acid-dependent but uncoupled channel-like anion conductance with a preference SCN(-) >> NO3(-) > I(-) > Cl(-) (PubMed:10698697). Through binding of the fusogenic protein syncytin-1/ERVW-1 may mediate trophoblasts syncytialization, the spontaneous fusion of their plasma membranes, an essential process in placental development (By similarity)., [UniProtKB, PubMed, UniProtKB]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 2,
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        "predicted_c_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "total_s_glycosites": 0,
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        "reported_phosphosites": 5,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 7,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "1.8.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.8.-.-",
                "type": "external"
            },
            {
                "id": "1.8.5.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.8.5.1",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0015175 neutral L-amino acid transmembrane transporter activity;GO:0015186 L-glutamine transmembrane transporter activity;GO:0015194 L-serine transmembrane transporter activity;GO:0015293 symporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0042470 melanosome;GO:0009925 basal plasma membrane",
        "go_biological_process": "GO:0015825 L-serine transport;GO:0030218 erythrocyte differentiation;GO:0006868 glutamine transport;GO:0010585 glutamine secretion;GO:0015804 neutral amino acid transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D3ZJ25-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000010001.001.00000",
        "kg_view_protein": true
    },
    {
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            {
                "id": "D3ZXX3_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZXX3",
                "type": "external"
            }
        ],
        "mass": 370837.0,
        "length": 3332,
        "protein_name": "Unc-80 homolog, NALCN channel complex subunit",
        "gene_name": "Unc80",
        "organism": "Rat",
        "refseq_name": "protein unc-80 homolog isoform X7",
        "refseq_ac": [
            {
                "id": "XP_038940528",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_038940528",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Unc80",
        "gene_names_refseq": "Unc80",
        "protein_names_uniprotkb": "Unc-80 homolog, NALCN channel complex subunit",
        "protein_names_refseq": "protein unc-80 homolog isoform X7",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-2672351)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "38843836",
        "class_list": "",
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        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0005261 monoatomic cation channel activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0034706 sodium channel complex;GO:0001518 voltage-gated sodium channel complex;GO:0034703 cation channel complex;GO:0030424 axon",
        "go_biological_process": "GO:0035725 sodium ion transmembrane transport;GO:0098908 regulation of neuronal action potential;GO:0055080 monoatomic cation homeostasis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "D3ZXX3-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.001000.000000000000001000.0100000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "F1LS35-1",
        "uniprot_id": [
            {
                "id": "F1LS35_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LS35",
                "type": "external"
            }
        ],
        "mass": 126282.0,
        "length": 1126,
        "protein_name": "Hermansky-Pudlak syndrome 5 protein homolog",
        "gene_name": "Hps5",
        "organism": "Rat",
        "refseq_name": "BLOC-2 complex member HPS5",
        "refseq_ac": [
            {
                "id": "NP_001129084",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001129084",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Hps5; Saa4",
        "gene_names_refseq": "Aa2-028; Ab1-018; Hps5",
        "protein_names_uniprotkb": "Hermansky-Pudlak syndrome 5 protein homolog",
        "protein_names_refseq": "BLOC-2 complex member HPS5; Hermansky-Pudlak syndrome 5",
        "tax_id": 10116,
        "disease": "Hermansky-Pudlak syndrome 5 (Disease Ontology:DOID:0060543); platelet storage pool deficiency (Disease Ontology:DOID:2223); Hermansky-Pudlak syndrome (Disease Ontology:DOID:3753)",
        "pathway": " (rno:308598)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
        "function": "May regulate the synthesis and function of lysosomes and of highly specialized organelles, such as melanosomes and platelet dense granules. Regulates intracellular vesicular trafficking in fibroblasts. May be involved in the regulation of general functions of integrins., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_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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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005829 cytosol;GO:0031084 BLOC-2 complex;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0007596 blood coagulation;GO:0043473 pigmentation;GO:0048066 developmental pigmentation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F1LS35-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.010000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZXB0-1",
        "uniprot_id": [
            {
                "id": "D3ZXB0_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZXB0",
                "type": "external"
            }
        ],
        "mass": 47381.0,
        "length": 424,
        "protein_name": "Probable thioesterase PNKD",
        "gene_name": "Pnkd",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Pnkd",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Probable thioesterase PNKD; Myofibrillogenesis regulator 1; Paroxysmal nonkinesiogenic dyskinesia protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "paroxysmal nonkinesigenic dyskinesia 1 (Disease Ontology:DOID:0090049)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "38843836",
        "class_list": "",
        "function": "Probable thioesterase that may play a role in cellular detoxification processes; it likely acts on a yet-unknown alpha-hydroxythioester substrate. In vitro, it is able to catalyze the hydrolysis of S-D-lactoyl-glutathione to form glutathione and D-lactic acid at very low rate, though this reaction is not physiologically relevant in vivo., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 2,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0004416 hydroxyacylglutathione hydrolase activity;GO:0046872 metal ion binding;GO:0016790 thiolester hydrolase activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005886 plasma membrane;GO:0016020 membrane;GO:0099523 presynaptic cytosol",
        "go_biological_process": "GO:0019243 methylglyoxal catabolic process to D-lactate via S-lactoyl-glutathione;GO:0032225 regulation of synaptic transmission, dopaminergic;GO:0042053 regulation of dopamine metabolic process;GO:0046929 negative regulation of neurotransmitter secretion;GO:0050884 neuromuscular process controlling posture",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "D3ZXB0-1",
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        "filter_code": "0000000.0000110.100000.000000000000001000.0100000001000.001.00000",
        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
                "id": "E9PU41_RAT",
                "url": "https://www.uniprot.org/uniprot/E9PU41",
                "type": "external"
            }
        ],
        "mass": 83121.0,
        "length": 707,
        "protein_name": "Zinc finger protein 846",
        "gene_name": "Znf846",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein LOC304336 isoform X1",
        "refseq_ac": [
            {
                "id": "XP_038945325",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_038945325",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Znf846; RGD1566386",
        "gene_names_refseq": "RGD1566386; Znf846",
        "protein_names_uniprotkb": "Zinc finger protein 846",
        "protein_names_refseq": "uncharacterized protein LOC304336 isoform X1",
        "tax_id": 10116,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription",
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        "record_id": "E9PU41-1",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A1B0GWT9-1",
        "uniprot_id": [
            {
                "id": "A0A1B0GWT9_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A1B0GWT9",
                "type": "external"
            }
        ],
        "mass": 56038.0,
        "length": 485,
        "protein_name": "Tripartite motif containing 68",
        "gene_name": "Trim68",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase TRIM68",
        "refseq_ac": [
            {
                "id": "NP_001388433",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001388433",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Trim68",
        "gene_names_refseq": "Trim68",
        "protein_names_uniprotkb": "Tripartite motif containing 68",
        "protein_names_refseq": "E3 ubiquitin-protein ligase TRIM68",
        "tax_id": 10116,
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        "pathway": " (rno:684189)",
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        "reported_c_glycosites_with_glycan": 0,
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        "total_o_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:0008270 zinc ion binding;GO:0042802 identical protein binding;GO:0061630 ubiquitin protein ligase activity;GO:0004842 ubiquitin-protein transferase activity;GO:0050681 nuclear androgen receptor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0045087 innate immune response;GO:0010468 regulation of gene expression;GO:0051865 protein autoubiquitination;GO:0060765 regulation of androgen receptor signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A1B0GWT9-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D4A6Y0-1",
        "uniprot_id": [
            {
                "id": "D4A6Y0_RAT",
                "url": "https://www.uniprot.org/uniprot/D4A6Y0",
                "type": "external"
            }
        ],
        "mass": 32848.0,
        "length": 295,
        "protein_name": "Leukocyte immunoglobulin like receptor A5",
        "gene_name": "Lilra5",
        "organism": "Rat",
        "refseq_name": "leukocyte immunoglobulin-like receptor subfamily A member 5 isoform 1 precursor",
        "refseq_ac": [
            {
                "id": "NP_001070261",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001070261",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Lilra5",
        "gene_names_refseq": "Lilra5; Lilrc1",
        "protein_names_uniprotkb": "Leukocyte immunoglobulin like receptor A5",
        "protein_names_refseq": "leukocyte immunoglobulin-like receptor subfamily A member 5 isoform 1 precursor; leukocyte immunoglobulin-like receptor subfamily A member 5; leukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:691533)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "16041585",
        "class_list": "",
        "function": "LILRC1 and LILRC2 both have two extracellular Ig-like domains and a cytoplasmic tail devoid of any known signaling motifs. The transmembrane regions contain an arginine residue., [RefSeq, PubMed]",
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            {
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        ],
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        "protein_name": "Cytoplasmic dynein 2 intermediate chain 2",
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        ],
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        "go_molecular_function": "GO:0045503 dynein light chain binding;GO:0045504 dynein heavy chain binding",
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        "gene_names_refseq": "Lrwd1",
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        "kg_view_protein": true
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            {
                "id": "D3Z8X4_RAT",
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            }
        ],
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        "length": 2283,
        "protein_name": "DNA polymerase epsilon catalytic subunit",
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            {
                "id": "NP_001100622",
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            }
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        "disease": "mismatch repair cancer syndrome (Disease Ontology:DOID:0112182); duodenum cancer (Disease Ontology:DOID:10021); prostate cancer (Disease Ontology:DOID:10283); lung cancer (Disease Ontology:DOID:1324); endometrial cancer (Disease Ontology:DOID:1380); cancer (Disease Ontology:DOID:162); ascending colon cancer (Disease Ontology:DOID:218); ovarian cancer (Disease Ontology:DOID:2394); kidney cancer (Disease Ontology:DOID:263); endometrial carcinoma (Disease Ontology:DOID:2871); glioblastoma (Disease Ontology:DOID:3068); high grade glioma (Disease Ontology:DOID:3070); anaplastic astrocytoma (Disease Ontology:DOID:3078); breast carcinoma (Disease Ontology:DOID:3459); liver cancer (Disease Ontology:DOID:3571); gastric adenocarcinoma (Disease Ontology:DOID:3717); lung squamous cell carcinoma (Disease Ontology:DOID:3907); lung non-small cell carcinoma (Disease Ontology:DOID:3908); pleomorphic xanthoastrocytoma (Disease Ontology:DOID:4852); endometrial serous adenocarcinoma (Disease Ontology:DOID:5750); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:304573);  (R-RNO-110314);  (R-RNO-5651801);  (R-RNO-5656169);  (R-RNO-5685942);  (R-RNO-5693537);  (R-RNO-5696397);  (R-RNO-5696400);  (R-RNO-6782135);  (R-RNO-6782210);  (R-RNO-68952);  (R-RNO-68962)",
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        "publication_id_list": "16641100;29393594",
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        "function": "DNA polymerase II participates in chromosomal DNA replication., [UniProtKB, UniProtKB, UniProtKB]",
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        "biomarker_type": "",
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                "id": "3.1.11.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.11.-",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
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            },
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                "id": "4.2.99.-",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.23",
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            },
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            },
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                "id": "3.6.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.-.-",
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            }
        ],
        "go_molecular_function": "GO:0003887 DNA-directed DNA polymerase activity;GO:0008310 single-stranded DNA 3'-5' DNA exonuclease activity;GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0008622 epsilon DNA polymerase complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0071897 DNA biosynthetic process;GO:0006272 leading strand elongation;GO:0006297 nucleotide-excision repair, DNA gap filling;GO:0006287 base-excision repair, gap-filling;GO:0045004 DNA replication proofreading",
        "synthesized_glycan_count": 0,
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        "kg_view_protein": true
    },
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            {
                "id": "D3Z930_RAT",
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            }
        ],
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        "protein_name": "Ribosome assembly protein METTL17, mitochondrial",
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        "refseq_name": "methyltransferase-like protein 17, mitochondrial",
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            {
                "id": "NP_001414183",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414183",
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            }
        ],
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        "protein_names_uniprotkb": "Ribosome assembly protein METTL17, mitochondrial; Methyltransferase-like protein 17",
        "protein_names_refseq": "methyltransferase 11 domain containing 1; methyltransferase-like protein 17, mitochondrial",
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        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005759 mitochondrial matrix",
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        ],
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            {
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        "protein_names_refseq": "rho GTPase-activating protein 11A",
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        ],
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        "protein_name": "KIAA1549 homolog",
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            {
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        ],
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        "gene_names_refseq": "Kiaa1549",
        "protein_names_uniprotkb": "KIAA1549 homolog",
        "protein_names_refseq": "UPF0606 protein KIAA1549 homolog isoform X1",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa 86 (Disease Ontology:DOID:0112143)",
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        "go_cellular_component": "GO:0032391 photoreceptor connecting cilium",
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        "protein_name": "Acylglycerol transacylase",
        "gene_name": "Pnpla3",
        "organism": "Rat",
        "refseq_name": "1-acylglycerol-3-phosphate O-acyltransferase PNPLA3",
        "refseq_ac": [
            {
                "id": "NP_001269253",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001269253",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Pnpla3",
        "gene_names_refseq": "Adpn; Pnpla3",
        "protein_names_uniprotkb": "Acylglycerol transacylase; 2.3.1.51; 3.1.1.3; 3.1.1.4; Adiponutrin; Calcium-independent phospholipase A2-epsilon; Lysophosphatidic acid acyltransferase; Patatin-like phospholipase domain-containing protein 3",
        "protein_names_refseq": "1-acylglycerol-3-phosphate O-acyltransferase PNPLA3; adiponutrin; patatin-like phospholipase domain containing 3; patatin-like phospholipase domain-containing protein 3",
        "tax_id": 10116,
        "disease": "Chanarin-Dorfman syndrome (Disease Ontology:DOID:0050729); acquired metabolic disease (Disease Ontology:DOID:0060158); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); hypothyroidism (Disease Ontology:DOID:1459); coronary artery disease (Disease Ontology:DOID:3393); liver cirrhosis (Disease Ontology:DOID:5082); hepatocellular carcinoma (Disease Ontology:DOID:684); diabetes mellitus (Disease Ontology:DOID:9351); type 2 diabetes mellitus (Disease Ontology:DOID:9352); steatotic liver disease (Disease Ontology:DOID:9452); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:362972);  (R-RNO-1482883)",
        "pathway_count": 2,
        "publication_count": 6,
        "publication_id_list": "12565853;17372308;19619606;22673903;28433418;35908495",
        "class_list": "",
        "function": "Adiponutrin expression is highly regulated by feeding conditions in the different adipose tissue depots, but this regulation is impaired in obese rats., [RefSeq, PubMed]; Data suggest that adiponutrin could be involved in overall energy homeostasis, as is leptin., [RefSeq, PubMed]; Histone acetylation plays a role in the modulation of PNPLA3 levels in the liver exposed to binge ethanol drinking., [RefSeq, PubMed]; Inulin may prevent steatosis by suppressing cannabinoid receptor-1 and patatin-like phospholipase-3 expression in liver., [RefSeq, PubMed]; PNPLA3 mRNA expression is upregulated by tri-iodothyronine in adipocytes in vitro, in humans and rats, and in vivo in rat white adipose tissue., [RefSeq, PubMed]; Specifically catalyzes coenzyme A (CoA)-dependent acylation of 1-acyl-sn-glycerol 3-phosphate (2-lysophosphatidic acid/LPA) to generate phosphatidic acid (PA), an important metabolic intermediate and precursor for both triglycerides and glycerophospholipids. Does not esterify other lysophospholipids. Acyl donors are long chain (at least C16) fatty acyl-CoAs: arachidonoyl-CoA, linoleoyl-CoA, oleoyl-CoA and at a lesser extent palmitoyl-CoA. Additionally possesses low triacylglycerol lipase and CoA-independent acylglycerol transacylase activities and thus may play a role in acyl-chain remodeling of triglycerides. In vitro may express hydrolytic activity against glycerolipids triacylglycerol, diacylglycerol and monoacylglycerol, with a strong preference for oleic acid as the acyl moiety. However, the triacylglycerol hydrolase activity is controversial and may be very low. Possesses phospholipase A2 activity., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 11,
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        "ec_number_list": [
            {
                "id": "3.1.1.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.3",
                "type": "external"
            },
            {
                "id": "3.1.1.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.4",
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            },
            {
                "id": "3.1.1.32",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.32",
                "type": "external"
            },
            {
                "id": "2.3.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.-",
                "type": "external"
            },
            {
                "id": "2.3.1.51",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.51",
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            },
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.15",
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            },
            {
                "id": "3.1.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.-",
                "type": "external"
            },
            {
                "id": "3.1.1.5",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.5",
                "type": "external"
            },
            {
                "id": "3.1.1.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.23",
                "type": "external"
            },
            {
                "id": "3.1.1.79",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.79",
                "type": "external"
            },
            {
                "id": "3.1.1.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.6",
                "type": "external"
            },
            {
                "id": "1.11.1.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.11.1.27",
                "type": "external"
            },
            {
                "id": "2.3.1.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.23",
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            },
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                "id": "3.1.1.13",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.13",
                "type": "external"
            },
            {
                "id": "2.3.1.67",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.67",
                "type": "external"
            },
            {
                "id": "2.3.1.25",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.25",
                "type": "external"
            },
            {
                "id": "3.1.1.116",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.116",
                "type": "external"
            },
            {
                "id": "3.1.1.26",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.26",
                "type": "external"
            },
            {
                "id": "3.1.2.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.2.2",
                "type": "external"
            },
            {
                "id": "3.1.1.34",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.34",
                "type": "external"
            },
            {
                "id": "2.3.1.n7",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.n7",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0003841 1-acylglycerol-3-phosphate O-acyltransferase activity;GO:0042171 lysophosphatidic acid acyltransferase activity;GO:0004623 phospholipase A2 activity;GO:0036042 long-chain fatty acyl-CoA binding;GO:0004806 triacylglycerol lipase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005811 lipid droplet;GO:0016020 membrane",
        "go_biological_process": "GO:0006650 glycerophospholipid metabolic process;GO:0001676 long-chain fatty acid metabolic process;GO:0006654 phosphatidic acid biosynthetic process;GO:0032869 cellular response to insulin stimulus;GO:0050872 white fat cell differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "D3Z9J9-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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        ],
        "mass": 25715.0,
        "length": 225,
        "protein_name": "Phospholipid scramblase",
        "gene_name": "Plscr1l1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Phospholipid scramblase",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:102551265)",
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        "publication_count": 0,
        "publication_id_list": "",
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        "function": "May mediate accelerated ATP-independent bidirectional transbilayer migration of phospholipids upon binding calcium ions that results in a loss of phospholipid asymmetry in the plasma membrane., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0017128 phospholipid scramblase activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
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    },
    {
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        ],
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        "protein_name": "Maestro heat-like repeat family member 8",
        "gene_name": "Mroh8",
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            {
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001418728",
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            }
        ],
        "gene_names_uniprotkb": "Mroh8; LOC100360777",
        "gene_names_refseq": "Mroh8",
        "protein_names_uniprotkb": "Maestro heat-like repeat family member 8",
        "protein_names_refseq": "maestro heat-like repeat family member 8 isoform 1",
        "tax_id": 10116,
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        "pathway": " (rno:100360777)",
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        "go_cellular_component": "GO:0005737 cytoplasm",
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    },
    {
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            {
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        ],
        "mass": 34921.0,
        "length": 319,
        "protein_name": "Zinc finger protein 688",
        "gene_name": "Zfp688",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Zfp688",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 688",
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        "tax_id": 10116,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription",
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    },
    {
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        ],
        "mass": 68376.0,
        "length": 609,
        "protein_name": "Actin-related protein 5",
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        "refseq_name": "actin-related protein 5",
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            {
                "id": "NP_001382533",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001382533",
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            }
        ],
        "gene_names_uniprotkb": "Actr5",
        "gene_names_refseq": "Actr5",
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        "protein_names_refseq": "ARP5 actin-related protein 5 homolog; actin-related protein 5",
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        "pathway": " (rno:362258);  (R-RNO-5689603);  (R-RNO-5696394)",
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        "function": "Proposed core component of the chromatin remodeling INO80 complex which is involved in transcriptional regulation, DNA replication and probably DNA repair. Involved in DNA double-strand break repair and UV-damage excision repair., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0030234 enzyme regulator activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0031011 Ino80 complex",
        "go_biological_process": "GO:0060382 regulation of DNA strand elongation;GO:0033044 regulation of chromosome organization;GO:0006310 DNA recombination;GO:0006338 chromatin remodeling;GO:0006351 DNA-templated transcription",
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    {
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        ],
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        "protein_name": "Transcription factor binding to IGHM enhancer 3",
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        ],
        "gene_names_uniprotkb": "Tfe3",
        "gene_names_refseq": "RGD1559642; Tcfe3; Tfe3",
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            {
                "id": "NP_001101307",
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        "function": "Knockdown of Lhx6 during embryonic development results in neurophysiological alterations and behavioral deficits analogous to schizophrenia in adult rats., [RefSeq, PubMed]; LIM homeobox 6 (Lhx6)+ neurons in the ventral zona incerta project to the core portion of the lateral supramammillary nucleus in the rat., [RefSeq, PubMed]; Studied the DNA binding activity of human CDX2. Three CDX2-binding proteins were found in rat gastric tissue, and those proteins were identified to the homeobox protein Hox-D8, LIM homeobox protein 6, and SMC1L1 protein., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005634 nucleus",
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        ],
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        "go_molecular_function": "GO:0042803 protein homodimerization 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:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000785 chromatin;GO:0090571 RNA polymerase II transcription repressor complex",
        "go_biological_process": "GO:0001708 cell fate specification;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045893 positive regulation of DNA-templated transcription",
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        "refseq_name": "protein CIMAP1D",
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            {
                "id": "NP_001178706",
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        "protein_names_refseq": "outer dense fiber of sperm tails 3-like 2; outer dense fiber protein 3-like protein 2; protein CIMAP1D",
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        "protein_name": "MORC family CW-type zinc finger protein 1",
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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": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell",
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    },
    {
        "uniprot_canonical_ac": "D3ZMY7-1",
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            {
                "id": "5NTC_RAT",
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                "type": "external"
            }
        ],
        "mass": 64866.0,
        "length": 560,
        "protein_name": "Cytosolic purine 5'-nucleotidase",
        "gene_name": "Nt5c2",
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        "refseq_name": "cytosolic purine 5'-nucleotidase",
        "refseq_ac": [
            {
                "id": "NP_001388640",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001388640",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Nt5c2",
        "gene_names_refseq": "Nt5c2",
        "protein_names_uniprotkb": "Cytosolic purine 5'-nucleotidase; 2.7.1.77; 3.1.3.5; 3.1.3.99; Cytosolic nucleoside phosphotransferase 5'N",
        "protein_names_refseq": "cytosolic nucleoside phosphotransferase 5'N; cytosolic purine 5'-nucleotidase",
        "tax_id": 10116,
        "disease": "hereditary spastic paraplegia 45 (Disease Ontology:DOID:0110797); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:100363253);  (R-RNO-2161541);  (R-RNO-74259);  (R-RNO-9755088)",
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        "function": "Broad specificity cytosolic 5'-nucleotidase that catalyzes the dephosphorylation of 6-hydroxypurine nucleoside 5'-monophosphates (PubMed:6260203). In addition, possesses a phosphotransferase activity by which it can transfer a phosphate from a donor nucleoside monophosphate to an acceptor nucleoside, preferably inosine, deoxyinosine and guanosine (By similarity). Has the highest activities for IMP and GMP followed by dIMP, dGMP and XMP (PubMed:6260203). Could also catalyze the transfer of phosphates from pyrimidine monophosphates but with lower efficiency (By similarity). Through these activities regulates the purine nucleoside/nucleotide pools within the cell (PubMed:6260203)., [UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "biomarker_type": "",
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            {
                "id": "3.1.3.5",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.5",
                "type": "external"
            },
            {
                "id": "2.7.1.77",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.77",
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            },
            {
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            },
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            },
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.48",
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            },
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.91",
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            },
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                "id": "3.1.3.89",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.89",
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            },
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                "id": "3.1.3.35",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.35",
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            },
            {
                "id": "3.6.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.-",
                "type": "external"
            },
            {
                "id": "3.1.4.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.4.1",
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            },
            {
                "id": "3.6.1.9",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.9",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0005524 ATP binding;GO:0042802 identical protein binding;GO:0046872 metal ion binding;GO:0008253 5'-nucleotidase activity;GO:0050146 nucleoside phosphotransferase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0050689 negative regulation of defense response to virus by host;GO:0046054 dGMP metabolic process;GO:0046037 GMP metabolic process;GO:0046040 IMP metabolic process;GO:0046085 adenosine metabolic process",
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    },
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            }
        ],
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        "protein_name": "Large ribosomal subunit protein P2",
        "gene_name": "Rplp2l3",
        "organism": "Rat",
        "refseq_name": "large ribosomal subunit protein P2-like",
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            {
                "id": "XP_038948670",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_038948670",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Rplp2l3; LOC100362751",
        "gene_names_refseq": "Rplp2l3",
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        "protein_names_refseq": "large ribosomal subunit protein P2-like",
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        "function": "Plays an important role in the elongation step of protein synthesis., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0022625 cytosolic large ribosomal subunit",
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    },
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            {
                "id": "D3ZN41_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZN41",
                "type": "external"
            }
        ],
        "mass": 158841.0,
        "length": 1417,
        "protein_name": "Phospholipid-transporting ATPase",
        "gene_name": "Atp10d",
        "organism": "Rat",
        "refseq_name": "phospholipid-transporting ATPase VD",
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            {
                "id": "NP_001414735",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414735",
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            }
        ],
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        "gene_names_refseq": "Atp10d",
        "protein_names_uniprotkb": "Phospholipid-transporting ATPase; 7.6.2.1",
        "protein_names_refseq": "ATPase, class V, type 10D; phospholipid-transporting ATPase VD; probable phospholipid-transporting ATPase VD",
        "tax_id": 10116,
        "disease": "progressive familial intrahepatic cholestasis (Disease Ontology:DOID:0070221)",
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        ],
        "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0005524 ATP binding;GO:0016887 ATP hydrolysis activity;GO:0140326 ATPase-coupled intramembrane lipid transporter activity;GO:0140351 glycosylceramide flippase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005886 plasma membrane;GO:0005789 endoplasmic reticulum membrane;GO:1990531 phospholipid-translocating ATPase complex",
        "go_biological_process": "GO:0045332 phospholipid translocation",
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        "hit_score": 0.1,
        "record_id": "D3ZN41-1",
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    },
    {
        "uniprot_canonical_ac": "D3ZNC0-1",
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            {
                "id": "D3ZNC0_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZNC0",
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            }
        ],
        "mass": 49064.0,
        "length": 455,
        "protein_name": "OTU domain-containing protein 1",
        "gene_name": "Otud1",
        "organism": "Rat",
        "refseq_name": "OTU domain-containing protein 1",
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            {
                "id": "NP_001387701",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001387701",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Otud1",
        "gene_names_refseq": "Otud1; RGD1563344",
        "protein_names_uniprotkb": "OTU domain-containing protein 1; 3.4.19.12",
        "protein_names_refseq": "OTU domain containing 1; OTU domain-containing protein 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:498803);  (R-RNO-5357786);  (R-RNO-5357905);  (R-RNO-5357956)",
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        "function": "Deubiquitinating enzyme that specifically hydrolyzes 'Lys-63'-linked polyubiquitin to monoubiquitin. Required for the stability and translation of a subset mRNAs with a high abundance of rare codons by mediating deubiquitination of 40S ribosomal protein RPS10/eS10, thereby antagonizing ZNF598-mediated 40S ubiquitination. The abundance of rare codons in mRNAs can limit the translation rate and can lead to ribosome collisions that trigger activation of ribosome quality control (RQC) pathway by ZNF598. OTUD1-mediated deubiquitination prevents activation of the RQC and subsequent dissociation of ribosomes and stimulates formation of polysomes and translation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
            },
            {
                "id": "2.3.2.31",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.31",
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            {
                "id": "2.7.11.10",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.10",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.25",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0004843 cysteine-type deubiquitinase activity",
        "go_cellular_component": "",
        "go_biological_process": "GO:0006508 proteolysis;GO:0070536 protein K63-linked deubiquitination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZNC0-1",
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        "filter_code": "0000000.0000001.100000.000000000000001000.0000000001000.001.00000",
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    },
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        "uniprot_id": [
            {
                "id": "D3ZNC9_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZNC9",
                "type": "external"
            }
        ],
        "mass": 45265.0,
        "length": 409,
        "protein_name": "RING-type E3 ubiquitin transferase",
        "gene_name": "Marchf4",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase MARCHF4",
        "refseq_ac": [
            {
                "id": "NP_001414713",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414713",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Marchf4; March4",
        "gene_names_refseq": "March4; Marchf4",
        "protein_names_uniprotkb": "RING-type E3 ubiquitin transferase; 2.3.2.27",
        "protein_names_refseq": "E3 ubiquitin-protein ligase MARCH4; E3 ubiquitin-protein ligase MARCHF4; membrane-associated ring finger (C3HC4) 4, E3 ubiquitin protein ligase",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:367295)",
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            },
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            },
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            {
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            },
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            },
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        ],
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    },
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            {
                "id": "D3ZTQ2_RAT",
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            }
        ],
        "mass": 26273.0,
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        "protein_name": "T-cell immunoreceptor with Ig and ITIM domains",
        "gene_name": "Tigit",
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        "refseq_name": "T cell immunoreceptor with Ig and ITIM domains precursor",
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            {
                "id": "NP_001417720",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001417720",
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        ],
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        "protein_names_uniprotkb": "T-cell immunoreceptor with Ig and ITIM domains; V-set and transmembrane domain-containing protein 3",
        "protein_names_refseq": "T cell immunoreceptor with Ig and ITIM domains precursor",
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        "function": "Animals deficient in Vstm3 are more sensitive to autoimmune challenges indicating that this new member of the CD28 family is an important regulator of T-cell responses, [RefSeq, PubMed]; Inhibitory receptor that plays a role in the modulation of immune responses. Suppresses T-cell activation by promoting the generation of mature immunoregulatory dendritic cells. Upon binding to its ligands PVR/CD155 or NECTIN2/CD112, which are expressed on antigen-presenting cells, sends inhibitory signals to the T-cell or NK cell. Mechanistically, interaction with ligand leads to phosphorylation of the cytoplasmic tail by Src family tyrosine kinases such as FYN or LCK, allowing subsequent binding to adapter GRB2 and SHIP1/INPP5D. In turn, inhibits PI3K and MAPK signaling cascades. In addition, associates with beta-arrestin-2/ARRB2 to recruit SHIP1/INPP5D that suppresses autoubiquitination of TRAF6 and subsequently inhibits NF-kappa-B signaling pathway. Also acts as a receptor for NECTIN4 to inhibit NK cell cytotoxicity., [UniProtKB, UniProtKB]",
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        "refseq_name": "double homeobox 4",
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            {
                "id": "NP_001419931",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001419931",
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        "protein_names_uniprotkb": "Double homeobox 4",
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        "protein_name": "DNA excision repair protein ERCC-5",
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        "protein_names_uniprotkb": "DNA excision repair protein ERCC-5",
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        "tax_id": 10116,
        "disease": "disease by infectious agent (Disease Ontology:DOID:0050117); cerebrooculofacioskeletal syndrome 3 (Disease Ontology:DOID:0080913); xeroderma pigmentosum group G (Disease Ontology:DOID:0110849); stomach cancer (Disease Ontology:DOID:10534); lung cancer (Disease Ontology:DOID:1324); melanoma (Disease Ontology:DOID:1909); larynx cancer (Disease Ontology:DOID:2596); Cockayne syndrome (Disease Ontology:DOID:2962); high grade glioma (Disease Ontology:DOID:3070); coronary artery disease (Disease Ontology:DOID:3393); lung non-small cell carcinoma (Disease Ontology:DOID:3908)",
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        "protein_name": "Tripartite motif-containing protein 67",
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            {
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        ],
        "gene_names_uniprotkb": "Trim67",
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        "protein_names_refseq": "tripartite motif-containing protein 67 isoform X3",
        "tax_id": 10116,
        "disease": "Opitz GBBB syndrome (Disease Ontology:DOID:0080697)",
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        "go_molecular_function": "GO:0008270 zinc ion binding",
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        ],
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        "protein_name": "Sucrase-isomaltase, intestinal",
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        "organism": "Rat",
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            {
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        ],
        "gene_names_uniprotkb": "Mgam2; Mgam; Mgam2",
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        "protein_names_uniprotkb": "Sucrase-isomaltase, intestinal",
        "protein_names_refseq": "maltase-glucoamylase, intestinal-like; maltase-glucoamylase",
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        "function": "Plays an important role in the final stage of carbohydrate digestion. Isomaltase activity is specific for both alpha-1,4- and alpha-1,6-oligosaccharides., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004558 alpha-1,4-glucosidase activity;GO:0016160 amylase activity;GO:0030246 carbohydrate binding;GO:0090599 alpha-glucosidase activity",
        "go_cellular_component": "GO:0016324 apical plasma membrane;GO:0016020 membrane",
        "go_biological_process": "GO:0000025 maltose catabolic process;GO:1901027 dextrin catabolic process;GO:0005975 carbohydrate metabolic process",
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        ],
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        "protein_name": "EF hand domain family, member B",
        "gene_name": "Efhb",
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        "gene_names_uniprotkb": "Efhb",
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        "protein_names_uniprotkb": "EF hand domain family, member B",
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0061891 calcium ion sensor activity",
        "go_cellular_component": "GO:0036126 sperm flagellum;GO:0005879 axonemal microtubule;GO:0160111 axonemal A tubule inner sheath",
        "go_biological_process": "GO:0070884 regulation of calcineurin-NFAT signaling cascade;GO:0030317 flagellated sperm motility;GO:2001256 regulation of store-operated calcium entry",
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                "url": "https://www.uniprot.org/uniprot/D3ZU55",
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            }
        ],
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        "protein_name": "Forkhead box protein K1",
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        "refseq_name": "forkhead box protein K1",
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            {
                "id": "NP_001032296",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0071889 14-3-3 protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0030154 cell differentiation;GO:0042594 response to starvation;GO:0010906 regulation of glucose metabolic process",
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    },
    {
        "uniprot_canonical_ac": "D3ZUD3-1",
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            {
                "id": "D3ZUD3_RAT",
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            }
        ],
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        "refseq_name": "WAS/WASL-interacting protein family member 2",
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            {
                "id": "NP_001178754",
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            }
        ],
        "gene_names_uniprotkb": "Wipf2",
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        "go_molecular_function": "GO:0003779 actin binding",
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    },
    {
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            {
                "id": "D3ZUV9_RAT",
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        ],
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        "protein_names_uniprotkb": "CCR4-NOT transcription complex subunit 3; CCR4-associated factor 3",
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        "tax_id": 10116,
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        "function": "Component of the CCR4-NOT complex which is one of the major cellular mRNA deadenylases and is linked to various cellular processes including bulk mRNA degradation, miRNA-mediated repression, translational repression during translational initiation and general transcription regulation. Additional complex functions may be a consequence of its influence on mRNA expression. May be involved in metabolic regulation; may be involved in recruitment of the CCR4-NOT complex to deadenylation target mRNAs involved in energy metabolism. Involved in mitotic progression and regulation of the spindle assembly checkpoint by regulating the stability of MAD1L1 mRNA. Can repress transcription and may link the CCR4-NOT complex to transcriptional regulation; the repressive function may involve histone deacetylases. Involved in the maintenance of embryonic stem (ES) cell identity., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0000932 P-body;GO:0030014 CCR4-NOT complex;GO:0030015 CCR4-NOT core complex",
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        ],
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        "protein_name": "Olfactory receptor",
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        "refseq_name": "olfactory receptor Olr610",
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            {
                "id": "NP_001000336",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000336",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Or5d41b; LOC100909611; Or5d41",
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        "protein_names_uniprotkb": "Olfactory receptor",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "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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    },
    {
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        ],
        "mass": 102983.0,
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        "protein_name": "Periodic tryptophan protein 2 homolog",
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        "refseq_name": "periodic tryptophan protein 2 homolog",
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            {
                "id": "NP_001162124",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001162124",
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        ],
        "gene_names_uniprotkb": "Pwp2",
        "gene_names_refseq": "Pwp2",
        "protein_names_uniprotkb": "Periodic tryptophan protein 2 homolog",
        "protein_names_refseq": "PWP2 periodic tryptophan protein homolog; PWP2, UTPB SSU processome subunit; periodic tryptophan protein 2 homolog",
        "tax_id": 10116,
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        "go_cellular_component": "GO:0034388 Pwp2p-containing subcomplex of 90S preribosome;GO:0005730 nucleolus;GO:0032040 small-subunit processome",
        "go_biological_process": "GO:0000462 maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA);GO:0042274 ribosomal small subunit biogenesis;GO:0000028 ribosomal small subunit assembly",
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        ],
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        "protein_name": "RING finger protein 150",
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        "refseq_name": "RING finger protein 150 precursor",
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            {
                "id": "NP_001178022",
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        ],
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity",
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        ],
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        "protein_name": "Large ribosomal subunit protein eL31",
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            {
                "id": "XP_063130886",
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        ],
        "gene_names_uniprotkb": "LOC120096991; ENSRNOG00000065077",
        "gene_names_refseq": "LOC120096991",
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        "protein_names_refseq": "large ribosomal subunit protein eL31-like",
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        "function": "E3 Ubiquitin ligase proteins mediate ubiquitination and subsequent proteasomal degradation of target proteins. E3 ubiquitin ligases accept ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. Able to specifically bind RNA., [UniProtKB, UniProtKB, UniProtKB]",
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            {
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            {
                "id": "2.3.2.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.23",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.24",
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                "id": "2.3.2.-",
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                "type": "external"
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        ],
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        "protein_names_uniprotkb": "Patatin like phospholipase domain containing 4",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005811 lipid droplet;GO:0016020 membrane",
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        ],
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        "protein_name": "15-oxoprostaglandin 13-reductase",
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        "refseq_name": "prostaglandin reductase 3",
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            {
                "id": "NP_001099599",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099599",
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        "protein_names_uniprotkb": "15-oxoprostaglandin 13-reductase; 1.3.1.48; 15-oxoprostaglandin 13-reductase; Zinc-binding alcohol dehydrogenase domain-containing protein 2",
        "protein_names_refseq": "prostaglandin reductase 3; zinc binding alcohol dehydrogenase, domain containing 2; zinc-binding alcohol dehydrogenase domain-containing protein 2",
        "tax_id": 10116,
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        "function": "Functions as 15-oxo-prostaglandin 13-reductase and acts on 15-keto-PGE1, 15-keto-PGE2, 15-keto-PGE1-alpha and 15-keto-PGE2-alpha with highest efficiency towards 15-keto-PGE2-alpha. Overexpression represses transcriptional activity of PPARG and inhibits adipocyte differentiation., [UniProtKB, UniProtKB]",
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            {
                "id": "1.3.1.74",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.3.1.74",
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        "go_cellular_component": "GO:0005777 peroxisome",
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        "length": 175,
        "protein_name": "TNF receptor superfamily member 13C",
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        "refseq_name": "TNF receptor superfamily member 13C",
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            {
                "id": "NP_001418900",
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        ],
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        "protein_names_uniprotkb": "TNF receptor superfamily member 13C",
        "protein_names_refseq": "TNF receptor superfamily member 13C; tumor necrosis factor receptor superfamily, member 13c",
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        "disease": "common variable immunodeficiency 4 (Disease Ontology:DOID:0081147)",
        "pathway": " (rno:500910);  (R-RNO-5668541);  (R-RNO-5676594)",
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        "publication_id_list": "22124120;22391142",
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        "function": "BAFF/BAFF-R involved in autoantibody production in rats with collagen-induced arthritis via PI3K-Akt-mTOR signaling and the regulation of paeoniflorin., [RefSeq, PubMed]; Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0038023 signaling receptor activity",
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        "synthesized_glycan_count": 0,
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        ],
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        "length": 1198,
        "protein_name": "Tubulin tyrosine ligase like 4",
        "gene_name": "Ttll4",
        "organism": "Rat",
        "refseq_name": "tubulin monoglutamylase TTLL4",
        "refseq_ac": [
            {
                "id": "NP_001414011",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414011",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ttll4",
        "gene_names_refseq": "Ttll4",
        "protein_names_uniprotkb": "Tubulin tyrosine ligase like 4",
        "protein_names_refseq": "tubulin monoglutamylase TTLL4; tubulin polyglutamylase TTLL4; tubulin tyrosine ligase-like family, member 4",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0070740 tubulin-glutamic acid ligase activity;GO:0005524 ATP binding;GO:0015631 tubulin binding;GO:0070739 protein-glutamic acid ligase activity",
        "go_cellular_component": "GO:0005874 microtubule;GO:0036064 ciliary basal body;GO:0097731 9+0 non-motile cilium",
        "go_biological_process": "GO:0000226 microtubule cytoskeleton organization;GO:0018095 protein polyglutamylation;GO:0018200 peptidyl-glutamic acid modification;GO:0120222 regulation of blastocyst development",
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        ],
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        "protein_name": "Endoplasmic reticulum membrane sensor NFE2L1",
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        "refseq_name": "endoplasmic reticulum membrane sensor NFE2L1 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001101763",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001101763",
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        ],
        "gene_names_uniprotkb": "Nfe2l1",
        "gene_names_refseq": "Nfe2l1",
        "protein_names_uniprotkb": "Endoplasmic reticulum membrane sensor NFE2L1; Nuclear factor erythroid 2-related factor 1; Nuclear factor, erythroid derived 2, like 1",
        "protein_names_refseq": "endoplasmic reticulum membrane sensor NFE2L1 isoform 1; endoplasmic reticulum membrane sensor NFE2L1; nuclear factor erythroid 2-related factor 1; nuclear factor, erythroid 2-like 1; nuclear factor, erythroid derived 2,-like 1",
        "tax_id": 10116,
        "disease": "hepatocellular carcinoma (Disease Ontology:DOID:684); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": " (rno:360610)",
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        "function": "This gene encodes a protein that is involved in globin gene expression in erythrocytes. Confusion has occurred in bibliographic databases for genes in the 'nuclear respiratory factor' and 'nuclear factor (erythroid-derived 2)' families due to a shared symbol or alias pattern of NRF*. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003682 chromatin binding;GO:0003713 transcription coactivator activity;GO:0019904 protein domain specific binding;GO:0042802 identical protein binding;GO:0046982 protein heterodimerization activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane;GO:0090575 RNA polymerase II transcription regulator complex;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0021781 glial cell fate commitment;GO:0070417 cellular response to cold;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II",
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                "url": "https://www.uniprot.org/uniprot/D4A3D6",
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            }
        ],
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        "length": 486,
        "protein_name": "ETS transcription factor ERG",
        "gene_name": "Erg",
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        "refseq_name": "transcriptional regulator ERG isoform 5",
        "refseq_ac": [
            {
                "id": "NP_001424636",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001424636",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Erg",
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        "protein_names_uniprotkb": "ETS transcription factor ERG",
        "protein_names_refseq": "ERG, ETS transcription factor; avian erythroblastosis virus E-26 (v-ets) oncogene related; transcriptional regulator ERG isoform 5; transcriptional regulator ERG; v-ets avian erythroblastosis virus E26 oncogene; v-ets erythroblastosis virus E26 oncogene homolog; v-ets erythroblastosis virus E26 oncogene like",
        "tax_id": 10116,
        "disease": "hereditary lymphedema (Disease Ontology:DOID:0050580); pulmonary venoocclusive disease (Disease Ontology:DOID:5453); osteoarthritis (Disease Ontology:DOID:8398); myeloid leukemia (Disease Ontology:DOID:8692)",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:1990904 ribonucleoprotein complex",
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    },
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            }
        ],
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        "length": 317,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or52e8b",
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        "refseq_name": "olfactory receptor Olr184",
        "refseq_ac": [
            {
                "id": "NP_001000182",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000182",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Or52e8b",
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        "protein_names_refseq": "olfactory receptor 184; olfactory receptor Olr184; olfactory receptor gene Olr184",
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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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        ],
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        "protein_name": "Omega-hydroxyceramide transacylase",
        "gene_name": "Pnpla1",
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        "gene_names_uniprotkb": "Pnpla1",
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        "protein_names_uniprotkb": "Omega-hydroxyceramide transacylase; 2.3.1.296; Patatin-like phospholipase domain-containing protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Chanarin-Dorfman syndrome (Disease Ontology:DOID:0050729); acquired metabolic disease (Disease Ontology:DOID:0060158); autosomal recessive congenital ichthyosis 10 (Disease Ontology:DOID:0060719); diabetes mellitus (Disease Ontology:DOID:9351); obesity (Disease Ontology:DOID:9970)",
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        "function": "Omega-hydroxyceramide transacylase involved in the synthesis of omega-O-acylceramides (esterified omega-hydroxyacyl-sphingosine; EOS), which are extremely hydrophobic lipids involved in skin barrier formation. Catalyzes the last step of the synthesis of omega-O-acylceramides by transferring linoleic acid from triglycerides to an omega-hydroxyceramide. Omega-O-acylceramides, are required for the biogenesis of lipid lamellae in the stratum corneum and the formation of the cornified lipid envelope which are essential for the epidermis barrier function. These lipids also play a role in keratinocyte differentiation. May also act on omega-hydroxylated ultra-long chain fatty acids (omega-OH ULCFA) and acylglucosylceramides (GlcEOS)., [UniProtKB, UniProtKB]",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.296",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0004806 triacylglycerol lipase activity;GO:0016747 acyltransferase activity, transferring groups other than amino-acyl groups;GO:0030280 structural constituent of skin epidermis;GO:0106341 omega-hydroxyceramide transacylase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005811 lipid droplet;GO:0016020 membrane",
        "go_biological_process": "GO:0046513 ceramide biosynthetic process;GO:0055088 lipid homeostasis;GO:0061436 establishment of skin barrier;GO:0030216 keratinocyte differentiation;GO:0019433 triglyceride catabolic process",
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            {
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        ],
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        "protein_name": "SHC adaptor protein 4",
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        "refseq_name": "SHC-transforming protein 4",
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            {
                "id": "NP_001177994",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001177994",
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            }
        ],
        "gene_names_uniprotkb": "Shc4",
        "gene_names_refseq": "RGD1309182; Shc4",
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        "function": "ShcD shows relatively widespread distribution in the adult brain and spinal cord, with prominent levels of staining throughout the olfactory bulb, as well as in sub-structures of the cerebellum and hippocampus, including the subgranular zone. Co-localization studies confirm the expression of ShcD in mature neurons and progenitor cells. ShcD immunoreactivity is primarily localized to axons and somata. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0019904 protein domain specific binding;GO:0030971 receptor tyrosine kinase binding",
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    {
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        "protein_names_uniprotkb": "F-box protein 24",
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        "go_molecular_function": "GO:1990756 ubiquitin-like ligase-substrate adaptor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0019005 SCF ubiquitin ligase complex",
        "go_biological_process": "GO:0007283 spermatogenesis;GO:0007338 single fertilization;GO:0006325 chromatin organization;GO:0007005 mitochondrion organization;GO:0030163 protein catabolic process",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "MTSS I-BAR domain containing 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "intellectual developmental disorder with ocular anomalies and distinctive facial features (Disease Ontology:DOID:0081301)",
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        "go_molecular_function": "GO:0003779 actin binding;GO:0003785 actin monomer binding;GO:0005096 GTPase activator activity;GO:0005543 phospholipid binding;GO:0005546 phosphatidylinositol-4,5-bisphosphate binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005925 focal adhesion;GO:0015629 actin cytoskeleton;GO:0030027 lamellipodium;GO:0032587 ruffle membrane",
        "go_biological_process": "GO:0007009 plasma membrane organization;GO:0061024 membrane organization;GO:0090630 activation of GTPase activity;GO:0036120 cellular response to platelet-derived growth factor stimulus;GO:0097581 lamellipodium organization",
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                "url": "https://www.uniprot.org/uniprot/D4A447",
                "type": "external"
            }
        ],
        "mass": 161886.0,
        "length": 1442,
        "protein_name": "CD109 antigen",
        "gene_name": "Cd109",
        "organism": "Rat",
        "refseq_name": "CD109 antigen precursor",
        "refseq_ac": [
            {
                "id": "NP_001102241",
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        "gene_names_refseq": "Cd109",
        "protein_names_uniprotkb": "CD109 antigen",
        "protein_names_refseq": "CD109 antigen precursor; CD109 antigen",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363104);  (R-RNO-114608);  (R-RNO-163125)",
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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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        "function": "Component of the telomerase ribonucleoprotein (RNP) complex that is essential for the replication of chromosome termini. May have a general role in telomere regulation. Promotes in vitro the ability of TERT to elongate telomeres. Overexpression induces telomere uncapping, chromosomal end-to-end fusions (telomeric DNA persists at the fusion points) and did not perturb TRF2 telomeric localization. Binds to the single-stranded 5'-(GTGTGG)(4)GTGT-3' telomeric DNA, but not to a telomerase RNA template component (TER)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Mechanism of circRNA_SMG6 mediating lung macrophage ECM degradation via miR-570-3p in microplastics-induced emphysema., [RefSeq, PubMed]; Plays a role in nonsense-mediated mRNA decay. Is thought to provide a link to the mRNA degradation machinery as it has endonuclease activity required to initiate NMD, and to serve as an adapter for UPF1 to protein phosphatase 2A (PP2A), thereby triggering UPF1 dephosphorylation. Degrades single-stranded RNA (ssRNA), but not ssDNA or dsRNA., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.8.5",
                "type": "external"
            }
        ],
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        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0005783 endoplasmic reticulum",
        "go_biological_process": "GO:0032049 cardiolipin biosynthetic process",
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    },
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            {
                "id": "NP_001178043",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001178043",
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        ],
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        "go_cellular_component": "",
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        "refseq_name": "protein associated with UVRAG as autophagy enhancer isoform X1",
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            {
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        ],
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        "protein_names_refseq": "BANF family member 2; barrier to autointegration factor 2",
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        ],
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        ],
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        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0001502 cartilage condensation",
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        "protein_names_refseq": "cytochrome P450 26C1",
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            {
                "id": "1.14.14.-",
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                "type": "external"
            },
            {
                "id": "1.14.13.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.14.13.-",
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            }
        ],
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        "go_cellular_component": "GO:0016020 membrane",
        "go_biological_process": "GO:0048284 organelle fusion;GO:0007417 central nervous system development;GO:0009952 anterior/posterior pattern specification;GO:0014032 neural crest cell development;GO:0034653 retinoic acid catabolic process",
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        "kg_view_protein": true
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            {
                "id": "D4ABD3_RAT",
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            }
        ],
        "mass": 81681.0,
        "length": 740,
        "protein_name": "Arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein",
        "gene_name": "Acap1",
        "organism": "Rat",
        "refseq_name": "arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 1",
        "refseq_ac": [
            {
                "id": "NP_001099266",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099266",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Acap1",
        "gene_names_refseq": "Acap1; Centb1",
        "protein_names_uniprotkb": "Arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein; Centaurin-beta; Cnt-b",
        "protein_names_refseq": "arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 1; centaurin, beta 1",
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        "function": "GTPase-activating protein (GAP) for ADP ribosylation factor 6 (ARF6) required for clathrin-dependent export of proteins from recycling endosomes to trans-Golgi network and cell surface. Required for regulated export of ITGB1 from recycling endosomes to the cell surface and ITGB1-dependent cell migration., [UniProtKB, UniProtKB, UniProtKB]; GTPase-activating protein for the ADP ribosylation factor family., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0055038 recycling endosome membrane;GO:0010008 endosome membrane",
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        "kg_view_protein": true
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    {
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            {
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        ],
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            {
                "id": "NP_001000743",
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        "gene_names_uniprotkb": "Or52z12",
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        "protein_names_refseq": "olfactory receptor 110; olfactory receptor Olr110; olfactory receptor gene Olr110",
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        "go_cellular_component": "GO:0005902 microvillus;GO:0120043 stereocilium shaft;GO:0120044 stereocilium base",
        "go_biological_process": "GO:0007605 sensory perception of sound;GO:0060088 auditory receptor cell stereocilium organization;GO:0060122 inner ear receptor cell stereocilium organization",
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        "function": "Converts 1-acyl-sn-glycerol-3-phosphate (lysophosphatidic acid or LPA) into 1,2-diacyl-sn-glycerol-3-phosphate (phosphatidic acid or PA) by incorporating an acyl moiety at the sn-2 position of the glycerol backbone., [UniProtKB, UniProtKB]",
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                "id": "2.3.1.-",
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        "go_biological_process": "GO:0006654 phosphatidic acid biosynthetic process;GO:0008544 epidermis development;GO:0001819 positive regulation of cytokine production;GO:0009410 response to xenobiotic stimulus;GO:0019432 triglyceride biosynthetic process",
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    },
    {
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            {
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            }
        ],
        "mass": 20902.0,
        "length": 182,
        "protein_name": "Ferritin heavy chain-like",
        "gene_name": "LOC108352322",
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        "refseq_name": "ferritin heavy chain-like",
        "refseq_ac": [
            {
                "id": "XP_038944683",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_038944683",
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            }
        ],
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        "protein_names_uniprotkb": "Ferritin heavy chain-like",
        "protein_names_refseq": "ferritin heavy chain-like",
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            {
                "id": "NP_001419561",
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        ],
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        "protein_names_refseq": "BTB (POZ) domain containing 11; BTB domain containing 11; ankyrin repeat and BTB/POZ domain-containing protein 3; ankyrin repeat and BTB/POZ domain-containing protein BTBD11 isoform 1; ankyrin repeat and BTB/POZ domain-containing protein BTBD11",
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        "protein_name": "Keratin-associated protein",
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        ],
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        "protein_name": "Zinc finger protein 788",
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        ],
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            {
                "id": "XP_006235324",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006235324",
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        ],
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        "go_molecular_function": "GO:0005102 signaling receptor binding;GO:0008201 heparin binding",
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        ],
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        "protein_name": "Rho guanine nucleotide exchange factor 38",
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            {
                "id": "NP_001414563",
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        ],
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        "protein_names_refseq": "Rho guanine nucleotide exchange factor (GEF) 38; rho guanine nucleotide exchange factor 38-like; rho guanine nucleotide exchange factor 38",
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        "go_molecular_function": "GO:0005085 guanyl-nucleotide exchange factor activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
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    {
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        ],
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        "protein_name": "Polyamine-transporter SLC45A4",
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        "gene_names_uniprotkb": "Slc45a4",
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            {
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        "protein_names_uniprotkb": "Sodium channel protein type 7 subunit alpha; Glial sodium channel alpha subunit; Na-G; Nax channel; SCL-11; Voltage-gated sodium channel-like protein",
        "protein_names_refseq": "glial sodium channel alpha subunit; nax channel; sodium channel protein type 7 subunit alpha; sodium channel voltage-gated type VI alpha polypeptide; sodium channel, voltage-gated, type 6, alpha polypeptide; sodium channel, voltage-gated, type VII, alpha subunit; voltage-gated sodium channel-like protein",
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        "disease": "generalized epilepsy with febrile seizures plus (Disease Ontology:DOID:0060170); Dravet syndrome (Disease Ontology:DOID:0080422); generalized epilepsy with febrile seizures plus 2 (Disease Ontology:DOID:0111294); epilepsy (Disease Ontology:DOID:1826); anxiety disorder (Disease Ontology:DOID:2030); brain infarction (Disease Ontology:DOID:3454)",
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        "pathway": " (rno:306618);  (R-RNO-193648);  (R-RNO-416482);  (R-RNO-8980692);  (R-RNO-9013026);  (R-RNO-9013106);  (R-RNO-9013148);  (R-RNO-9013149)",
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            {
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        "function": "Identify HMCN1 as a new molecule involved in the dynamic changes of podocyte foot processes in glomerular disease., [RefSeq, PubMed]; Involved in transforming growth factor beta-mediated rearrangement of the podocyte cytoskeleton which includes reduction of F-actin fibers and broadening, flattening and elongation of podocytes. Plays a role in basement membrane organization. May promote cleavage furrow maturation during cytokinesis in preimplantation embryos. May play a role in the architecture of adhesive and flexible epithelial cell junctions. May play a role during myocardial remodeling by imparting an effect on cardiac fibroblast migration., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Myelin expression factor 2",
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        "function": "Calcium, potassium:sodium antiporter that transports 1 Ca(2+) and 1 K(+) to the melanosome in exchange for 4 cytoplasmic Na(+). Involved in pigmentation, possibly by participating in ion transport in melanosomes. Predominant sodium-calcium exchanger in melanocytes., [UniProtKB, UniProtKB]; Transcriptional repressor of the myelin basic protein gene (MBP). Binds to the proximal MB1 element 5'-TTGTCC-3' of the MBP promoter. Its binding to MB1 and function are inhibited by PURA., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        ],
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.11.-",
                "type": "external"
            },
            {
                "id": "2.7.13.3",
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            },
            {
                "id": "2.7.4.18",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.18",
                "type": "external"
            },
            {
                "id": "3.1.24.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.24.-",
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            },
            {
                "id": "3.4.19.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.19.12",
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            },
            {
                "id": "2.7.11.39",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.39",
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            },
            {
                "id": "2.4.99.18",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.4.99.18",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.10",
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            }
        ],
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        "go_biological_process": "GO:0042149 cellular response to glucose starvation",
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            }
        ],
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            {
                "id": "NP_001414083",
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            }
        ],
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        "pathway": " (rno:682937);  (R-RNO-2029482);  (R-RNO-4420097);  (R-RNO-5663213);  (R-RNO-9013149)",
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        "function": "Downstream effector molecule involved in the transmission of signals from tyrosine kinase receptors and small GTPases to the actin cytoskeleton. Promotes formation of actin filaments. Part of the WAVE complex that regulates lamellipodia formation. The WAVE complex regulates actin filament reorganization via its interaction with the Arp2/3 complex., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0098885 modification of postsynaptic actin cytoskeleton;GO:0030036 actin cytoskeleton organization;GO:2000601 positive regulation of Arp2/3 complex-mediated actin nucleation;GO:0030032 lamellipodium assembly;GO:0014003 oligodendrocyte development",
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            {
                "id": "3.1.1.71",
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        ],
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        "go_cellular_component": "GO:0005811 lipid droplet",
        "go_biological_process": "GO:0016042 lipid catabolic process;GO:0016125 sterol metabolic process;GO:0019915 lipid storage",
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                "id": "NP_001178029",
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        ],
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        "go_biological_process": "GO:0010831 positive regulation of myotube differentiation;GO:0010830 regulation of myotube differentiation;GO:0006397 mRNA processing;GO:0030154 cell differentiation;GO:0048255 mRNA stabilization",
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        "mass": 30938.0,
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        "protein_name": "Peptidase S1 domain-containing protein",
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        "protein_names_uniprotkb": "Peptidase S1 domain-containing protein",
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        "go_molecular_function": "GO:0004252 serine-type endopeptidase activity",
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        ],
        "mass": 86315.0,
        "length": 791,
        "protein_name": "ATR interacting protein",
        "gene_name": "Atrip",
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        "disease": "Seckel syndrome (Disease Ontology:DOID:0050569)",
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        "go_molecular_function": "GO:0070530 K63-linked polyubiquitin modification-dependent protein binding",
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        ],
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        "protein_name": "Olfactory receptor",
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        ],
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        "gene_names_refseq": "Or5d14l1",
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        "protein_names_refseq": "olfactory receptor 5D14; rCG27063-like",
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        "function": "Coreceptor for SEMA3A and SEMA6A. Necessary for signaling by SEMA6A and class 3 semaphorins and subsequent remodeling of the cytoskeleton. Plays a role in axon guidance, invasive growth and cell migration. Class 3 semaphorins bind to a complex composed of a neuropilin and a plexin. The plexin modulates the affinity of the complex for specific semaphorins, and its cytoplasmic domain is required for the activation of down-stream signaling events in the cytoplasm., [UniProtKB, UniProtKB]; MiR-145a-5p/Plexin-A2 promotes the migration of OECs and transplantation of miR-145a-5p engineered OECs enhances the functional recovery in rats with SCI., [RefSeq, PubMed]; PLXNA2 knockdown promotes M2 microglia polarization through mTOR/STAT3 signaling to improve functional recovery in rats after cerebral ischemia/reperfusion injury., [RefSeq, PubMed]",
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        "go_biological_process": "GO:0045087 innate immune response;GO:0051607 defense response to virus;GO:0090090 negative regulation of canonical Wnt signaling pathway;GO:0034063 stress granule assembly;GO:0032481 positive regulation of type I interferon production",
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            {
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001386394",
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            }
        ],
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            {
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        "protein_name": "Hepatitis A virus cellular receptor 1 like 1",
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        "tax_id": 10116,
        "disease": "essential hypertension (Disease Ontology:DOID:10825); hydronephrosis (Disease Ontology:DOID:11111); acute kidney tubular necrosis (Disease Ontology:DOID:12556); renovascular hypertension (Disease Ontology:DOID:1591); hyperuricemia (Disease Ontology:DOID:1920); relapsing-remitting multiple sclerosis (Disease Ontology:DOID:2378); asthma (Disease Ontology:DOID:2841); IgA glomerulonephritis (Disease Ontology:DOID:2986); acute kidney failure (Disease Ontology:DOID:3021); atopic dermatitis (Disease Ontology:DOID:3310); renal cell carcinoma (Disease Ontology:DOID:4450); kidney disease (Disease Ontology:DOID:557); hepatocellular carcinoma (Disease Ontology:DOID:684); vesicoureteral reflux (Disease Ontology:DOID:9620)",
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        "refseq_name": "spectrin alpha chain, erythrocytic 1",
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            {
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        "protein_names_uniprotkb": "Spectrin alpha chain, erythrocytic 1; Erythroid alpha-spectrin",
        "protein_names_refseq": "erythroid spectrin alpha; spectrin alpha chain, erythrocyte; spectrin alpha chain, erythrocytic 1; spectrin, alpha, erythrocytic 1 (elliptocytosis 2)",
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        "disease": "hereditary pyropoikilocytosis (Disease Ontology:DOID:0061026); hereditary spherocytosis type 1 (Disease Ontology:DOID:0110916); hereditary spherocytosis type 3 (Disease Ontology:DOID:0110918); sickle cell anemia (Disease Ontology:DOID:10923); hereditary spherocytosis (Disease Ontology:DOID:12971)",
        "pathway": " (rno:289257);  (R-RNO-375165);  (R-RNO-445095);  (R-RNO-5673001);  (R-RNO-6807878)",
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        "function": "Cytoskeletal protein SPTA1 mediating the decrease in erectile function induced by high-fat diet via Hippo signaling pathway., [RefSeq, PubMed]; Spectrin is the major constituent of the cytoskeletal network underlying the erythrocyte plasma membrane. It associates with band 4.1 and actin to form the cytoskeletal superstructure of the erythrocyte plasma membrane., [UniProtKB, UniProtKB]",
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        "length": 398,
        "protein_name": "Stomatin-like protein 1",
        "gene_name": "Stoml1",
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        "refseq_name": "stomatin-like protein 1",
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            {
                "id": "NP_001292167",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001292167",
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        "gene_names_uniprotkb": "Stoml1",
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        "protein_names_refseq": "stomatin (EPB72)-like 1; stomatin-like protein 1",
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        "go_molecular_function": "GO:0008200 ion channel inhibitor activity",
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        "protein_name": "Protein N-lysine methyltransferase METTL21A",
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        "refseq_name": "protein N-lysine methyltransferase METTL21A",
        "refseq_ac": [
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001386380",
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        "gene_names_refseq": "Fam119a; Mettl21a; RGD1311824",
        "protein_names_uniprotkb": "Protein N-lysine methyltransferase METTL21A; Methyltransferase-like protein 21A",
        "protein_names_refseq": "family with sequence similarity 119, member A; methyltransferase like 21A; protein N-lysine methyltransferase METTL21A-like; protein N-lysine methyltransferase METTL21A",
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        "pathway": " (rno:102553119);  (R-RNO-8876725)",
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        "function": "Protein-lysine methyltransferase that selectively trimethylates residues in heat shock protein 70 (HSP70) family members. Contributes to the in vivo trimethylation of Lys residues in HSPA1 and HSPA8. In vitro methylates 'Lys-561' in HSPA1, 'Lys-564' in HSPA2, 'Lys-585' in HSPA5, 'Lys-563' in HSPA6 and 'Lys-561' in HSPA8., [UniProtKB, UniProtKB]",
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        "ec_number_list": [
            {
                "id": "2.1.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.-",
                "type": "external"
            },
            {
                "id": "2.1.1.359",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.359",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.372",
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        "pathway": " (rno:299112);  (R-RNO-110314);  (R-RNO-5651801);  (R-RNO-5656169);  (R-RNO-5685942);  (R-RNO-5693537);  (R-RNO-5696397);  (R-RNO-5696400);  (R-RNO-6782135);  (R-RNO-6782210);  (R-RNO-68952);  (R-RNO-68962)",
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        "protein_names_refseq": "large ribosomal subunit protein eL38-like",
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        "go_molecular_function": "GO:0003735 structural constituent of ribosome",
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        "protein_name": "Peptidoglycan recognition protein 4",
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            {
                "id": "XP_063137890",
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        "gene_names_refseq": "Pglyrp4",
        "protein_names_uniprotkb": "Peptidoglycan recognition protein 4",
        "protein_names_refseq": "peptidoglycan recognition protein 4 isoform X1",
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        "go_molecular_function": "GO:0042834 peptidoglycan binding;GO:0008745 N-acetylmuramoyl-L-alanine amidase activity;GO:0008270 zinc ion binding;GO:0046982 protein heterodimerization activity;GO:0016019 peptidoglycan immune receptor activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0032991 protein-containing complex",
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        "protein_names_refseq": "G protein-coupled receptor 89B; G protein-coupled receptor 89",
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        "disease": "cold-induced sweating syndrome 2 (Disease Ontology:DOID:0080330); severe acute respiratory syndrome (Disease Ontology:DOID:2945)",
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    },
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            {
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        ],
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        "kg_view_protein": true
    },
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            {
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        ],
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        "disease": "limb-girdle muscular dystrophy (Disease Ontology:DOID:11724)",
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        "function": "Calcium/phospholipid-binding protein which is essential for proper development of skeletal and cardiac muscle., [UniProtKB, UniProtKB]",
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            {
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        ],
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        "protein_name": "Asteroid homolog 1",
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            {
                "id": "XP_063121879",
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            }
        ],
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        ],
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        "protein_name": "Phosphoserine aminotransferase",
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        "function": "Involved in L-serine biosynthesis via the phosphorylated pathway, a three-step pathway converting the glycolytic intermediate 3-phospho-D-glycerate into L-serine. Catalyzes the second step, that is the pyridoxal 5'-phosphate-dependent transamination of 3-phosphohydroxypyruvate and L-glutamate to O-phosphoserine (OPS) and alpha-ketoglutarate. Acts as an inhibitor of ferroptosis in response to interferon-gamma (IFNG) by promoting GPX4 stability: following phosphorylation by CAMK2A, PSAT1 interacts with GPX4 and provides 2-oxoglutarate to EGLN3, leading to GPX4 hydroxylation and stability., [UniProtKB, UniProtKB, UniProtKB]",
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            {
                "id": "A0A0G2JVD2_RAT",
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                "type": "external"
            }
        ],
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        "length": 467,
        "protein_name": "Mitochondrial adenyl nucleotide antiporter SLC25A23",
        "gene_name": "Slc25a23",
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        "refseq_name": "mitochondrial adenyl nucleotide antiporter SLC25A23",
        "refseq_ac": [
            {
                "id": "NP_001100343",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100343",
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            }
        ],
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        "gene_names_refseq": "Slc25a23",
        "protein_names_uniprotkb": "Mitochondrial adenyl nucleotide antiporter SLC25A23; Short calcium-binding mitochondrial carrier protein 3; Solute carrier family 25 member 23",
        "protein_names_refseq": "calcium-binding mitochondrial carrier protein SCaMC-3; mitochondrial adenyl nucleotide antiporter SLC25A23; phosphate carrier), member 23; solute carrier family 25 (mitochondrial carrier",
        "tax_id": 10116,
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        "pathway": " (rno:301113)",
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        "function": "Electroneutral antiporter that mediates the transport of adenine nucleotides through the inner mitochondrial membrane. Originally identified as an ATP-magnesium/inorganic phosphate antiporter, it also acts as a broad specificity adenyl nucleotide antiporter. By regulating the mitochondrial matrix adenine nucleotide pool could adapt to changing cellular energetic demands and indirectly regulate adenine nucleotide-dependent metabolic pathways. Also acts as a regulator of mitochondrial calcium uptake and can probably transport trace amounts of other divalent metal cations in complex with ATP. In vitro, a low activity is also observed with guanyl and pyrimidine nucleotides., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0000295 adenine nucleotide transmembrane transporter activity;GO:0005347 ATP transmembrane transporter activity;GO:0140987 ATP:phosphate antiporter activity;GO:0140988 ADP:phosphate antiporter activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane",
        "go_biological_process": "GO:0043457 regulation of cellular respiration;GO:0071277 cellular response to calcium ion;GO:0006851 mitochondrial calcium ion transmembrane transport;GO:0015866 ADP transport;GO:0036444 calcium import into the mitochondrion",
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            {
                "id": "A0A0G2JXM5_RAT",
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                "type": "external"
            }
        ],
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        "protein_name": "Polymerase delta-interacting protein 3",
        "gene_name": "Poldip3",
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        "refseq_name": "polymerase delta-interacting protein 3",
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            {
                "id": "NP_001123978",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001123978",
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        ],
        "gene_names_uniprotkb": "Poldip3",
        "gene_names_refseq": "Poldip3",
        "protein_names_uniprotkb": "Polymerase delta-interacting protein 3; S6K1 Aly/REF-like target",
        "protein_names_refseq": "polymerase (DNA) delta interacting protein 3; polymerase (DNA-directed), delta interacting protein 3; polymerase delta-interacting protein 3",
        "tax_id": 10116,
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        "pathway": " (rno:315170);  (R-RNO-159236)",
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        "function": "Is involved in regulation of translation. Is preferentially associated with CBC-bound spliced mRNA-protein complexes during the pioneer round of mRNA translation. Contributes to enhanced translational efficiency of spliced over nonspliced mRNAs. Recruits activated ribosomal protein S6 kinase beta-1 I/RPS6KB1 to newly synthesized mRNA. Involved in nuclear mRNA export; probably mediated by association with the TREX complex., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003729 mRNA binding;GO:0044877 protein-containing complex binding;GO:0003723 RNA binding",
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        "go_biological_process": "GO:0016973 poly(A)+ mRNA export from nucleus;GO:0045727 positive regulation of translation;GO:0006417 regulation of translation;GO:0051028 mRNA transport",
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            }
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    },
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        ],
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        ],
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            {
                "id": "NP_001099696",
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            }
        ],
        "gene_names_uniprotkb": "Bicra; Gltscr1",
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        ],
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            {
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001119757",
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            }
        ],
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        "protein_names_refseq": "organic anion transporter 10; organic cation transporter-like 3; solute carrier family 22 (organic anion transporter), member 13; solute carrier family 22 (organic anion/urate transporter), member 13; solute carrier family 22 (organic cation transporter), member 13; solute carrier family 22 member 13",
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        "function": "Anion antiporter that mediates the transport of nicotinate (PubMed:35144162). Possibly involved in nicotinate intestinal reabsorption (By similarity)., [UniProtKB, PubMed, UniProtKB]; Expression of SLC22A13 in basolateral membrane of renal collecting duct stimulates efflux of aspartate and glutamate., [RefSeq, PubMed]; SLC22A13 is a new urate and high affinity nicotinate transporter, [RefSeq, PubMed]",
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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:0016020 membrane",
        "go_biological_process": "GO:0045922 negative regulation of fatty acid metabolic process;GO:2001142 nicotinate transport;GO:0015747 urate transport;GO:0002854 positive regulation of T cell mediated cytotoxicity directed against tumor cell target",
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        ],
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        "protein_name": "Galectin",
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        ],
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        "protein_name": "Alpha-L-iduronidase",
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        "protein_names_uniprotkb": "Alpha-L-iduronidase; 3.2.1.76",
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        "disease": "Scheie syndrome (Disease Ontology:DOID:0060222); mucopolysaccharidosis Ih/s (Disease Ontology:DOID:0111389); mucopolysaccharidosis Ih (Disease Ontology:DOID:0111390); otitis media (Disease Ontology:DOID:10754); gastric ulcer (Disease Ontology:DOID:10808); mucopolysaccharidosis I (Disease Ontology:DOID:12802)",
        "pathway": " (rno:360904);  (R-RNO-2024096);  (R-RNO-2024101)",
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            }
        ],
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        "go_biological_process": "GO:0030209 dermatan sulfate proteoglycan catabolic process;GO:0005975 carbohydrate metabolic process;GO:0006027 glycosaminoglycan catabolic process;GO:0030200 heparan sulfate proteoglycan catabolic process;GO:0030211 heparin proteoglycan catabolic process",
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            {
                "id": "D3ZMB0_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZMB0",
                "type": "external"
            }
        ],
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        "protein_name": "ADAM metallopeptidase with thrombospondin type 1 motif, 9",
        "gene_name": "Adamts9",
        "organism": "Rat",
        "refseq_name": "A disintegrin and metalloproteinase with thrombospondin motifs 9 precursor",
        "refseq_ac": [
            {
                "id": "NP_001416065",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001416065",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Adamts9",
        "gene_names_refseq": "Adamts9",
        "protein_names_uniprotkb": "ADAM metallopeptidase with thrombospondin type 1 motif, 9",
        "protein_names_refseq": "A disintegrin and metalloproteinase with thrombospondin motifs 9 precursor; A disintegrin and metalloproteinase with thrombospondin motifs 9; a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 9",
        "tax_id": 10116,
        "disease": "scoliosis (Disease Ontology:DOID:0060249); type 2 diabetes mellitus (Disease Ontology:DOID:9352); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:312566);  (R-RNO-5173214)",
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        "publication_id_list": "19348733",
        "class_list": "",
        "function": "Study indicates that ADAMTS-9 expression is modulated in response to cerebral ischaemia in vivo, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0004222 metalloendopeptidase activity;GO:0008270 zinc ion binding;GO:0004175 endopeptidase activity;GO:0008237 metallopeptidase activity",
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        "go_biological_process": "GO:0006508 proteolysis;GO:0030198 extracellular matrix organization;GO:0009617 response to bacterium;GO:0048593 camera-type eye morphogenesis;GO:0045636 positive regulation of melanocyte differentiation",
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    },
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        ],
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        "protein_name": "Zinc finger protein 26",
        "gene_name": "Zfp26",
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        "refseq_name": "zinc finger protein 26 isoform X2",
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            {
                "id": "XP_038937759",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_038937759",
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            }
        ],
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        "protein_names_refseq": "zinc finger protein 26 isoform X2",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription",
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            {
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        ],
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        "length": 1277,
        "protein_name": "Paired amphipathic helix protein Sin3a",
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        "gene_names_uniprotkb": "Sin3a",
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        "protein_names_uniprotkb": "Paired amphipathic helix protein Sin3a; Histone deacetylase complex subunit Sin3a; Transcriptional corepressor Sin3a",
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        "tax_id": 10116,
        "disease": "developmental disorder of mental health (Disease Ontology:DOID:0060037); chromosome 15q24 deletion syndrome (Disease Ontology:DOID:0060395); Huntington's disease (Disease Ontology:DOID:12858); cancer (Disease Ontology:DOID:162); transient cerebral ischemia (Disease Ontology:DOID:224)",
        "pathway": " (R-RNO-3899300);  (R-RNO-400206);  (R-RNO-8936459);  (R-RNO-9022692);  (R-RNO-9707564);  (R-RNO-9824594);  (R-RNO-9825892)",
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        "function": "Acts as a transcriptional repressor. Corepressor for REST. Interacts with MXI1 to repress MYC responsive genes and antagonize MYC oncogenic activities. Also interacts with MXD1-MAX heterodimers to repress transcription by tethering SIN3A to DNA. Acts cooperatively with OGT to repress transcription in parallel with histone deacetylation. Involved in the control of the circadian rhythms. Required for the transcriptional repression of circadian target genes, such as PER1, mediated by the large PER complex through histone deacetylation. Cooperates with FOXK1 to regulate cell cycle progression probably by repressing cell cycle inhibitor genes expression. Required for cortical neuron differentiation and callosal axon elongation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003714 transcription corepressor activity;GO:0061629 RNA polymerase II-specific DNA-binding transcription factor binding;GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0003723 RNA binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005694 chromosome;GO:0032991 protein-containing complex;GO:0005634 nucleus",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0048511 rhythmic process;GO:0051726 regulation of cell cycle;GO:0001701 in utero embryonic development",
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    {
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            {
                "id": "A0A0G2K9R9_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2K9R9",
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            }
        ],
        "mass": 211185.0,
        "length": 1843,
        "protein_name": "Proteasome activator complex subunit 4",
        "gene_name": "Psme4",
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        "refseq_name": "proteasome activator complex subunit 4",
        "refseq_ac": [
            {
                "id": "NP_001020311",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001020311",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Psme4",
        "gene_names_refseq": "Psme4",
        "protein_names_uniprotkb": "Proteasome activator complex subunit 4; Proteasome activator PA200; Protein BLM10 homolog",
        "protein_names_refseq": "proteasome (prosome, macropain) activator subunit 4; proteasome activator complex subunit 4",
        "tax_id": 10116,
        "disease": "visceral heterotaxy (Disease Ontology:DOID:0050545)",
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        "function": "Associated component of the proteasome that specifically recognizes acetylated histones and promotes ATP- and ubiquitin-independent degradation of core histones during spermatogenesis and DNA damage response. Recognizes and binds acetylated histones via its bromodomain-like (BRDL) region and activates the proteasome by opening the gated channel for substrate entry. Binds to the core proteasome via its C-terminus, which occupies the same binding sites as the proteasomal ATPases, opening the closed structure of the proteasome via an active gating mechanism. Component of the spermatoproteasome, a form of the proteasome specifically found in testis: binds to acetylated histones and promotes degradation of histones, thereby participating actively to the exchange of histones during spermatogenesis. Also involved in DNA damage response in somatic cells, by promoting degradation of histones following DNA double-strand breaks., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0016504 peptidase activator activity;GO:0070628 proteasome binding",
        "go_cellular_component": "GO:1990111 spermatoproteasome complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0016607 nuclear speck",
        "go_biological_process": "GO:0006281 DNA repair;GO:0006974 DNA damage response;GO:0010499 proteasomal ubiquitin-independent protein catabolic process;GO:0035092 sperm DNA condensation",
        "synthesized_glycan_count": 0,
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    {
        "uniprot_canonical_ac": "D4AC02-1",
        "uniprot_id": [
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                "id": "D4AC02_RAT",
                "url": "https://www.uniprot.org/uniprot/D4AC02",
                "type": "external"
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        ],
        "mass": 107060.0,
        "length": 972,
        "protein_name": "Signal peptide, CUB and EGF-like domain-containing protein 2",
        "gene_name": "Scube2",
        "organism": "Rat",
        "refseq_name": "signal peptide, CUB and EGF-like domain-containing protein 2 precursor",
        "refseq_ac": [
            {
                "id": "NP_001414533",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414533",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Scube2",
        "gene_names_refseq": "RGD1563998; Scube2-ps1; Scube2",
        "protein_names_uniprotkb": "Signal peptide, CUB and EGF-like domain-containing protein 2; Protein CEGP1; Scube/You",
        "protein_names_refseq": "signal peptide, CUB and EGF-like domain-containing protein 2 precursor; signal peptide, CUB and EGF-like domain-containing protein 2; signal peptide, CUB domain, EGF-like 2, pseudogene 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499241);  (R-RNO-5362798)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "31734396",
        "class_list": "",
        "function": "Matrix metalloproteinase-9 regulates the blood brain barrier via the hedgehog pathway in a rat model of traumatic brain injury., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0097108 hedgehog family protein binding;GO:0008289 lipid binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0009986 cell surface",
        "go_biological_process": "GO:0045880 positive regulation of smoothened signaling pathway;GO:0007165 signal transduction;GO:0045669 positive regulation of osteoblast differentiation;GO:1902732 positive regulation of chondrocyte proliferation;GO:0003413 chondrocyte differentiation involved in endochondral bone morphogenesis",
        "synthesized_glycan_count": 0,
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        "record_id": "D4AC02-1",
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        "filter_code": "0000000.0000101.010000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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            {
                "id": "A0A0G2K1F8_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2K1F8",
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            }
        ],
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        "length": 225,
        "protein_name": "Membrane spanning 4-domains A7",
        "gene_name": "Ms4a7",
        "organism": "Rat",
        "refseq_name": "membrane-spanning 4-domains subfamily A member 7",
        "refseq_ac": [
            {
                "id": "NP_001397220",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001397220",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ms4a7",
        "gene_names_refseq": "Ms4a7",
        "protein_names_uniprotkb": "Membrane spanning 4-domains A7",
        "protein_names_refseq": "membrane-spanning 4-domains subfamily A member 7; membrane-spanning 4-domains, subfamily A, member 7",
        "tax_id": 10116,
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        "pathway": " (rno:293744)",
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        ],
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        "protein_names_refseq": "acyl-CoA dehydrogenase family member 9, mitochondrial; acyl-Coenzyme A dehydrogenase family, member 9; complex I assembly factor ACAD9, mitochondrial",
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        "function": "Accumulation of 3-hydroxylated intermediates of long-chain fatty acids may contribute to the pathogenesis of retinopathy in MTP deficiencies., [RefSeq, PubMed]; Results suggested that Glu389 could function as the catalytic base that abstracted the alpha-proton of the acyl-CoA substrate in a proposed catalytic mechanism., [RefSeq, PubMed]; Together with NDUFAF1 and ECSIT, forms part of the mitochondrial complex I (MCIA),which is required for the biogenesis of respiratory Complex I (CI) and is therefore crucial for the activation of the oxidative phosphorylation system. ECSIT binding triggers a large conformational change, switching ACAD9 from a fatty acid oxidation (FAO) enzyme to a CI assembly factor. The function in CI assembly is independent of the fatty acid oxidation (FAO) activity of the protein. As FAO enzyme, it catalyzes the first step in mitochondrial FAO, which consists in the proR-proR stereospecific alpha, beta-dehydrogenation of fatty acyl-CoA thioesters using the electron transfer flavoprotein (ETF) as their physiologic electron acceptor, resulting in the formation of trans-2-enoyl-CoA ((2E)-enoyl-CoA). Its preferred substrates are both saturated and unsaturated long-chain acyl-CoA substrates, with optimum activity toward the latter. In addition, based on its established catalytic mechanism, and combined genetic interaction or mutant phenotype evidence, it is predicted to act also on substrates that have not been tested experimentally but are metabolized by mitochondrial FAO, including long-chain unsaturated fatty acids such as linoleate (9Z,12Z-octadecadienoate), linolenate (9Z,12Z,15Z-octadecatrienoate), and others. Among the different mitochondrial acyl-CoA dehydrogenases, its FAO activity overlaps with that of ACADV and ACADL, but plays a primary role in tissues where it is the main long-chain ACAD expressed. It differs significantly from ACADVL in the use of polyunsaturated substrates in vitro, especially docosahexaenoic acid (which is not primarily used for energy but mainly beta-oxidized in the peroxisomes)., [UniProtKB, UniProtKB]",
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        "protein_name": "Sosondowah ankyrin repeat domain family member D",
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        "protein_name": "Histone RNA hairpin-binding protein",
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            {
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        "pathway": " (rno:681062);  (R-RNO-159230);  (R-RNO-73856);  (R-RNO-77588)",
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        "protein_name": "CD2 antigen cytoplasmic tail-binding protein 2",
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        "disease": "Parkinson's disease (Disease Ontology:DOID:14330); clear cell renal cell carcinoma (Disease Ontology:DOID:4467)",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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            }
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        "length": 709,
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            {
                "id": "NP_001100334",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100334",
                "type": "external"
            }
        ],
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        "gene_names_refseq": "Ltf",
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        "disease": "inflammatory bowel disease (Disease Ontology:DOID:0050589); chromosome 3q29 microdeletion syndrome (Disease Ontology:DOID:0060419); prostate calculus (Disease Ontology:DOID:13689); candidiasis (Disease Ontology:DOID:1508); lung non-small cell carcinoma (Disease Ontology:DOID:3908); renal cell carcinoma (Disease Ontology:DOID:4450); connective tissue disease (Disease Ontology:DOID:65)",
        "pathway": " (rno:301034);  (R-RNO-6798695);  (R-RNO-6799990);  (R-RNO-6803157)",
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        "function": "Lactoferrin ameliorates the prostaglandin E2 inhibition of Na(+)-glucose cotransport most likely via the Ca(2+)- and cAMP-signaling pathways. Erratum:[Can J Physiol Pharmacol. 2014 Jun;92(6):519], [RefSeq, PubMed]; Lactoferrin promotes the autophagy activity during osteoblast formation via BCL2-Beclin1 signaling., [RefSeq, PubMed]; Lf supplemented in food during lactation attenuated acute and long-term cerebral LPS-induced alterations. This provides a new evidence for a promising use of Lf as a preventive neuroprotective approach in preterm encephalopathy., [RefSeq, PubMed]; The lactotransferrin transferrin-like domain 1 functions as a serine protease of the peptidase S60 family that cuts arginine rich regions. This function contributes to the antimicrobial activity. Shows a preferential cleavage at -Arg-Ser-Arg-Arg-|- and -Arg-Arg-Ser-Arg-|-, and of Z-Phe-Arg-|-aminomethylcoumarin sites., [UniProtKB, UniProtKB, UniProtKB]; Transferrins are iron binding transport proteins which can bind two Fe(3+) ions in association with the binding of an anion, usually bicarbonate., [UniProtKB, UniProtKB, UniProtKB]",
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        ],
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        "function": "May act as an inhibitor of TGF-beta signaling., [UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045893 positive regulation of DNA-templated transcription;GO:0044726 epigenetic programing of female pronucleus;GO:0044027 negative regulation of gene expression via chromosomal CpG island methylation",
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        "protein_name": "Neutral alpha-glucosidase AB",
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            {
                "id": "XP_063142985",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_063142985",
                "type": "external"
            }
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        "gene_names_refseq": "G2an; Ganab",
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        "disease": "polycystic liver disease (Disease Ontology:DOID:0050770); polycystic kidney disease (Disease Ontology:DOID:0080322); polycystic kidney disease 3 (Disease Ontology:DOID:0110860)",
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        ],
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        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0017177 glucosidase II complex;GO:0005794 Golgi apparatus;GO:0042470 melanosome",
        "go_biological_process": "GO:0005975 carbohydrate metabolic process;GO:0006491 N-glycan processing",
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        "protein_name": "Nucleolar protein 7",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Nucleolar protein 7",
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        "go_molecular_function": "GO:0051015 actin filament binding;GO:0005521 lamin binding",
        "go_cellular_component": "GO:0005635 nuclear envelope;GO:0005654 nucleoplasm;GO:0031965 nuclear membrane;GO:0032541 cortical endoplasmic reticulum;GO:0005637 nuclear inner membrane",
        "go_biological_process": "GO:0090435 protein localization to nuclear envelope;GO:0001525 angiogenesis;GO:0010595 positive regulation of endothelial cell migration;GO:0006998 nuclear envelope organization;GO:0010761 fibroblast migration",
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                "id": "D3ZC04_RAT",
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        ],
        "mass": 100289.0,
        "length": 890,
        "protein_name": "Extended synaptotagmin-3",
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            {
                "id": "NP_001416359",
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        "gene_names_uniprotkb": "Esyt3",
        "gene_names_refseq": "Esyt3; Fam62c; RGD1561304",
        "protein_names_uniprotkb": "Extended synaptotagmin-3",
        "protein_names_refseq": "extended synaptotagmin protein 3; extended synaptotagmin-3; extended synaptotagmin-like protein 3; family with sequence similarity 62 (C2 domain containing), member C",
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        "protein_names_refseq": "essential meiotic endonuclease 1 homolog 2; probable crossover junction endonuclease EME2 isoform 1; probable crossover junction endonuclease EME2",
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        "gene_name": "Steap1",
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            {
                "id": "NP_001100099",
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        "gene_names_refseq": "Olr821; Or2a57",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 821; olfactory receptor Olr821; olfactory receptor gene Olr821",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:405131)",
        "pathway_count": 1,
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        "publication_id_list": "",
        "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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        "ec_number_list": [],
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0050911 detection of chemical stimulus involved in sensory perception of smell",
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    },
    {
        "uniprot_canonical_ac": "D3ZFM2-1",
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            {
                "id": "D3ZFM2_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZFM2",
                "type": "external"
            }
        ],
        "mass": 169526.0,
        "length": 1546,
        "protein_name": "Tubby-related protein 4",
        "gene_name": "Tulp4",
        "organism": "Rat",
        "refseq_name": "tubby-related protein 4",
        "refseq_ac": [
            {
                "id": "NP_001102607",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102607",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tulp4",
        "gene_names_refseq": "RGD1564487; Tulp4",
        "protein_names_uniprotkb": "Tubby-related protein 4; Tubby superfamily protein; Tubby-like protein 4",
        "protein_names_refseq": "tubby like protein 4; tubby-related protein 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499016);  (R-RNO-8951664)",
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        "publication_id_list": "16641100",
        "class_list": "",
        "function": "May be a substrate-recognition component of a SCF-like ECS (Elongin-Cullin-SOCS-box protein) E3 ubiquitin ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0016567 protein ubiquitination",
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        "hit_score": 0.2,
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        "record_type": "protein",
        "filter_code": "0000000.0000101.010000.000000000000001000.0000000000000.000.00000",
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    },
    {
        "uniprot_canonical_ac": "D3ZFM4-1",
        "uniprot_id": [
            {
                "id": "D3ZFM4_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZFM4",
                "type": "external"
            }
        ],
        "mass": 33304.0,
        "length": 293,
        "protein_name": "Dehydrodolichyl diphosphate synthase complex subunit NUS1",
        "gene_name": "Nus1",
        "organism": "Rat",
        "refseq_name": "dehydrodolichyl diphosphate synthase complex subunit NUS1",
        "refseq_ac": [
            {
                "id": "NP_001157629",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001157629",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Nus1",
        "gene_names_refseq": "Nus1; RGD1307879",
        "protein_names_uniprotkb": "Dehydrodolichyl diphosphate synthase complex subunit NUS1; 2.5.1.87; Dehydrodolichyl diphosphate synthase complex subunit nus1; Nogo-B receptor; Nuclear undecaprenyl pyrophosphate synthase 1 homolog",
        "protein_names_refseq": "dehydrodolichyl diphosphate synthase complex subunit NUS1; nogo-B receptor; nuclear undecaprenyl pyrophosphate synthase 1 homolog",
        "tax_id": 10116,
        "disease": "autosomal dominant intellectual developmental disorder 55 (Disease Ontology:DOID:0080227); congenital disorder of glycosylation Iaa (Disease Ontology:DOID:0080553); Parkinson's disease (Disease Ontology:DOID:14330); epilepsy (Disease Ontology:DOID:1826); congenital disorder of glycosylation (Disease Ontology:DOID:5212)",
        "pathway": " (rno:294400);  (R-RNO-446199)",
        "pathway_count": 2,
        "publication_count": 3,
        "publication_id_list": "31154456;31442237;34662809",
        "class_list": "",
        "function": "NUS1 was upregulated in IUAs tissues, and the high expression level of NUS1 was positively correlated with the severity of IUAs. NUS1 promoted cell proliferation in vitro. NUS1 overexpression on cell migration and invasion promoted the EMT process in vitro and in vivo. Publication Status: Online-Only, [RefSeq, PubMed]; Silencing Nogo-B improves the integrity of blood-retinal barrier in diabetic retinopathy via regulating Src, PI3K/Akt and ERK pathways., [RefSeq, PubMed]; The results found that capillaries and vascular smooth muscle cell content reduced, and nogo-B receptor and ICAM-1 were elevated in rats with diabetic erectile dysfunction. Publication Status: Online-Only, [RefSeq, PubMed]; With DHDDS, forms the dehydrodolichyl diphosphate synthase (DDS) complex, an essential component of the dolichol monophosphate (Dol-P) biosynthetic machinery. Both subunits contribute to enzymatic activity, i.e. condensation of multiple copies of isopentenyl pyrophosphate (IPP) to farnesyl pyrophosphate (FPP) to produce dehydrodolichyl diphosphate (Dedol-PP), a precursor of dolichol phosphate which is utilized as a sugar carrier in protein glycosylation in the endoplasmic reticulum (ER). Synthesizes long-chain polyprenols, mostly of C95 and C100 chain length. Regulates the glycosylation and stability of nascent NPC2, thereby promoting trafficking of LDL-derived cholesterol. Acts as a specific receptor for the N-terminus of Nogo-B, a neural and cardiovascular regulator., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": [
            {
                "id": "2.5.1.87",
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                "type": "external"
            },
            {
                "id": "2.5.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.5.1.-",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0004659 prenyltransferase activity;GO:0045547 ditrans,polycis-polyprenyl diphosphate synthase [(2E,6E)-farnesyl diphosphate specific] activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0005789 endoplasmic reticulum membrane;GO:1904423 dehydrodolichyl diphosphate synthase complex",
        "go_biological_process": "GO:0001525 angiogenesis;GO:0030154 cell differentiation;GO:0032383 regulation of intracellular cholesterol transport;GO:0042632 cholesterol homeostasis;GO:0090050 positive regulation of cell migration involved in sprouting angiogenesis",
        "synthesized_glycan_count": 0,
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    },
    {
        "uniprot_canonical_ac": "D3ZFR1-1",
        "uniprot_id": [
            {
                "id": "D3ZFR1_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZFR1",
                "type": "external"
            }
        ],
        "mass": 43454.0,
        "length": 393,
        "protein_name": "Sulfotransferase",
        "gene_name": "Hs3st3a1",
        "organism": "Rat",
        "refseq_name": "heparan sulfate glucosamine 3-O-sulfotransferase 3A1",
        "refseq_ac": [
            {
                "id": "NP_001165538",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001165538",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Hs3st3a1",
        "gene_names_refseq": "Hs3st3a1; Hs3st3a; RGD1561262",
        "protein_names_uniprotkb": "Sulfotransferase; 2.8.2.-",
        "protein_names_refseq": "heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1; heparan sulfate (glucosamine) 3-O-sulfotransferase 3A; heparan sulfate glucosamine 3-O-sulfotransferase 3A1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363618);  (R-RNO-2022928)",
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                "id": "2.8.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.8.2.-",
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            },
            {
                "id": "2.8.2.29",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.8.2.29",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0008467 [heparan sulfate]-glucosamine 3-sulfotransferase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane",
        "go_biological_process": "GO:0006024 glycosaminoglycan biosynthetic process;GO:0001658 branching involved in ureteric bud morphogenesis;GO:0015012 heparan sulfate proteoglycan biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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    },
    {
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        "uniprot_id": [
            {
                "id": "D3ZG05_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZG05",
                "type": "external"
            }
        ],
        "mass": 14509.0,
        "length": 132,
        "protein_name": "40S ribosomal protein S12",
        "gene_name": "LOC120100003",
        "organism": "Rat",
        "refseq_name": "small ribosomal subunit protein eS12-like",
        "refseq_ac": [
            {
                "id": "XP_063136246",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_063136246",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "LOC120100003",
        "gene_names_refseq": "LOC120100003",
        "protein_names_uniprotkb": "40S ribosomal protein S12",
        "protein_names_refseq": "small ribosomal subunit protein eS12-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:120100003)",
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        "class_list": "",
        "function": "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. Subunit of the 40S ribosomal complex., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0022627 cytosolic small ribosomal subunit",
        "go_biological_process": "GO:1990145 maintenance of translational fidelity;GO:0042274 ribosomal small subunit biogenesis",
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        "hit_score": 0.1,
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    },
    {
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            {
                "id": "D3ZGG8_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZGG8",
                "type": "external"
            }
        ],
        "mass": 113533.0,
        "length": 1002,
        "protein_name": "Hermansky-Pudlak syndrome 3 protein homolog",
        "gene_name": "Hps3",
        "organism": "Rat",
        "refseq_name": "BLOC-2 complex member HPS3",
        "refseq_ac": [
            {
                "id": "NP_001101134",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001101134",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Hps3",
        "gene_names_refseq": "Hps3",
        "protein_names_uniprotkb": "Hermansky-Pudlak syndrome 3 protein homolog",
        "protein_names_refseq": "BLOC-2 complex member HPS3; Hermansky-Pudlak syndrome 3 homolog",
        "tax_id": 10116,
        "disease": "Hermansky-Pudlak syndrome 3 (Disease Ontology:DOID:0060541); platelet storage pool deficiency (Disease Ontology:DOID:2223); Hermansky-Pudlak syndrome (Disease Ontology:DOID:3753)",
        "pathway": " (rno:310288)",
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        "publication_id_list": "29393594",
        "class_list": "",
        "function": "Involved in early stages of melanosome biogenesis and maturation., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0031084 BLOC-2 complex",
        "go_biological_process": "GO:0043473 pigmentation",
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    {
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        "uniprot_id": [
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                "id": "D3ZGJ3_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZGJ3",
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001386261",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Klhl30",
        "gene_names_refseq": "Klhl30; RGD1309644",
        "protein_names_uniprotkb": "Kelch-like family member 30",
        "protein_names_refseq": "kelch-like 30; kelch-like protein 30",
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        "pathway": " (rno:316624)",
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        "go_molecular_function": "GO:1990756 ubiquitin-like ligase-substrate adaptor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0031463 Cul3-RING ubiquitin ligase complex",
        "go_biological_process": "GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process",
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    },
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            {
                "id": "D3ZHK9_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZHK9",
                "type": "external"
            }
        ],
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        "length": 482,
        "protein_name": "mRNA decay activator protein ZFP36",
        "gene_name": "Zfp36l2",
        "organism": "Rat",
        "refseq_name": "mRNA decay activator protein ZFP36L2",
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            {
                "id": "NP_001031703",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001031703",
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            }
        ],
        "gene_names_uniprotkb": "Zfp36l2",
        "gene_names_refseq": "Zfp36l2",
        "protein_names_uniprotkb": "mRNA decay activator protein ZFP36; Zinc finger protein 36",
        "protein_names_refseq": "butyrate response factor 2; mRNA decay activator protein ZFP36L2; zinc finger protein 36, C3H1 type-like 2-like; zinc finger protein 36, C3H1 type-like 2",
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        "function": "Zinc-finger RNA-binding protein that destabilizes several cytoplasmic AU-rich element (ARE)-containing mRNA transcripts by promoting their poly(A) tail removal or deadenylation, and hence provide a mechanism for attenuating protein synthesis. Acts as a 3'-untranslated region (UTR) ARE mRNA-binding adapter protein to communicate signaling events to the mRNA decay machinery. Functions by recruiting the CCR4-NOT deadenylase complex and probably other components of the cytoplasmic RNA decay machinery to the bound ARE-containing mRNAs, and hence promotes ARE-mediated mRNA deadenylation and decay processes. Binds to 3'-UTR ARE of numerous mRNAs., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0000900 mRNA regulatory element binding translation repressor activity;GO:0008270 zinc ion binding;GO:0035925 mRNA 3'-UTR AU-rich region binding;GO:0160134 protein-RNA sequence-specific adaptor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0000932 P-body;GO:1990904 ribonucleoprotein complex",
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            {
                "id": "NP_001178700",
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            }
        ],
        "gene_names_uniprotkb": "Prox2",
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        "protein_names_refseq": "prospero homeobox protein 2",
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        "function": "The prominent but limited distribution of Prox-1 in the brain suggests its potentially important role during postnatal brain development., [RefSeq, PubMed]",
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        "go_biological_process": "GO:0060059 embryonic retina morphogenesis in camera-type eye;GO:0035295 tube development;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007417 central nervous system development",
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        ],
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        "length": 418,
        "protein_name": "Nucleoporin NUP42",
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        "refseq_name": "nucleoporin NUP42",
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                "id": "NP_001102687",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102687",
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            }
        ],
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        "protein_names_uniprotkb": "Nucleoporin NUP42; Nucleoporin-like protein 2",
        "protein_names_refseq": "nucleoporin NUP42; nucleoporin like 2; nucleoporin-like protein 2",
        "tax_id": 10116,
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        "pathway": " (rno:499974);  (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-4551638);  (R-RNO-4570464);  (R-RNO-4615885)",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0005049 nuclear export signal receptor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005635 nuclear envelope;GO:0005643 nuclear pore;GO:0005654 nucleoplasm;GO:0031965 nuclear membrane",
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        ],
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        "protein_name": "Serine peptidase inhibitor, Kazal type 8",
        "gene_name": "Spink8",
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        "refseq_name": "serine protease inhibitor Kazal-type 8",
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        ],
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        "protein_names_refseq": "serine protease inhibitor Kazal-type 8",
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        ],
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        "length": 461,
        "protein_name": "Ribitol-5-phosphate transferase",
        "gene_name": "Fktn",
        "organism": "Rat",
        "refseq_name": "ribitol-5-phosphate transferase FKTN isoform a",
        "refseq_ac": [
            {
                "id": "NP_001102137",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102137",
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        ],
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        "gene_names_refseq": "Fcmd; Fktn",
        "protein_names_uniprotkb": "Ribitol-5-phosphate transferase",
        "protein_names_refseq": "Fukuyama type congenital muscular dystrophy (fukutin); Fukuyama type congenital muscular dystrophy homolog; ribitol-5-phosphate transferase FKTN isoform a; ribitol-5-phosphate transferase FKTN",
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        "disease": "Fukuyama congenital muscular dystrophy (Disease Ontology:DOID:0050559); Walker-Warburg syndrome (Disease Ontology:DOID:0050560); muscular dystrophy-dystroglycanopathy type B1 (Disease Ontology:DOID:0050588); autosomal recessive limb-girdle muscular dystrophy type 2L (Disease Ontology:DOID:0110284); autosomal recessive limb-girdle muscular dystrophy type 2M (Disease Ontology:DOID:0110296); dilated cardiomyopathy 1B (Disease Ontology:DOID:0110443); dilated cardiomyopathy 1X (Disease Ontology:DOID:0110444); muscular dystrophy-dystroglycanopathy type B4 (Disease Ontology:DOID:0112379); muscular dystrophy (Disease Ontology:DOID:9884)",
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        "go_molecular_function": "GO:0004867 serine-type endopeptidase inhibitor activity",
        "go_cellular_component": "GO:0005615 extracellular space",
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        "hit_score": 0.1,
        "record_id": "D3ZJI7-1",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZJP9-1",
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            {
                "id": "D3ZJP9_RAT",
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                "type": "external"
            }
        ],
        "mass": 22704.0,
        "length": 194,
        "protein_name": "Ferritin",
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        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Ftdc2; LOC680520",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ferritin",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "function": "Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Has ferroxidase activity. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation., [UniProtKB, UniProtKB]; Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation., [UniProtKB, UniProtKB]",
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            {
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            {
                "id": "1.11.1.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.11.1.27",
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            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:1.11.1.9",
                "type": "external"
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            {
                "id": "1.16.3.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.16.3.4",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0004322 ferroxidase activity;GO:0008199 ferric iron binding",
        "go_cellular_component": "",
        "go_biological_process": "GO:0006879 intracellular iron ion homeostasis;GO:0006826 iron ion transport",
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        "hit_score": 0.1,
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        "uniprot_canonical_ac": "D3ZJQ3-1",
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            {
                "id": "D3ZJQ3_RAT",
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                "type": "external"
            }
        ],
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        "length": 312,
        "protein_name": "Olfactory receptor",
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        "refseq_name": "olfactory receptor Olr1063",
        "refseq_ac": [
            {
                "id": "NP_001000064",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000064",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Or6c33",
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        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1063; olfactory receptor Olr1063; olfactory receptor gene Olr1063",
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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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            {
                "id": "NP_001417355",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001417355",
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        ],
        "gene_names_uniprotkb": "Wdr76",
        "gene_names_refseq": "RGD1309616; Wdr76",
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        "protein_names_refseq": "WD repeat domain 76 isoform 2; WD repeat-containing protein 76",
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        "function": "Specifically binds 5-hydroxymethylcytosine (5hmC), suggesting that it acts as a specific reader of 5hmC., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0019899 enzyme binding",
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        ],
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            {
                "id": "NP_001100420",
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        ],
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        "pathway": " (rno:302495);  (R-RNO-6798695)",
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        "function": "Identification and functional analysis of the human Rap2C ortholog., [RefSeq, PubMed]; Small GTP-binding protein which cycles between a GDP-bound inactive and a GTP-bound active form., [UniProtKB, UniProtKB]; Study found that SCII upregulated the expression of miR-204 and downregulated the expression of RAP2C; that hypoxia increased the expression of miR-204 and decreased the expression of RAP2C, and overexpression of RAP2C attenuates the effect of hypoxia on apoptosis rate; and miR-204 could directly bind to RAP2C, and could regulate the expression of RAP2C., [RefSeq, PubMed]",
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        "ec_number_list": [
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                "id": "3.6.5.2",
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            {
                "id": "3.6.1.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.1",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.-",
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                "id": "3.6.5.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.3",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.5",
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            {
                "id": "3.6.1.5",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.5",
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            {
                "id": "3.6.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.-",
                "type": "external"
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            {
                "id": "3.6.5.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.4",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0019003 GDP binding;GO:0003925 G protein activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0005923 bicellular tight junction;GO:0016020 membrane",
        "go_biological_process": "GO:0032486 Rap protein signal transduction;GO:0030336 negative regulation of cell migration;GO:0090557 establishment of endothelial intestinal barrier;GO:0031954 positive regulation of protein autophosphorylation;GO:0061097 regulation of protein tyrosine kinase activity",
        "synthesized_glycan_count": 0,
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    {
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        "uniprot_id": [
            {
                "id": "D3ZKF6_RAT",
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                "type": "external"
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        ],
        "mass": 87770.0,
        "length": 750,
        "protein_name": "EF-hand domain-containing family member C2",
        "gene_name": "Efhc2",
        "organism": "Rat",
        "refseq_name": "EF-hand domain-containing family member C2",
        "refseq_ac": [
            {
                "id": "NP_001100422",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100422",
                "type": "external"
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        ],
        "gene_names_uniprotkb": "Efhc2",
        "gene_names_refseq": "Efhc2; RGD1563388",
        "protein_names_uniprotkb": "EF-hand domain-containing family member C2",
        "protein_names_refseq": "EF-hand domain (C-terminal) containing 2; EF-hand domain-containing family member C2",
        "tax_id": 10116,
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        "pathway": " (rno:302507)",
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        "class_list": "",
        "function": "Microtubule inner protein (MIP) part of the dynein-decorated doublet microtubules (DMTs) in cilia axoneme, which is required for motile cilia beating., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_cellular_component": "GO:0036126 sperm flagellum;GO:0036064 ciliary basal body;GO:0005879 axonemal microtubule;GO:0160111 axonemal A tubule inner sheath",
        "go_biological_process": "GO:0048814 regulation of dendrite morphogenesis;GO:0030317 flagellated sperm motility;GO:1990830 cellular response to leukemia inhibitory factor",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZKF6-1",
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        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
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    {
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        ],
        "mass": 39894.0,
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        "protein_name": "BPI fold containing family A, member 6",
        "gene_name": "Bpifa6",
        "organism": "Rat",
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        "refseq_ac": [],
        "gene_names_uniprotkb": "Bpifa6",
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        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZMB1-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    }
]
