[
    {
        "uniprot_canonical_ac": "A0ABZ3NNP9-1",
        "uniprot_id": [
            {
                "id": "A0ABZ3NNP9_RAT",
                "url": "https://www.uniprot.org/uniprot/A0ABZ3NNP9",
                "type": "external"
            }
        ],
        "mass": 97032.0,
        "length": 862,
        "protein_name": "Leucine-zipper-like transcriptional regulator 1",
        "gene_name": "Lztr1",
        "organism": "Rat",
        "refseq_name": "leucine-zipper-like transcriptional regulator 1 isoform X1",
        "refseq_ac": [
            {
                "id": "XP_006248769",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006248769",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Lztr1",
        "gene_names_refseq": "Lztr1",
        "protein_names_uniprotkb": "Leucine-zipper-like transcriptional regulator 1",
        "protein_names_refseq": "leucine-zipper-like transcriptional regulator 1 isoform X1",
        "tax_id": 10116,
        "disease": "Noonan syndrome 2 (Disease Ontology:DOID:0060580); Noonan syndrome 10 (Disease Ontology:DOID:0060588); schwannomatosis 2 (Disease Ontology:DOID:0070481); stomach cancer (Disease Ontology:DOID:10534); hypertrophic cardiomyopathy (Disease Ontology:DOID:11984); glioblastoma (Disease Ontology:DOID:3068); neurilemmoma (Disease Ontology:DOID:3192); schwannomatosis (Disease Ontology:DOID:3204); Noonan syndrome (Disease Ontology:DOID:3490); hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (rno:360745)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complex that mediates ubiquitination of Ras (K-Ras/KRAS, N-Ras/NRAS and H-Ras/HRAS). Is a negative regulator of RAS-MAPK signaling that acts by controlling Ras levels and decreasing Ras association with membranes., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 10,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0031267 small GTPase binding;GO:1990756 ubiquitin-like ligase-substrate adaptor activity",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0012505 endomembrane system;GO:0055038 recycling endosome membrane;GO:0031463 Cul3-RING ubiquitin ligase complex",
        "go_biological_process": "GO:0046580 negative regulation of Ras protein signal transduction;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0016567 protein ubiquitination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABZ3NNP9-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0ABK0M8C9-1",
        "uniprot_id": [
            {
                "id": "A0ABK0M8C9_RAT",
                "url": "https://www.uniprot.org/uniprot/A0ABK0M8C9",
                "type": "external"
            }
        ],
        "mass": 18911.0,
        "length": 166,
        "protein_name": "Trafficking protein particle complex subunit",
        "gene_name": "Trappc2l",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Trappc2l",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Trafficking protein particle complex subunit",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May play a role in vesicular transport from endoplasmic reticulum to Golgi., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
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        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_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:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0048471 perinuclear region of cytoplasm;GO:0030008 TRAPP complex;GO:0005829 cytosol",
        "go_biological_process": "GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M8C9-1",
        "record_type": "protein",
        "filter_code": "0000000.0000000.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0ABZ3NN98-1",
        "uniprot_id": [
            {
                "id": "A0ABZ3NN98_RAT",
                "url": "https://www.uniprot.org/uniprot/A0ABZ3NN98",
                "type": "external"
            }
        ],
        "mass": 43884.0,
        "length": 389,
        "protein_name": "Double C2-like domain-containing protein",
        "gene_name": "Doc2g",
        "organism": "Rat",
        "refseq_name": "double C2-like domain-containing protein gamma isoform X1",
        "refseq_ac": [
            {
                "id": "XP_006230797",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006230797",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Doc2g; Doc2gp",
        "gene_names_refseq": "Doc2gp; Doc2g",
        "protein_names_uniprotkb": "Double C2-like domain-containing protein",
        "protein_names_refseq": "double C2-like domain-containing protein gamma isoform X1",
        "tax_id": 10116,
        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); chromosome 16p11.2 deletion syndrome, 593-kb (Disease Ontology:DOID:0070515)",
        "pathway": " (rno:293654)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
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        "total_o_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0016020 membrane;GO:0098793 presynapse",
        "go_biological_process": "GO:0007269 neurotransmitter secretion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABZ3NN98-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0ABK0M9J5-1",
        "uniprot_id": [
            {
                "id": "A0ABK0M9J5_RAT",
                "url": "https://www.uniprot.org/uniprot/A0ABK0M9J5",
                "type": "external"
            }
        ],
        "mass": 58815.0,
        "length": 523,
        "protein_name": "RAR-related orphan receptor A",
        "gene_name": "Rora",
        "organism": "Rat",
        "refseq_name": "nuclear receptor ROR-alpha isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001414296",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414296",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Rora",
        "gene_names_refseq": "Rora",
        "protein_names_uniprotkb": "RAR-related orphan receptor A",
        "protein_names_refseq": "RAR-related orphan receptor alpha; nuclear receptor ROR-alpha isoform 1; nuclear receptor ROR-alpha-like; nuclear receptor ROR-alpha",
        "tax_id": 10116,
        "disease": "idiopathic pulmonary fibrosis (Disease Ontology:DOID:0050156); childhood-onset asthma (Disease Ontology:DOID:0080815); nocturnal asthma (Disease Ontology:DOID:0080826); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); coronary artery disease (Disease Ontology:DOID:3393); lung non-small cell carcinoma (Disease Ontology:DOID:3908); tuberculosis (Disease Ontology:DOID:399); allergic rhinitis (Disease Ontology:DOID:4481); myocardial infarction (Disease Ontology:DOID:5844); acute myocardial infarction (Disease Ontology:DOID:9408)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "The protein encoded by this gene is a member of the NR1 subfamily of nuclear hormone receptors. It can bind as a monomer or as a homodimer to hormone response elements upstream of several genes to enhance the expression of those genes. The encoded protein has been shown to interact with NM23-2, a nucleoside diphosphate kinase involved in organogenesis and differentiation, as well as with NM23-1, the product of a tumor metastasis suppressor candidate gene. Also, it has been shown to aid in the transcriptional regulation of some genes involved in circadian rhythm. [provided by RefSeq, Feb 2014]., [RefSeq]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0043565 sequence-specific DNA binding;GO:0004879 nuclear receptor activity;GO:0008142 oxysterol binding;GO:0003677 DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005730 nucleolus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0001525 angiogenesis;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M9J5-1",
        "record_type": "protein",
        "filter_code": "0000000.0000010.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0ABK0M8H4-1",
        "uniprot_id": [
            {
                "id": "A0ABK0M8H4_RAT",
                "url": "https://www.uniprot.org/uniprot/A0ABK0M8H4",
                "type": "external"
            }
        ],
        "mass": 96596.0,
        "length": 852,
        "protein_name": "Nitric oxide synthase, inducible",
        "gene_name": "",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Nitric oxide synthase, inducible; 1.14.13.39; Inducible NO synthase; NOS type II; Peptidyl-cysteine S-nitrosylase NOS2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
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        "predicted_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "1.14.13.39",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.14.13.39",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0004517 nitric-oxide synthase activity;GO:0005516 calmodulin binding;GO:0046872 metal ion binding;GO:0050660 flavin adenine dinucleotide binding;GO:0020037 heme binding",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0006809 nitric oxide biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M8H4-1",
        "record_type": "protein",
        "filter_code": "0000000.0000000.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0ABK0M8N4-1",
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            {
                "id": "A0ABK0M8N4_RAT",
                "url": "https://www.uniprot.org/uniprot/A0ABK0M8N4",
                "type": "external"
            }
        ],
        "mass": 131128.0,
        "length": 1201,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "Hipk2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Hipk2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway_count": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
            },
            {
                "id": "2.7.12.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.12.1",
                "type": "external"
            },
            {
                "id": "2.7.1.153",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.153",
                "type": "external"
            },
            {
                "id": "2.7.1.137",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.137",
                "type": "external"
            },
            {
                "id": "2.7.11.24",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.24",
                "type": "external"
            },
            {
                "id": "2.7.11.25",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.25",
                "type": "external"
            },
            {
                "id": "2.7.11.22",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.22",
                "type": "external"
            },
            {
                "id": "2.7.11.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.23",
                "type": "external"
            },
            {
                "id": "2.7.4.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.6",
                "type": "external"
            },
            {
                "id": "2.7.1.154",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.154",
                "type": "external"
            },
            {
                "id": "2.7.11.38",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.38",
                "type": "external"
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        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Tvp23b; Fam18b2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Golgi apparatus membrane protein TVP23 homolog",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:687358)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "22673903;29393594",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus;GO:0016020 membrane",
        "go_biological_process": "GO:0016192 vesicle-mediated transport;GO:0009306 protein secretion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "A0A8I5ZVP7-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P48450-1",
        "uniprot_id": [
            {
                "id": "LSS_RAT",
                "url": "https://www.uniprot.org/uniprot/P48450",
                "type": "external"
            }
        ],
        "mass": 83301.0,
        "length": 733,
        "protein_name": "Lanosterol synthase",
        "gene_name": "Lss; Spatc1l",
        "organism": "Rat",
        "refseq_name": "lanosterol synthase",
        "refseq_ac": [
            {
                "id": "NP_112311",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_112311",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Lss; Spatc1l; Lss; Osc; Spatc1l",
        "gene_names_refseq": "Lss",
        "protein_names_uniprotkb": "Lanosterol synthase; 2,3-epoxysqualene--lanosterol cyclase; 5.4.99.7; OSC; Oxidosqualene--lanosterol cyclase",
        "protein_names_refseq": "2,3-epoxysqualene--lanosterol cyclase; 2,3-oxidosqualene: lanosterol cyclase; OSC; lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase); lanosterol synthase; oxidosqualene--lanosterol cyclase",
        "tax_id": 10116,
        "disease": "hypotrichosis 14 (Disease Ontology:DOID:0080582); alopecia-mental retardation syndrome 4 (Disease Ontology:DOID:0080950); cataract 44 (Disease Ontology:DOID:0110267); cataract (Disease Ontology:DOID:83)",
        "pathway": " (rno:499418);  (rno:81681);  (R-RNO-9969896)",
        "pathway_count": 3,
        "publication_count": 4,
        "publication_id_list": "16440058;38079167;7568116;7735243",
        "class_list": "",
        "function": "Key enzyme in the cholesterol biosynthesis pathway. Catalyzes the cyclization of (S)-2,3 oxidosqualene to lanosterol, a reaction that forms the sterol nucleus (PubMed:7568116). Through the production of lanosterol may regulate lens protein aggregation and increase transparency (By similarity)., [UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Lanosterol Synthase Prevents EMT During Lens Epithelial Fibrosis Via Regulating SREBP1., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 4,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "Q62811",
        "ec_number_list": [
            {
                "id": "5.4.99.7",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.4.99.7",
                "type": "external"
            },
            {
                "id": "5.4.99.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.4.99.-",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0000250 lanosterol synthase activity;GO:0042802 identical protein binding;GO:0034237 protein kinase A regulatory subunit binding",
        "go_cellular_component": "GO:0098554 cytoplasmic side of endoplasmic reticulum membrane;GO:0005811 lipid droplet;GO:0005789 endoplasmic reticulum membrane;GO:0005737 cytoplasm;GO:0005813 centrosome",
        "go_biological_process": "GO:0006695 cholesterol biosynthetic process;GO:0031647 regulation of protein stability;GO:0016125 sterol metabolic process;GO:0006694 steroid biosynthetic process;GO:0033489 cholesterol biosynthetic process via desmosterol",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "P48450-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q6IE24-1",
        "uniprot_id": [
            {
                "id": "UBP54_RAT",
                "url": "https://www.uniprot.org/uniprot/Q6IE24",
                "type": "external"
            }
        ],
        "mass": 176155.0,
        "length": 1588,
        "protein_name": "Ubiquitin carboxyl-terminal hydrolase 54",
        "gene_name": "Usp54",
        "organism": "Rat",
        "refseq_name": "ubiquitin carboxyl-terminal hydrolase 54",
        "refseq_ac": [
            {
                "id": "NP_001008863",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001008863",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Usp54",
        "gene_names_refseq": "Usp54",
        "protein_names_uniprotkb": "Ubiquitin carboxyl-terminal hydrolase 54; 3.4.19.12; Ubiquitin-specific peptidase 54",
        "protein_names_refseq": "inactive ubiquitin carboxyl-terminal hydrolase 54; inactive ubiquitin-specific peptidase 54; ubiquitin carboxyl-terminal hydrolase 54; ubiquitin specific protease 54",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:408223)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "15060002;22673903",
        "class_list": "",
        "function": "Deubiquitinase that specifically mediates 'Lys-63'-linked deubiquitination of substrates with a polyubiquitin chain composed of at least 3 ubiquitins. Specifically recognizes ubiquitin chain in position S2 and catalyzes cleavage of polyubiquitin within 'Lys-63'-linked chains. Not able to deubiquitinate substrates with shorter ubiquitin chains. Mediates deubiquitination of PLK4, maintaining PLK4 stability by reducing its ubiquitination-mediated degradation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_mutagensis": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "Q4QQU8",
        "ec_number_list": [],
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0004843 cysteine-type deubiquitinase activity;GO:0061578 K63-linked deubiquitinase activity",
        "go_cellular_component": "",
        "go_biological_process": "GO:0006508 proteolysis;GO:0016579 protein deubiquitination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "Q6IE24-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.010000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "F1LW30-1",
        "uniprot_id": [
            {
                "id": "UNC5D_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LW30",
                "type": "external"
            }
        ],
        "mass": 106520.0,
        "length": 956,
        "protein_name": "Netrin receptor UNC5D",
        "gene_name": "Unc5d",
        "organism": "Rat",
        "refseq_name": "netrin receptor UNC5D precursor",
        "refseq_ac": [
            {
                "id": "NP_001100789",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100789",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Unc5d",
        "gene_names_refseq": "Unc5d",
        "protein_names_uniprotkb": "Netrin receptor UNC5D; Protein unc-5 homolog D",
        "protein_names_refseq": "netrin receptor UNC5D precursor; netrin receptor UNC5D; protein unc-5 homolog D; unc-5 homolog D",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:306534)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "25374360",
        "class_list": "",
        "function": "Receptor for netrin required for axon guidance. Mediates axon repulsion of neuronal growth cones in the developing nervous system upon ligand binding., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Receptor for the netrin NTN4 that promotes neuronal cell survival. Plays a role in cell-cell adhesion and cell guidance. Receptor for netrin involved in cell migration. Plays a role in axon guidance by mediating axon repulsion of neuronal growth cones in the developing nervous system upon ligand binding. May play a role in apoptosis in response to DNA damage. It also acts as a dependence receptor required for apoptosis induction when not associated with netrin ligand (By similarity). Mediates cell-cell adhesion via its interaction with FLRT3 on an adjacent cell (By similarity)., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 2,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 2,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 2,
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        "total_reported_c_glycosites": 2,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 4,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0005042 netrin receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface",
        "go_biological_process": "GO:0006915 apoptotic process;GO:0098609 cell-cell adhesion;GO:0007411 axon guidance;GO:2001222 regulation of neuron migration;GO:0021859 pyramidal neuron differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "F1LW30-1",
        "record_type": "protein",
        "filter_code": "0000000.0100101.010000.000000000000001000.1010000000000.100.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "B2RZ59-1",
        "uniprot_id": [
            {
                "id": "SH21A_RAT",
                "url": "https://www.uniprot.org/uniprot/B2RZ59",
                "type": "external"
            }
        ],
        "mass": 13992.0,
        "length": 126,
        "protein_name": "SH2 domain-containing protein 1A",
        "gene_name": "Sh2d1a",
        "organism": "Rat",
        "refseq_name": "SH2 domain-containing protein 1A",
        "refseq_ac": [
            {
                "id": "NP_001102783",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102783",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Sh2d1a",
        "gene_names_refseq": "RGD1562408; Sh2d1a",
        "protein_names_uniprotkb": "SH2 domain-containing protein 1A",
        "protein_names_refseq": "SH2 domain protein 1A; SH2 domain-containing protein 1A",
        "tax_id": 10116,
        "disease": "X-linked lymphoproliferative syndrome 1 (Disease Ontology:DOID:0060705)",
        "pathway": " (rno:501502)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "16223723;22673903",
        "class_list": "",
        "function": "Cytoplasmic adapter regulating receptors of the signaling lymphocytic activation molecule (SLAM) family such as SLAMF1, CD244, LY9, CD84, SLAMF6 and SLAMF7. In SLAM signaling seems to cooperate with SH2D1B/EAT-2. Initially it has been proposed that association with SLAMF1 prevents SLAMF1 binding to inhibitory effectors including INPP5D/SHIP1 and PTPN11/SHP-2. However, by simultaneous interactions, recruits FYN which subsequently phosphorylates and activates SLAMF1. Positively regulates CD244/2B4- and CD84-mediated natural killer (NK) cell functions. Can also promote CD48-, SLAMF6 -, LY9-, and SLAMF7-mediated NK cell activation. In the context of NK cell-mediated cytotoxicity enhances conjugate formation with target cells (By similarity). May also regulate the activity of the neurotrophin receptors NTRK1, NTRK2 and NTRK3 (PubMed:16223723)., [UniProtKB, UniProtKB, UniProtKB, PubMed]; SAP may serve as a negative regulator of Trk receptor activation and downstream signaling, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "reported_mutagensis": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0007267 cell-cell signaling;GO:0045087 innate immune response;GO:0006968 cellular defense response;GO:0050776 regulation of immune response;GO:0002250 adaptive immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "B2RZ59-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P21463-1",
        "uniprot_id": [
            {
                "id": "TSHR_RAT",
                "url": "https://www.uniprot.org/uniprot/P21463",
                "type": "external"
            }
        ],
        "mass": 86475.0,
        "length": 764,
        "protein_name": "Thyrotropin receptor",
        "gene_name": "Tshr",
        "organism": "Rat",
        "refseq_name": "thyrotropin receptor precursor",
        "refseq_ac": [
            {
                "id": "NP_037020",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_037020",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tshr; TSHR",
        "gene_names_refseq": "TSHRA; Tshr",
        "protein_names_uniprotkb": "Thyrotropin receptor; TSH-R; Thyroid-stimulating hormone receptor",
        "protein_names_refseq": "TSH-R; thyrotropin receptor precursor; thyrotropin receptor",
        "tax_id": 10116,
        "disease": "congenital hypothyroidism (Disease Ontology:DOID:0050328); cardiomyopathy (Disease Ontology:DOID:0050700); congenital nongoitrous hypothyroidism 1 (Disease Ontology:DOID:0070126); nonautoimmune hyperthyroidism (Disease Ontology:DOID:0081101); familial gestational hyperthyroidism (Disease Ontology:DOID:0081102); Graves ophthalmopathy (Disease Ontology:DOID:0081120); Graves' disease (Disease Ontology:DOID:12361); hyperthyroidism (Disease Ontology:DOID:7998); mitral valve prolapse (Disease Ontology:DOID:988)",
        "pathway": " (rno:25360);  (R-RNO-375281)",
        "pathway_count": 2,
        "publication_count": 7,
        "publication_id_list": "12045258;1332945;1696008;27059392;31439949;33191870;36857434",
        "class_list": "",
        "function": "Allylpyrocatechol, isolated from betel leaf ameliorates thyrotoxicosis in rats by altering thyroid peroxidase and thyrotropin receptors. Publication Status: Online-Only, [RefSeq, PubMed]; Data suggest that functional thyroid-stimulating hormone receptor is present in the caudal brainstem and hypothalamic nuclei of relevance for feeding control as a possibly uncleaved holoreceptor, and highlights a hindbrain component to central thyroid-stimulating hormone inhibition of food intake., [RefSeq, PubMed]; Expression and Role of Thyrotropin Receptors in Proopiomelanocortin-Producing Pituitary Cells., [RefSeq, PubMed]; Receptor for the thyroid-stimulating hormone (TSH) or thyrotropin (PubMed:1696008). Also acts as a receptor for the heterodimeric glycoprotein hormone (GPHA2:GPHB5) or thyrostimulin (PubMed:12045258). TSHR is coupled to G(s) proteins and mediates the activation of adenylate cyclase. This leads to the generation of cyclic adenosine monophosphate (cAMP), which in turn activates protein kinase A (PKA). PKA subsequently phosphorylates downstream targets involved in thyroid hormone biosynthesis and secretion, including thyroid peroxidase (TPO) and the sodium/iodide symporter (NIS) (By similarity). Additionally, plays a central role in controlling thyroid cell metabolism (PubMed:12045258)., [UniProtKB, PubMed, PubMed, UniProtKB]; Receptor for the thyroid-stimulating hormone (TSH) or thyrotropin. Also acts as a receptor for the heterodimeric glycoprotein hormone (GPHA2:GPHB5) or thyrostimulin. TSHR is coupled to G(s) proteins and mediates the activation of adenylate cyclase. This leads to the generation of cyclic adenosine monophosphate (cAMP), which in turn activates protein kinase A (PKA). PKA subsequently phosphorylates downstream targets involved in thyroid hormone biosynthesis and secretion, including thyroid peroxidase (TPO) and the sodium/iodide symporter (NIS). Additionally, plays a central role in controlling thyroid cell metabolism., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Thyroid-stimulating hormone receptor signaling restores skeletal muscle stem cell regeneration in rats with muscular dystrophy., [RefSeq, PubMed]",
        "predicted_glycosites": 5,
        "predicted_n_glycosites": 5,
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        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 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,
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        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 2,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 9,
        "glyco_site_count": 5,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0004996 thyroid-stimulating hormone receptor activity;GO:0004930 G protein-coupled receptor activity;GO:0044877 protein-containing complex binding;GO:0008528 G protein-coupled peptide receptor activity;GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane;GO:0043235 receptor complex;GO:0016020 membrane",
        "go_biological_process": "GO:0007166 cell surface receptor signaling pathway;GO:0007189 adenylate cyclase-activating G protein-coupled receptor signaling pathway;GO:0008284 positive regulation of cell population proliferation;GO:0008344 adult locomotory behavior;GO:0040012 regulation of locomotion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.8,
        "record_id": "P21463-1",
        "record_type": "protein",
        "filter_code": "0000000.0100111.100000.000000000000001000.0000000010000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P30082-1",
        "uniprot_id": [
            {
                "id": "GLR_RAT",
                "url": "https://www.uniprot.org/uniprot/P30082",
                "type": "external"
            }
        ],
        "mass": 55038.0,
        "length": 485,
        "protein_name": "Glucagon receptor",
        "gene_name": "Gcgr",
        "organism": "Rat",
        "refseq_name": "glucagon receptor isoform a precursor",
        "refseq_ac": [
            {
                "id": "NP_742088",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_742088",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Gcgr",
        "gene_names_refseq": "Gcgr",
        "protein_names_uniprotkb": "Glucagon receptor; GL-R",
        "protein_names_refseq": "GL-R; glucagon receptor isoform a precursor; glucagon receptor perhaps same as Niddm3",
        "tax_id": 10116,
        "disease": "Mahvash Disease (Disease Ontology:DOID:0112306); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": " (rno:24953);  (R-RNO-163359);  (R-RNO-416476);  (R-RNO-420092)",
        "pathway_count": 4,
        "publication_count": 6,
        "publication_id_list": "22673903;23918690;26975347;8082779;8384375;8384842",
        "class_list": "",
        "function": "G protein-coupled receptor for glucagon that plays a central role in the regulation of blood glucose levels and glucose homeostasis. Regulates the rate of hepatic glucose production by promoting glycogen hydrolysis and gluconeogenesis. Plays an important role in mediating the responses to fasting. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors, such as adenylate cyclase. Promotes activation of adenylate cyclase. Besides, plays a role in signaling via a phosphatidylinositol-calcium second messenger system., [UniProtKB, PubMed]; G-protein coupled receptor for glucagon that plays a central role in the regulation of blood glucose levels and glucose homeostasis. Regulates the rate of hepatic glucose production by promoting glycogen hydrolysis and gluconeogenesis. Plays an important role in mediating the responses to fasting. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors, such as adenylate cyclase. Promotes activation of adenylate cyclase. Besides, plays a role in signaling via a phosphatidylinositol-calcium second messenger system., [UniProtKB, UniProtKB]; Significant higher GluR density (mRNA and proteins) following exercise and fasting than in the control group., [RefSeq, PubMed]; The vasodilatation due to glucagon evokes via the glucagon-receptor, but also via the receptor for GLP-1, and it is endothelium-independent., [RefSeq, PubMed]",
        "predicted_glycosites": 4,
        "predicted_n_glycosites": 4,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "total_o_glycosites": 0,
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        "reported_phosphosites": 2,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 2,
        "glyco_site_count": 4,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0017046 peptide hormone binding;GO:0004967 glucagon receptor activity",
        "go_cellular_component": "GO:0005768 endosome;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007166 cell surface receptor signaling pathway;GO:0007186 G protein-coupled receptor signaling pathway;GO:0007189 adenylate cyclase-activating G protein-coupled receptor signaling pathway;GO:0010628 positive regulation of gene expression;GO:0042594 response to starvation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "P30082-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000010001.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q8VHT6-1",
        "uniprot_id": [
            {
                "id": "AS3MT_RAT",
                "url": "https://www.uniprot.org/uniprot/Q8VHT6",
                "type": "external"
            }
        ],
        "mass": 41056.0,
        "length": 369,
        "protein_name": "Arsenite methyltransferase",
        "gene_name": "As3mt",
        "organism": "Rat",
        "refseq_name": "arsenite methyltransferase",
        "refseq_ac": [
            {
                "id": "NP_543166",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_543166",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "As3mt; Cyt19",
        "gene_names_refseq": "As3mt; Cyt19",
        "protein_names_uniprotkb": "Arsenite methyltransferase; 2.1.1.137; Methylarsonite methyltransferase; S-adenosyl-L-methionine:arsenic(III) methyltransferase",
        "protein_names_refseq": "S-adenosyl-L-methionine:arsenic(III) methyltransferase; S-adenosylmethionine:arsenic (III) methyltransferase; arsenic (+3 oxidation state) methyltransferase; arsenite methyltransferase; methylarsonite methyltransferase; methyltransferase Cyt19",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:140925);  (R-RNO-156581)",
        "pathway_count": 2,
        "publication_count": 4,
        "publication_id_list": "11790780;15606138;15808521;22673903",
        "class_list": "",
        "function": "Catalyzes the transfer of a methyl group from AdoMet to trivalent arsenicals producing methylated and dimethylated arsenicals. It methylates arsenite to form methylarsonate, Me-AsO(3)H(2), which is reduced by methylarsonate reductase to methylarsonite, Me-As(OH)2. Methylarsonite is also a substrate and it is converted into the much less toxic compound dimethylarsinate (cacodylate), Me(2)As(O)-OH., [UniProtKB, PubMed]; Enzyme catalyzing the conversion of inorganic arsenic to volatile arsenicals., [RefSeq, PubMed]; In rat AS3MT, Cys156 located in a well-defined cavity structure may be situated to participate in the binding of substrates which contain A(III)., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "2.1.1.137",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.137",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0008276 protein methyltransferase activity;GO:0008757 S-adenosylmethionine-dependent methyltransferase activity;GO:0030791 arsenite methyltransferase activity",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0046685 response to arsenic-containing substance;GO:0009404 toxin metabolic process;GO:0018872 arsonoacetate metabolic process;GO:0032259 methylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "Q8VHT6-1",
        "record_type": "protein",
        "filter_code": "0000000.0100101.100000.000000000000001000.0000000001001.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P28647-1",
        "uniprot_id": [
            {
                "id": "AA3R_RAT",
                "url": "https://www.uniprot.org/uniprot/P28647",
                "type": "external"
            }
        ],
        "mass": 36629.0,
        "length": 320,
        "protein_name": "Adenosine receptor A3",
        "gene_name": "Adora3",
        "organism": "Rat",
        "refseq_name": "adenosine receptor A3 isoform a",
        "refseq_ac": [
            {
                "id": "NP_001289679",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001289679",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Adora3",
        "gene_names_refseq": "A3; Adora3; TGPCR1",
        "protein_names_uniprotkb": "Adenosine receptor A3; TGPCR1",
        "protein_names_refseq": "Adenosine receptor A3; adenosine receptor A3 isoform a; adenosine receptor A3-like; putative G-protein coupled receptor",
        "tax_id": 10116,
        "disease": "autosomal recessive nonsyndromic deafness 116 (Disease Ontology:DOID:0112162)",
        "pathway": " (rno:100911796);  (R-RNO-417973);  (R-RNO-418594)",
        "pathway_count": 3,
        "publication_count": 11,
        "publication_id_list": "10692494;11278110;1323836;16005018;1647979;31556103;32461578;33007835;33472058;35775127;8612733",
        "class_list": "",
        "function": "Activation of Adenosine A3 Receptor Inhibits Microglia Reactivity Elicited by Elevated Pressure. Publication Status: Online-Only, [RefSeq, PubMed]; Activation of adenosine A3 receptor attenuates progression of osteoarthritis through inhibiting the NLRP3/caspase-1/GSDMD induced signalling., [RefSeq, PubMed]; Activation of adenosine A3 receptor protects retinal ganglion cells from degeneration induced by ocular hypertension. Publication Status: Online-Only, [RefSeq, PubMed]; Acupuncture induces adenosine in fibroblasts through energy metabolism and promotes proliferation by activating MAPK signaling pathway via adenosine3 receptor., [RefSeq, PubMed]; G protein-coupled receptor (GPCR) for adenosine that plays significant roles in various physiological processes including immune regulation, cardioprotection and neuroprotection (PubMed:1323836). Also acts as a receptor for adenosines containing N(6)-methylated adenine (m6A) post-transcriptional modification, which are derived from the degradation of RNAs (mRNAs, rRNAs and tRNAs): activated by N(6)-methyladenosine (m6A), N(6),N(6)-dimethyladenosine (m6,6A) and N(6)-isopentenyladenosine (i6A) (PubMed:33472058). Preferentially couples to the inhibitory G protein (Gi), leading to the suppression of adenylate cyclase activity and a reduction in intracellular cyclic AMP levels (By similarity). Upon adenosine binding, mediates cardioprotection in cardiomyocytes through anti-apoptotic effects primarily via the ERK1/2 pathway as well as the PI3K pathway (PubMed:16005018). In the central nervous system, participates in the modulation of synaptic plasticity, including long-term potentiation (LTP) and long-term depression (LTD) in the hippocampus (PubMed:11278110). In lung mast cells, receptor activation contributes to the type I allergic response by facilitating mast cell degranulation and histamine release (PubMed:33472058). Highly expressed in inflammatory cells such as neutrophils and mast cells, inhibits neutrophil degranulation and reduces superoxide production, thereby modulating inflammatory responses (By similarity)., [UniProtKB, PubMed, PubMed, UniProtKB, PubMed, UniProtKB, PubMed]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 2,
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        "reported_o_glycosites_with_glycan": 0,
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        "reported_phosphosites": 3,
        "reported_mutagensis": 5,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "Q63792",
        "ec_number_list": [],
        "go_molecular_function": "GO:0001609 G protein-coupled adenosine receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0030425 dendrite;GO:0031594 neuromuscular junction;GO:0045202 synapse;GO:0042734 presynaptic membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007193 adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway;GO:0008285 negative regulation of cell population proliferation;GO:0051897 positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0014061 regulation of norepinephrine secretion",
        "synthesized_glycan_count": 0,
        "hit_score": 1.2,
        "record_id": "P28647-1",
        "record_type": "protein",
        "filter_code": "0000000.0100111.100000.000000000000001000.0000000010001.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZK93-1",
        "uniprot_id": [
            {
                "id": "GSG1L_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZK93",
                "type": "external"
            }
        ],
        "mass": 35903.0,
        "length": 322,
        "protein_name": "Germ cell-specific gene 1-like protein",
        "gene_name": "Gsg1l",
        "organism": "Rat",
        "refseq_name": "germ cell-specific gene 1-like protein",
        "refseq_ac": [
            {
                "id": "NP_001406591",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001406591",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Gsg1l",
        "gene_names_refseq": "Gsg1l; RGD1562278",
        "protein_names_uniprotkb": "Germ cell-specific gene 1-like protein; GSG1-like protein",
        "protein_names_refseq": "GSG1-like protein; germ cell-specific gene 1-like protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499263)",
        "pathway_count": 1,
        "publication_count": 5,
        "publication_id_list": "22632720;22673903;22813734;26932439;27707810",
        "class_list": "",
        "function": "As a component of the inner core of AMPAR complexes, modifies AMPA receptor (AMPAR) gating., [UniProtKB, PubMed]; The current work reveals that GSG1L regulates strength of AMPAR-mediated synaptic transmission but not the receptor kinetic properties in hippocampal dentate granule neurons., [RefSeq, PubMed]; The interactomes of native AMPA-Rs and KA-Rs were compared and identified an AMPA-R auxiliary subunit, GSG1L., [RefSeq, PubMed]; These data demonstrate that GSG1L represents a new class of auxiliary subunit with distinct functional properties for AMPA receptors. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "reported_phosphosites": 1,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005886 plasma membrane;GO:0032279 asymmetric synapse;GO:0098839 postsynaptic density membrane;GO:0098685 Schaffer collateral - CA1 synapse",
        "go_biological_process": "GO:0048172 regulation of short-term neuronal synaptic plasticity;GO:0050808 synapse organization;GO:0019226 transmission of nerve impulse;GO:2000311 regulation of AMPA receptor activity;GO:0099149 regulation of postsynaptic neurotransmitter receptor internalization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "D3ZK93-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q4G075-1",
        "uniprot_id": [
            {
                "id": "ILEUA_RAT",
                "url": "https://www.uniprot.org/uniprot/Q4G075",
                "type": "external"
            }
        ],
        "mass": 42727.0,
        "length": 379,
        "protein_name": "Leukocyte elastase inhibitor A",
        "gene_name": "Serpinb1a",
        "organism": "Rat",
        "refseq_name": "leukocyte elastase inhibitor A",
        "refseq_ac": [
            {
                "id": "NP_001026812",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001026812",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Serpinb1a",
        "gene_names_refseq": "Serpinb1a; Serpinb1",
        "protein_names_uniprotkb": "Leukocyte elastase inhibitor A; Serine protease inhibitor EIA; Serpin B1a",
        "protein_names_refseq": "leukocyte elastase inhibitor A; serine (or cysteine) proteinase inhibitor, clade B, member 1a; serine protease inhibitor EIA; serpin B1a",
        "tax_id": 10116,
        "disease": "familial encephalopathy with neuroserpin inclusion bodies (Disease Ontology:DOID:0050831); alpha 1-antitrypsin deficiency (Disease Ontology:DOID:13372)",
        "pathway": " (rno:291091);  (R-RNO-6798695)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "22673903;35291946",
        "class_list": "",
        "function": "Regulates the activity of the neutrophil proteases., [UniProtKB]; SERPINB1 overexpression protects myocardial damage induced by acute myocardial infarction through AMPK/mTOR pathway. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "missing_score": 10000,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0004867 serine-type endopeptidase inhibitor activity;GO:0030414 peptidase inhibitor activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0005769 early endosome;GO:0036464 cytoplasmic ribonucleoprotein granule;GO:0044194 cytolytic granule",
        "go_biological_process": "GO:0006954 inflammatory response;GO:0019725 cellular homeostasis;GO:0030336 negative regulation of cell migration;GO:0032691 negative regulation of interleukin-1 beta production;GO:0010951 negative regulation of endopeptidase activity",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "Q4G075-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P02770-1",
        "uniprot_id": [
            {
                "id": "ALBU_RAT",
                "url": "https://www.uniprot.org/uniprot/P02770",
                "type": "external"
            }
        ],
        "mass": 68731.0,
        "length": 608,
        "protein_name": "Albumin",
        "gene_name": "Alb",
        "organism": "Rat",
        "refseq_name": "albumin precursor",
        "refseq_ac": [
            {
                "id": "NP_599153",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_599153",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Alb",
        "gene_names_refseq": "Alb1; Albza; Alb",
        "protein_names_uniprotkb": "Albumin",
        "protein_names_refseq": "albumin precursor; serum albumin",
        "tax_id": 10116,
        "disease": "biliary tract benign neoplasm (Disease Ontology:DOID:0050625); Zollinger-Ellison syndrome (Disease Ontology:DOID:0050782); stroke (Disease Ontology:DOID:0051061); COVID-19 (Disease Ontology:DOID:0080600); pre-eclampsia (Disease Ontology:DOID:10591); esophageal varix (Disease Ontology:DOID:112); Hantavirus hemorrhagic fever with renal syndrome (Disease Ontology:DOID:11266); heart disease (Disease Ontology:DOID:114); familial hyperlipidemia (Disease Ontology:DOID:1168); protein-energy malnutrition (Disease Ontology:DOID:11801); nephrotic syndrome (Disease Ontology:DOID:1184); alcoholic hepatitis (Disease Ontology:DOID:12351); leukemia (Disease Ontology:DOID:1240); twin-to-twin transfusion syndrome (Disease Ontology:DOID:13576); cholestasis (Disease Ontology:DOID:13580); obstructive jaundice (Disease Ontology:DOID:13603); root caries (Disease Ontology:DOID:14089); Reye syndrome (Disease Ontology:DOID:14525); pancreatic cancer (Disease Ontology:DOID:1793); hyperthyroxinemia (Disease Ontology:DOID:2855); middle cerebral artery infarction (Disease Ontology:DOID:3525); pancreatic ductal carcinoma (Disease Ontology:DOID:3587); lung non-small cell carcinoma (Disease Ontology:DOID:3908); cholangiocarcinoma (Disease Ontology:DOID:4947); liver cirrhosis (Disease Ontology:DOID:5082); pneumonia (Disease Ontology:DOID:552); proteinuria (Disease Ontology:DOID:576); congestive heart failure (Disease Ontology:DOID:6000); blood protein disease (Disease Ontology:DOID:620); gastric cardia adenocarcinoma (Disease Ontology:DOID:6271); hepatocellular carcinoma (Disease Ontology:DOID:684); end stage renal disease (Disease Ontology:DOID:783); psoriasis (Disease Ontology:DOID:8893); autoimmune thrombocytopenic purpura (Disease Ontology:DOID:8924); type 2 diabetes mellitus (Disease Ontology:DOID:9352); multiple myeloma (Disease Ontology:DOID:9538); pulmonary emphysema (Disease Ontology:DOID:9675)",
        "pathway": " (rno:24186);  (R-RNO-114608);  (R-RNO-159418);  (R-RNO-189451);  (R-RNO-189483);  (R-RNO-2168880);  (R-RNO-381426);  (R-RNO-8957275);  (R-RNO-8964058);  (R-RNO-9707564);  (R-RNO-9749641);  (R-RNO-9757110);  (R-RNO-9793528)",
        "pathway_count": 13,
        "publication_count": 9,
        "publication_id_list": "22673903;2437111;31691325;564345;7017712;7358734;80265;893447;956149",
        "class_list": "",
        "function": "Binds water, Ca(2+), Na(+), K(+), fatty acids, hormones, bilirubin and drugs. Its main function is the regulation of the colloidal osmotic pressure of blood. Major zinc transporter in plasma, typically binds about 80% of all plasma zinc (By similarity). Major calcium and magnesium transporter in plasma, binds approximately 45% of circulating calcium and magnesium in plasma (By similarity). Potentially has more than two calcium-binding sites and might additionally bind calcium in a non-specific manner (By similarity). The shared binding site between zinc and calcium at residue Asp-273 suggests a crosstalk between zinc and calcium transport in the blood (By similarity). The rank order of affinity is zinc > calcium > magnesium (By similarity). Binds to the bacterial siderophore enterobactin and inhibits enterobactin-mediated iron uptake of E.coli from ferric transferrin, and may thereby limit the utilization of iron and growth of enteric bacteria such as E.coli (By similarity). Does not prevent iron uptake by the bacterial siderophore aerobactin (By similarity)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Predictive value of ischaemia-modified albumin in spermatogenesis in an experimental testicular torsion model., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 8,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 37,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "P11382;Q5U3X3",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0005504 fatty acid binding;GO:0008270 zinc ion binding;GO:0015643 toxic substance binding;GO:0019899 enzyme binding",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0005737 cytoplasm;GO:0070062 extracellular exosome;GO:0005604 basement membrane",
        "go_biological_process": "GO:0007584 response to nutrient;GO:0031667 response to nutrient levels;GO:0042311 vasodilation;GO:0009267 cellular response to starvation;GO:0046689 response to mercury ion",
        "synthesized_glycan_count": 0,
        "hit_score": 1.0,
        "record_id": "P02770-1",
        "record_type": "protein",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P09117-1",
        "uniprot_id": [
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                "id": "ALDOC_RAT",
                "url": "https://www.uniprot.org/uniprot/P09117",
                "type": "external"
            }
        ],
        "mass": 39284.0,
        "length": 363,
        "protein_name": "Fructose-bisphosphate aldolase C",
        "gene_name": "Aldoc",
        "organism": "Rat",
        "refseq_name": "fructose-bisphosphate aldolase C",
        "refseq_ac": [
            {
                "id": "NP_036629",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_036629",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Aldoc",
        "gene_names_refseq": "ALDCAA; Aldoc; F16dip7; RATALDCAA",
        "protein_names_uniprotkb": "Fructose-bisphosphate aldolase C; 4.1.2.13; Brain-type aldolase",
        "protein_names_refseq": "aldolase C, fructose-biphosphate; aldolase C, fructose-bisphosphate; brain-type aldolase; fructose-bisphosphate aldolase C",
        "tax_id": 10116,
        "disease": "stroke (Disease Ontology:DOID:0051061); chromosome 16p11.2 deletion syndrome, 593-kb (Disease Ontology:DOID:0070515); autoimmune disease of the nervous system (Disease Ontology:DOID:438); borna disease (Disease Ontology:DOID:5154); hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (rno:24191);  (R-RNO-6798695);  (R-RNO-70171);  (R-RNO-70263)",
        "pathway_count": 4,
        "publication_count": 8,
        "publication_id_list": "18683930;1993044;21280042;22420779;22673903;2831050;3830170;9443807",
        "class_list": "",
        "function": "Catalyzes the reversible conversion of beta-D-fructose 1,6-bisphosphate (FBP) into two triose phosphate and plays a key role in glycolysis and gluconeogenesis., [UniProtKB, UniProtKB]; Data show statistically significant altered levels of Tpi1 and alteration of Hk1, Aldoc, Pgam1 and Gapdh with borderline significance in phencyclidine (PCP) rats compared to controls. Publication Status: Online-Only, [RefSeq, PubMed]; Dorsal column nuclei (DCN)-cerebellar axons project to multiple compartments with terminals clustered mainly in the conventional spinocerebellar region with a coarse topography, which relates to the cortical compartments defined by aldolase C., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "predicted_c_glycosites": 0,
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        "mined_o_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "reported_fully_resolved_glycans": 1,
        "reported_phosphosites": 4,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 5,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "Q54AI4;Q63037",
        "ec_number_list": [
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            {
                "id": "3.5.1.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.5.1.23",
                "type": "external"
            },
            {
                "id": "3.5.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.5.1.-",
                "type": "external"
            },
            {
                "id": "3.6.1.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.6",
                "type": "external"
            },
            {
                "id": "3.4.25.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.25.1",
                "type": "external"
            },
            {
                "id": "3.4.18.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.18.1",
                "type": "external"
            },
            {
                "id": "1.11.1.24",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.11.1.24",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0044877 protein-containing complex binding;GO:0008092 cytoskeletal protein binding;GO:0004332 fructose-bisphosphate aldolase activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0030424 axon;GO:0099524 postsynaptic cytosol",
        "go_biological_process": "GO:0030855 epithelial cell differentiation;GO:0001666 response to hypoxia;GO:0006094 gluconeogenesis;GO:0031100 animal organ regeneration;GO:0006096 glycolytic process",
        "synthesized_glycan_count": 0,
        "hit_score": 1.1,
        "record_id": "P09117-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0100000001001.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P15943-1",
        "uniprot_id": [
            {
                "id": "APLP2_RAT",
                "url": "https://www.uniprot.org/uniprot/P15943",
                "type": "external"
            }
        ],
        "mass": 86883.0,
        "length": 765,
        "protein_name": "Amyloid beta precursor like protein 2",
        "gene_name": "Aplp2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Aplp2; APPL2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Amyloid beta precursor like protein 2; APLP-2; Amyloid beta (A4) precursor-like protein 2; Amyloid protein homolog; Amyloid-like protein 2; CDEBP; CDEI box-binding protein; Sperm membrane protein YWK-II",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Alzheimer's disease 1 (Disease Ontology:DOID:0080348); Alzheimer's disease (Disease Ontology:DOID:10652); neurodegenerative disease (Disease Ontology:DOID:1289)",
        "pathway": " (rno:64312);  (R-RNO-114608);  (R-RNO-381426);  (R-RNO-8957275)",
        "pathway_count": 4,
        "publication_count": 3,
        "publication_id_list": "1690887;22673903;8086458",
        "class_list": "",
        "function": "May play a role in the regulation of hemostasis. The soluble form may have inhibitory properties towards coagulation factors. May interact with cellular G-protein signaling pathways. May bind to the DNA 5'-GTCACATG-3'(CDEI box). Inhibits trypsin, chymotrypsin, plasmin, factor XIA and plasma and glandular kallikrein. Modulates the Cu/Zn nitric oxide-catalyzed autodegradation of GPC1 heparan sulfate side chains in fibroblasts., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 2,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 2,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 3,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0004867 serine-type endopeptidase inhibitor activity;GO:0008201 heparin binding;GO:0042802 identical protein binding;GO:0046914 transition metal ion binding;GO:0140677 molecular function activator activity",
        "go_cellular_component": "GO:0099503 secretory vesicle;GO:0005634 nucleus;GO:0009986 cell surface;GO:0016020 membrane;GO:0097444 spine apparatus",
        "go_biological_process": "GO:0001967 suckling behavior;GO:0006878 intracellular copper ion homeostasis;GO:0007409 axonogenesis;GO:0007617 mating behavior;GO:0007626 locomotory behavior",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "P15943-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000001001.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P15337-2",
        "uniprot_id": [
            {
                "id": "CREB1_RAT",
                "url": "https://www.uniprot.org/uniprot/P15337",
                "type": "external"
            }
        ],
        "mass": 35081.0,
        "length": 327,
        "protein_name": "Cyclic AMP-responsive element-binding protein 1",
        "gene_name": "Creb1",
        "organism": "Rat",
        "refseq_name": "cyclic AMP-responsive element-binding protein 1 isoform B",
        "refseq_ac": [
            {
                "id": "NP_112279",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_112279",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Creb1; Creb-1",
        "gene_names_refseq": "Creb1; Creb",
        "protein_names_uniprotkb": "Cyclic AMP-responsive element-binding protein 1; CREB-1; cAMP-responsive element-binding protein 1",
        "protein_names_refseq": "CREB-1; Y protein; cAMP response element binding protein 1; cyclic AMP-responsive element-binding protein 1 isoform B; cyclic AMP-responsive element-binding protein 1",
        "tax_id": 10116,
        "disease": "alcohol dependence (Disease Ontology:DOID:0050741); nicotine dependence (Disease Ontology:DOID:0050742); withdrawal disorder (Disease Ontology:DOID:0060001); autism spectrum disorder (Disease Ontology:DOID:0060041); hypertension (Disease Ontology:DOID:10763); amnestic disorder (Disease Ontology:DOID:10914); obsessive-compulsive disorder (Disease Ontology:DOID:10933); opioid abuse (Disease Ontology:DOID:11206); sciatic neuropathy (Disease Ontology:DOID:11446); Pick's disease (Disease Ontology:DOID:11870); Huntington's disease (Disease Ontology:DOID:12858); Parkinson's disease (Disease Ontology:DOID:14330); alcohol use disorder (Disease Ontology:DOID:1574); depressive disorder (Disease Ontology:DOID:1596); anxiety disorder (Disease Ontology:DOID:2030); transient cerebral ischemia (Disease Ontology:DOID:224); brain ischemia (Disease Ontology:DOID:2316); morphine dependence (Disease Ontology:DOID:2560); middle cerebral artery infarction (Disease Ontology:DOID:3525); schizophrenia (Disease Ontology:DOID:5419); congestive heart failure (Disease Ontology:DOID:6000); amphetamine abuse (Disease Ontology:DOID:670); cocaine abuse (Disease Ontology:DOID:809); vascular dementia (Disease Ontology:DOID:8725); substance dependence (Disease Ontology:DOID:9973); drug dependence (Disease Ontology:DOID:9974); cocaine dependence (Disease Ontology:DOID:9975); heroin dependence (Disease Ontology:DOID:9976)",
        "pathway": " (rno:81646);  (R-RNO-198693);  (R-RNO-199920);  (R-RNO-375165);  (R-RNO-442742);  (R-RNO-881907);  (R-RNO-9031628);  (R-RNO-9634638)",
        "pathway_count": 8,
        "publication_count": 24,
        "publication_id_list": "10222196;11796524;12162494;12769553;1646483;17692820;17696880;1831258;20657584;22267118;22673903;24722832;2521922;30566056;36642184;37891366;38552745;38679120;38838971;38929606;7603449;7612187;7958915;8621702",
        "class_list": "",
        "function": "CBP Expression Contributes to Neuropathic Pain via CREB and MeCP2 Regulation in the Spared Nerve Injury Rat Model. Publication Status: Online-Only, [RefSeq, PubMed]; CREB1 Silencing Protects Against Inflammatory Response in Rats with Deep Vein Thrombosis Through Reducing RPL9 Expression and Blocking NF-kappaB Signaling., [RefSeq, PubMed]; Divergent effects of chronic continuous and intermittent social defeat stress on emotional behaviors: Impact on phosphorylated CREB and BDNF protein levels in the rat hippocampus., [RefSeq, PubMed]; Neonatal nociceptive stimulation results in pain sensitization, reduction of hippocampal 5-HT1A receptor, and p-CREB expression in adult female rats., [RefSeq, PubMed]; Phosphorylation-dependent transcription factor that stimulates transcription upon binding to the DNA cAMP response element (CRE), a sequence present in many viral and cellular promoters (By similarity). Transcription activation is enhanced by the TORC coactivators which act independently of Ser-119 phosphorylation (By similarity). Involved in different cellular processes including the synchronization of circadian rhythmicity and the differentiation of adipose cells (By similarity). Regulates the expression of apoptotic and inflammatory response factors in cardiomyocytes in response to ERFE-mediated activation of AKT signaling (PubMed:30566056)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, PubMed]; Role of cAMP/pCREB and GSK-3beta/NF-kappaB p65 signaling pathways in the renoprotective effect of mirabegron against renal ischemia-reperfusion injury in rats., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 4,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 4,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 4,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 1,
        "reported_phosphosites": 5,
        "reported_mutagensis": 2,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 28,
        "glyco_site_count": 4,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0019899 enzyme binding;GO:0042802 identical protein binding;GO:1990763 arrestin family protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005759 mitochondrial matrix;GO:0030424 axon;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:1990910 response to hypobaric hypoxia;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006468 protein phosphorylation;GO:0007409 axonogenesis;GO:0007613 memory",
        "synthesized_glycan_count": 0,
        "hit_score": 3.0,
        "record_id": "P15337-2",
        "record_type": "protein",
        "filter_code": "0000000.0100111.100000.000000000000001000.0100000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P50503-1",
        "uniprot_id": [
            {
                "id": "F10A1_RAT",
                "url": "https://www.uniprot.org/uniprot/P50503",
                "type": "external"
            }
        ],
        "mass": 41280.0,
        "length": 368,
        "protein_name": "Hsc70-interacting protein",
        "gene_name": "Slc25a17; St13",
        "organism": "Rat",
        "refseq_name": "hsc70-interacting protein",
        "refseq_ac": [
            {
                "id": "NP_112384",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_112384",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Slc25a17; St13; Fam10a1; Hip; Slc25a17",
        "gene_names_refseq": "St13",
        "protein_names_uniprotkb": "Hsc70-interacting protein; Hip; Protein FAM10A1; Protein ST13 homolog",
        "protein_names_refseq": "hip; hsc70-interacting protein; protein ST13 homolog; suppression of tumorigenicity 13 (colon carcinoma) Hsp70-interacting protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:81800);  (R-RNO-3371453)",
        "pathway_count": 2,
        "publication_count": 4,
        "publication_id_list": "22673903;23812373;29393594;7585962",
        "class_list": "",
        "function": "One HIP oligomer binds the ATPase domains of at least two HSC70 molecules dependent on activation of the HSC70 ATPase by HSP40. Stabilizes the ADP state of HSC70 that has a high affinity for substrate protein. Through its own chaperone activity, it may contribute to the interaction of HSC70 with various target proteins., [UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB]; Peroxisomal transporter for multiple cofactors like coenzyme A (CoA), flavin adenine dinucleotide (FAD), flavin mononucleotide (FMN) and nucleotide adenosine monophosphate (AMP), and to a lesser extent for nicotinamide adenine dinucleotide (NAD(+)), adenosine diphosphate (ADP) and adenosine 3',5'-diphosphate (PAP). May catalyze the transport of free CoA, FAD and NAD(+) from the cytosol into the peroxisomal matrix by a counter-exchange mechanism., [UniProtKB, UniProtKB]; The tetratricopeptide repeat domain of rat Hip with the Hsp70 ATPase domain through an extensive interface, to form a bracket that locks ADP in the binding cleft., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 1,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "3.1.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.-.-",
                "type": "external"
            },
            {
                "id": "5.6.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.3",
                "type": "external"
            },
            {
                "id": "3.6.4.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.12",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0032564 dATP binding;GO:0019904 protein domain specific binding;GO:0042802 identical protein binding;GO:0046983 protein dimerization activity;GO:0051082 unfolded protein binding",
        "go_cellular_component": "GO:0005829 cytosol;GO:0032991 protein-containing complex;GO:0005737 cytoplasm;GO:0005777 peroxisome;GO:0005778 peroxisomal membrane",
        "go_biological_process": "GO:1903334 positive regulation of protein folding;GO:0009617 response to bacterium;GO:0006457 protein folding;GO:0061084 negative regulation of protein refolding;GO:0006635 fatty acid beta-oxidation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "P50503-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q4G005-1",
        "uniprot_id": [
            {
                "id": "ERCC3_RAT",
                "url": "https://www.uniprot.org/uniprot/Q4G005",
                "type": "external"
            }
        ],
        "mass": 89099.0,
        "length": 782,
        "protein_name": "General transcription and DNA repair factor IIH helicase/translocase subunit XPB",
        "gene_name": "Ercc3",
        "organism": "Rat",
        "refseq_name": "general transcription and DNA repair factor IIH helicase/translocase subunit XPB",
        "refseq_ac": [
            {
                "id": "NP_001026814",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001026814",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ercc3",
        "gene_names_refseq": "Ercc3",
        "protein_names_uniprotkb": "General transcription and DNA repair factor IIH helicase/translocase subunit XPB; 5.6.2.4; DNA 3'-5' helicase/translocase XPB; DNA excision repair protein ERCC-3; TFIIH subunit XPB",
        "protein_names_refseq": "DNA 3'-5' helicase/translocase XPB; DNA excision repair protein ERCC-3; TFIIH basal transcription factor complex helicase XPB subunit; TFIIH subunit XPB; excision repair cross-complementation group 3; excision repair cross-complementing rodent repair deficiency, complementation group 3; general transcription and DNA repair factor IIH helicase subunit XPB; general transcription and DNA repair factor IIH helicase/translocase subunit XPB",
        "tax_id": 10116,
        "disease": "xeroderma pigmentosum (Disease Ontology:DOID:0050427); xeroderma pigmentosum group B (Disease Ontology:DOID:0110850); trichothiodystrophy (Disease Ontology:DOID:0111866); photosensitive trichothiodystrophy 2 (Disease Ontology:DOID:0111869); Alzheimer's disease (Disease Ontology:DOID:10652); asphyxia neonatorum (Disease Ontology:DOID:11088); Down syndrome (Disease Ontology:DOID:14250); Cockayne syndrome (Disease Ontology:DOID:2962); lung non-small cell carcinoma (Disease Ontology:DOID:3908); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:291703);  (R-RNO-112382);  (R-RNO-113418);  (R-RNO-5696395);  (R-RNO-5696400);  (R-RNO-674695);  (R-RNO-6781823);  (R-RNO-6782135);  (R-RNO-6782210);  (R-RNO-6796648);  (R-RNO-72086);  (R-RNO-73762);  (R-RNO-73772);  (R-RNO-73776);  (R-RNO-73779);  (R-RNO-73863);  (R-RNO-75953);  (R-RNO-75955);  (R-RNO-76042);  (R-RNO-77075)",
        "pathway_count": 20,
        "publication_count": 2,
        "publication_id_list": "22673903;29393594",
        "class_list": "",
        "function": "ATP-dependent 3'-5' DNA helicase/translocase; binds dsDNA rather than ssDNA, unzipping it in a translocase rather than classical helicase activity. Component of the general transcription and DNA repair factor IIH (TFIIH) core complex. When complexed to CDK-activating kinase (CAK), involved in RNA transcription by RNA polymerase II. The ATPase activity of XPB/ERCC3, but not its helicase activity, is required for DNA opening; it may wrap around the damaged DNA wedging it open, causing localized melting and twisting that allows XPD/ERCC2 helicase to anchor. The ATP-dependent helicase activity of XPB/ERCC3 may be required for promoter escape. Also involved in transcription-coupled nucleotide excision repair (NER) of damaged DNA. In NER, TFIIH acts by opening DNA around the lesion to allow the excision of the damaged oligonucleotide and its replacement by a new DNA fragment. The structure of the TFIIH transcription complex differs from the NER-TFIIH complex; large movements by XPD/ERCC2 and XPB/ERCC3 are stabilized by XPA., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 3,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 10,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "5.6.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.3",
                "type": "external"
            },
            {
                "id": "6.5.1.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.5.1.1",
                "type": "external"
            },
            {
                "id": "3.6.4.13",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.13",
                "type": "external"
            },
            {
                "id": "2.3.2.32",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.32",
                "type": "external"
            },
            {
                "id": "3.6.4.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.12",
                "type": "external"
            },
            {
                "id": "3.1.3.16",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.16",
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                "id": "2.3.1.48",
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                "id": "1.14.11.-",
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                "id": "2.1.1.56",
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                "id": "3.4.24.-",
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                "id": "3.6.-.-",
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                "id": "3.4.21.53",
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        "go_cellular_component": "GO:0097550 transcription preinitiation complex;GO:0005654 nucleoplasm;GO:0005675 transcription factor TFIIH holo complex;GO:0005669 transcription factor TFIID complex;GO:0000112 nucleotide-excision repair factor 3 complex",
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            {
                "id": "NP_001006987",
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        "pathway": " (rno:300447);  (R-RNO-166058);  (R-RNO-6799198);  (R-RNO-975138);  (R-RNO-975871)",
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        "function": "Adapter protein that plays a role in different signaling pathways including TLRs and IL-1 pathways or innate antiviral induction signaling. Plays a role in the activation of NF-kappa-B by forming a signal complex with TRAF6 and TAK1/MAP3K7 to activate TAK1/MAP3K7 leading to activation of IKKs. Once ubiquitinated, interacts with the dissociated RELA and NFKB1 proteins and translocates to the nucleus where it induces NF-kappa-B-dependent gene expression. Plays a role in innate antiviral immune response by bridging the pattern recognition receptors RIGI and MDA5/IFIT1 to the MAVS complex at the mitochondrion. Promotes proteolytic activation of MAP3K1. Involved in the BMP signaling pathway. Required for normal embryonic development., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; As part of the MCIA complex, involved in the assembly of the mitochondrial complex I., [UniProtKB, UniProtKB, UniProtKB, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0060090 molecular adaptor activity;GO:0003682 chromatin binding;GO:0003700 DNA-binding transcription factor activity;GO:0004857 enzyme inhibitor activity;GO:0030674 protein-macromolecule adaptor activity",
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            {
                "id": "NP_851602",
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            }
        ],
        "gene_names_uniprotkb": "Whrn; Cip98; Dfnb31",
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        "protein_names_uniprotkb": "Whirlin; CASK-interacting protein CIP98",
        "protein_names_refseq": "CASK-interacting protein CIP98; deafness, autosomal recessive 31; whirlin isoform 1",
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        "disease": "autosomal recessive nonsyndromic deafness 31 (Disease Ontology:DOID:0110490); Usher syndrome type 2D (Disease Ontology:DOID:0110840); sensorineural hearing loss (Disease Ontology:DOID:10003)",
        "pathway": " (rno:313255)",
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        "publication_id_list": "12641734;16434480;17584769;23055499;26516054",
        "class_list": "",
        "function": "CIP98, a novel protein (98 kDa) consisting of three PDZ domains and a proline-rich region, is widely expressed in the central nervous system and interacts with CASK (calmodulin-dependent serine kinase), [RefSeq, PubMed]; Findings indicate that Whirlin and TRPV1 are associated in a subset of nociceptors and that TRPV1 protein stability is increased through the interaction with the cytoskeletal scaffold protein., [RefSeq, PubMed]; Involved in hearing and vision as member of the USH2 complex. Necessary for elongation and maintenance of inner and outer hair cell stereocilia in the organ of Corti in the inner ear. Involved in the maintenance of the hair bundle ankle region, which connects stereocilia in cochlear hair cells of the inner ear. In retina photoreceptors, required for the maintenance of periciliary membrane complex that seems to play a role in regulating intracellular protein transport., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0019904 protein domain specific binding;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005884 actin filament;GO:0005886 plasma membrane;GO:0005929 cilium;GO:0030426 growth cone",
        "go_biological_process": "GO:0010628 positive regulation of gene expression;GO:0050910 detection of mechanical stimulus involved in sensory perception of sound;GO:0001895 retina homeostasis;GO:0045184 establishment of protein localization;GO:0007605 sensory perception of sound",
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    },
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        "protein_name": "Lysoplasmalogenase TMEM86B",
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        "refseq_name": "lysoplasmalogenase TMEM86B isoform X1",
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            {
                "id": "XP_063130864",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_063130864",
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            }
        ],
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        "gene_names_refseq": "Tmem86b",
        "protein_names_uniprotkb": "Lysoplasmalogenase TMEM86B; 3.3.2.2; Transmembrane protein 86B",
        "protein_names_refseq": "lysoplasmalogenase TMEM86B isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-1482788)",
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        "publication_id_list": "21515882",
        "class_list": "",
        "function": "Catalyzes the hydrolysis of the vinyl ether bond of choline or ethanolamine lysoplasmalogens, forming fatty aldehyde and glycerophosphocholine or glycerophosphoethanolamine, respectively and is specific for the sn-2-deacylated (lyso) form of plasmalogen., [UniProtKB, PubMed]",
        "predicted_glycosites": 0,
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            }
        ],
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        "go_biological_process": "GO:0046485 ether lipid metabolic process",
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        "hit_score": 0.2,
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    },
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                "id": "VTI1A_RAT",
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            }
        ],
        "mass": 26043.0,
        "length": 224,
        "protein_name": "Vesicle transport through interaction with t-SNAREs homolog 1A",
        "gene_name": "Vti1a",
        "organism": "Rat",
        "refseq_name": "vesicle transport through interaction with t-SNAREs homolog 1A",
        "refseq_ac": [
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                "id": "NP_075589",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_075589",
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            }
        ],
        "gene_names_uniprotkb": "Vti1a; Vti1l2",
        "gene_names_refseq": "DD6A4-2(1); Vti1a; Vti1",
        "protein_names_uniprotkb": "Vesicle transport through interaction with t-SNAREs homolog 1A; Vesicle transport v-SNARE protein Vti1-like 2; Vti1-rp2",
        "protein_names_refseq": "SNARE Vti1a-beta protein; vesicle transport through interaction with t-SNAREs homolog 1A; vesicle transport v-SNARE protein Vti1-like 2; vti1-rp2",
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        "disease": "",
        "pathway": " (rno:65277);  (R-RNO-6811438);  (R-RNO-6811440)",
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        "publication_id_list": "10908612;12067063;17159904;9705316",
        "class_list": "",
        "function": "Data describe a novel SNARE complex containing vti1a and vti1b, found on small synaptic vesicles and clathrin-coated vesicles isolated from nerve terminals., [RefSeq, PubMed]; V-SNARE that mediates vesicle transport pathways through interactions with t-SNAREs on the target membrane. These interactions are proposed to mediate aspects of the specificity of vesicle trafficking and to promote fusion of the lipid bilayers. Involved in vesicular transport from the late endosomes to the trans-Golgi network. Along with VAMP7, involved in an non-conventional RAB1-dependent traffic route to the cell surface used by KCNIP1 and KCND2 (By similarity). May be concerned with increased secretion of cytokines associated with cellular senescence., [UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 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": "Q9JI52",
        "ec_number_list": [],
        "go_molecular_function": "GO:0000149 SNARE binding;GO:0005484 SNAP receptor activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005768 endosome;GO:0005794 Golgi apparatus;GO:0005829 cytosol;GO:0043025 neuronal cell body",
        "go_biological_process": "GO:0050882 voluntary musculoskeletal movement;GO:0006886 intracellular protein transport;GO:0016236 macroautophagy;GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport;GO:0006914 autophagy",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "Q9JI51-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q5XHX6-1",
        "uniprot_id": [
            {
                "id": "TXND2_RAT",
                "url": "https://www.uniprot.org/uniprot/Q5XHX6",
                "type": "external"
            }
        ],
        "mass": 61103.0,
        "length": 550,
        "protein_name": "Thioredoxin domain-containing protein 2",
        "gene_name": "Txndc2",
        "organism": "Rat",
        "refseq_name": "thioredoxin domain-containing protein 2 isoform 2",
        "refseq_ac": [
            {
                "id": "NP_001005559",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001005559",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Txndc2; Sptrx1; Sptrx",
        "gene_names_refseq": "Txndc2",
        "protein_names_uniprotkb": "Thioredoxin domain-containing protein 2; Spermatid-specific thioredoxin-1; Sptrx-1",
        "protein_names_refseq": "spermatid-specific thioredoxin-1; sptrx-1; thioredoxin domain containing 2 (spermatozoa); thioredoxin domain-containing protein 2 isoform 2; thioredoxin domain-containing protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:316777)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "12390887;22673903",
        "class_list": "",
        "function": "Probably plays a regulatory role in sperm development. May participate in regulation of fibrous sheath (FS) assembly by supporting the formation of disulfide bonds during sperm tail morphogenesis. May also be required to rectify incorrect disulfide pairing and generate suitable pairs between the FS constituents. Can reduce disulfide bonds in vitro in the presence of NADP and thioredoxin reductase (By similarity)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
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        "reported_phosphosites": 6,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "Q6AY11",
        "ec_number_list": [],
        "go_molecular_function": "GO:0004791 thioredoxin-disulfide reductase (NADPH) activity;GO:0003756 protein disulfide isomerase activity",
        "go_cellular_component": "GO:0001520 outer dense fiber;GO:0005737 cytoplasm;GO:0036126 sperm flagellum",
        "go_biological_process": "GO:0007283 spermatogenesis;GO:0030154 cell differentiation;GO:0030317 flagellated sperm motility;GO:0034614 cellular response to reactive oxygen species",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "Q5XHX6-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q924B5-1",
        "uniprot_id": [
            {
                "id": "TX101_RAT",
                "url": "https://www.uniprot.org/uniprot/Q924B5",
                "type": "external"
            }
        ],
        "mass": 27004.0,
        "length": 250,
        "protein_name": "Testis-expressed protein 101",
        "gene_name": "Tex101",
        "organism": "Rat",
        "refseq_name": "testis-expressed protein 101 precursor",
        "refseq_ac": [
            {
                "id": "NP_620606",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_620606",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tex101",
        "gene_names_refseq": "Tec21; Tex101",
        "protein_names_uniprotkb": "Testis-expressed protein 101; Lipid raft-associated glycoprotein TEC-21",
        "protein_names_refseq": "36-42 kDa in RBL cells and 30-36 kDa in testicular cells; GPI-anchored surface glycoprotein; heavily glycosylated protein; lipid raft-associated glycoprotein TEC-21; testis expressed gene 101; testis-expressed protein 101 precursor; testis-expressed protein 101; testis-expressed sequence 101 protein-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:207113);  (R-RNO-163125)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "11809740",
        "class_list": "",
        "function": "Plays a role in fertilization by controlling binding of sperm to zona pellucida and migration of spermatozoa into the oviduct (By similarity). May play a role in signal transduction and promote protein tyrosine phosphorylation (PubMed:11809740)., [UniProtKB, UniProtKB, PubMed]",
        "predicted_glycosites": 4,
        "predicted_n_glycosites": 4,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0044853 plasma membrane raft;GO:0001669 acrosomal vesicle",
        "go_biological_process": "GO:0007339 binding of sperm to zona pellucida;GO:0009566 fertilization;GO:0030317 flagellated sperm motility;GO:0051480 regulation of cytosolic calcium ion concentration;GO:0045575 basophil activation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "Q924B5-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000010000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "O89049-1",
        "uniprot_id": [
            {
                "id": "TRXR1_RAT",
                "url": "https://www.uniprot.org/uniprot/O89049",
                "type": "external"
            }
        ],
        "mass": 54670.0,
        "length": 499,
        "protein_name": "Thioredoxin reductase 1, cytoplasmic",
        "gene_name": "Txnrd1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Txnrd1; Trxr1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Thioredoxin reductase 1, cytoplasmic; 1.11.1.2; 1.8.1.9; NADPH-dependent thioredoxin reductase; Peroxidase TXNRD1; TR; Thioredoxin reductase TR1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "amyotrophic lateral sclerosis (Disease Ontology:DOID:332); myocardial infarction (Disease Ontology:DOID:5844)",
        "pathway": " (R-RNO-3299685);  (R-RNO-499943);  (R-RNO-5263617);  (R-RNO-5628897)",
        "pathway_count": 4,
        "publication_count": 4,
        "publication_id_list": "10333487;10849437;11481439;9535831",
        "class_list": "",
        "function": "Reduces disulfide protein thioredoxin (Trx) to its dithiol-containing form. Homodimeric flavoprotein involved in the regulation of cellular redox reactions, growth and differentiation. A selenocysteine residue at the C-terminal active site is essential for catalysis (PubMed:10849437). Also has reductase activity on hydrogen peroxide (H2O2) (PubMed:10849437)., [UniProtKB, PubMed, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_c_glycosites": 0,
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        "reported_phosphosites": 1,
        "reported_mutagensis": 2,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "Q5U344;Q9JKZ3;Q9JKZ4;Q9R1I3",
        "ec_number_list": [
            {
                "id": "1.8.1.9",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.8.1.9",
                "type": "external"
            },
            {
                "id": "1.11.1.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.11.1.2",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0004791 thioredoxin-disulfide reductase (NADPH) activity;GO:0042802 identical protein binding;GO:0071949 FAD binding;GO:0016174 NAD(P)H oxidase H2O2-forming activity;GO:0045340 mercury ion binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005829 cytosol",
        "go_biological_process": "GO:0006979 response to oxidative stress;GO:0008283 cell population proliferation;GO:0043065 positive regulation of apoptotic process;GO:0010269 response to selenium ion;GO:0045454 cell redox homeostasis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "O89049-1",
        "record_type": "protein",
        "filter_code": "0000000.0100111.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P01134-1",
        "uniprot_id": [
            {
                "id": "TGFA_RAT",
                "url": "https://www.uniprot.org/uniprot/P01134",
                "type": "external"
            }
        ],
        "mass": 16960.0,
        "length": 159,
        "protein_name": "Protransforming growth factor alpha",
        "gene_name": "Tgfa",
        "organism": "Rat",
        "refseq_name": "protransforming growth factor alpha preproprotein",
        "refseq_ac": [
            {
                "id": "NP_036803",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_036803",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tgfa",
        "gene_names_refseq": "RATTGFAA; TGFAA; Tgfa",
        "protein_names_uniprotkb": "Protransforming growth factor alpha; EGF-like TGF; ETGF; TGF type 1",
        "protein_names_refseq": "protransforming growth factor alpha preproprotein; protransforming growth factor alpha",
        "tax_id": 10116,
        "disease": "stroke (Disease Ontology:DOID:0051061); pancreatic cancer (Disease Ontology:DOID:1793); gastroenteritis (Disease Ontology:DOID:2326); acute kidney failure (Disease Ontology:DOID:3021); insulinoma (Disease Ontology:DOID:3892); gallbladder carcinoma (Disease Ontology:DOID:4948); hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (rno:24827);  (R-RNO-1257604);  (R-RNO-177929);  (R-RNO-179812);  (R-RNO-180292);  (R-RNO-180336);  (R-RNO-182971);  (R-RNO-204005);  (R-RNO-212718);  (R-RNO-5673001);  (R-RNO-5694530);  (R-RNO-6811558);  (R-RNO-8856825);  (R-RNO-8856828);  (R-RNO-9009391)",
        "pathway_count": 15,
        "publication_count": 7,
        "publication_id_list": "2325647;24595367;26804134;34968668;3855503;6320373;6605968",
        "class_list": "",
        "function": "5-HT stimulates DNA synthesis and proliferation in primary cultures of adult rat hepatocytes by acting via autocrine secretion of TGF-alpha induced by the serotonin 5-HT2B receptor/Gq/PLC/Ca2+ pathway., [RefSeq, PubMed]; Lipopolysaccharide exposure led to a suppression of both HDAC1 and HDAC2 expression and activity, induced TGFa expression, and disrupted alveolar morphology. Publication Status: Online-Only, [RefSeq, PubMed]; TGF alpha is a mitogenic polypeptide that is able to bind to the EGF receptor/EGFR and to act synergistically with TGF beta to promote anchorage-independent cell proliferation in soft agar., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Transforming Growth Factor-alpha Acts in Hypothalamic Paraventricular Nucleus to Upregulate ERK1/2 Signaling and Expression of Sympathoexcitatory Mediators in Heart Failure Rats., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 1,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 7,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "Q63749",
        "ec_number_list": [],
        "go_molecular_function": "GO:0005154 epidermal growth factor receptor binding;GO:0008083 growth factor activity;GO:0048018 receptor ligand activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0009986 cell surface;GO:0016323 basolateral plasma membrane;GO:0048471 perinuclear region of cytoplasm;GO:0031410 cytoplasmic vesicle",
        "go_biological_process": "GO:0072574 hepatocyte proliferation;GO:0001525 angiogenesis;GO:0007166 cell surface receptor signaling pathway;GO:0008284 positive regulation of cell population proliferation;GO:0043066 negative regulation of apoptotic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.8,
        "record_id": "P01134-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000010000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q5GH61-1",
        "uniprot_id": [
            {
                "id": "XK_RAT",
                "url": "https://www.uniprot.org/uniprot/Q5GH61",
                "type": "external"
            }
        ],
        "mass": 51050.0,
        "length": 445,
        "protein_name": "Endoplasmic reticulum membrane adapter protein XK",
        "gene_name": "Xk",
        "organism": "Rat",
        "refseq_name": "endoplasmic reticulum membrane adapter protein XK",
        "refseq_ac": [
            {
                "id": "NP_001012227",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001012227",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Xk; Xkh; Xkr1; Xrg1",
        "gene_names_refseq": "Xk",
        "protein_names_uniprotkb": "Endoplasmic reticulum membrane adapter protein XK; Membrane transport protein XK; XK homolog; XK-related protein 1",
        "protein_names_refseq": "Kell blood group precursor (McLeod phenotype) homolog; X-linked Kx blood group (McLeod syndrome) homolog; XK homolog; XK-related protein 1; endoplasmic reticulum membrane adapter protein XK; membrane transport protein XK",
        "tax_id": 10116,
        "disease": "McLeod syndrome (Disease Ontology:DOID:0112107); hematopoietic system disease (Disease Ontology:DOID:74)",
        "pathway": " (rno:497078);  (R-RNO-375276)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "17379193;22673903",
        "class_list": "",
        "function": "Immunohistochemical experiments using adult rat brain indicated widespread XK immunoreactivity in the cerebral cortex, hippocampus, striatum, diencephalon and cerebellum., [RefSeq, PubMed]; Recruits the lipid transfer protein VPS13A from lipid droplets to the endoplasmic reticulum (ER) membrane., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 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,
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        "reported_phosphosites": 1,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006874 intracellular calcium ion homeostasis;GO:0042552 myelination;GO:0048741 skeletal muscle fiber development;GO:0006865 amino acid transport;GO:0010961 intracellular magnesium ion homeostasis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "Q5GH61-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q7TPK6-1",
        "uniprot_id": [
            {
                "id": "WNK4_RAT",
                "url": "https://www.uniprot.org/uniprot/Q7TPK6",
                "type": "external"
            }
        ],
        "mass": 132833.0,
        "length": 1222,
        "protein_name": "Serine/threonine-protein kinase WNK4",
        "gene_name": "Wnk4",
        "organism": "Rat",
        "refseq_name": "serine/threonine-protein kinase WNK4",
        "refseq_ac": [
            {
                "id": "NP_783169",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_783169",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Wnk4; Prkwnk4",
        "gene_names_refseq": "Ac2-059; Prkwnk4; Wnk4",
        "protein_names_uniprotkb": "Serine/threonine-protein kinase WNK4; 2.7.11.1; Protein kinase lysine-deficient 4; Protein kinase with no lysine 4",
        "protein_names_refseq": "WNK4 Ser/Thr kinase; protein kinase lysine-deficient 4; protein kinase with no lysine 4; serine/threonine-protein kinase WNK4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:287715)",
        "pathway_count": 1,
        "publication_count": 8,
        "publication_id_list": "12642508;14608358;15883153;16083423;22513846;22673903;24811174;28493961",
        "class_list": "",
        "function": "Gene analysis of rat chromosome 10 suggest that Wnk4 does not have a role in polygenic hypertension., [RefSeq, PubMed]; In addition to SPAK and OSR1, WNK4 is able to anchor itself to the N-terminal domain of NKCC1 and to promote cotransporter activation., [RefSeq, PubMed]; Serine/threonine-protein kinase component of the WNK4-SPAK/OSR1 kinase cascade, which acts as a key regulator of ion transport in the distal nephron and blood pressure (By similarity). The WNK4-SPAK/OSR1 kinase cascade is composed of WNK4, which mediates phosphorylation and activation of downstream kinases OXSR1/OSR1 and STK39/SPAK (PubMed:16083423). Following activation, OXSR1/OSR1 and STK39/SPAK catalyze phosphorylation of ion cotransporters, such as SLC12A1/NKCC2, SLC12A2/NKCC1, SLC12A3/NCC, SLC12A5/KCC2 or SLC12A6/KCC3, regulating their activity (By similarity). Acts as a molecular switch that regulates the balance between renal salt reabsorption and K(+) secretion by modulating the activities of renal transporters and channels, including the Na-Cl cotransporter SLC12A3/NCC and the K(+) channel, KCNJ1/ROMK (By similarity). Regulates NaCl reabsorption in the distal nephron by activating the thiazide-sensitive Na-Cl cotransporter SLC12A3/NCC in distal convoluted tubule cells of kidney: activates SLC12A3/NCC in a OXSR1/OSR1- and STK39/SPAK-dependent process (By similarity). Also acts as a scaffold protein independently of its protein kinase activity: negatively regulates cell membrane localization of various transporters and channels (CFTR, KCNJ1/ROMK, SLC4A4, SLC26A9 and TRPV4) by clathrin-dependent endocytosis (By similarity). Also inhibits the activity of the epithelial Na(+) channel (ENaC) SCNN1A, SCNN1B, SCNN1D in a inase-independent mechanism (By similarity). May also phosphorylate NEDD4L (By similarity)., [UniProtKB, UniProtKB, UniProtKB, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 8,
        "reported_mutagensis": 2,
        "reported_glycation": 0,
        "reported_snv": 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": "Q810H4;Q811R5",
        "ec_number_list": [
            {
                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
            },
            {
                "id": "2.7.12.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.12.1",
                "type": "external"
            },
            {
                "id": "2.7.1.153",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.153",
                "type": "external"
            },
            {
                "id": "2.7.1.137",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.137",
                "type": "external"
            },
            {
                "id": "2.7.11.24",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.24",
                "type": "external"
            },
            {
                "id": "2.7.11.25",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.25",
                "type": "external"
            },
            {
                "id": "2.7.11.22",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.22",
                "type": "external"
            },
            {
                "id": "2.7.11.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.23",
                "type": "external"
            },
            {
                "id": "2.7.4.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.6",
                "type": "external"
            },
            {
                "id": "2.7.1.154",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.154",
                "type": "external"
            },
            {
                "id": "2.7.11.38",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.38",
                "type": "external"
            },
            {
                "id": "2.7.11.17",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.17",
                "type": "external"
            },
            {
                "id": "2.7.11.21",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.21",
                "type": "external"
            },
            {
                "id": "2.7.12.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.12.2",
                "type": "external"
            },
            {
                "id": "2.7.1.40",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.40",
                "type": "external"
            },
            {
                "id": "2.7.11.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.12",
                "type": "external"
            },
            {
                "id": "2.7.11.26",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.26",
                "type": "external"
            },
            {
                "id": "2.7.11.34",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.34",
                "type": "external"
            },
            {
                "id": "2.7.10.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.10.2",
                "type": "external"
            },
            {
                "id": "2.7.1.150",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.150",
                "type": "external"
            },
            {
                "id": "2.7.11.13",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.13",
                "type": "external"
            },
            {
                "id": "4.1.1.32",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.1.1.32",
                "type": "external"
            },
            {
                "id": "2.7.11.19",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.19",
                "type": "external"
            },
            {
                "id": "2.7.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.2.3",
                "type": "external"
            },
            {
                "id": "2.7.11.11",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.11",
                "type": "external"
            },
            {
                "id": "2.7.11.31",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.31",
                "type": "external"
            },
            {
                "id": "3.1.3.16",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.16",
                "type": "external"
            },
            {
                "id": "2.7.11.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.4",
                "type": "external"
            },
            {
                "id": "2.3.1.48",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.48",
                "type": "external"
            },
            {
                "id": "3.1.11.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.11.-",
                "type": "external"
            },
            {
                "id": "2.7.13.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.13.3",
                "type": "external"
            },
            {
                "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.-",
                "type": "external"
            },
            {
                "id": "3.4.19.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.19.12",
                "type": "external"
            },
            {
                "id": "2.7.11.39",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.39",
                "type": "external"
            },
            {
                "id": "2.4.99.18",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.4.99.18",
                "type": "external"
            },
            {
                "id": "2.7.11.10",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.10",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0019870 potassium channel inhibitor activity;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0031404 chloride ion binding;GO:0008200 ion channel inhibitor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005923 bicellular tight junction;GO:0016020 membrane;GO:0044297 cell body",
        "go_biological_process": "GO:0030644 intracellular chloride ion homeostasis;GO:0003096 renal sodium ion transport;GO:0006468 protein phosphorylation;GO:0006954 inflammatory response;GO:0007165 signal transduction",
        "synthesized_glycan_count": 0,
        "hit_score": 0.9,
        "record_id": "Q7TPK6-1",
        "record_type": "protein",
        "filter_code": "0000000.0100101.010000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q99376-1",
        "uniprot_id": [
            {
                "id": "TFR1_RAT",
                "url": "https://www.uniprot.org/uniprot/Q99376",
                "type": "external"
            }
        ],
        "mass": 85876.0,
        "length": 761,
        "protein_name": "Transferrin receptor protein 1",
        "gene_name": "Tfrc",
        "organism": "Rat",
        "refseq_name": "transferrin receptor protein 1",
        "refseq_ac": [
            {
                "id": "NP_073203",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_073203",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tfrc; Trfr",
        "gene_names_refseq": "Tfrc; Trfr",
        "protein_names_uniprotkb": "Transferrin receptor protein 1; TR; TfR1; TfR; Trfr",
        "protein_names_refseq": "TR; tfR1; tfR; transferrin receptor protein 1",
        "tax_id": 10116,
        "disease": "metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); immunodeficiency 46 (Disease Ontology:DOID:0111948); prostate cancer (Disease Ontology:DOID:10283); iron deficiency anemia (Disease Ontology:DOID:11758); breast cancer (Disease Ontology:DOID:1612); duodenal ulcer (Disease Ontology:DOID:1724); ovarian cancer (Disease Ontology:DOID:2394); transitional cell carcinoma (Disease Ontology:DOID:2671); breast carcinoma (Disease Ontology:DOID:3459); cervical adenocarcinoma (Disease Ontology:DOID:3702); nutrition disease (Disease Ontology:DOID:374); Weissenbacher-Zweymuller syndrome (Disease Ontology:DOID:4258); renal cell carcinoma (Disease Ontology:DOID:4450); hepatocellular carcinoma (Disease Ontology:DOID:684); muscular atrophy (Disease Ontology:DOID:767); multiple myeloma (Disease Ontology:DOID:9538)",
        "pathway": " (rno:64678);  (R-RNO-432722);  (R-RNO-8856825);  (R-RNO-8856828);  (R-RNO-8980692);  (R-RNO-9013026);  (R-RNO-9013106);  (R-RNO-9013149);  (R-RNO-9013404);  (R-RNO-9013406);  (R-RNO-9013407);  (R-RNO-9013408);  (R-RNO-9013423);  (R-RNO-917977);  (R-RNO-9696270);  (R-RNO-9696273)",
        "pathway_count": 16,
        "publication_count": 8,
        "publication_id_list": "2126342;21454685;35038133;37105375;37683766;38241836;38843836;39251905",
        "class_list": "",
        "function": "Cellular uptake of iron occurs via receptor-mediated endocytosis of ligand-occupied transferrin receptor into specialized endosomes. Endosomal acidification leads to iron release. The apotransferrin-receptor complex is then recycled to the cell surface with a return to neutral pH and the concomitant loss of affinity of apotransferrin for its receptor. Transferrin receptor is necessary for development of erythrocytes and the nervous system. Acts as a lipid sensor that regulates mitochondrial fusion by regulating activation of the JNK pathway., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Endothelial transferrin receptor 1 contributes to thrombogenesis through cascade ferroptosis., [RefSeq, PubMed]; Exosome-Derived lncRNA NEAT1 Exacerbates Sepsis-Associated Encephalopathy by Promoting Ferroptosis Through Regulating miR-9-5p/TFRC and GOT1 Axis. Erratum:[Mol Neurobiol. 2022 Aug;59(8):5252. doi: 10.1007/s12035-022-02931-2. PMID: 35727437], [RefSeq, PubMed]; METTL3 silenced inhibited the ferroptosis development via regulating the TFRC levels in the Intracerebral hemorrhage progression., [RefSeq, PubMed]; NAT10-mediated ac[4]C acetylation of TFRC promotes sepsis-induced pulmonary injury through regulating ferroptosis. Publication Status: Online-Only, [RefSeq, PubMed]; TFEB regulates cellular labile iron and prevents ferroptosis in a TfR1-dependent manner., [RefSeq, PubMed]",
        "predicted_glycosites": 5,
        "predicted_n_glycosites": 5,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 1,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 1,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 1,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 1,
        "reported_phosphosites": 5,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 16,
        "glyco_site_count": 5,
        "binding_glycan_count": 0,
        "secondary_ac_list": "G3V679",
        "ec_number_list": [],
        "go_molecular_function": "GO:0019901 protein kinase binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0051087 protein-folding chaperone binding;GO:0044877 protein-containing complex binding",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0005768 endosome;GO:0005769 early endosome",
        "go_biological_process": "GO:0030316 osteoclast differentiation;GO:0007166 cell surface receptor signaling pathway;GO:0007584 response to nutrient;GO:0010628 positive regulation of gene expression;GO:0031623 receptor internalization",
        "synthesized_glycan_count": 0,
        "hit_score": 1.1,
        "record_id": "Q99376-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0100000010001.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q9JIH7-1",
        "uniprot_id": [
            {
                "id": "WNK1_RAT",
                "url": "https://www.uniprot.org/uniprot/Q9JIH7",
                "type": "external"
            }
        ],
        "mass": 225112.0,
        "length": 2126,
        "protein_name": "Serine/threonine-protein kinase WNK1",
        "gene_name": "Wnk1",
        "organism": "Rat",
        "refseq_name": "serine/threonine-protein kinase WNK1 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001002823",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001002823",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Wnk1; Hsn2; Prkwnk1",
        "gene_names_refseq": "Hsn2; Prkwnk1; Wnk1",
        "protein_names_uniprotkb": "Serine/threonine-protein kinase WNK1; 2.7.11.1; Protein kinase lysine-deficient 1; Protein kinase with no lysine 1",
        "protein_names_refseq": "protein kinase with no lysine 1; serine/threonine-protein kinase WNK1 isoform 1",
        "tax_id": 10116,
        "disease": "hereditary sensory and autonomic neuropathy (Disease Ontology:DOID:0050548); hereditary sensory and autonomic neuropathy type 2A (Disease Ontology:DOID:0070155); hypertension (Disease Ontology:DOID:10763); transient cerebral ischemia (Disease Ontology:DOID:224); pseudohypoaldosteronism (Disease Ontology:DOID:4479)",
        "pathway": " (rno:116477)",
        "pathway_count": 1,
        "publication_count": 30,
        "publication_id_list": "10828064;12374799;12671053;15060842;15242606;15340146;15350218;16006511;16081417;16083423;16204408;16403833;17673510;17975670;18683930;20525693;22544747;22673903;23376100;24803536;27595330;28771350;29393594;31085334;31561038;32314908;33439774;33689398;36318922;38843836",
        "class_list": "",
        "function": "A Phosphorylated Intermediate in the Activation of WNK Kinases., [RefSeq, PubMed]; Kinase-defective isoform produced by alternative promoter usage and alternative splicing., [UniProtKB, PubMed]; Kinase-defective isoform specifically expressed in kidney, which acts as a dominant-negative regulator of the longer isoform 1 (PubMed:16204408). Does not directly inhibit WNK4 and has no direct effect on sodium and chloride ion transport (PubMed:16204408). Down-regulates sodium-chloride cotransporter activity indirectly by inhibiting isoform 1, it associates with isoform 1 and attenuates its kinase activity (PubMed:16204408). In kidney, may play an important role regulating sodium and potassium balance (PubMed:16204408)., [UniProtKB, PubMed]; Osmosensing by WNK Kinases., [RefSeq, PubMed]; Regulation of CFTR Bicarbonate Channel Activity by WNK1: Implications for Pancreatitis and CFTR-Related Disorders., [RefSeq, PubMed]; Serine/threonine-protein kinase component of the WNK1-SPAK/OSR1 kinase cascade, which acts as a key regulator of blood pressure and regulatory volume increase by promoting ion influx (PubMed:10828064, PubMed:12374799, PubMed:16083423, PubMed:17975670, PubMed:24803536, PubMed:36318922). WNK1 mediates regulatory volume increase in response to hyperosmotic stress by acting as a molecular crowding sensor, which senses cell shrinkage and mediates formation of a membraneless compartment by undergoing liquid-liquid phase separation (PubMed:36318922). The membraneless compartment concentrates WNK1 with its substrates, OXSR1/OSR1 and STK39/SPAK, promoting WNK1-dependent phosphorylation and activation of downstream kinases OXSR1/OSR1 and STK39/SPAK (PubMed:16083423, PubMed:36318922). Following activation, OXSR1/OSR1 and STK39/SPAK catalyze phosphorylation of ion cotransporters SLC12A1/NKCC2, SLC12A2/NKCC1, SLC12A5/KCC2 and SLC12A6/KCC3, regulating their activity (PubMed:22544747, PubMed:36318922). Phosphorylation of Na-K-Cl cotransporters SLC12A2/NKCC1 and SLC12A2/NKCC1 promote their activation and ion influx; simultaneously, phosphorylation of K-Cl cotransporters SLC12A5/KCC2 and SLC12A6/KCC3 inhibit their activity, blocking ion efflux (PubMed:36318922). Also acts as a regulator of angiogenesis in endothelial cells (By similarity). Also acts independently of the WNK1-SPAK/OSR1 kinase cascade by catalyzing phosphorylation of other substrates, such as SYT2, PCF11 and NEDD4L (PubMed:15350218, PubMed:20525693). Mediates phosphorylation of SYT2, regulating SYT2 association with phospholipids and membrane-binding (PubMed:15350218). Regulates mRNA export in the nucleus by mediating phosphorylation of PCF11, thereby decreasing the association between PCF11 and POLR2A/RNA polymerase II and promoting mRNA export to the cytoplasm (By similarity). Acts as a negative regulator of autophagy (By similarity). Required for the abscission step during mitosis, independently of the WNK1-SPAK/OSR1 kinase cascade (By similarity). WNK1 may also play a role in actin cytoskeletal reorganization (By similarity). Also acts as a scaffold protein independently of its protein kinase activity: negatively regulates cell membrane localization of various transporters and channels, such as SLC4A4, SLC26A6, SLC26A9, TRPV4 and CFTR (PubMed:16403833, PubMed:17673510). Involved in the regulation of epithelial Na(+) channel (ENaC) by promoting activation of SGK1 in a kinase-independent manner (PubMed:16006511, PubMed:16081417). Probably activates SGK1 by acting as a scaffold protein that promotes the recruitment of SGK1 to the mTORC2 complex in response to chloride, leading to mTORC2-dependent phosphorylation and activation of SGK1 (By similarity). Acts as an assembly factor for the ER membrane protein complex independently of its protein kinase activity: associates with EMC2 in the cytoplasm via its amphipathic alpha-helix, and prevents EMC2 ubiquitination and subsequent degradation, thereby promoting EMC2 stabilization (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed, PubMed]; Suppression of WNK1-SPAK/OSR1 Attenuates Bone Cancer Pain by Regulating NKCC1 and KCC2., [RefSeq, PubMed]; WNK1 has a role in the sodium regulatory pathway of the distal, [RefSeq, PubMed]",
        "predicted_glycosites": 4,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 4,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 1,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 1,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 1,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 1,
        "reported_phosphosites": 20,
        "reported_mutagensis": 20,
        "reported_glycation": 0,
        "reported_snv": 1,
        "reported_interactions": 0,
        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 5,
        "glyco_site_count": 4,
        "binding_glycan_count": 0,
        "secondary_ac_list": "Q3S2I2;Q6IFS7",
        "ec_number_list": [
            {
                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
            },
            {
                "id": "2.7.12.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.12.1",
                "type": "external"
            },
            {
                "id": "2.7.1.153",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.153",
                "type": "external"
            },
            {
                "id": "2.7.1.137",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.137",
                "type": "external"
            },
            {
                "id": "2.7.11.24",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.24",
                "type": "external"
            },
            {
                "id": "2.7.11.25",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.25",
                "type": "external"
            },
            {
                "id": "2.7.11.22",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.22",
                "type": "external"
            },
            {
                "id": "2.7.11.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.23",
                "type": "external"
            },
            {
                "id": "2.7.4.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.6",
                "type": "external"
            },
            {
                "id": "2.7.1.154",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.154",
                "type": "external"
            },
            {
                "id": "2.7.11.38",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.38",
                "type": "external"
            },
            {
                "id": "2.7.11.17",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.17",
                "type": "external"
            },
            {
                "id": "2.7.11.21",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.21",
                "type": "external"
            },
            {
                "id": "2.7.12.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.12.2",
                "type": "external"
            },
            {
                "id": "2.7.1.40",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.40",
                "type": "external"
            },
            {
                "id": "2.7.11.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.12",
                "type": "external"
            },
            {
                "id": "2.7.11.26",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.26",
                "type": "external"
            },
            {
                "id": "2.7.11.34",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.34",
                "type": "external"
            },
            {
                "id": "2.7.10.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.10.2",
                "type": "external"
            },
            {
                "id": "2.7.1.150",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.150",
                "type": "external"
            },
            {
                "id": "2.7.11.13",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.13",
                "type": "external"
            },
            {
                "id": "4.1.1.32",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.1.1.32",
                "type": "external"
            },
            {
                "id": "2.7.11.19",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.19",
                "type": "external"
            },
            {
                "id": "2.7.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.2.3",
                "type": "external"
            },
            {
                "id": "2.7.11.11",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.11",
                "type": "external"
            },
            {
                "id": "2.7.11.31",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.31",
                "type": "external"
            },
            {
                "id": "3.1.3.16",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.16",
                "type": "external"
            },
            {
                "id": "2.7.11.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.4",
                "type": "external"
            },
            {
                "id": "2.3.1.48",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.48",
                "type": "external"
            },
            {
                "id": "3.1.11.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.11.-",
                "type": "external"
            },
            {
                "id": "2.7.13.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.13.3",
                "type": "external"
            },
            {
                "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.-",
                "type": "external"
            },
            {
                "id": "3.4.19.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.19.12",
                "type": "external"
            },
            {
                "id": "2.7.11.39",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.39",
                "type": "external"
            },
            {
                "id": "2.4.99.18",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.4.99.18",
                "type": "external"
            },
            {
                "id": "2.7.11.10",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.10",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0019870 potassium channel inhibitor activity;GO:0000287 magnesium ion binding;GO:0004672 protein kinase activity;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding",
        "go_cellular_component": "GO:0098982 GABA-ergic synapse;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0016020 membrane",
        "go_biological_process": "GO:1990869 cellular response to chemokine;GO:0030644 intracellular chloride ion homeostasis;GO:0033633 negative regulation of cell-cell adhesion mediated by integrin;GO:0006468 protein phosphorylation;GO:0006811 monoatomic ion transport",
        "synthesized_glycan_count": 0,
        "hit_score": 3.3,
        "record_id": "Q9JIH7-1",
        "record_type": "protein",
        "filter_code": "0000000.1100111.010000.000000000000001000.0100000001001.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "F1LNJ2-1",
        "uniprot_id": [
            {
                "id": "U520_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LNJ2",
                "type": "external"
            }
        ],
        "mass": 244875.0,
        "length": 2139,
        "protein_name": "U5 small nuclear ribonucleoprotein 200 kDa helicase",
        "gene_name": "Snrnp200",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Snrnp200",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "U5 small nuclear ribonucleoprotein 200 kDa helicase; 3.6.4.13; BRR2 homolog; U5 snRNP-specific 200 kDa protein; U5-200KD",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa 33 (Disease Ontology:DOID:0110366); retinitis pigmentosa (Disease Ontology:DOID:10584)",
        "pathway": " (rno:296126);  (R-RNO-72163);  (R-RNO-72165)",
        "pathway_count": 3,
        "publication_count": 2,
        "publication_id_list": "16641100;22673903",
        "class_list": "",
        "function": "Catalyzes the ATP-dependent unwinding of U4/U6 RNA duplices, an essential step in the assembly of a catalytically active spliceosome. Plays a role in pre-mRNA splicing as core component of precatalytic, catalytic and postcatalytic spliceosomal complexes. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (By similarity). Involved in spliceosome assembly, activation and disassembly. Mediates changes in the dynamic network of RNA-RNA interactions in the spliceosome., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 11,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "5.6.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.3",
                "type": "external"
            },
            {
                "id": "3.6.4.13",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.13",
                "type": "external"
            },
            {
                "id": "3.6.4.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.12",
                "type": "external"
            },
            {
                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
            },
            {
                "id": "3.6.1.5",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.5",
                "type": "external"
            },
            {
                "id": "3.6.4.10",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.10",
                "type": "external"
            },
            {
                "id": "3.6.4.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.-",
                "type": "external"
            },
            {
                "id": "2.3.2.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
                "type": "external"
            },
            {
                "id": "5.6.2.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.4",
                "type": "external"
            },
            {
                "id": "5.2.1.8",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.2.1.8",
                "type": "external"
            },
            {
                "id": "3.6.5.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.-",
                "type": "external"
            },
            {
                "id": "5.6.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.-",
                "type": "external"
            },
            {
                "id": "3.1.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.-.-",
                "type": "external"
            },
            {
                "id": "2.7.7.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.6",
                "type": "external"
            },
            {
                "id": "2.7.7.7",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.7",
                "type": "external"
            },
            {
                "id": "2.7.7.49",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.49",
                "type": "external"
            },
            {
                "id": "3.1.13.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.13.1",
                "type": "external"
            },
            {
                "id": "4.2.99.18",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.2.99.18",
                "type": "external"
            },
            {
                "id": "7.6.2.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.6.2.2",
                "type": "external"
            },
            {
                "id": "7.6.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.6.2.3",
                "type": "external"
            },
            {
                "id": "7.6.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.6.2.-",
                "type": "external"
            },
            {
                "id": "5.6.1.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.1.6",
                "type": "external"
            },
            {
                "id": "7.2.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.2.2.-",
                "type": "external"
            },
            {
                "id": "3.6.1.15",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.15",
                "type": "external"
            },
            {
                "id": "3.6.4.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.6",
                "type": "external"
            },
            {
                "id": "3.1.3.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.1",
                "type": "external"
            },
            {
                "id": "3.9.1.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.9.1.1",
                "type": "external"
            },
            {
                "id": "6.1.1.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.1.1.12",
                "type": "external"
            },
            {
                "id": "3.6.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.-",
                "type": "external"
            },
            {
                "id": "2.7.4.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.3",
                "type": "external"
            },
            {
                "id": "3.1.4.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.4.-",
                "type": "external"
            },
            {
                "id": "3.4.24.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.24.-",
                "type": "external"
            },
            {
                "id": "3.6.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.-.-",
                "type": "external"
            },
            {
                "id": "3.4.21.53",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.21.53",
                "type": "external"
            },
            {
                "id": "5.6.2.5",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.5",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0003723 RNA binding;GO:0005524 ATP binding;GO:0042802 identical protein binding;GO:0016887 ATP hydrolysis activity;GO:0004386 helicase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005681 spliceosomal complex;GO:0071013 catalytic step 2 spliceosome;GO:0071011 precatalytic spliceosome",
        "go_biological_process": "GO:0000398 mRNA splicing, via spliceosome;GO:0000388 spliceosome conformational change to release U4 (or U4atac) and U1 (or U11)",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "F1LNJ2-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.010000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q8R5K6-1",
        "uniprot_id": [
            {
                "id": "TOB1_RAT",
                "url": "https://www.uniprot.org/uniprot/Q8R5K6",
                "type": "external"
            }
        ],
        "mass": 40461.0,
        "length": 365,
        "protein_name": "Protein Tob1",
        "gene_name": "Tob1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Tob1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein Tob1; Transducer of erbB-2 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:170842)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "21336257",
        "class_list": "",
        "function": "Anti-proliferative protein; the function is mediated by association with deadenylase subunits of the CCR4-NOT complex. Mediates CPEB3-accelerated mRNA deadenylation by binding to CPEB3 and recruiting CNOT7 which leads to target mRNA deadenylation and decay., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 1,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003714 transcription corepressor activity;GO:0030971 receptor tyrosine kinase binding;GO:0046332 SMAD binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0030014 CCR4-NOT complex",
        "go_biological_process": "GO:0060390 regulation of SMAD protein signal transduction;GO:0008285 negative regulation of cell population proliferation;GO:0030514 negative regulation of BMP signaling pathway;GO:0017148 negative regulation of translation;GO:0010468 regulation of gene expression",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "Q8R5K6-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P04633-1",
        "uniprot_id": [
            {
                "id": "UCP1_RAT",
                "url": "https://www.uniprot.org/uniprot/P04633",
                "type": "external"
            }
        ],
        "mass": 33212.0,
        "length": 307,
        "protein_name": "Mitochondrial brown fat uncoupling protein 1",
        "gene_name": "Ucp1",
        "organism": "Rat",
        "refseq_name": "mitochondrial brown fat uncoupling protein 1",
        "refseq_ac": [
            {
                "id": "NP_036814",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_036814",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ucp1; Slc25a7; Ucp",
        "gene_names_refseq": "Ucp1; Ucpa; Ucp; Uncp",
        "protein_names_uniprotkb": "Mitochondrial brown fat uncoupling protein 1; Solute carrier family 25 member 7; Thermogenin; UCP 1",
        "protein_names_refseq": "UCP 1; mitochondrial brown fat uncoupling protein 1-like; mitochondrial brown fat uncoupling protein 1; solute carrier family 25 member 7; thermogenin; uncoupling protein 1 (mitochondrial, proton carrier)",
        "tax_id": 10116,
        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652); hypertension (Disease Ontology:DOID:10763); prediabetes syndrome (Disease Ontology:DOID:11716); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": " (rno:24860);  (R-RNO-166187);  (R-RNO-167826)",
        "pathway_count": 3,
        "publication_count": 14,
        "publication_id_list": "12479871;16814247;22531154;22952235;2421800;3012461;30624981;3202878;33202085;33441773;33815288;36650072;3753702;7691596",
        "class_list": "",
        "function": "Instead of UCP1-mediated mitochondrial uncoupling, cold acclimation increased the capacity of Sc Ing adipocytes to export fatty acids., [RefSeq, PubMed]; Maternal Roux-en-Y gastric bypass surgery reduces lipid deposition and increases UCP1 expression in the brown adipose tissue of male offspring. Publication Status: Online-Only, [RefSeq, PubMed]; Mitochondrial protein responsible for thermogenic respiration, a specialized capacity of brown adipose tissue and beige fat that participates in non-shivering adaptive thermogenesis to temperature and diet variations and more generally to the regulation of energy balance (By similarity). Functions as a long-chain fatty acid/LCFA and proton symporter, simultaneously transporting one LCFA and one proton through the inner mitochondrial membrane. However, LCFAs remaining associated with the transporter via their hydrophobic tails, it results in an apparent transport of protons activated by LCFAs (PubMed:12479871, PubMed:16814247, PubMed:22952235). Thereby, dissipates the mitochondrial proton gradient and converts the energy of substrate oxydation into heat instead of ATP. Regulates the production of reactive oxygen species/ROS by mitochondria (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed]; NT3/TrkC Pathway Modulates the Expression of UCP-1 and Adipocyte Size in Human and Rodent Adipose Tissue. Publication Status: Online-Only, [RefSeq, PubMed]; Rats lacking Ucp1 present a novel translational tool for the investigation of thermogenic adaptation during cold challenge., [RefSeq, PubMed]; Structural models of mitochondrial uncoupling proteins obtained in DPC micelles are not functionally relevant., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 6,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 4,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0036041 long-chain fatty acid binding;GO:0005525 GTP binding;GO:0022857 transmembrane transporter activity;GO:0019003 GDP binding;GO:0015078 proton transmembrane transporter activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005740 mitochondrial envelope;GO:0005743 mitochondrial inner membrane",
        "go_biological_process": "GO:0070417 cellular response to cold;GO:0009893 positive regulation of metabolic process;GO:0006091 generation of precursor metabolites and energy;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006839 mitochondrial transport",
        "synthesized_glycan_count": 0,
        "hit_score": 1.5,
        "record_id": "P04633-1",
        "record_type": "protein",
        "filter_code": "0000000.0100111.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P21643-1",
        "uniprot_id": [
            {
                "id": "T23O_RAT",
                "url": "https://www.uniprot.org/uniprot/P21643",
                "type": "external"
            }
        ],
        "mass": 47857.0,
        "length": 406,
        "protein_name": "Tryptophan 2,3-dioxygenase",
        "gene_name": "Tdo2",
        "organism": "Rat",
        "refseq_name": "tryptophan 2,3-dioxygenase",
        "refseq_ac": [
            {
                "id": "NP_071798",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_071798",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tdo2; Tdo",
        "gene_names_refseq": "TO; Tdo2; Tdo",
        "protein_names_uniprotkb": "Tryptophan 2,3-dioxygenase; 1.13.11.11; TDO; TO; TRPO; Tryptamin 2,3-dioxygenase; Tryptophan oxygenase; Tryptophan pyrrolase; Tryptophanase",
        "protein_names_refseq": "TRPO; tryptamin 2,3-dioxygenase; tryptophan 2,3-dioxygenase A; tryptophan 2,3-dioxygenase; tryptophan oxygenase; tryptophan pyrrolase; tryptophan-23-dioxygenase; tryptophanase",
        "tax_id": 10116,
        "disease": "familial hypertryptophanemia (Disease Ontology:DOID:0111703); Gilles de la Tourette syndrome (Disease Ontology:DOID:11119); diabetes mellitus (Disease Ontology:DOID:9351)",
        "pathway": " (rno:64206);  (R-RNO-71240)",
        "pathway_count": 2,
        "publication_count": 5,
        "publication_id_list": "1511007;22673903;2372286;3582368;6327261",
        "class_list": "",
        "function": "Heme-dependent dioxygenase that catalyzes the oxidative cleavage of the L-tryptophan (L-Trp) pyrrole ring and converts L-tryptophan to N-formyl-L-kynurenine. Catalyzes the oxidative cleavage of the indole moiety., [UniProtKB, HAMAP]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 1,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 3,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "Q5EBC2;Q6LBW3",
        "ec_number_list": [
            {
                "id": "1.13.11.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.13.11.-",
                "type": "external"
            },
            {
                "id": "1.13.11.11",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.13.11.11",
                "type": "external"
            },
            {
                "id": "1.13.11.52",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.13.11.52",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0046872 metal ion binding;GO:0016597 amino acid binding;GO:0020037 heme binding;GO:0019825 oxygen binding",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0019441 L-tryptophan catabolic process to kynurenine;GO:0045471 response to ethanol;GO:0051289 protein homotetramerization;GO:0006568 L-tryptophan metabolic process;GO:0051414 response to cortisol",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "P21643-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P63045-1",
        "uniprot_id": [
            {
                "id": "VAMP2_RAT",
                "url": "https://www.uniprot.org/uniprot/P63045",
                "type": "external"
            }
        ],
        "mass": 12691.0,
        "length": 116,
        "protein_name": "Vesicle-associated membrane protein 2",
        "gene_name": "Vamp2",
        "organism": "Rat",
        "refseq_name": "vesicle-associated membrane protein 2 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_036795",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_036795",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Vamp2; Syb2",
        "gene_names_refseq": "RATVAMPB; RATVAMPIR; SYB; Syb2; Vamp2",
        "protein_names_uniprotkb": "Vesicle-associated membrane protein 2; Synaptobrevin-2; VAMP-2",
        "protein_names_refseq": "Synaptobrevin 2 (vesicle-associated membrane protein VAMP-2); VAMP-2; Vesicle-associated membrane protein (synaptobrevin 2); synaptobrevin-2; vesicle-associated membrane protein 2 isoform 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:24803);  (R-RNO-181429);  (R-RNO-181430);  (R-RNO-199992);  (R-RNO-210500);  (R-RNO-212676);  (R-RNO-264642);  (R-RNO-432720);  (R-RNO-432722);  (R-RNO-449836);  (R-RNO-8856825);  (R-RNO-8856828);  (R-RNO-888590);  (R-RNO-9609523)",
        "pathway_count": 14,
        "publication_count": 15,
        "publication_id_list": "11832227;12496247;1331807;19196426;19690160;2472388;28770820;32210233;32467162;33513363;34496238;7910017;8175689;8505288;9759724",
        "class_list": "",
        "function": "By using in-cell NMR spectroscopy study described the dynamic membrane association of rat VAMP2 SNARE motif in mammalian cells, and the structural change of VAMP2 upon the change of intracellular lipis. In contrast to the non-raft region, the membrane region of cholesterol-rich lipid raft markedly weakens the membrane association of VAMP2 SNARE motif, which releases the SNARE motif and facilitates the SNARE assembly. Publication Status: Online-Only, [RefSeq, PubMed]; Interneuronal exchange and functional integration of synaptobrevin via extracellular vesicles., [RefSeq, PubMed]; PI(4,5)P2-dependent regulation of exocytosis by amisyn, the vertebrate-specific competitor of synaptobrevin 2., [RefSeq, PubMed]; SNAREs (soluble N-ethylmaleimide-sensitive factor-attachment protein receptors) are essential proteins for intracellular membrane fusion. SNAREs localized on opposing membranes assemble to form a trans-SNARE complex, an extended, parallel four-helix bundle whose assembly releases energy that drives membrane fusion. The core SNARE complex typically consists of four alpha-helical domains, three from target membrane SNAREs (t-SNAREs) and one from a vesicle SNARE (v-SNARE) (PubMed:12496247, PubMed:19690160, PubMed:9759724). VAMP2 is a v-SNARE assembling into a SNARE complex with the t-SNAREs SNAP25 and STX1A to mediate the fusion of synaptic vesicles with the presynaptic plasma membrane in neurotransmitter release (PubMed:1331807). Also functions in compensatory endocytosis for synaptic vesicle recycling (By similarity). In adipocytes, it is involved in the insulin-dependent exocytosis of GLUT4 storage vesicles (By similarity). Independently of its SNARE activity, it could modulate the gating characteristics of the delayed rectifier voltage-dependent potassium channel KCNB1 (PubMed:19690160)., [UniProtKB, PubMed, UniProtKB, PubMed, PubMed, PubMed]; The vSNAREs VAMP2 and VAMP4 control recycling and intracellular sorting of post-synaptic receptors in neuronal dendrites., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "Q64357",
        "ec_number_list": [],
        "go_molecular_function": "GO:0060090 molecular adaptor activity;GO:0005516 calmodulin binding;GO:0005543 phospholipid binding;GO:0042802 identical protein binding;GO:0048306 calcium-dependent protein binding",
        "go_cellular_component": "GO:0070032 synaptobrevin 2-SNAP-25-syntaxin-1a-complexin I complex;GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0014069 postsynaptic density",
        "go_biological_process": "GO:1902259 regulation of delayed rectifier potassium channel activity;GO:0015031 protein transport;GO:0032869 cellular response to insulin stimulus;GO:0045055 regulated exocytosis;GO:0090316 positive regulation of intracellular protein transport",
        "synthesized_glycan_count": 0,
        "hit_score": 1.6,
        "record_id": "P63045-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q5FVR2-1",
        "uniprot_id": [
            {
                "id": "TYPH_RAT",
                "url": "https://www.uniprot.org/uniprot/Q5FVR2",
                "type": "external"
            }
        ],
        "mass": 49901.0,
        "length": 476,
        "protein_name": "Thymidine phosphorylase",
        "gene_name": "Sco2; Tymp",
        "organism": "Rat",
        "refseq_name": "thymidine phosphorylase",
        "refseq_ac": [
            {
                "id": "NP_001012122",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001012122",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Sco2; Tymp; Ecgf1; Tymp",
        "gene_names_refseq": "Ecgf1; TP; Tymp",
        "protein_names_uniprotkb": "Thymidine phosphorylase; 2.4.2.4; TP; TdRPase",
        "protein_names_refseq": "endothelial cell growth factor 1 (platelet-derived); tdRPase; thymidine phosphorylase",
        "tax_id": 10116,
        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); ductal carcinoma in situ (Disease Ontology:DOID:0060074); mitochondrial DNA depletion syndrome 1 (Disease Ontology:DOID:0080119); mitochondrial complex IV deficiency nuclear type 2 (Disease Ontology:DOID:0080357); urinary bladder cancer (Disease Ontology:DOID:11054); myopia (Disease Ontology:DOID:11830); hypertrophic cardiomyopathy (Disease Ontology:DOID:11984); endometrial cancer (Disease Ontology:DOID:1380); pancreatic cancer (Disease Ontology:DOID:1793); ovarian cancer (Disease Ontology:DOID:2394); transitional cell carcinoma (Disease Ontology:DOID:2671); teratoma (Disease Ontology:DOID:3307); pancreatic ductal carcinoma (Disease Ontology:DOID:3587); cervical squamous cell carcinoma (Disease Ontology:DOID:3744); cytochrome-c oxidase deficiency disease (Disease Ontology:DOID:3762); lung non-small cell carcinoma (Disease Ontology:DOID:3908); liver disease (Disease Ontology:DOID:409); seminoma (Disease Ontology:DOID:4440); renal cell carcinoma (Disease Ontology:DOID:4450); common bile duct neoplasm (Disease Ontology:DOID:4608); gallbladder carcinoma (Disease Ontology:DOID:4948); mitochondrial metabolism disease (Disease Ontology:DOID:700); mitochondrial encephalomyopathy (Disease Ontology:DOID:890)",
        "pathway": " (rno:315219);  (R-RNO-73614);  (R-RNO-73621)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Catalyzes the reversible phosphorolysis of thymidine. The produced molecules are then utilized as carbon and energy sources or in the rescue of pyrimidine bases for nucleotide synthesis (By similarity)., [UniProtKB]; Copper metallochaperone essential for the synthesis and maturation of cytochrome c oxidase subunit II (MT-CO2/COX2)., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 2,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 23,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "2.4.2.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.4.2.4",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0042803 protein homodimerization activity;GO:0004645 1,4-alpha-oligoglucan phosphorylase activity;GO:0009032 thymidine phosphorylase activity;GO:0005507 copper ion binding;GO:0016531 copper chaperone activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005743 mitochondrial inner membrane",
        "go_biological_process": "GO:0006213 pyrimidine nucleoside metabolic process;GO:0006206 pyrimidine nucleobase metabolic process;GO:0046074 dTMP catabolic process;GO:0006878 intracellular copper ion homeostasis;GO:0008535 respiratory chain complex IV assembly",
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    },
    {
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            {
                "id": "COX2_RAT",
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            }
        ],
        "mass": 25928.0,
        "length": 227,
        "protein_name": "Cytochrome c oxidase subunit 2",
        "gene_name": "Mt-co2",
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        "refseq_name": "cytochrome c oxidase subunit II",
        "refseq_ac": [
            {
                "id": "YP_665632",
                "url": "https://www.ncbi.nlm.nih.gov/protein/YP_665632",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Mt-co2; COX2; Coii; Mtco2",
        "gene_names_refseq": "COII; COX2",
        "protein_names_uniprotkb": "Cytochrome c oxidase subunit 2; 7.1.1.9; Cytochrome c oxidase polypeptide II",
        "protein_names_refseq": "cytochrome c oxidase subunit II",
        "tax_id": 10116,
        "disease": "colorectal carcinoma (Disease Ontology:DOID:0080199); stomach cancer (Disease Ontology:DOID:10534); Huntington's disease (Disease Ontology:DOID:12858); type 2 diabetes mellitus (Disease Ontology:DOID:9352); acute myocardial infarction (Disease Ontology:DOID:9408)",
        "pathway": " (rno:26198);  (R-RNO-5419276);  (R-RNO-5628897);  (R-RNO-611105);  (R-RNO-9707564);  (R-RNO-9864848)",
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        "publication_id_list": "1848093;22673903;2504926;6091655;6285344;7981121",
        "class_list": "",
        "function": "Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane transport and the ATP synthase. Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Electrons originating from reduced cytochrome c in the intermembrane space (IMS) are transferred via the dinuclear copper A center (CU(A)) of subunit 2 and heme A of subunit 1 to the active site in subunit 1, a binuclear center (BNC) formed by heme A3 and copper B (CU(B)). The BNC reduces molecular oxygen to 2 water molecules using 4 electrons from cytochrome c in the IMS and 4 protons from the mitochondrial matrix., [UniProtKB, UniProtKB]",
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        "secondary_ac_list": "Q37738;Q80WI7",
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            {
                "id": "3.1.1.29",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.29",
                "type": "external"
            },
            {
                "id": "7.1.1.9",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.1.1.9",
                "type": "external"
            },
            {
                "id": "7.1.1.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.1.1.2",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0016491 oxidoreductase activity;GO:0005507 copper ion binding;GO:0004129 cytochrome-c oxidase activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0031966 mitochondrial membrane;GO:0045277 respiratory chain complex IV",
        "go_biological_process": "GO:0042773 ATP synthesis coupled electron transport;GO:0045471 response to ethanol;GO:0001666 response to hypoxia;GO:0045907 positive regulation of vasoconstriction;GO:0007595 lactation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "P00406-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q5BJK8-1",
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            {
                "id": "GOLI4_RAT",
                "url": "https://www.uniprot.org/uniprot/Q5BJK8",
                "type": "external"
            }
        ],
        "mass": 76597.0,
        "length": 653,
        "protein_name": "Golgi integral membrane protein 4",
        "gene_name": "Golim4",
        "organism": "Rat",
        "refseq_name": "Golgi integral membrane protein 4 isoform 2",
        "refseq_ac": [
            {
                "id": "NP_001386398",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001386398",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Golim4; Gimpc; Golph4",
        "gene_names_refseq": "Golim4; Golph4",
        "protein_names_uniprotkb": "Golgi integral membrane protein 4; GIMPc; Golgi integral membrane protein, cis; Golgi phosphoprotein 4",
        "protein_names_refseq": "GIMPc; Golgi integral membrane protein 4 isoform 2; golgi integral membrane protein, cis; golgi phosphoprotein 4",
        "tax_id": 10116,
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        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus;GO:0016020 membrane;GO:0010008 endosome membrane;GO:0032580 Golgi cisterna membrane",
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    },
    {
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            {
                "id": "A0A8I6AAL4_RAT",
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        ],
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        "protein_name": "Cilia- and flagella-associated protein HOATZ",
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            {
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        ],
        "gene_names_uniprotkb": "Hoatz; LOC100359479",
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        "protein_names_uniprotkb": "Cilia- and flagella-associated protein HOATZ",
        "protein_names_refseq": "cilia- and flagella-associated protein HOATZ isoform X1",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005929 cilium",
        "go_biological_process": "GO:0060271 cilium assembly;GO:0007283 spermatogenesis;GO:0030317 flagellated sperm motility;GO:0035082 axoneme assembly",
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    },
    {
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        ],
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Guanidinoacetate N-methyltransferase; 2.1.1.2",
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        "tax_id": 10116,
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        "function": "Converts guanidinoacetate to creatine, using S-adenosylmethionine as the methyl donor. Important in nervous system development., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.2",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0030731 guanidinoacetate N-methyltransferase activity;GO:0042802 identical protein binding;GO:0008757 S-adenosylmethionine-dependent methyltransferase activity;GO:0008168 methyltransferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:1990402 embryonic liver development;GO:0007283 spermatogenesis;GO:0040014 regulation of multicellular organism growth;GO:0009887 animal organ morphogenesis;GO:0032259 methylation",
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    },
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        ],
        "mass": 15979.0,
        "length": 147,
        "protein_name": "Hemoglobin subunit beta-1",
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        "refseq_name": "hemoglobin subunit beta-1",
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            {
                "id": "NP_150237",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_150237",
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            }
        ],
        "gene_names_uniprotkb": "Hbb",
        "gene_names_refseq": "Hbb-b1; Hbb",
        "protein_names_uniprotkb": "Hemoglobin subunit beta-1; Beta-1-globin; Hemoglobin beta chain, major-form; Hemoglobin beta-1 chain",
        "protein_names_refseq": "III beta-1 globin; III beta-2 globin; beta-1-globin; hemoglobin beta chain complex; hemoglobin beta chain, major-form; hemoglobin beta-1 chain; hemoglobin subunit beta-1; hemoglobin subunit beta; hemoglobin, beta",
        "tax_id": 10116,
        "disease": "autosomal dominant beta thalassemia (Disease Ontology:DOID:0080770); delta beta-thalassemia (Disease Ontology:DOID:0080773); sickle cell disease (Disease Ontology:DOID:0081445); Heinz body anemia (Disease Ontology:DOID:0111363); familial erythrocytosis 6 (Disease Ontology:DOID:0111632); sickle cell anemia (Disease Ontology:DOID:10923); alpha thalassemia (Disease Ontology:DOID:1099); beta thalassemia (Disease Ontology:DOID:12241); malaria (Disease Ontology:DOID:12365); Parkinson's disease (Disease Ontology:DOID:14330); acute chest syndrome (Disease Ontology:DOID:1584); anemia (Disease Ontology:DOID:2355); hemoglobin C disease (Disease Ontology:DOID:2859); hemoglobinopathy (Disease Ontology:DOID:2860); congenital hemolytic anemia (Disease Ontology:DOID:589); polycythemia (Disease Ontology:DOID:8432)",
        "pathway": " (rno:24440);  (R-RNO-1237044);  (R-RNO-1247673);  (R-RNO-2168880);  (R-RNO-6798695);  (R-RNO-9707564);  (R-RNO-9707616)",
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        "function": "Involved in oxygen transport from the lung to the various peripheral tissues., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "P33584",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0044877 protein-containing complex binding;GO:0030492 hemoglobin binding;GO:0020037 heme binding;GO:0031721 hemoglobin alpha binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005833 hemoglobin complex;GO:0031838 haptoglobin-hemoglobin complex",
        "go_biological_process": "GO:0006954 inflammatory response;GO:0042542 response to hydrogen peroxide;GO:0030097 hemopoiesis;GO:0042744 hydrogen peroxide catabolic process;GO:0015670 carbon dioxide transport",
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    {
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        ],
        "mass": 14119.0,
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        "protein_name": "Histone H2A type 1-E",
        "gene_name": "",
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            {
                "id": "NP_001302421",
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        ],
        "gene_names_uniprotkb": "",
        "gene_names_refseq": "H2A.1; Hist1h2ah",
        "protein_names_uniprotkb": "Histone H2A type 1-E",
        "protein_names_refseq": "histone H2A type 1-E; histone cluster 1, H2ah",
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        "pathway": " (rno:103690190);  (rno:502125);  (R-RNO-3214815);  (R-RNO-3214858);  (R-RNO-5689603);  (R-RNO-5689880);  (R-RNO-5689901)",
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        "publication_id_list": "1268188;19343714;21239733",
        "class_list": "",
        "function": "Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling., [UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0019899 enzyme binding;GO:0046982 protein heterodimerization activity;GO:0030527 structural constituent of chromatin",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0070062 extracellular exosome;GO:0000786 nucleosome",
        "go_biological_process": "GO:0008285 negative regulation of cell population proliferation;GO:0031507 heterochromatin formation",
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        "hit_score": 0.4,
        "record_id": "P0C170-1",
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        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P11517-1",
        "uniprot_id": [
            {
                "id": "HBB2_RAT",
                "url": "https://www.uniprot.org/uniprot/P11517",
                "type": "external"
            }
        ],
        "mass": 15982.0,
        "length": 147,
        "protein_name": "Hemoglobin subunit beta-2",
        "gene_name": "",
        "organism": "Rat",
        "refseq_name": "hemoglobin subunit beta-2",
        "refseq_ac": [
            {
                "id": "NP_001104739",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001104739",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "",
        "gene_names_refseq": "Hbb-bs; Hbb-bt",
        "protein_names_uniprotkb": "Hemoglobin subunit beta-2; Beta-2-globin; Hemoglobin beta chain, minor-form; Hemoglobin beta-2 chain",
        "protein_names_refseq": "III beta-3 globin; beta-2-globin; beta-globin; beta-hemoglobin; hemoglobin beta chain, minor-form; hemoglobin beta-2 chain; hemoglobin subunit beta-2; hemoglobin, beta adult s chain",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100134871);  (rno:120093065);  (rno:689064)",
        "pathway_count": 3,
        "publication_count": 6,
        "publication_id_list": "22673903;2587229;2748344;29393594;3357786;3453111",
        "class_list": "",
        "function": "Involved in oxygen transport from the lung to the various peripheral tissues., [UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0020037 heme binding;GO:0031721 hemoglobin alpha binding;GO:0019825 oxygen binding;GO:0005344 oxygen carrier activity",
        "go_cellular_component": "GO:0005833 hemoglobin complex;GO:0031838 haptoglobin-hemoglobin complex",
        "go_biological_process": "GO:0015670 carbon dioxide transport;GO:0048821 erythrocyte development;GO:0045646 regulation of erythrocyte differentiation;GO:0045639 positive regulation of myeloid cell differentiation;GO:0015671 oxygen transport",
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        "hit_score": 0.7,
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        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P31392-1",
        "uniprot_id": [
            {
                "id": "ACKR5_RAT",
                "url": "https://www.uniprot.org/uniprot/P31392",
                "type": "external"
            }
        ],
        "mass": 45188.0,
        "length": 398,
        "protein_name": "Atypical chemokine receptor 5",
        "gene_name": "Ackr5",
        "organism": "Rat",
        "refseq_name": "atypical chemokine receptor 5",
        "refseq_ac": [
            {
                "id": "NP_445754",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_445754",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ackr5; Admr; Gpr182",
        "gene_names_refseq": "Ackr5; Admr; Gpr182",
        "protein_names_uniprotkb": "Atypical chemokine receptor 5; G protein-coupled receptor 182; G10D; NOW",
        "protein_names_refseq": "G protein-coupled receptor 182; G10D; NOW; adrenomedullin receptor; atypical chemokine receptor 5",
        "tax_id": 10116,
        "disease": "pulmonary hypertension (Disease Ontology:DOID:6432)",
        "pathway": " (rno:29307)",
        "pathway_count": 1,
        "publication_count": 14,
        "publication_id_list": "11676473;11967020;17898545;17982694;18401014;20431304;21454685;22673903;25061099;29393594;7592696;8382168;8390839;9535752",
        "class_list": "",
        "function": "Adrenomedullin inhibits CaCl(2)-induced contraction, without affecting calcium influx, through a CGRP(8-37)-sensitive receptor, but not using the cyclic adenosine monophosphate pathway, probably through activation of protein phosphatases., [RefSeq, PubMed]; Atypical chemokine receptor that regulates chemokine levels and localization through chemokine binding, independently of activating classical ligand-induced signaling pathways such as G protein activation and Ca(2+) mobilization. Instead, it mediates chemokine sequestration, transport, or internalization to control their availability. Acts as a scavenger for a broad range of chemokines from CXC, CC and XC chemokine ligand families including CXCL9, CXCL10, CXCL12, CXCL13, CXCL11, CXCL14, CCL1, CCL11, CCL19, CCL25, CCL28 and XCL1. Is the only atypical receptor for chemokines CXCL13 and CCL28. Has a strong constitutive association with beta-arrestins, which is essential for intracellular receptor trafficking and chemokine scavenging, and occurs independently of ligand binding. Cooperates with ACKR3 and ACKR4 in regulating serum levels of CXCL12 and CCL19, respectively (By similarity). Acts as an important modulator of cellular immunity (By similarity)., [UniProtKB, UniProtKB, UniProtKB]; Data indicate that the adrenomedullin receptor subtypes AM1-R and AM2-R are up-regulated in enucleated adrenals, and that this effect depends on the increased local production of AM., [RefSeq, PubMed]; Data suggest that stimulation of adrenomedullin/adrenomedullin receptor signaling enhances trophoblast stem cell differentiation; this stimulation involves CALCRL (calcitonin receptor-like receptor) and RAMP2 (receptor activity-modifying protein 2)., [RefSeq, PubMed]; Nitric oxide increases adrenomedullin receptor function in rat mesangial cells, [RefSeq, PubMed]; Study demonstrates that glomerular gene expression of ADM and its receptors are downregulated during anti-Thy1 glomerulonephritis, [RefSeq, PubMed]; The increase in functional adrenomedullin receptor during phenotypic change may in part contribute to the development of vascular lesions, [RefSeq, PubMed]; The presence of ADM and the gene expression of ADM and its receptor components in the female reproductive system suggest a paracrine effect of ADM on ovarian steroidogenesis., [RefSeq, PubMed]",
        "predicted_glycosites": 2,
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        "missing_score": 10000,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "A0A8I6AT50;A1L1I2;A6HQX3;D3ZC02;Q64166",
        "ec_number_list": [],
        "go_molecular_function": "GO:0019957 C-C chemokine binding;GO:0019958 C-X-C chemokine binding;GO:0001605 adrenomedullin receptor activity;GO:0140319 receptor decoy activity",
        "go_cellular_component": "GO:0005768 endosome;GO:0005886 plasma membrane;GO:0010008 endosome membrane",
        "go_biological_process": "GO:0001666 response to hypoxia",
        "synthesized_glycan_count": 0,
        "hit_score": 1.5,
        "record_id": "P31392-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000010001.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q64298-1",
        "uniprot_id": [
            {
                "id": "MCSP_RAT",
                "url": "https://www.uniprot.org/uniprot/Q64298",
                "type": "external"
            }
        ],
        "mass": 15148.0,
        "length": 145,
        "protein_name": "Sperm mitochondrial-associated cysteine-rich protein",
        "gene_name": "Smcp",
        "organism": "Rat",
        "refseq_name": "sperm mitochondrial-associated cysteine-rich protein",
        "refseq_ac": [
            {
                "id": "NP_113724",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_113724",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Smcp; Mcsp; Mcs",
        "gene_names_refseq": "Mcsp; Mcs; Smcp",
        "protein_names_uniprotkb": "Sperm mitochondrial-associated cysteine-rich protein",
        "protein_names_refseq": "sperm mitochondrial-associated cysteine-rich protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:24899)",
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        "publication_count": 5,
        "publication_id_list": "16159880;19423663;22673903;8634143;8916043",
        "class_list": "",
        "function": "Involved in sperm motility. Its absence is associated with genetic background dependent male infertility. Infertility may be due to reduced sperm motility in the female reproductive tract and inability to penetrate the oocyte zona pellucida (By similarity)., [UniProtKB, UniProtKB]; PHGPx interacts with SMCP; the cysteine motif of PHGPx is a new substrate of the selenoperoxidase, [RefSeq, PubMed]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 2,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0031966 mitochondrial membrane",
        "go_biological_process": "GO:0007339 binding of sperm to zona pellucida;GO:0030317 flagellated sperm motility;GO:0007341 penetration of zona pellucida",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "Q64298-1",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q9R1K8-1",
        "uniprot_id": [
            {
                "id": "GRP1_RAT",
                "url": "https://www.uniprot.org/uniprot/Q9R1K8",
                "type": "external"
            }
        ],
        "mass": 90245.0,
        "length": 795,
        "protein_name": "RAS guanyl-releasing protein 1",
        "gene_name": "Rasgrp1",
        "organism": "Rat",
        "refseq_name": "RAS guanyl-releasing protein 1",
        "refseq_ac": [
            {
                "id": "NP_062084",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_062084",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Rasgrp1; Rasgrp",
        "gene_names_refseq": "Rasgrp1; Rasgrp",
        "protein_names_uniprotkb": "RAS guanyl-releasing protein 1; CalDAG-GEFII; Calcium and DAG-regulated guanine nucleotide exchange factor II; Ras guanyl-releasing protein",
        "protein_names_refseq": "CalDAG-GEF1; RAS guanyl releasing protein 1 (calcium and DAG-regulated); RAS guanyl-releasing protein 1; calDAG-GEFII; calcium and DAG-regulated guanine nucleotide exchange factor II",
        "tax_id": 10116,
        "disease": "immunodeficiency 64 (Disease Ontology:DOID:0111980); systemic lupus erythematosus (Disease Ontology:DOID:9074)",
        "pathway": " (rno:29434);  (R-RNO-1169092);  (R-RNO-354192);  (R-RNO-392517);  (R-RNO-5673001)",
        "pathway_count": 5,
        "publication_count": 8,
        "publication_id_list": "10779365;11279364;11738253;12626538;15064353;22673903;9582122;9789079",
        "class_list": "",
        "function": "Functions as a calcium- and diacylglycerol (DAG)-regulated nucleotide exchange factor specifically activating Ras through the exchange of bound GDP for GTP (PubMed:9582122, PubMed:9789079). Activates the Erk/MAP kinase cascade. Regulates T-cell/B-cell development, homeostasis and differentiation by coupling T-lymphocyte/B-lymphocyte antigen receptors to Ras. Regulates NK cell cytotoxicity and ITAM-dependent cytokine production by activation of Ras-mediated ERK and JNK pathways (By similarity). Functions in mast cell degranulation and cytokine secretion, regulating FcERI-evoked allergic responses. May also function in differentiation of other cell types. Proto-oncogene, which promotes T-cell lymphomagenesis when its expression is deregulated (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "O88469",
        "ec_number_list": [],
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0042802 identical protein binding;GO:0005509 calcium ion binding;GO:0005085 guanyl-nucleotide exchange factor activity;GO:0031210 phosphatidylcholine binding",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0051896 regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0046579 positive regulation of Ras protein signal transduction;GO:0001934 positive regulation of protein phosphorylation;GO:0030154 cell differentiation;GO:0002437 inflammatory response to antigenic stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.9,
        "record_id": "Q9R1K8-1",
        "record_type": "protein",
        "filter_code": "0000000.0100111.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "Q9Z1B2-1",
        "uniprot_id": [
            {
                "id": "GSTM5_RAT",
                "url": "https://www.uniprot.org/uniprot/Q9Z1B2",
                "type": "external"
            }
        ],
        "mass": 26629.0,
        "length": 225,
        "protein_name": "Glutathione S-transferase Mu 5",
        "gene_name": "Gstm5",
        "organism": "Rat",
        "refseq_name": "glutathione S-transferase Mu 5",
        "refseq_ac": [
            {
                "id": "NP_742035",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_742035",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Gstm5",
        "gene_names_refseq": "Gstm3; Gstm5",
        "protein_names_uniprotkb": "Glutathione S-transferase Mu 5; 2.5.1.18; GST class-mu 5",
        "protein_names_refseq": "GST class-mu 5; glutathione S-transferase Mu 5; glutathione S-transferase mu 3",
        "tax_id": 10116,
        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652); cystic fibrosis (Disease Ontology:DOID:1485); multiple sclerosis (Disease Ontology:DOID:2377); larynx cancer (Disease Ontology:DOID:2596); asthma (Disease Ontology:DOID:2841); high grade glioma (Disease Ontology:DOID:3070); osteosarcoma (Disease Ontology:DOID:3347); meningioma (Disease Ontology:DOID:3565); macular degeneration (Disease Ontology:DOID:4448); pulmonary emphysema (Disease Ontology:DOID:9675); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:64352);  (R-RNO-156590)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "22673903;9545290",
        "class_list": "",
        "function": "Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles., [UniProtKB]",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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            {
                "id": "NP_001386034",
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        "function": "Astrocytes with TDP-43 inclusions exhibit reduced noradrenergic cAMP and Ca(2+) signaling and dysregulated cell metabolism. Publication Status: Online-Only, [RefSeq, PubMed]; C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD., [RefSeq, PubMed]; Inactivation of cGAS signaling pathway mediated by TDP-43 deficiency protects microglia from hypoxia/reoxygenation induced injury., [RefSeq, PubMed]; TDP-43 was Involved in Radiation-induced Neuronal Damage and May Not Through the BDNF/TrkB Pathway., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005726 perichromatin fibrils;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005739 mitochondrion;GO:0016607 nuclear speck",
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        "protein_name": "Oxysterol-binding protein",
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            {
                "id": "XP_008761156",
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        "protein_name": "Olfactory receptor",
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        "gene_names_refseq": "Or1e1fl1",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "function": "Authors determined that transcytosis of three classes of newly synthesized apical residents showed similar responses to rab17 mutant expression, indicating that rab17 is a general component of the transcytotic machinery required for apically destined vesicle docking and fusion., [RefSeq, PubMed]; These data suggest that Rab17 mediates the dendritic trafficking of Syntaxin-4 to selectively regulate dendritic surface insertion of GluK2-containing KARs in rat hippocampal neurons., [RefSeq, PubMed]",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.31",
                "type": "external"
            },
            {
                "id": "2.3.2.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.23",
                "type": "external"
            },
            {
                "id": "2.3.2.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
                "type": "external"
            },
            {
                "id": "2.3.2.34",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.34",
                "type": "external"
            },
            {
                "id": "2.3.2.24",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.24",
                "type": "external"
            },
            {
                "id": "2.3.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.-",
                "type": "external"
            },
            {
                "id": "2.3.2.25",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.25",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity;GO:0004842 ubiquitin-protein transferase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005768 endosome;GO:0005829 cytosol;GO:0016020 membrane;GO:0005764 lysosome",
        "go_biological_process": "GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0070936 protein K48-linked ubiquitination;GO:0034145 positive regulation of toll-like receptor 4 signaling pathway;GO:0160177 positive regulation of autophagosome-lysosome fusion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZUZ1-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "F7FAJ9-1",
        "uniprot_id": [
            {
                "id": "F7FAJ9_RAT",
                "url": "https://www.uniprot.org/uniprot/F7FAJ9",
                "type": "external"
            }
        ],
        "mass": 39660.0,
        "length": 355,
        "protein_name": "Carbonic anhydrase",
        "gene_name": "Ca12",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Ca12; Car12",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Carbonic anhydrase; 4.2.1.1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "colorectal adenocarcinoma (Disease Ontology:DOID:0050861); colorectal carcinoma (Disease Ontology:DOID:0080199); isolated hyperchlorhidrosis (Disease Ontology:DOID:0111371); lung cancer (Disease Ontology:DOID:1324); colon adenocarcinoma (Disease Ontology:DOID:234); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); Lynch syndrome (Disease Ontology:DOID:3883); lung non-small cell carcinoma (Disease Ontology:DOID:3908); fibrolamellar carcinoma (Disease Ontology:DOID:5015); hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (R-RNO-1475029)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Reversible hydration of carbon dioxide., [UniProtKB, UniProtKB, UniProtKB]",
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            {
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    },
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            {
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        ],
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        "length": 1884,
        "protein_name": "Proteasome adapter and scaffold protein ECM29",
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        "refseq_ac": [],
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Proteasome adapter and scaffold protein ECM29; Proteasome-associated protein ECM29 homolog",
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        "function": "Adapter/scaffolding protein that binds to the 26S proteasome, motor proteins and other compartment specific proteins. May couple the proteasome to different compartments including endosome, endoplasmic reticulum and centrosome. May play a role in ERAD and other enhanced proteolysis. Promotes proteasome dissociation under oxidative stress., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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    },
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            {
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        ],
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            {
                "id": "XP_038956357",
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        ],
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        "function": "Induces gene transcription activation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Involved in neural development, regulating the establishment of proper connectivity within the nervous system. May function as a cellular signal transducer., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Plays a role in the regulation of neuroplasticity in the limbic system. Mediates a rapid reorganization of actin- and tubulin-based cytoskeleton elements with an increase in dendritic arborization and spine density formation of neurons in the hippocampus and amygdala. Induces BDNF transcription inhibition in neurons. Activates the mitogen-activated protein (MAP) kinase 2 (MEK2) and extracellular signal-regulated kinase (ERK) cascade. Also acts as a bioactive neuroprotective peptide on limbic neurons of the brain and regulates stress-induced behavior: attenuates alkalosis-associated necrotic cell death and the effects of corticotropin-releasing factor (CRF) on c-fos/FOS induction and on the reinstatement of cocaine seeking., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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    },
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        "protein_name": "P-type phospholipid transporter",
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            {
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            }
        ],
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        "go_biological_process": "GO:0006911 phagocytosis, engulfment;GO:0007186 G protein-coupled receptor signaling pathway;GO:0007189 adenylate cyclase-activating G protein-coupled receptor signaling pathway;GO:0007584 response to nutrient;GO:0008203 cholesterol metabolic process",
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        ],
        "mass": 36902.0,
        "length": 335,
        "protein_name": "Apolipoprotein L3 like 1",
        "gene_name": "LOC120093819",
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        "protein_names_uniprotkb": "Apolipoprotein L3 like 1",
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        "disease": "kidney disease (Disease Ontology:DOID:557)",
        "pathway": " (R-RNO-2168880);  (R-RNO-381426);  (R-RNO-8957275)",
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        ],
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        "protein_name": "Eukaryotic translation initiation factor 4C",
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            {
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            }
        ],
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        "gene_names_refseq": "Eif1ax; Eif1ay; RGD1560198",
        "protein_names_uniprotkb": "Eukaryotic translation initiation factor 4C",
        "protein_names_refseq": "eukaryotic translation initiation factor 1A, X-chromosomal; eukaryotic translation initiation factor 1A, Y-linked",
        "tax_id": 10116,
        "disease": "uveal melanoma (Disease Ontology:DOID:6039)",
        "pathway": " (rno:302697);  (R-RNO-156827);  (R-RNO-72649);  (R-RNO-72689);  (R-RNO-72695);  (R-RNO-72702)",
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        "function": "Component of the 43S pre-initiation complex (43S PIC), which binds to the mRNA cap-proximal region, scans mRNA 5'-untranslated region, and locates the initiation codon. This protein enhances formation of the cap-proximal complex. Together with EIF1, facilitates scanning, start codon recognition, promotion of the assembly of 48S complex at the initiation codon (43S PIC becomes 48S PIC after the start codon is reached), and dissociation of aberrant complexes. After start codon location, together with EIF5B orients the initiator methionine-tRNA in a conformation that allows 60S ribosomal subunit joining to form the 80S initiation complex. Is released after 80S initiation complex formation, just after GTP hydrolysis by EIF5B, and before release of EIF5B. Its globular part is located in the A site of the 40S ribosomal subunit. Its interaction with EIF5 during scanning contribute to the maintenance of EIF1 within the open 43S PIC. In contrast to yeast orthologs, does not bind EIF1., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0000049 tRNA binding;GO:0003743 translation initiation factor activity",
        "go_cellular_component": "GO:0045202 synapse;GO:0016282 eukaryotic 43S preinitiation complex;GO:0033290 eukaryotic 48S preinitiation complex;GO:0043614 multi-eIF complex;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006413 translational initiation;GO:0042255 ribosome assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7EZM1-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZYW3-1",
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            {
                "id": "A0A8I5ZYW3_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A8I5ZYW3",
                "type": "external"
            }
        ],
        "mass": 50217.0,
        "length": 458,
        "protein_name": "Lymphocyte-specific protein 1",
        "gene_name": "Lsp1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Lsp1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Lymphocyte-specific protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "breast cancer (Disease Ontology:DOID:1612)",
        "pathway": "",
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        "missing_score": 10000,
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        "go_molecular_function": "GO:0003779 actin binding",
        "go_cellular_component": "",
        "go_biological_process": "GO:0007165 signal transduction;GO:0006935 chemotaxis;GO:0006952 defense response;GO:0098761 cellular response to interleukin-7",
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        "hit_score": 0.2,
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        "kg_view_protein": true
    },
    {
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            {
                "id": "A0A8L2QRU2_RAT",
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                "type": "external"
            }
        ],
        "mass": 7554.0,
        "length": 68,
        "protein_name": "Guanine nucleotide-binding protein subunit gamma",
        "gene_name": "Gng5-ps5",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Gng5-ps5; Gng5-ps3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Guanine nucleotide-binding protein subunit gamma",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "obesity (Disease Ontology:DOID:9970)",
        "pathway": "",
        "pathway_count": 0,
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        "function": "Guanine nucleotide-binding proteins (G proteins) are involved as a modulator or transducer in various transmembrane signaling systems. The beta and gamma chains are required for the GTPase activity, for replacement of GDP by GTP, and for G protein-effector interaction., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0031681 G-protein beta-subunit binding",
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        "kg_view_protein": true
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            {
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            }
        ],
        "mass": 55977.0,
        "length": 493,
        "protein_name": "Ubiquitin carboxyl-terminal hydrolase",
        "gene_name": "Usp14",
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        "refseq_name": "ubiquitin carboxyl-terminal hydrolase 14",
        "refseq_ac": [
            {
                "id": "NP_001008302",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001008302",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Usp14",
        "gene_names_refseq": "Usp14",
        "protein_names_uniprotkb": "Ubiquitin carboxyl-terminal hydrolase; 3.4.19.12",
        "protein_names_refseq": "ubiquitin carboxyl-terminal hydrolase 14; ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase); ubiquitin specific protease 14",
        "tax_id": 10116,
        "disease": "prion disease (Disease Ontology:DOID:649)",
        "pathway": " (rno:291796);  (R-RNO-5689880);  (R-RNO-9758274)",
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        "publication_id_list": "26969276;27545607;28372990",
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        "function": "Activation of proteasome degradation by IU-1, which is an inhibitor for the deubiquitinating activity of USP14, decreased only the quantity of TH molecules phosphorylated at their Ser19., [RefSeq, PubMed]; Deubiquitinating enzyme that removes conjugated ubiquitin from specific proteins to regulate different cellular processes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Mediates the development of cardiac hypertrophy by promoting GSK-3beta phosphorylation., [RefSeq, PubMed]; Pharmacologically inhibiting (with low or high IU1 concentrations) or genetically down-regulating USP14 fail to enhance proteasomal degradation of Ub-proteins or Tau in neurons., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "ec_number_list": [
            {
                "id": "3.4.19.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.19.12",
                "type": "external"
            },
            {
                "id": "2.7.11.10",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.10",
                "type": "external"
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            {
                "id": "3.4.25.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.25.1",
                "type": "external"
            },
            {
                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
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            }
        ],
        "go_molecular_function": "GO:0004866 endopeptidase inhibitor activity;GO:0070628 proteasome binding;GO:0004843 cysteine-type deubiquitinase activity;GO:0061578 K63-linked deubiquitinase activity;GO:0101005 deubiquitinase activity",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0009986 cell surface",
        "go_biological_process": "GO:0006954 inflammatory response;GO:0007268 chemical synaptic transmission;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0050920 regulation of chemotaxis;GO:2000059 negative regulation of ubiquitin-dependent protein catabolic process",
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        "kg_view_protein": true
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            {
                "id": "F7ETC0_RAT",
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            }
        ],
        "mass": 69633.0,
        "length": 626,
        "protein_name": "Sphingomyelin phosphodiesterase",
        "gene_name": "Smpd1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Smpd1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Sphingomyelin phosphodiesterase; 3.1.4.12",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Niemann-Pick disease type A (Disease Ontology:DOID:0070111); Niemann-Pick disease type B (Disease Ontology:DOID:0070112); Niemann-Pick disease (Disease Ontology:DOID:14504); Wilson disease (Disease Ontology:DOID:893)",
        "pathway": " (R-RNO-9769739);  (R-RNO-9840310)",
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        "function": "Converts sphingomyelin to ceramide. Exists as two enzymatic forms that arise from alternative trafficking of a single protein precursor, one that is targeted to the endolysosomal compartment, whereas the other is released extracellularly. However, in response to various forms of stress, lysosomal exocytosis may represent a major source of the secretory form., [UniProtKB, UniProtKB]; In the lysosomes, converts sphingomyelin to ceramide. Plays an important role in the export of cholesterol from the intraendolysosomal membranes. Also has phospholipase C activities toward 1,2-diacylglycerolphosphocholine and 1,2-diacylglycerolphosphoglycerol. Modulates stress-induced apoptosis through the production of ceramide., [UniProtKB, UniProtKB]; This form is generated following cleavage by CASP7 in the extracellular milieu in response to bacterial infection. It shows increased ability to convert sphingomyelin to ceramide and promotes plasma membrane repair. Plasma membrane repair by ceramide counteracts the action of gasdermin-D (GSDMD) perforin (PRF1) pores that are formed in response to bacterial infection., [UniProtKB, UniProtKB]; When secreted, modulates cell signaling with its ability to reorganize the plasma membrane by converting sphingomyelin to ceramide. Secreted form is increased in response to stress and inflammatory mediators such as IL1B, IFNG or TNF as well as upon infection with bacteria and viruses. Produces the release of ceramide in the outer leaflet of the plasma membrane playing a central role in host defense. Ceramide reorganizes these rafts into larger signaling platforms that are required to internalize P.aeruginosa, induce apoptosis and regulate the cytokine response in infected cells. In wounded cells, the lysosomal form is released extracellularly in the presence of Ca(2+) and promotes endocytosis and plasma membrane repair., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "ec_number_list": [
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.4.12",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0004767 sphingomyelin phosphodiesterase activity;GO:0016798 hydrolase activity, acting on glycosyl bonds;GO:0061750 acid sphingomyelin phosphodiesterase activity;GO:0034480 phosphatidylcholine phospholipase C activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005768 endosome;GO:0005811 lipid droplet;GO:0005886 plasma membrane;GO:0005764 lysosome",
        "go_biological_process": "GO:0001778 plasma membrane repair;GO:0008203 cholesterol metabolic process;GO:0034612 response to tumor necrosis factor;GO:0043065 positive regulation of apoptotic process;GO:0046513 ceramide biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7ETC0-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
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                "url": "https://www.uniprot.org/uniprot/F7EWF8",
                "type": "external"
            }
        ],
        "mass": 102333.0,
        "length": 897,
        "protein_name": "Anaphase-promoting complex subunit 2",
        "gene_name": "Anapc2",
        "organism": "Rat",
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        "refseq_ac": [],
        "gene_names_uniprotkb": "Anapc2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Anaphase-promoting complex subunit 2",
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        "tax_id": 10116,
        "disease": "aplastic anemia (Disease Ontology:DOID:12449); primary angle-closure glaucoma (Disease Ontology:DOID:1405); lung adenocarcinoma (Disease Ontology:DOID:3910); lung adenoma (Disease Ontology:DOID:5386); acute myeloid leukemia (Disease Ontology:DOID:9119)",
        "pathway": " (R-RNO-141430);  (R-RNO-174048);  (R-RNO-174084);  (R-RNO-174154);  (R-RNO-174178);  (R-RNO-174184);  (R-RNO-176407);  (R-RNO-176408);  (R-RNO-176412);  (R-RNO-179409);  (R-RNO-2467813);  (R-RNO-2559582);  (R-RNO-68867);  (R-RNO-69017);  (R-RNO-983168)",
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        "missing_score": 10000,
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        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005680 anaphase-promoting complex",
        "go_biological_process": "GO:0010629 negative regulation of gene expression;GO:0051301 cell division;GO:0031145 anaphase-promoting complex-dependent catabolic process;GO:0031915 positive regulation of synaptic plasticity;GO:0045773 positive regulation of axon extension",
        "synthesized_glycan_count": 0,
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            {
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        "length": 163,
        "protein_name": "Myb/SANT DNA binding domain containing 5",
        "gene_name": "Msantd5",
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        "refseq_name": "Myb/SANT DNA binding domain containing 5",
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            {
                "id": "NP_001017472",
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            }
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        "protein_names_refseq": "Myb/SANT DNA binding domain containing 5",
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    {
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            {
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            }
        ],
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        "protein_name": "Tektin-5",
        "gene_name": "Tekt5",
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            {
                "id": "NP_001014246",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001014246",
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            }
        ],
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            {
                "id": "NP_001099503",
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        "go_cellular_component": "GO:0005615 extracellular space;GO:0005764 lysosome;GO:0097208 alveolar lamellar body",
        "go_biological_process": "GO:0006508 proteolysis;GO:0043129 surfactant homeostasis;GO:0033619 membrane protein proteolysis",
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        ],
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                "id": "M0RCG9_RAT",
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                "type": "external"
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        ],
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        "protein_name": "RNA polymerase II subunit I",
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        "pathway": " (rno:292778);  (R-RNO-112382);  (R-RNO-113418);  (R-RNO-5578749);  (R-RNO-674695);  (R-RNO-6781823);  (R-RNO-6782135);  (R-RNO-6782210);  (R-RNO-6796648);  (R-RNO-6803529);  (R-RNO-6807505);  (R-RNO-72086);  (R-RNO-72163);  (R-RNO-72165);  (R-RNO-72203);  (R-RNO-73776);  (R-RNO-73779);  (R-RNO-75953);  (R-RNO-75955);  (R-RNO-76042);  (R-RNO-77075);  (R-RNO-9018519);  (R-RNO-9770562)",
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        "function": "DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0003899 DNA-directed RNA polymerase activity;GO:0008270 zinc ion binding;GO:0003676 nucleic acid binding",
        "go_cellular_component": "GO:0005665 RNA polymerase II, core complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus",
        "go_biological_process": "GO:0006367 transcription initiation at RNA polymerase II promoter;GO:0006368 transcription elongation by RNA polymerase II;GO:0001193 maintenance of transcriptional fidelity during transcription elongation by RNA polymerase II;GO:0006366 transcription by RNA polymerase II;GO:0006283 transcription-coupled nucleotide-excision repair",
        "synthesized_glycan_count": 0,
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    },
    {
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            {
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        ],
        "mass": 73605.0,
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        "protein_name": "Kinetochore protein NDC80",
        "gene_name": "Ndc80",
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        "refseq_name": "",
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        "gene_names_uniprotkb": "Ndc80",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Kinetochore protein NDC80",
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        "tax_id": 10116,
        "disease": "stomach cancer (Disease Ontology:DOID:10534); cancer (Disease Ontology:DOID:162); lung non-small cell carcinoma (Disease Ontology:DOID:3908); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (R-RNO-141430);  (R-RNO-141444);  (R-RNO-2467813);  (R-RNO-2500257);  (R-RNO-5663220);  (R-RNO-68877);  (R-RNO-9648025)",
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        "function": "Acts as a component of the essential kinetochore-associated NDC80 complex, which is required for chromosome segregation and spindle checkpoint activity. Required for kinetochore integrity and the organization of stable microtubule binding sites in the outer plate of the kinetochore. The NDC80 complex synergistically enhances the affinity of the SKA1 complex for microtubules and may allow the NDC80 complex to track depolymerizing microtubules. Plays a role in chromosome congression and is essential for the end-on attachment of the kinetochores to spindle microtubules., [UniProtKB, UniProtKB]",
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        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Miller-Dieker lissencephaly syndrome (Disease Ontology:DOID:0060469); diphthamide deficiency syndrome (Disease Ontology:DOID:0070476); diphthamide deficiency syndrome 1 (Disease Ontology:DOID:0070477)",
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            {
                "id": "2.5.1.108",
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            }
        ],
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0051536 iron-sulfur cluster binding;GO:0090560 2-(3-amino-3-carboxypropyl)histidine synthase activity",
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        "go_biological_process": "GO:0008283 cell population proliferation;GO:0017183 protein histidyl modification to diphthamide",
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    {
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            {
                "id": "A0A0G2K6D8_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A0G2K6D8",
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        ],
        "mass": 36028.0,
        "length": 319,
        "protein_name": "NAD-dependent protein lipoamidase sirtuin-4, mitochondrial",
        "gene_name": "Sirt4",
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        "refseq_name": "NAD-dependent protein lipoamidase sirtuin-4, mitochondrial",
        "refseq_ac": [
            {
                "id": "NP_001100617",
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            }
        ],
        "gene_names_uniprotkb": "Sirt4; SIRT4",
        "gene_names_refseq": "Sirt4",
        "protein_names_uniprotkb": "NAD-dependent protein lipoamidase sirtuin-4, mitochondrial; 2.3.1.-; 2.3.1.286; 2.4.2.-; NAD-dependent ADP-ribosyltransferase sirtuin-4; NAD-dependent protein biotinylase sirtuin-4; NAD-dependent protein deacetylase sirtuin-4; Regulatory protein SIR2 homolog 4; SIR2-like protein 4",
        "protein_names_refseq": "NAD-dependent ADP-ribosyltransferase sirtuin-4; NAD-dependent protein deacetylase sirtuin-4; NAD-dependent protein lipoamidase sirtuin-4, mitochondrial",
        "tax_id": 10116,
        "disease": "metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208)",
        "pathway": " (rno:304539)",
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        "function": "Acts as NAD-dependent protein lipoamidase, biotinylase, deacetylase and ADP-ribosyl transferase. Catalyzes more efficiently removal of lipoyl- and biotinyl- than acetyl-lysine modifications. Inhibits the pyruvate dehydrogenase complex (PDH) activity via the enzymatic hydrolysis of the lipoamide cofactor from the E2 component, DLAT, in a phosphorylation-independent manner. Catalyzes the transfer of ADP-ribosyl groups onto target proteins, including mitochondrial GLUD1, inhibiting GLUD1 enzyme activity. Acts as a negative regulator of mitochondrial glutamine metabolism by mediating mono ADP-ribosylation of GLUD1: expressed in response to DNA damage and negatively regulates anaplerosis by inhibiting GLUD1, leading to block metabolism of glutamine into tricarboxylic acid cycle and promoting cell cycle arrest. In response to mTORC1 signal, SIRT4 expression is repressed, promoting anaplerosis and cell proliferation. Acts as a tumor suppressor. Also acts as a NAD-dependent protein deacetylase: mediates deacetylation of 'Lys-471' of MLYCD, inhibiting its activity, thereby acting as a regulator of lipid homeostasis. Does not seem to deacetylate PC. Controls fatty acid oxidation by inhibiting PPARA transcriptional activation. Impairs SIRT1-PPARA interaction probably through the regulation of NAD(+) levels. Down-regulates insulin secretion., [UniProtKB, HAMAP]; Physiological profile regulation during weight gain and loss by ovariectomized females: importance of SIRT1 and SIRT4., [RefSeq, PubMed]; SIRT4 regulates rat dental papilla cell differentiation by promoting mitochondrial functions., [RefSeq, PubMed]; The association between recovery of olfactory function and the increase in bulbar SIRT1 and SIRT4 expression, is reported., [RefSeq, PubMed]",
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                "id": "2.3.1.-",
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            {
                "id": "2.3.1.286",
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            }
        ],
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0070403 NAD+ binding;GO:0003950 NAD+ poly-ADP-ribosyltransferase activity;GO:0061690 lipoamidase activity;GO:0034979 NAD-dependent protein lysine deacetylase activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0005759 mitochondrial matrix",
        "go_biological_process": "GO:0046322 negative regulation of fatty acid oxidation;GO:0046889 positive regulation of lipid biosynthetic process;GO:0071456 cellular response to hypoxia;GO:0006974 DNA damage response;GO:0046676 negative regulation of insulin secretion",
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        "protein_name": "Leucine rich repeat containing 45",
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        ],
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        "protein_name": "HMG box domain-containing protein",
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        "protein_names_refseq": "upstream-binding factor 1-like protein 1",
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        "go_molecular_function": "GO:0001164 RNA polymerase I core promoter sequence-specific DNA binding;GO:0001181 RNA polymerase I general transcription initiation factor activity",
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        ],
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        "protein_name": "Attractin-like protein 1",
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        "organism": "Rat",
        "refseq_name": "attractin like 1 isoform 1",
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            {
                "id": "NP_001418043",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001418043",
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        ],
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        "protein_names_uniprotkb": "Attractin-like protein 1",
        "protein_names_refseq": "attractin like 1 isoform 1; attractin-like protein 1",
        "tax_id": 10116,
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        "pathway": " (R-RNO-163125)",
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        "class_list": "",
        "function": "May play a role in melanocortin signaling pathways that regulate energy homeostasis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "Trafficking kinesin protein 1",
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        "disease": "developmental and epileptic encephalopathy 68 (Disease Ontology:DOID:0112204); neurodegenerative disease (Disease Ontology:DOID:1289); Stiff-Person syndrome (Disease Ontology:DOID:13366)",
        "pathway": " (rno:316085);  (R-RNO-9013419)",
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        "function": "Proposed effector of Rab5. Binds to phosphatidylinositol 3-phosphate (PI[3]P). Involved in homotypic early endosome fusion and to a lesser extent in heterotypic fusion of clathrin-coated vesicles with early endosomes. Involved in macropinocytosis; the function is dependent on Rab5-GTP. Required for correct endosomal localization. Involved in the internalization and trafficking of activated tyrosine kinase receptors such as PDGFRB. Regulates the subcellular localization of the retromer complex in a EHD1-dependent manner. Involved in endosome-to-Golgi transport and biosynthetic transport to late endosomes and lysosomes indicative for a regulation of retromer complex-mediated retrograde transport. Required for podocyte migration., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_refseq": "catalytic phosphatidylinositol 3-kinase delta; phosphatidylinositol 3-kinase catalytic delta polypeptide; phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform isoform b; phosphoinositide-3-kinase, catalytic, delta polypeptide",
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        "disease": "immunodeficiency 14 (Disease Ontology:DOID:0111936); heart disease (Disease Ontology:DOID:114); endometrial cancer (Disease Ontology:DOID:1380); alcohol use disorder (Disease Ontology:DOID:1574); cancer (Disease Ontology:DOID:162); glioblastoma (Disease Ontology:DOID:3068); high grade glioma (Disease Ontology:DOID:3070); glucose metabolism disease (Disease Ontology:DOID:4194); schizophrenia (Disease Ontology:DOID:5419); colorectal cancer (Disease Ontology:DOID:9256); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": " (rno:366508);  (R-RNO-1257604);  (R-RNO-1660499);  (R-RNO-389357);  (R-RNO-512988);  (R-RNO-6811558);  (R-RNO-8853659);  (R-RNO-9027276);  (R-RNO-912526);  (R-RNO-912631);  (R-RNO-983695);  (R-RNO-9927354)",
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        "function": "Inhibition of mitochondrial fission alters neo-intimal hyperplasia via PI3K/Akt signaling in arteriovenous fistulas., [RefSeq, PubMed]; Upregulation of SEMP1 Contributes to Improving the Biological Functions of Trophoblast via the PI3K/AKT Pathway in Preeclampsia., [RefSeq, PubMed]",
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        ],
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        "protein_name": "Protein eva-1 homolog C",
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            {
                "id": "NP_001417718",
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        ],
        "gene_names_uniprotkb": "Eva1c; Fam176c",
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        "protein_names_uniprotkb": "Protein eva-1 homolog C; Protein FAM176C",
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        "function": "Binds heparin., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0030246 carbohydrate binding;GO:0008201 heparin binding",
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        ],
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        "protein_name": "Polypyrimidine tract binding protein 1, pseudogene 3",
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        "protein_names_uniprotkb": "Polypyrimidine tract binding protein 1, pseudogene 3",
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        "function": "Plays a role in pre-mRNA splicing and in the regulation of alternative splicing events. Activates exon skipping of its own pre-mRNA during muscle cell differentiation. Binds to the polypyrimidine tract of introns. May promote RNA looping when bound to two separate polypyrimidine tracts in the same pre-mRNA. May promote the binding of U2 snRNP to pre-mRNA. Cooperates with RAVER1 to modulate switching between mutually exclusive exons during maturation of the TPM1 pre-mRNA. Represses the splicing of MAPT/Tau exon 10. Binds to polypyrimidine-rich controlling element (PCE) of CFTR and promotes exon skipping of CFTR exon 9, thereby antagonizing TIA1 and its role in exon inclusion of CFTR exon 9. Plays a role in the splicing of pyruvate kinase PKM by binding repressively to a polypyrimidine tract flanking PKM exon 9, inhibiting exon 9 inclusion and resulting in exon 10 inclusion and production of the PKM M2 isoform., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003729 mRNA binding",
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        ],
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        "protein_name": "Guanylate kinase",
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        "protein_names_uniprotkb": "Guanylate kinase; 2.7.4.8; GMP kinase; Guanylate kinase 1",
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        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005829 cytosol;GO:0001917 photoreceptor inner segment",
        "go_biological_process": "GO:0019673 GDP-mannose metabolic process;GO:0006185 dGDP biosynthetic process;GO:0046054 dGMP metabolic process;GO:0046060 dATP metabolic process;GO:0046711 GDP biosynthetic process",
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        ],
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        "go_cellular_component": "GO:0097227 sperm annulus;GO:0036126 sperm flagellum",
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            {
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        "function": "Initiates repair of AP sites in DNA by catalyzing hydrolytic incision of the phosphodiester backbone immediately adjacent to the damage, generating a single-strand break with 5'-deoxyribose phosphate and 3'-hydroxyl ends., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane;GO:0045277 respiratory chain complex IV",
        "go_biological_process": "GO:0006123 mitochondrial electron transport, cytochrome c to oxygen",
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        "kg_view_protein": true
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        ],
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            {
                "id": "NP_001426893",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001426893",
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        ],
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        "protein_names_uniprotkb": "Ciliary microtubule inner protein 2B",
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            {
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            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.4",
                "type": "external"
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.259",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.80",
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        ],
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        ],
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            {
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        "go_cellular_component": "GO:0005634 nucleus;GO:0002102 podosome;GO:0032154 cleavage furrow;GO:0030496 midbody;GO:0042995 cell projection",
        "go_biological_process": "GO:0007010 cytoskeleton organization;GO:0061061 muscle structure development;GO:0051016 barbed-end actin filament capping;GO:0008154 actin polymerization or depolymerization;GO:0051014 actin filament severing",
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    },
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            {
                "id": "B0BNB9_RAT",
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        ],
        "mass": 49094.0,
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        "protein_name": "Serine protease HTRA2, mitochondrial",
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        "refseq_name": "serine protease HTRA2, mitochondrial",
        "refseq_ac": [
            {
                "id": "NP_001100069",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100069",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Htra2",
        "gene_names_refseq": "Htra2; Prss25",
        "protein_names_uniprotkb": "Serine protease HTRA2, mitochondrial; 3.4.21.108; High temperature requirement protein A2; Omi stress-regulated endoprotease; Serine protease 25; Serine proteinase OMI",
        "protein_names_refseq": "high temperature requirement protein A2; protease, serine, 25; serine protease HTRA2, mitochondrial",
        "tax_id": 10116,
        "disease": "3-methylglutaconic aciduria type 8 (Disease Ontology:DOID:0070000); prostate cancer (Disease Ontology:DOID:10283); stomach cancer (Disease Ontology:DOID:10534); Alzheimer's disease (Disease Ontology:DOID:10652); asphyxia neonatorum (Disease Ontology:DOID:11088); cryptorchidism (Disease Ontology:DOID:11383); endometrial cancer (Disease Ontology:DOID:1380); Parkinson's disease (Disease Ontology:DOID:14330); status epilepticus (Disease Ontology:DOID:1824); transient cerebral ischemia (Disease Ontology:DOID:224); motor neuron disease (Disease Ontology:DOID:231); ovarian cancer (Disease Ontology:DOID:2394); middle cerebral artery infarction (Disease Ontology:DOID:3525); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:297376);  (R-RNO-9837999)",
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        "publication_id_list": "29581019;30286467;32945404;34677809",
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        "function": "Inhibition of HtrA2 alleviates inflammatory response and cell apoptosis in lipopolysaccharideinduced acute pneumonia in rats., [RefSeq, PubMed]; Local high expression of Apo-J in the peripheral regions may play a neuroprotective role by inhibiting apoptosis via the Omi/HtrA2 pathway after hemorrhage, [RefSeq, PubMed]; Omi inhibition ameliorates neuron apoptosis and neurological deficit after subarachnoid hemorrhage in rats., [RefSeq, PubMed]; Serine protease that shows proteolytic activity against a non-specific substrate beta-casein. Promotes apoptosis by either relieving the inhibition of BIRC proteins on caspases, leading to an increase in caspase activity; or by a BIRC inhibition-independent, caspase-independent and serine protease activity-dependent mechanism. Cleaves BIRC6 and relieves its inhibition on CASP3, CASP7 and CASP9, but it is also prone to inhibition by BIRC6. Cleaves THAP5 and promotes its degradation during apoptosis., [UniProtKB, UniProtKB]; The inhibition of Omi/HtrA2 by UCF-101 leads to neuroprotection by inhibiting the cytosolic translocation of Omi/HtrA2 and antagonizing the caspase-dependent apoptosis pathway., [RefSeq, PubMed]",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.21.108",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005739 mitochondrion;GO:0005758 mitochondrial intermembrane space;GO:0005829 cytosol;GO:0005856 cytoskeleton",
        "go_biological_process": "GO:0006508 proteolysis;GO:0008344 adult locomotory behavior;GO:0030900 forebrain development;GO:0035556 intracellular signal transduction;GO:0040014 regulation of multicellular organism growth",
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            {
                "id": "XP_008764624",
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        "go_molecular_function": "GO:0005178 integrin binding;GO:0005200 structural constituent of cytoskeleton;GO:0051015 actin filament binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005856 cytoskeleton;GO:0005886 plasma membrane;GO:0005925 focal adhesion;GO:0001726 ruffle",
        "go_biological_process": "GO:0030036 actin cytoskeleton organization;GO:0098609 cell-cell adhesion;GO:0007155 cell adhesion;GO:0099140 presynaptic actin cytoskeleton organization",
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    },
    {
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        ],
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        "protein_name": "E3 ubiquitin-protein ligase ARIH1",
        "gene_name": "Arih1",
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            {
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            }
        ],
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        "gene_names_refseq": "Arih1",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase ARIH1; 2.3.2.31; E3 ubiquitin-protein ligase arih1; Protein ariadne-1 homolog; UbcH7-binding protein; Ubiquitin-conjugating enzyme E2-binding protein 1",
        "protein_names_refseq": "E3 ubiquitin-protein ligase ARIH1; ariadne homolog, ubiquitin-conjugating enzyme E2 binding protein, 1; ariadne ubiquitin-conjugating enzyme E2 binding protein homolog 1",
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        "pathway": " (rno:300756);  (R-RNO-1169408);  (R-RNO-9833482);  (R-RNO-9909505)",
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            },
            {
                "id": "3.6.4.13",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.13",
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            },
            {
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            },
            {
                "id": "2.3.2.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
                "type": "external"
            },
            {
                "id": "6.3.2.n3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.3.2.n3",
                "type": "external"
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                "id": "3.1.4.11",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.4.11",
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            {
                "id": "2.7.11.24",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.24",
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            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.16",
                "type": "external"
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            {
                "id": "2.7.10.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.10.2",
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            {
                "id": "2.7.11.1",
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            }
        ],
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0031625 ubiquitin protein ligase binding;GO:0061630 ubiquitin protein ligase activity;GO:0031624 ubiquitin conjugating enzyme binding;GO:0004842 ubiquitin-protein transferase activity",
        "go_cellular_component": "GO:0031464 Cul4A-RING E3 ubiquitin ligase complex;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0016604 nuclear body;GO:0019005 SCF ubiquitin ligase complex",
        "go_biological_process": "GO:0016567 protein ubiquitination;GO:0006511 ubiquitin-dependent protein catabolic process",
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        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
                "id": "RBPMS_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A8I6G705",
                "type": "external"
            }
        ],
        "mass": 21816.0,
        "length": 197,
        "protein_name": "RNA-binding protein with multiple splicing",
        "gene_name": "Rbpms",
        "organism": "Rat",
        "refseq_name": "RNA-binding protein with multiple splicing isoform 2",
        "refseq_ac": [
            {
                "id": "NP_001258173",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001258173",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Rbpms",
        "gene_names_refseq": "RBP-MS; RGD1561067; Rbpms",
        "protein_names_uniprotkb": "RNA-binding protein with multiple splicing; RBP-MS; RBPMS",
        "protein_names_refseq": "RNA binding protein gene with multiple splicing; RNA binding protein with multiple splicing; RNA-binding protein with multiple splicing isoform 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:498642)",
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        "publication_id_list": "19737887;31283468;37548402",
        "class_list": "",
        "function": "Acts as a regulator of pre-mRNA alternative splicing (AS) (PubMed:31283468). Binds mRNA (By similarity). Regulates AS of ACTN1, FLNB, although with lower efficiency than isoform 1 (PubMed:31283468). Acts as coactivator of SMAD transcriptional activity in a TGFB1-dependent manner, possibly through increased phosphorylation of SMAD2 and SMAD3 at the C-terminal SSXS regions and promotion of the nuclear accumulation of SMAD proteins (By similarity)., [UniProtKB, UniProtKB, PubMed]; Data indicate RNA-Binding Protein with Multiple Splicing (RBPMS) as a critical regulator of numerous alternative splicing (AS) events in vascular smooth muscle cells (SMCs) Publication Status: Online-Only, [RefSeq, PubMed]; RNA binding protein that mediates pre-mRNA alternative splicing (AS) regulation (PubMed:31283468, PubMed:37548402). Acts either as activator (FLNB, HSPG2, LIPA1, MYOCD, PTPRF and PPFIBP1) or repressor (TPM1, ACTN1, ITGA7, PIEZO1, LSM14B, MBNL1 and MBML2) of splicing events on specific pre-mRNA targets (PubMed:31283468, PubMed:37548402). Together with RNA binding proteins RBFOX2 and MBNL1/2, activates a splicing program associated with differentiated contractile vascular smooth muscle cells (SMC) by regulating AS of numerous pre-mRNA involved in actin cytoskeleton and focal adhesion machineries, suggesting a role in promoting a cell differentiated state (PubMed:31283468, PubMed:37548402). Binds to introns, exons and 3'-UTR associated with tandem CAC trinucleotide motifs separated by a variable spacer region, at a minimum as a dimer. The minimal length of RNA required for RBPMS-binding tandem CAC motifs is 15 nt, with spacing ranging from 1 to 9 nt. Can also bind to CA dinucleotide repeats (By similarity). Mediates repression of TPM1 exon 3 by binding to CAC tandem repeats in the flanking intronic regions, followed by higher-order oligomerization and heterotypic interactions with other splicing regulators including MBNL1 and RBFOX2, which prevents assembly of ATP-dependent splicing complexes (PubMed:37548402)., [UniProtKB, UniProtKB, PubMed, PubMed]; The data indicate that in the retina RBPMS is selectively expressed in RGCs and therefore could serve as a marker for RGC quantification in normal retinas and for estimation of RGC loss in ocular neuropathies., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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            {
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        ],
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        "disease": "developmental and epileptic encephalopathy 31B (Disease Ontology:DOID:0070376); developmental and epileptic encephalopathy 31A (Disease Ontology:DOID:0080437); Alzheimer's disease (Disease Ontology:DOID:10652); adult respiratory distress syndrome (Disease Ontology:DOID:11394); Creutzfeldt-Jakob disease (Disease Ontology:DOID:11949); cystic fibrosis (Disease Ontology:DOID:1485); generalized epilepsy (Disease Ontology:DOID:1827); severe acute respiratory syndrome (Disease Ontology:DOID:2945); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); lung adenocarcinoma (Disease Ontology:DOID:3910); collagen disease (Disease Ontology:DOID:854); vasculitis (Disease Ontology:DOID:865)",
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        "protein_name": "NADH:ubiquinone oxidoreductase complex assembly factor 2",
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            {
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001385981",
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        "function": "Mimitin overexpression protected INS1E pancreatic beta cells against cytokine-induced caspase 3 activation, mitochondrial membrane potential reduction and ATP production inhibition., [RefSeq, PubMed]",
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    },
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            {
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        ],
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        "protein_name": "Claudin 34B4",
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            {
                "id": "XP_002730287",
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            }
        ],
        "gene_names_uniprotkb": "Cldn34b4; LOC100362173",
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        ],
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        "protein_name": "tRNA pseudouridine synthase Pus10",
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        "refseq_name": "tRNA pseudouridine synthase Pus10 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001388093",
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            }
        ],
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        "protein_names_uniprotkb": "tRNA pseudouridine synthase Pus10; 5.4.99.25; Coiled-coil domain-containing protein 139; tRNA pseudouridine 55 synthase; tRNA pseudouridylate synthase; tRNA-uridine isomerase",
        "protein_names_refseq": "pseudouridylate synthase 10; putative tRNA pseudouridine synthase Pus10-like; putative tRNA pseudouridine synthase Pus10; tRNA pseudouridine synthase Pus10 isoform 1",
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        "function": "Protein with different functions depending on its subcellular location: involved in miRNA processing in the nucleus and acts as a tRNA pseudouridylate synthase in the cytoplasm. In the cytoplasm, acts as a pseudouridylate synthase by catalyzing synthesis of pseudouridine(54) and pseudouridine(55) from uracil-54 and uracil-55, respectively, in the psi GC loop of a subset of tRNAs. tRNA pseudouridylate synthase activity is enhanced by the presence of 1-methyladenosine at position 53-61 of tRNAs. Does not show tRNA pseudouridylate synthase activity in the nucleus. In the nucleus, promotes primary microRNAs (pri-miRNAs) processing independently of its RNA pseudouridylate synthase activity. Binds pri-miRNAs. Modulator of TRAIL/TNFSF10-induced cell death via activation of procaspase-8 and BID cleavage. Required for the progression of the apoptotic signal through intrinsic mitochondrial cell death., [UniProtKB, UniProtKB, UniProtKB]",
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            {
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            },
            {
                "id": "5.4.99.-",
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            }
        ],
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol",
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        "protein_name": "Radial spoke head 14 homolog",
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        "protein_names_uniprotkb": "Radial spoke head 14 homolog",
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        "go_cellular_component": "GO:0001534 radial spoke",
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            {
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        ],
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        "protein_name": "Olfactory receptor",
        "gene_name": "Or4a73",
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        "refseq_name": "olfactory receptor Olr709",
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            {
                "id": "NP_001001066",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001001066",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Or4a73",
        "gene_names_refseq": "Olr709; Or4a73",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 709; olfactory receptor Olr709; olfactory receptor gene Olr709",
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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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        ],
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        "length": 176,
        "protein_name": "Ferritin",
        "gene_name": "Fthl17b",
        "organism": "Rat",
        "refseq_name": "ferritin, heavy polypeptide-like 17, member B",
        "refseq_ac": [
            {
                "id": "NP_001103837",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001103837",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Fthl17b; Fthl17cl1; LOC120099271; LOC691895",
        "gene_names_refseq": "Fthl17b",
        "protein_names_uniprotkb": "Ferritin",
        "protein_names_refseq": "ferritin, heavy polypeptide-like 17, member B",
        "tax_id": 10116,
        "disease": "candidiasis (Disease Ontology:DOID:1508)",
        "pathway": " (rno:691895)",
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        "function": "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]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0008198 ferrous iron binding;GO:0008199 ferric iron binding",
        "go_cellular_component": "GO:0005737 cytoplasm",
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        ],
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        "protein_name": "tRNA-splicing endonuclease subunit SEN15",
        "gene_name": "Tsen15",
        "organism": "Rat",
        "refseq_name": "tRNA-splicing endonuclease subunit Sen15 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001388243",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001388243",
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            }
        ],
        "gene_names_uniprotkb": "Tsen15",
        "gene_names_refseq": "RGD1308584; Tsen15",
        "protein_names_uniprotkb": "tRNA-splicing endonuclease subunit SEN15; tRNA-intron endonuclease SEN15; tRNA-splicing endonuclease subunit Sen15",
        "protein_names_refseq": "TSEN15 tRNA splicing endonuclease subunit; tRNA splicing endonuclease 15 homolog; tRNA-splicing endonuclease subunit Sen15 isoform 1; tRNA-splicing endonuclease subunit Sen15",
        "tax_id": 10116,
        "disease": "pontocerebellar hypoplasia type 2F (Disease Ontology:DOID:0112329)",
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        "function": "Non-catalytic subunit of the tRNA-splicing endonuclease complex, a complex responsible for identification and cleavage of the splice sites in pre-tRNA. It cleaves pre-tRNA at the 5' and 3' splice sites to release the intron. The products are an intron and two tRNA half-molecules bearing 2',3' cyclic phosphate and 5'-OH termini. There are no conserved sequences at the splice sites, but the intron is invariably located at the same site in the gene, placing the splice sites an invariant distance from the constant structural features of the tRNA body. The tRNA splicing endonuclease is also involved in mRNA processing via its association with pre-mRNA 3'-end processing factors, establishing a link between pre-tRNA splicing and pre-mRNA 3'-end formation, suggesting that the endonuclease subunits function in multiple RNA-processing events., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
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        "function": "The branched-chain alpha-keto dehydrogenase complex catalyzes the overall conversion of alpha-keto acids to acyl-CoA and CO(2). It contains multiple copies of three enzymatic components: branched-chain alpha-keto acid decarboxylase (E1), lipoamide acyltransferase (E2) and lipoamide dehydrogenase (E3). Within this complex, the catalytic function of this enzyme is to accept, and to transfer to coenzyme A, acyl groups that are generated by the branched-chain alpha-keto acid decarboxylase component., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005829 cytosol;GO:0042645 mitochondrial nucleoid;GO:0160157 branched-chain alpha-ketoacid dehydrogenase complex",
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        "protein_names_refseq": "carbonyl reductase [NADPH] 3; monomeric carbonyl reductase 3; quinone reductase CBR3",
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        "go_cellular_component": "GO:0005829 cytosol",
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        "disease": "immunodeficiency 23 (Disease Ontology:DOID:0111953); cancer (Disease Ontology:DOID:162); teratoma (Disease Ontology:DOID:3307); cervical cancer (Disease Ontology:DOID:4362)",
        "pathway": " (rno:363109);  (R-RNO-446210)",
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        "disease": "autosomal recessive intellectual developmental disorder 73 (Disease Ontology:DOID:0081233)",
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        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "2.3.1.254",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.254",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0120518 protein N-terminal-methionine acetyltransferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0031416 NatB complex",
        "go_biological_process": "GO:0006474 N-terminal protein amino acid acetylation;GO:0018002 N-terminal peptidyl-glutamic acid acetylation;GO:0017190 N-terminal peptidyl-aspartic acid acetylation;GO:0017192 N-terminal peptidyl-glutamine acetylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B2RZ44-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "B4F778-1",
        "uniprot_id": [
            {
                "id": "B4F778_RAT",
                "url": "https://www.uniprot.org/uniprot/B4F778",
                "type": "external"
            }
        ],
        "mass": 39957.0,
        "length": 364,
        "protein_name": "Replication factor C subunit 4",
        "gene_name": "Rfc4",
        "organism": "Rat",
        "refseq_name": "replication factor C subunit 4",
        "refseq_ac": [
            {
                "id": "NP_001099339",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099339",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Rfc4",
        "gene_names_refseq": "Rfc4",
        "protein_names_uniprotkb": "Replication factor C subunit 4; Activator 1 subunit 4",
        "protein_names_refseq": "replication factor C (activator 1) 4; replication factor C subunit 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:288003);  (R-RNO-110312);  (R-RNO-110314);  (R-RNO-110320);  (R-RNO-174411);  (R-RNO-176187);  (R-RNO-5651801);  (R-RNO-5655862);  (R-RNO-5656121);  (R-RNO-5656169);  (R-RNO-5685938);  (R-RNO-5685942);  (R-RNO-5693537);  (R-RNO-5693607);  (R-RNO-5696397);  (R-RNO-5696400);  (R-RNO-6782135);  (R-RNO-6782210);  (R-RNO-6804756);  (R-RNO-69091);  (R-RNO-69473)",
        "pathway_count": 21,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Subunit of the replication factor C (RFC) complex which acts during elongation of primed DNA templates by DNA polymerases delta and epsilon, and is necessary for ATP-dependent loading of proliferating cell nuclear antigen (PCNA) onto primed DNA. The RFC4 subunit probably functions as a scaffold on which the other complex components can assemble., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0005524 ATP binding;GO:0019899 enzyme binding;GO:0016887 ATP hydrolysis activity;GO:0003689 DNA clamp loader activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0031390 Ctf18 RFC-like complex;GO:0031391 Elg1 RFC-like complex;GO:0005663 DNA replication factor C complex",
        "go_biological_process": "GO:0006281 DNA repair;GO:1900264 positive regulation of DNA-directed DNA polymerase activity;GO:0006261 DNA-templated DNA replication",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B4F778-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "B4F7C7-1",
        "uniprot_id": [
            {
                "id": "B4F7C7_RAT",
                "url": "https://www.uniprot.org/uniprot/B4F7C7",
                "type": "external"
            }
        ],
        "mass": 21124.0,
        "length": 190,
        "protein_name": "Heme-binding protein 1",
        "gene_name": "Hebp1",
        "organism": "Rat",
        "refseq_name": "heme-binding protein 1 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001385805",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001385805",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Hebp1",
        "gene_names_refseq": "Hebp1",
        "protein_names_uniprotkb": "Heme-binding protein 1; p22HBP",
        "protein_names_refseq": "heme-binding protein 1 isoform 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362454);  (R-RNO-418594);  (R-RNO-444473)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May bind free porphyrinogens that may be present in the cell and thus facilitate removal of these potentially toxic compound. Binds with a high affinity to one molecule of heme or porphyrins. It binds metalloporphyrins, free porphyrins and N-methylprotoporphyrin with similar affinities., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "F7EVC6",
        "ec_number_list": [],
        "go_molecular_function": "GO:0020037 heme binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B4F7C7-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "B4F7E7-1",
        "uniprot_id": [
            {
                "id": "PALS1_RAT",
                "url": "https://www.uniprot.org/uniprot/B4F7E7",
                "type": "external"
            }
        ],
        "mass": 77152.0,
        "length": 675,
        "protein_name": "Protein PALS1",
        "gene_name": "Pals1",
        "organism": "Rat",
        "refseq_name": "protein PALS1",
        "refseq_ac": [
            {
                "id": "NP_001101504",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001101504",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Pals1; Mpp5",
        "gene_names_refseq": "Mpp5; Pals1",
        "protein_names_uniprotkb": "Protein PALS1; MAGUK p55 subfamily member 5; Protein associated with Lin-7 1",
        "protein_names_refseq": "MAGUK p55 subfamily member 5; membrane palmitoylated protein 5; membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5); protein PALS1; protein associated with LIN7 1, MAGUK family member; protein associated with Lin-7 1",
        "tax_id": 10116,
        "disease": "Leber congenital amaurosis (Disease Ontology:DOID:14791); kidney disease (Disease Ontology:DOID:557)",
        "pathway": " (rno:314259)",
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        "publication_id_list": "20237282;22673903",
        "class_list": "",
        "function": "Plays a role in tight junction biogenesis and in the establishment of cell polarity in epithelial cells (By similarity). Also involved in adherens junction biogenesis by ensuring correct localization of the exocyst complex protein EXOC4/SEC8 which allows trafficking of adherens junction structural component CDH1 to the cell surface (By similarity). Plays a role through its interaction with CDH5 in vascular lumen formation and endothelial membrane polarity (By similarity). Required during embryonic and postnatal retinal development (By similarity). Required for the maintenance of cerebellar progenitor cells in an undifferentiated proliferative state, preventing premature differentiation, and is required for cerebellar histogenesis, fissure formation, cerebellar layer organization and cortical development (By similarity). Plays a role in neuronal progenitor cell survival, potentially via promotion of mTOR signaling (By similarity). Plays a role in the radial and longitudinal extension of the myelin sheath in Schwann cells (By similarity). May modulate SC6A1/GAT1-mediated GABA uptake by stabilizing the transporter (By similarity). May play a role in the T-cell receptor-mediated activation of NF-kappa-B (By similarity). Required for localization of EZR to the apical membrane of parietal cells and may play a role in the dynamic remodeling of the apical cytoskeleton (By similarity). Required for the normal polarized localization of the vesicular marker STX4 (By similarity). Required for the correct trafficking of the myelin proteins PMP22 and MAG (PubMed:20237282). Involved in promoting phosphorylation and cytoplasmic retention of transcriptional coactivators YAP1 and WWTR1/TAZ which leads to suppression of TGFB1-dependent transcription of target genes such as CCN2/CTGF, SERPINE1/PAI1, SNAI1/SNAIL1 and SMAD7 (By similarity)., [UniProtKB, PubMed, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0005524 ATP binding;GO:0019904 protein domain specific binding;GO:0042802 identical protein binding;GO:0016301 kinase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0005912 adherens junction;GO:0005923 bicellular tight junction",
        "go_biological_process": "GO:0017015 regulation of transforming growth factor beta receptor signaling pathway;GO:0016332 establishment or maintenance of polarity of embryonic epithelium;GO:0007009 plasma membrane organization;GO:0072659 protein localization to plasma membrane;GO:0021987 cerebral cortex development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "B4F7E7-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000001.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "B5DEJ6-1",
        "uniprot_id": [
            {
                "id": "B5DEJ6_RAT",
                "url": "https://www.uniprot.org/uniprot/B5DEJ6",
                "type": "external"
            }
        ],
        "mass": 27207.0,
        "length": 243,
        "protein_name": "Thiamine pyrophosphokinase",
        "gene_name": "Tpk1",
        "organism": "Rat",
        "refseq_name": "thiamin pyrophosphokinase 1",
        "refseq_ac": [
            {
                "id": "NP_001128466",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001128466",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tpk1",
        "gene_names_refseq": "Tpk1",
        "protein_names_uniprotkb": "Thiamine pyrophosphokinase; 2.7.6.2",
        "protein_names_refseq": "thiamin pyrophosphokinase 1; thiamine pyrophosphokinase",
        "tax_id": 10116,
        "disease": "cancer (Disease Ontology:DOID:162); inherited metabolic disorder (Disease Ontology:DOID:655)",
        "pathway": " (rno:680668);  (R-RNO-196819)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the phosphorylation of thiamine to thiamine pyrophosphate (TPP) utilizing UTP and therefore links the biosynthesis of TPP to pyrimidines metabolism. By producing thiamine pyrophosphate, a cofactor of the mitochondrial pyruvate dehydrogenase indirectly regulates pyruvate oxidation and lipogenesis. Although it can also catalyze thiamine phosphorylation using ATP and CTP in vitro, it does so with significantly lower efficiency and without physiological relevance evidence., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_s_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "F1LQE3",
        "ec_number_list": [
            {
                "id": "2.7.6.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.6.2",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0005524 ATP binding;GO:0042802 identical protein binding;GO:0016301 kinase activity;GO:0004788 thiamine diphosphokinase activity;GO:0030975 thiamine binding",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0009229 thiamine diphosphate biosynthetic process;GO:0006772 thiamine metabolic process;GO:0010510 regulation of pyruvate decarboxylation to acetyl-CoA",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B5DEJ6-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "B5DEZ6-1",
        "uniprot_id": [
            {
                "id": "B5DEZ6_RAT",
                "url": "https://www.uniprot.org/uniprot/B5DEZ6",
                "type": "external"
            }
        ],
        "mass": 30836.0,
        "length": 274,
        "protein_name": "Glucosamine-6-phosphate deaminase 2",
        "gene_name": "Gnpda2",
        "organism": "Rat",
        "refseq_name": "glucosamine-6-phosphate isomerase 2 isoform X1",
        "refseq_ac": [
            {
                "id": "XP_006251098",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006251098",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Gnpda2",
        "gene_names_refseq": "Gnpda2",
        "protein_names_uniprotkb": "Glucosamine-6-phosphate deaminase 2; 3.5.99.6; Glucosamine-6-phosphate isomerase 2",
        "protein_names_refseq": "glucosamine-6-phosphate isomerase 2 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:289608);  (R-RNO-70171)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "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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        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "3.5.99.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.5.99.6",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0004342 glucosamine-6-phosphate deaminase activity;GO:0042802 identical protein binding;GO:0016853 isomerase activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006043 glucosamine catabolic process;GO:0006046 N-acetylglucosamine catabolic process;GO:0005975 carbohydrate metabolic process;GO:0006048 UDP-N-acetylglucosamine biosynthetic process;GO:0019262 N-acetylneuraminate catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B5DEZ6-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "B5DFC3-1",
        "uniprot_id": [
            {
                "id": "B5DFC3_RAT",
                "url": "https://www.uniprot.org/uniprot/B5DFC3",
                "type": "external"
            }
        ],
        "mass": 86162.0,
        "length": 765,
        "protein_name": "Protein transport protein SEC23",
        "gene_name": "Sec23a",
        "organism": "Rat",
        "refseq_name": "protein transport protein Sec23A isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001099202",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099202",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Sec23a",
        "gene_names_refseq": "Sec23a",
        "protein_names_uniprotkb": "Protein transport protein SEC23",
        "protein_names_refseq": "Sec23 homolog A, COPII coat complex component; Sec23 homolog A, coat complex II component; protein transport protein Sec23A isoform 1; protein transport protein Sec23A",
        "tax_id": 10116,
        "disease": "craniolenticulosutural dysplasia (Disease Ontology:DOID:0070307); congenital dyserythropoietic anemia type II (Disease Ontology:DOID:0111401); Roberts syndrome (Disease Ontology:DOID:5325)",
        "pathway": " (rno:58817);  (R-RNO-204005);  (R-RNO-2132295);  (R-RNO-5694530);  (R-RNO-983170)",
        "pathway_count": 5,
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        "publication_id_list": "28801610;38843836",
        "class_list": "",
        "function": "Component of the coat protein complex II (COPII) which promotes the formation of transport vesicles from the endoplasmic reticulum (ER). The coat has two main functions, the physical deformation of the endoplasmic reticulum membrane into vesicles and the selection of cargo molecules., [UniProtKB, UniProtKB, UniProtKB]; Sec23A expression is upregulated via CREB3L2 during hepatic stellate cells activation.  Sec23A knockdown abrogated the activation. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005783 endoplasmic reticulum;GO:0005829 cytosol;GO:0030134 COPII-coated ER to Golgi transport vesicle;GO:0048471 perinuclear region of cytoplasm",
        "go_biological_process": "GO:0090110 COPII-coated vesicle cargo loading;GO:0006886 intracellular protein transport;GO:0072659 protein localization to plasma membrane;GO:0090114 COPII-coated vesicle budding",
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    },
    {
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            {
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            }
        ],
        "mass": 29553.0,
        "length": 262,
        "protein_name": "Carbonic anhydrase",
        "gene_name": "Ca13",
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        "refseq_name": "carbonic anhydrase 13",
        "refseq_ac": [
            {
                "id": "NP_001128465",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001128465",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ca13; Car13",
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        "protein_names_uniprotkb": "Carbonic anhydrase; 4.2.1.1",
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        "class_list": "",
        "function": "Reversible hydration of carbon dioxide., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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            {
                "id": "4.2.1.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.2.1.1",
                "type": "external"
            },
            {
                "id": "4.2.1.69",
                "url": "https://www.rhea-db.org/rhea/?query=ec:4.2.1.69",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0004089 carbonate dehydratase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "",
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        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000000.000.00000",
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    },
    {
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        ],
        "mass": 41084.0,
        "length": 405,
        "protein_name": "Pygopus family PHD finger 2",
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        "refseq_name": "pygopus homolog 2",
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            {
                "id": "NP_001099917",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099917",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Pygo2",
        "gene_names_refseq": "Pygo2; RGD1308535",
        "protein_names_uniprotkb": "Pygopus family PHD finger 2",
        "protein_names_refseq": "pygopus 2; pygopus homolog 2",
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        "disease": "heart conduction disease (Disease Ontology:DOID:10273)",
        "pathway": " (rno:295251);  (R-RNO-201722);  (R-RNO-3769402)",
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        "class_list": "",
        "function": "Involved in signal transduction through the Wnt pathway., [UniProtKB, UniProtKB]; Pygo2 is highly expressed in and promotes the growth of glioma cells by, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003682 chromatin binding;GO:0008270 zinc ion binding;GO:0042393 histone binding;GO:0035034 histone acetyltransferase regulator activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:1990907 beta-catenin-TCF complex",
        "go_biological_process": "GO:0001822 kidney development;GO:0007286 spermatid development;GO:0007420 brain development;GO:0060021 roof of mouth development;GO:0060070 canonical Wnt signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
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    },
    {
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                "id": "D3Z8A4_RAT",
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        ],
        "mass": 111917.0,
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        "protein_name": "TRPM8 channel-associated factor 1",
        "gene_name": "Tcaf1",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Tcaf1; Fam115a",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "TRPM8 channel-associated factor 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "secondary_ac_list": "D3ZFL9",
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        "go_molecular_function": "GO:0044325 transmembrane transporter binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0030336 negative regulation of cell migration;GO:0090314 positive regulation of protein targeting to membrane;GO:1901529 positive regulation of anion channel activity",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3Z8A4-1",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3Z8B6-1",
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            {
                "id": "D3Z8B6_RAT",
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                "type": "external"
            }
        ],
        "mass": 51286.0,
        "length": 459,
        "protein_name": "Protein ABHD15",
        "gene_name": "Abhd15",
        "organism": "Rat",
        "refseq_name": "protein ABHD15 precursor",
        "refseq_ac": [
            {
                "id": "NP_001100495",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100495",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Abhd15",
        "gene_names_refseq": "Abhd15; RGD1304598",
        "protein_names_uniprotkb": "Protein ABHD15; Alpha/beta hydrolase domain-containing protein 15",
        "protein_names_refseq": "abhydrolase domain-containing protein 15; alpha/beta hydrolase-1; lung alpha/beta hydrolase 1; protein ABHD15 precursor",
        "tax_id": 10116,
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        "pathway": " (rno:303343)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May regulate adipocyte lipolysis and liver lipid accumulation., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0047372 monoacylglycerol lipase activity;GO:0034338 short-chain carboxylesterase activity",
        "go_cellular_component": "GO:0005576 extracellular region",
        "go_biological_process": "GO:0006629 lipid metabolic process;GO:0060612 adipose tissue development;GO:0016042 lipid catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3Z8B6-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3Z8C4-1",
        "uniprot_id": [
            {
                "id": "D3Z8C4_RAT",
                "url": "https://www.uniprot.org/uniprot/D3Z8C4",
                "type": "external"
            }
        ],
        "mass": 98983.0,
        "length": 889,
        "protein_name": "Protein MCM10 homolog",
        "gene_name": "Mcm10",
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        "refseq_name": "protein MCM10 homolog",
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            {
                "id": "NP_001100836",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100836",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Mcm10",
        "gene_names_refseq": "Mcm10",
        "protein_names_uniprotkb": "Protein MCM10 homolog",
        "protein_names_refseq": "minichromosome maintenance complex component 10; minichromosome maintenance deficient 10; protein MCM10 homolog",
        "tax_id": 10116,
        "disease": "immunodeficiency 80 (Disease Ontology:DOID:0061051)",
        "pathway": " (rno:307126);  (R-RNO-176187);  (R-RNO-68962)",
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        "class_list": "",
        "function": "Acts as a replication initiation factor that brings together the MCM2-7 helicase and the DNA polymerase alpha/primase complex in order to initiate DNA replication. Additionally, plays a role in preventing DNA damage during replication. Key effector of the RBBP6 and ZBTB38-mediated regulation of DNA-replication and common fragile sites stability; acts as a direct target of transcriptional repression by ZBTB38., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0003688 DNA replication origin binding;GO:0008270 zinc ion binding;GO:0019899 enzyme binding;GO:0042802 identical protein binding;GO:0003697 single-stranded DNA binding",
        "go_cellular_component": "GO:0043596 nuclear replication fork;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus",
        "go_biological_process": "GO:0008283 cell population proliferation;GO:0006974 DNA damage response;GO:0006270 DNA replication initiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3Z8C4-1",
        "record_type": "protein",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3Z8C9-1",
        "uniprot_id": [
            {
                "id": "PDE6A_RAT",
                "url": "https://www.uniprot.org/uniprot/D3Z8C9",
                "type": "external"
            }
        ],
        "mass": 99752.0,
        "length": 860,
        "protein_name": "Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha",
        "gene_name": "Pde6a",
        "organism": "Rat",
        "refseq_name": "rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha",
        "refseq_ac": [
            {
                "id": "NP_001100856",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100856",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Pde6a",
        "gene_names_refseq": "Pde6a",
        "protein_names_uniprotkb": "Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha; 3.1.4.35",
        "protein_names_refseq": "phosphodiesterase 6A, cGMP-specific, rod, alpha; rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa 43 (Disease Ontology:DOID:0110379); retinitis pigmentosa (Disease Ontology:DOID:10584)",
        "pathway": " (rno:307401);  (R-RNO-2485179);  (R-RNO-2514859);  (R-RNO-4086398)",
        "pathway_count": 4,
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        "class_list": "",
        "function": "Catalytic alpha subunit of the rod-specific cGMP phosphodiesterase (PDE6) complex, which hydrolyzes 3',5'-cyclic GMP in the phototransduction cascade. The PDE6 holoenzyme consists of two catalytic subunits (PDE6A and PDE6B) and two inhibitory gamma subunits (PDE6G) (By similarity). Light-activated GNAT1 relieves gamma subunit-mediated inhibition, enabling the catalytic subunits to hydrolyze cGMP and thereby mediate visual signal transduction and amplification. Decreased cytosolic cGMP levels result in closure of cGMP-gated cation channels at the plasma membrane, leading to rod photoreceptor hyperpolarization (By similarity)., [UniProtKB, UniProtKB, UniProtKB]",
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        ],
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        ],
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        "go_biological_process": "GO:0016042 lipid catabolic process;GO:0050482 arachidonate secretion;GO:0046470 phosphatidylcholine metabolic process;GO:0046471 phosphatidylglycerol metabolic process;GO:0045299 otolith mineralization",
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        "protein_name": "Phosphatidylinositol-3,5-bisphosphate 3-phosphatase MTMR2",
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        ],
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        "protein_names_refseq": "myotubularin-related protein 2 isoform X1",
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        "disease": "Charcot-Marie-Tooth disease type 4B1 (Disease Ontology:DOID:0110191); centronuclear myopathy X-linked (Disease Ontology:DOID:0111225); Charcot-Marie-Tooth disease (Disease Ontology:DOID:10595); myopathy (Disease Ontology:DOID:423)",
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        "function": "Lipid phosphatase that specifically dephosphorylates the D-3 position of phosphatidylinositol 3-phosphate and phosphatidylinositol 3,5-bisphosphate, generating phosphatidylinositol and phosphatidylinositol 5-phosphate. Regulates the level of these phosphoinositides critical for various biological processes including autophagy initiation and autophagosome maturation., [UniProtKB, UniProtKB]",
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        "ec_number_list": [
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            },
            {
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            },
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        ],
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0014069 postsynaptic density;GO:0030424 axon",
        "go_biological_process": "GO:0016311 dephosphorylation;GO:0045806 negative regulation of endocytosis;GO:0060304 regulation of phosphatidylinositol dephosphorylation;GO:0048666 neuron development;GO:0002091 negative regulation of receptor internalization",
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        ],
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        "protein_name": "Gasdermin A",
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        ],
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        "protein_name": "Olfactory receptor",
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        "protein_names_refseq": "olfactory receptor 729; olfactory receptor Olr729; olfactory receptor gene Olr729",
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        ],
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0031849 olfactory receptor binding",
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        ],
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        "protein_name": "NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial",
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        "refseq_name": "NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial",
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        "gene_names_uniprotkb": "Ndufs6; LOC679739; Ndufs6l1",
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        "protein_names_uniprotkb": "NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial",
        "protein_names_refseq": "NADH dehydrogenase (ubiquinone) Fe-S protein 6; NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial-like; NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial; NADH:ubiquinone oxidoreductase subunit S6-like 1",
        "tax_id": 10116,
        "disease": "mitochondrial complex I deficiency (Disease Ontology:DOID:0060536); nuclear type mitochondrial complex I deficiency 9 (Disease Ontology:DOID:0112073); cervical cancer (Disease Ontology:DOID:4362)",
        "pathway": "",
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        "function": "Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "biomarker_type": "",
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        "secondary_ac_list": "A0A096MK72",
        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane;GO:0005739 mitochondrion;GO:0045271 respiratory chain complex I",
        "go_biological_process": "GO:0006120 mitochondrial electron transport, NADH to ubiquinone;GO:0072359 circulatory system development;GO:0097168 mesenchymal stem cell proliferation;GO:0006631 fatty acid metabolic process;GO:0006936 muscle contraction",
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        "kg_view_protein": true
    },
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            {
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            }
        ],
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        "length": 543,
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            {
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            }
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        "tax_id": 10116,
        "disease": "chromosome 1q21.1 deletion syndrome (Disease Ontology:DOID:0060411)",
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        "function": "Acts as a Baeyer-Villiger monooxygenase on a broad range of substrates. Catalyzes the insertion of an oxygen atom into a carbon-carbon bond adjacent to a carbonyl, which converts ketones to esters. Active on diverse carbonyl compounds, whereas soft nucleophiles are mostly non- or poorly reactive. In contrast with other forms of FMO it is non- or poorly active on 'classical' substrates such as drugs, pesticides, and dietary components containing soft nucleophilic heteroatoms. Able to oxidize drug molecules bearing a carbonyl group on an aliphatic chain, such as nabumetone and pentoxifylline. Also, in the absence of substrates, shows slow but yet significant NADPH oxidase activity. Acts as a positive modulator of cholesterol biosynthesis as well as glucose homeostasis, promoting metabolic aging via pleiotropic effects., [UniProtKB, UniProtKB]",
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            {
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                "type": "external"
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            {
                "id": "1.14.13.225",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.14.13.225",
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            },
            {
                "id": "1.-.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.-.-.-",
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            },
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                "id": "1.14.13.148",
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                "id": "1.14.13.8",
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                "id": "1.11.1.-",
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                "id": "1.14.13.32",
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            }
        ],
        "go_molecular_function": "GO:0050660 flavin adenine dinucleotide binding;GO:0016174 NAD(P)H oxidase H2O2-forming activity;GO:0050661 NADP binding;GO:0004499 N,N-dimethylaniline monooxygenase activity",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006629 lipid metabolic process",
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            {
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        ],
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            {
                "id": "NP_001099210",
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            }
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        "protein_names_refseq": "N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2; N-deacetylase/N-sulfotransferase 2; bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 2",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); intellectual disability (Disease Ontology:DOID:1059); azoospermia (Disease Ontology:DOID:14227); germ cell cancer (Disease Ontology:DOID:2994)",
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        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0030210 heparin proteoglycan biosynthetic process;GO:0015012 heparan sulfate proteoglycan biosynthetic process;GO:0002448 mast cell mediated immunity;GO:0002002 regulation of angiotensin levels in blood",
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        ],
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        "protein_names_refseq": "DEAD (Asp-Glu-Ala-Asp) box helicase 6; DEAD (Asp-Glu-Ala-Asp) box polypeptide 6; probable ATP-dependent RNA helicase DDX6",
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        "function": "Essential for the formation of P-bodies, cytosolic membrane-less ribonucleoprotein granules involved in RNA metabolism through the coordinated storage of mRNAs encoding regulatory functions. Plays a role in P-bodies to coordinate the storage of translationally inactive mRNAs in the cytoplasm and prevent their degradation. In the process of mRNA degradation, plays a role in mRNA decapping. Blocks autophagy in nutrient-rich conditions by repressing the expression of ATG-related genes through degradation of their transcripts., [UniProtKB, UniProtKB]",
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                "id": "5.6.2.-",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.6",
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                "id": "3.6.1.-",
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        ],
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        "go_cellular_component": "GO:0001520 outer dense fiber;GO:0097227 sperm annulus;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0019074 viral RNA genome packaging;GO:0007283 spermatogenesis;GO:0045665 negative regulation of neuron differentiation;GO:0017148 negative regulation of translation;GO:0019827 stem cell population maintenance",
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        ],
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        "protein_name": "Occludin/ELL domain containing 1",
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        "protein_names_refseq": "occludin/ELL domain-containing protein 1 isoform 3; occludin/ELL domain-containing protein 1",
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        "protein_name": "Sperm acrosome-associated protein 9",
        "gene_name": "Spaca9",
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        "protein_names_uniprotkb": "Sperm acrosome-associated protein 9",
        "protein_names_refseq": "Rsb-66 protein; sperm acrosome-associated protein 9 isoform 2; sperm acrosome-associated protein 9; uncharacterized protein C9orf9 homolog",
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                "id": "CYB5B_RAT",
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            }
        ],
        "mass": 16265.0,
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        "gene_name": "Cyb5b",
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        "refseq_name": "cytochrome b5 type B precursor",
        "refseq_ac": [
            {
                "id": "NP_085075",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_085075",
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        ],
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        "protein_names_uniprotkb": "Cytochrome b5 type B; Cytochrome b5 outer mitochondrial membrane isoform",
        "protein_names_refseq": "cytochrome b5 type B (outer mitochondrial membrane); cytochrome b5 type B precursor",
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        "disease": "",
        "pathway": " (rno:80773);  (R-RNO-1660661);  (R-RNO-203615);  (R-RNO-211945)",
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        "class_list": "",
        "function": "Comparison of X-ray crystal structures of human and rat CYB5B reveals a striking difference in packing involving the five-strand beta-sheet, which can be attributed to fully buried residue 21 in strand beta4, [RefSeq, PubMed]; Cytochrome b5 is a membrane-bound hemoprotein functioning as an electron carrier for several membrane-bound oxygenases., [UniProtKB]; Simulations provided qualitative microscopic explanations of many of the differences in physical properties between outer mitochondrial membrane CYB5 isoform and microsomal CYB5 and two mutants in terms of localized changes in structure and flexibility, [RefSeq, PubMed]; The presence of a novel reductive enzyme system of importance for lipid synthesis that is exclusively localized to the outer mitochondrial membrane and is composed of CYB5B, MOSC2, and a third unknown component (a CYB5B reductase)., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005741 mitochondrial outer membrane;GO:1903958 nitric-oxide synthase complex;GO:0016020 membrane",
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        "protein_name": "Phosphodiesterase",
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        "function": "Calcium/calmodulin-dependent cyclic nucleotide phosphodiesterase with a dual specificity for the second messengers cGMP and cAMP, which are key regulators of many important physiological processes. Has a higher efficiency with cGMP compared to cAMP., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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            {
                "id": "3.1.4.-",
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            },
            {
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            },
            {
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                "type": "external"
            },
            {
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            }
        ],
        "go_molecular_function": "GO:0005516 calmodulin binding;GO:0046872 metal ion binding;GO:0004117 calmodulin-activated dual specificity 3',5'-cyclic-GMP, 3',5'-cyclic-AMP phosphodiesterase activity;GO:0047555 3',5'-cyclic-GMP phosphodiesterase activity;GO:0004115 3',5'-cyclic-AMP phosphodiesterase activity",
        "go_cellular_component": "GO:0043025 neuronal cell body;GO:0036126 sperm flagellum",
        "go_biological_process": "GO:0007165 signal transduction;GO:0048660 regulation of smooth muscle cell proliferation;GO:0034391 regulation of smooth muscle cell apoptotic process;GO:0046069 cGMP catabolic process;GO:0141162 negative regulation of cAMP/PKA signal transduction",
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        ],
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        "protein_name": "A-kinase anchoring protein 8 like",
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            {
                "id": "XP_038939409",
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        "go_cellular_component": "GO:0016605 PML body;GO:0000785 chromatin;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016604 nuclear body",
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        ],
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        "protein_names_refseq": "CBP80/20-dependent translation initiation factor isoform X2",
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        "function": "Specifically required for the pioneer round of mRNA translation mediated by the cap-binding complex (CBC), that takes place during or right after mRNA export via the nuclear pore complex (NPC). Acts via its interaction with the NCBP1/CBP80 component of the CBC complex and recruits the 40S small subunit of the ribosome via eIF3. In contrast, it is not involved in steady state translation, that takes place when the CBC complex is replaced by cytoplasmic cap-binding protein eIF4E. Also required for nonsense-mediated mRNA decay (NMD), the pioneer round of mRNA translation mediated by the cap-binding complex playing a central role in nonsense-mediated mRNA decay (NMD)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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    {
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            {
                "id": "D4A7L4_RAT",
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            }
        ],
        "mass": 17634.0,
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        "protein_name": "NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial",
        "gene_name": "Ndufb11",
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        "refseq_name": "NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial",
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            {
                "id": "NP_001100226",
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            }
        ],
        "gene_names_uniprotkb": "Ndufb11",
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        "protein_names_uniprotkb": "NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial; Complex I-ESSS; NADH-ubiquinone oxidoreductase ESSS subunit",
        "protein_names_refseq": "NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 11; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial",
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        "function": "Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone., [UniProtKB, UniProtKB, UniProtKB]",
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        ],
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            {
                "id": "NP_001386494",
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        ],
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            {
                "id": "NP_001093977",
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        ],
        "gene_names_uniprotkb": "Zmiz2",
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        "protein_names_uniprotkb": "Zinc finger, MIZ-type containing 2",
        "protein_names_refseq": "zinc finger MIZ domain-containing protein 2",
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                "id": "D3ZJ77_RAT",
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        ],
        "mass": 39873.0,
        "length": 341,
        "protein_name": "Calcium binding protein 39",
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        "refseq_name": "calcium-binding protein 39 isoform 2",
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            {
                "id": "NP_001388554",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001388554",
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            }
        ],
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        "protein_names_uniprotkb": "Calcium binding protein 39",
        "protein_names_refseq": "calcium-binding protein 39 isoform 2",
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        "disease": "cancer (Disease Ontology:DOID:162); pancreatic cancer (Disease Ontology:DOID:1793); transient cerebral ischemia (Disease Ontology:DOID:224); hepatocellular carcinoma (Disease Ontology:DOID:684); hyperthyroidism (Disease Ontology:DOID:7998)",
        "pathway": " (rno:301574);  (R-RNO-380972);  (R-RNO-6798695)",
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        "function": "Cab39 differentially interacts with WNK4 and SPAK/OSR1 to switch the classic two kinase cascade into a signal kinase transduction, [RefSeq, PubMed]; Component of a complex that binds and activates STK11/LKB1. In the complex, required to stabilize the interaction between CAB39/MO25 (CAB39/MO25alpha or CAB39L/MO25beta) and STK11/LKB1., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Endurance training markedly increased skeletal muscle LKB1 and MO25 protein without increasing AMPKK activity., [RefSeq, PubMed]; Examine thyroid hormone effects on LKB1, MO25, phospho-AMPK, phospho-CREB, and PGC-1alpha in rat muscle., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:1902554 serine/threonine protein kinase complex;GO:0005737 cytoplasm;GO:0030018 Z disc;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0071476 cellular hypotonic response;GO:1901380 negative regulation of potassium ion transmembrane transport;GO:0007165 signal transduction;GO:0035556 intracellular signal transduction;GO:0032147 activation of protein kinase activity",
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    {
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        ],
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        "protein_name": "Mediator of RNA polymerase II transcription subunit 13",
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        "organism": "Rat",
        "refseq_name": "mediator of RNA polymerase II transcription subunit 13",
        "refseq_ac": [
            {
                "id": "NP_001402014",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001402014",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Med13",
        "gene_names_refseq": "Med13; Thrap1",
        "protein_names_uniprotkb": "Mediator of RNA polymerase II transcription subunit 13",
        "protein_names_refseq": "mediator of RNA polymerase II transcription subunit 13; thyroid hormone receptor associated protein 1",
        "tax_id": 10116,
        "disease": "autosomal dominant intellectual developmental disorder 61 (Disease Ontology:DOID:0061034); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:303403);  (R-RNO-9841922)",
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        "function": "Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors., [UniProtKB, UniProtKB, UniProtKB]; Exercise training can prevent weight gain and pathological cardiac hypertrophy via increased of cardiac MED13 by the regulation of miRNA-208a., [RefSeq, PubMed]",
        "predicted_glycosites": 5,
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        "go_molecular_function": "GO:0003712 transcription coregulator activity;GO:0003713 transcription coactivator activity;GO:0046966 nuclear thyroid hormone receptor binding",
        "go_cellular_component": "GO:0016592 mediator complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:1990508 CKM complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0060261 positive regulation of transcription initiation by RNA polymerase II;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
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    },
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        ],
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        "protein_name": "Mediator of RNA polymerase II transcription subunit 27",
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        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Med27",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Mediator of RNA polymerase II transcription subunit 27; Cofactor required for Sp1 transcriptional activation subunit 8; Mediator complex subunit 27",
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        "pathway": " (rno:296612);  (R-RNO-9841922)",
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        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0016567 protein ubiquitination;GO:0019827 stem cell population maintenance",
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        "filter_code": "0000000.0000101.010000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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            {
                "id": "D3ZLS2_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZLS2",
                "type": "external"
            }
        ],
        "mass": 44768.0,
        "length": 388,
        "protein_name": "Sulfotransferase",
        "gene_name": "Chst4",
        "organism": "Rat",
        "refseq_name": "carbohydrate sulfotransferase 4",
        "refseq_ac": [
            {
                "id": "NP_001100897",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100897",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Chst4",
        "gene_names_refseq": "Chst4",
        "protein_names_uniprotkb": "Sulfotransferase; 2.8.2.-",
        "protein_names_refseq": "carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 4; carbohydrate (chondroitin 6/keratan) sulfotransferase 4; carbohydrate sulfotransferase 4",
        "tax_id": 10116,
        "disease": "macular corneal dystrophy (Disease Ontology:DOID:2565)",
        "pathway": " (rno:307838);  (R-RNO-913709)",
        "pathway_count": 2,
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        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "ec_number_list": [
            {
                "id": "2.8.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.8.2.-",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0001517 N-acetylglucosamine 6-O-sulfotransferase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005802 trans-Golgi network",
        "go_biological_process": "GO:0006044 N-acetylglucosamine metabolic process;GO:0006477 protein sulfation;GO:1903238 positive regulation of leukocyte tethering or rolling;GO:0005975 carbohydrate metabolic process;GO:0050901 leukocyte tethering or rolling",
        "synthesized_glycan_count": 0,
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        "kg_view_protein": true
    },
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            {
                "id": "D3ZLV5_RAT",
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            }
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        "mass": 152615.0,
        "length": 1402,
        "protein_name": "AT-hook transcription factor",
        "gene_name": "Akna",
        "organism": "Rat",
        "refseq_name": "microtubule organization protein AKNA",
        "refseq_ac": [
            {
                "id": "NP_001102138",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102138",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Akna",
        "gene_names_refseq": "Akna",
        "protein_names_uniprotkb": "AT-hook transcription factor",
        "protein_names_refseq": "AT-hook-containing transcription factor; microtubule organization protein AKNA",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362530)",
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        "publication_id_list": "22673903;29079362;29393594",
        "class_list": "",
        "function": "T-2 toxin activates the PKA/CREB and NF-kappaB/p65 pathways, thereby promoting the direct binding of phospho-CREB and phospho-p65 to the AKNA promoter, thus inhibiting AKNA expression. GH and inflammatory cytokines (TNF-alpha, IL-1beta, and IL-6) expression were significantly downregulated after AKNA silencing., [RefSeq, PubMed]",
        "predicted_glycosites": 4,
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005813 centrosome;GO:0005874 microtubule;GO:0001650 fibrillar center;GO:0005814 centriole",
        "go_biological_process": "GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0050727 regulation of inflammatory response;GO:0001837 epithelial to mesenchymal transition;GO:0021849 neuroblast division in subventricular zone;GO:0060232 delamination",
        "synthesized_glycan_count": 0,
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZM36-1",
        "uniprot_id": [
            {
                "id": "D3ZM36_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZM36",
                "type": "external"
            }
        ],
        "mass": 41619.0,
        "length": 362,
        "protein_name": "Interleukin-10 receptor subunit beta",
        "gene_name": "Il10rb",
        "organism": "Rat",
        "refseq_name": "interleukin-10 receptor subunit beta isoform X2",
        "refseq_ac": [
            {
                "id": "XP_063126661",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_063126661",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Il10rb",
        "gene_names_refseq": "Il10rb; RGD1560373",
        "protein_names_uniprotkb": "Interleukin-10 receptor subunit beta; Coagulation factor III; Cytokine receptor class-II member 4; Cytokine receptor family 2 member 4; Interleukin-10 receptor subunit 2; Tissue factor",
        "protein_names_refseq": "interleukin-10 receptor subunit beta isoform X2",
        "tax_id": 10116,
        "disease": "graft-versus-host disease (Disease Ontology:DOID:0081267); inflammatory bowel disease 25 (Disease Ontology:DOID:0110909); hepatitis B (Disease Ontology:DOID:2043); perinatal necrotizing enterocolitis (Disease Ontology:DOID:8677)",
        "pathway": " (R-RNO-6783783);  (R-RNO-8854691)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Initiates blood coagulation by forming a complex with circulating factor VII or VIIa. The [TF:VIIa] complex activates factors IX or X by specific limited proteolysis. TF plays a role in normal hemostasis by initiating the cell-surface assembly and propagation of the coagulation protease cascade., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Shared cell surface receptor required for the activation of five class 2 cytokines: IL10, IL22, IL26, IL28, and IFNL1. The IFNLR1/IL10RB dimer is a receptor for the cytokine ligands IFNL2 and IFNL3 and mediates their antiviral activity. The ligand/receptor complex stimulate the activation of the JAK/STAT signaling pathway leading to the expression of IFN-stimulated genes (ISG), which contribute to the antiviral state., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0015026 coreceptor activity;GO:0004920 interleukin-10 receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0043235 receptor complex;GO:1905571 interleukin-10 receptor complex;GO:0016020 membrane",
        "go_biological_process": "GO:0007596 blood coagulation;GO:0046427 positive regulation of receptor signaling pathway via JAK-STAT;GO:0019221 cytokine-mediated signaling pathway;GO:1901857 positive regulation of cellular respiration;GO:0140105 interleukin-10-mediated signaling pathway",
        "synthesized_glycan_count": 0,
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        "record_id": "D3ZM36-1",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZMM8-1",
        "uniprot_id": [
            {
                "id": "YLAT2_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZMM8",
                "type": "external"
            }
        ],
        "mass": 56815.0,
        "length": 515,
        "protein_name": "Y+L amino acid transporter 2",
        "gene_name": "Slc7a6",
        "organism": "Rat",
        "refseq_name": "Y+L amino acid transporter 2",
        "refseq_ac": [
            {
                "id": "NP_001100894",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100894",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Slc7a6",
        "gene_names_refseq": "Slc7a6; Y+LAT2; y+LAT-2",
        "protein_names_uniprotkb": "Y+L amino acid transporter 2; Solute carrier family 7 member 6; Y+LAT2; y(+)L-type amino acid transporter 2; y+LAT-2",
        "protein_names_refseq": "Y+L amino acid transporter 2; solute carrier family 7 (amino acid transporter light chain, y+L system), member 6; solute carrier family 7 (cationic amino acid transporter, y+ system), member 6; y(+)L-type amino acid transporter 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:307811);  (R-RNO-210991);  (R-RNO-352230)",
        "pathway_count": 3,
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        "publication_id_list": "22401943;22673903;26448619",
        "class_list": "",
        "function": "Heterodimer with SLC3A2, that functions as an antiporter which operates as an efflux routeby exporting cationic amino acids such as L-arginine from inside the cells in exchange with neutral amino acids like L-leucine, L-glutamine and isoleucine, plus sodium ions and may participate in nitric oxide synthesis (PubMed:22401943, PubMed:26448619). Also exchanges L-arginine with L-lysine in a sodium-independent manner. The transport mechanism is electroneutral and operates with a stoichiometry of 1: 1 (By similarity). Contributes to ammonia-induced increase of L-arginine uptake in cerebral cortical astrocytes leading to ammonia-dependent increase of nitric oxide (NO) production via inducible nitric oxide synthase (iNOS) induction, and protein nitration (PubMed:22401943, PubMed:26448619). May mediate transport of ornithine in retinal pigment epithelial (RPE) cells (By similarity). May also transport glycine betaine in a sodium dependent manner from the cumulus granulosa into the enclosed oocyte (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed, UniProtKB]",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0015179 L-amino acid transmembrane transporter activity;GO:0034618 arginine binding;GO:0015174 basic amino acid transmembrane transporter activity;GO:0061459 L-arginine transmembrane transporter activity;GO:0106439 L-lysine:L-arginine antiporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:1902495 transmembrane transporter complex",
        "go_biological_process": "GO:0015820 L-leucine transport;GO:0031460 glycine betaine transport;GO:0015804 neutral amino acid transport;GO:0006809 nitric oxide biosynthetic process;GO:0003333 amino acid transmembrane transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "D3ZMM8-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZMP7-1",
        "uniprot_id": [
            {
                "id": "D3ZMP7_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZMP7",
                "type": "external"
            }
        ],
        "mass": 15361.0,
        "length": 133,
        "protein_name": "Cystatin domain containing 2",
        "gene_name": "Cstdc2",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein LOC689081 precursor",
        "refseq_ac": [
            {
                "id": "NP_001102992",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102992",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Cstdc2; LOC689081",
        "gene_names_refseq": "Cstdc2",
        "protein_names_uniprotkb": "Cystatin domain containing 2",
        "protein_names_refseq": "uncharacterized protein LOC689081 precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:689081)",
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        "go_molecular_function": "GO:0004869 cysteine-type endopeptidase inhibitor activity",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "GO:0019730 antimicrobial humoral response",
        "synthesized_glycan_count": 0,
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        "kg_view_protein": true
    },
    {
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                "id": "D3ZP23_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZP23",
                "type": "external"
            }
        ],
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        "length": 107,
        "protein_name": "Dehydrogenase/reductase member 2 like 1",
        "gene_name": "Dhrs2l1",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein LOC290217",
        "refseq_ac": [
            {
                "id": "NP_001099505",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099505",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Dhrs2l1; RGD1564324",
        "gene_names_refseq": "Dhrs2l1; RGD1564324",
        "protein_names_uniprotkb": "Dehydrogenase/reductase member 2 like 1",
        "protein_names_refseq": "uncharacterized protein LOC290217",
        "tax_id": 10116,
        "disease": "",
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        "go_molecular_function": "GO:0004090 carbonyl reductase (NADPH) activity",
        "go_cellular_component": "",
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        "protein_names_refseq": "AP-2 complex subunit alpha-1 isoform 1; AP-2 complex subunit alpha-1; adaptor protein complex AP-2, alpha 1 subunit; adaptor-related protein complex 2, alpha 1 subunit; alpha-adaptin A",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041)",
        "pathway": " (R-RNO-177504);  (R-RNO-2132295);  (R-RNO-416993);  (R-RNO-437239);  (R-RNO-5099900);  (R-RNO-5140745);  (R-RNO-8856825);  (R-RNO-8856828);  (R-RNO-8866427);  (R-RNO-8964038)",
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        "function": "Component of the adaptor protein complex 2 (AP-2). Adaptor protein complexes function in protein transport via transport vesicles in different membrane traffic pathways. Adaptor protein complexes are vesicle coat components and appear to be involved in cargo selection and vesicle formation. AP-2 is involved in clathrin-dependent endocytosis in which cargo proteins are incorporated into vesicles surrounded by clathrin (clathrin-coated vesicles, CCVs) which are destined for fusion with the early endosome. The clathrin lattice serves as a mechanical scaffold but is itself unable to bind directly to membrane components. Clathrin-associated adaptor protein (AP) complexes which can bind directly to both the clathrin lattice and to the lipid and protein components of membranes are considered to be the major clathrin adaptors contributing the CCV formation. AP-2 also serves as a cargo receptor to selectively sort the membrane proteins involved in receptor-mediated endocytosis. AP-2 seems to play a role in the recycling of synaptic vesicle membranes from the presynaptic surface. AP-2 recognizes Y-X-X-[FILMV] (Y-X-X-Phi) and [ED]-X-X-X-L-[LI] endocytosis signal motifs within the cytosolic tails of transmembrane cargo molecules. AP-2 may also play a role in maintaining normal post-endocytic trafficking through the ARF6-regulated, non-clathrin pathway. The AP-2 alpha subunit binds polyphosphoinositide-containing lipids, positioning AP-2 on the membrane. The AP-2 alpha subunit acts via its C-terminal appendage domain as a scaffolding platform for endocytic accessory proteins. The AP-2 alpha and AP-2 sigma subunits are thought to contribute to the recognition of the [ED]-X-X-X-L-[LI] motif., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Evidence on differential role for alpha 1 and alpha 2 subtypes of AP-2 adaptin in the central nervous system., [RefSeq, PubMed]; SP-A transiently enhances the basal protein expression of CHC and alpha-adaptin., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0035615 clathrin adaptor activity;GO:0019901 protein kinase binding;GO:0050750 low-density lipoprotein particle receptor binding;GO:0044877 protein-containing complex binding",
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        "refseq_name": "olfactory receptor Olr257",
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            {
                "id": "NP_001001038",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001001038",
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            }
        ],
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        ],
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        ],
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                "id": "NP_001000589",
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        "protein_names_refseq": "ecto-NOX disulfide-thiol exchanger 1 isoform X1",
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        "go_molecular_function": "GO:0003954 NADH dehydrogenase activity;GO:0003723 RNA binding;GO:0003756 protein disulfide isomerase activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0009897 external side of plasma membrane;GO:0005886 plasma membrane",
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        ],
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        "protein_name": "WAP four-disulfide core domain 5",
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        "organism": "Rat",
        "refseq_name": "WAP four-disulfide core domain protein 5 precursor",
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        ],
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        "gene_names_refseq": "Wfdc5",
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        "protein_names_refseq": "WAP four-disulfide core domain protein 5 precursor; WAP four-disulfide core domain protein 5",
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        "pathway": " (rno:296352)",
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        ],
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            {
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            {
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        ],
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        "protein_name": "Protein arginine N-methyltransferase 6",
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        "refseq_name": "protein arginine N-methyltransferase 6",
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            {
                "id": "NP_001380787",
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        ],
        "gene_names_uniprotkb": "Prmt6",
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        "protein_names_uniprotkb": "Protein arginine N-methyltransferase 6; 2.1.1.319; Histone-arginine N-methyltransferase PRMT6",
        "protein_names_refseq": "HMT1 hnRNP methyltransferase-like 6; protein arginine N-methyltransferase 6",
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        "disease": "cocaine dependence (Disease Ontology:DOID:9975)",
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            {
                "id": "3.5.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.5.1.-",
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            {
                "id": "3.5.1.98",
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            }
        ],
        "go_molecular_function": "GO:0003682 chromatin binding;GO:0016274 protein-arginine N-methyltransferase activity;GO:0035242 protein-arginine omega-N asymmetric methyltransferase activity;GO:0042054 histone methyltransferase activity;GO:0042393 histone binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus",
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        ],
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        "protein_names_refseq": "monocarboxylate transporter 6; solute carrier family 16 (monocarboxylate transporter), member 5; solute carrier family 16 (monocarboxylic acid transporters), member 5; solute carrier family 16, member 5 (monocarboxylic acid transporter 6)",
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        ],
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        "protein_name": "FHF complex subunit HOOK interacting protein 2A",
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    },
    {
        "uniprot_canonical_ac": "D4A3T5-1",
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            {
                "id": "D4A3T5_RAT",
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                "type": "external"
            }
        ],
        "mass": 26687.0,
        "length": 255,
        "protein_name": "Complement C1q like 3",
        "gene_name": "C1ql3",
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        "refseq_name": "complement C1q-like protein 3 precursor",
        "refseq_ac": [
            {
                "id": "NP_001102873",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102873",
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            }
        ],
        "gene_names_uniprotkb": "C1ql3",
        "gene_names_refseq": "Adij; C1ql3",
        "protein_names_uniprotkb": "Complement C1q like 3",
        "protein_names_refseq": "adiponectin j; complement C1q-like protein 3 precursor; complement C1q-like protein 3; complement component 1, q subcomponent-like 3",
        "tax_id": 10116,
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        "publication_id_list": "32554851",
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        "go_biological_process": "GO:0099558 maintenance of synapse structure;GO:0099550 trans-synaptic signaling, modulating synaptic transmission;GO:0097107 postsynaptic density assembly;GO:0050807 regulation of synapse organization;GO:0099645 neurotransmitter receptor localization to postsynaptic specialization membrane",
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        ],
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        "protein_name": "Protein Wnt",
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        "refseq_name": "protein Wnt-6 precursor",
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            {
                "id": "NP_001101696",
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        ],
        "gene_names_uniprotkb": "Wnt6",
        "gene_names_refseq": "Wnt6",
        "protein_names_uniprotkb": "Protein Wnt",
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        "disease": "",
        "pathway": " (rno:316526);  (R-RNO-3238698)",
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        "function": "Ligand for members of the frizzled family of seven transmembrane receptors., [UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0009798 axis specification;GO:0010628 positive regulation of gene expression;GO:0045893 positive regulation of DNA-templated transcription;GO:0030182 neuron differentiation;GO:0016055 Wnt signaling pathway",
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        ],
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        "protein_name": "Interleukin-7 receptor subunit alpha",
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        "protein_names_uniprotkb": "Interleukin-7 receptor subunit alpha",
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        "disease": "severe combined immunodeficiency 104 (Disease Ontology:DOID:0090014); stomach cancer (Disease Ontology:DOID:10534); colon cancer (Disease Ontology:DOID:219); middle cerebral artery infarction (Disease Ontology:DOID:3525); lung non-small cell carcinoma (Disease Ontology:DOID:3908); severe combined immunodeficiency (Disease Ontology:DOID:627); malignant pleural mesothelioma (Disease Ontology:DOID:7474)",
        "pathway": " (rno:294797);  (R-RNO-1266695);  (R-RNO-8856825);  (R-RNO-8856828)",
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        "function": "Receptor for interleukin-7. Also acts as a receptor for thymic stromal lymphopoietin (TSLP)., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004917 interleukin-7 receptor activity;GO:0004896 cytokine receptor activity",
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        "go_biological_process": "GO:0008284 positive regulation of cell population proliferation;GO:0010628 positive regulation of gene expression;GO:0019725 cellular homeostasis;GO:0050830 defense response to Gram-positive bacterium;GO:0000902 cell morphogenesis",
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    {
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        ],
        "mass": 338195.0,
        "length": 3083,
        "protein_name": "Basement membrane-specific heparan sulfate proteoglycan core protein",
        "gene_name": "Lama1",
        "organism": "Rat",
        "refseq_name": "laminin subunit alpha-1 precursor",
        "refseq_ac": [
            {
                "id": "NP_001101707",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001101707",
                "type": "external"
            }
        ],
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        "gene_names_refseq": "Lama1",
        "protein_names_uniprotkb": "Basement membrane-specific heparan sulfate proteoglycan core protein; Laminin A chain; Laminin M chain; Laminin subunit alpha-2; Laminin-12 subunit alpha; Laminin-2 subunit alpha; Laminin-4 subunit alpha; Merosin heavy chain; Perlecan",
        "protein_names_refseq": "laminin subunit alpha-1 precursor; laminin, alpha 1; laminin-1",
        "tax_id": 10116,
        "disease": "muscular dystrophy (Disease Ontology:DOID:9884)",
        "pathway": " (rno:316758)",
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        "publication_id_list": "21519634;30153280",
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        "function": "Anti-angiogenic and anti-tumor peptide that inhibits endothelial cell migration, collagen-induced endothelial tube morphogenesis and blood vessel growth in the chorioallantoic membrane. Blocks endothelial cell adhesion to fibronectin and type I collagen. Anti-tumor agent in neovascularization. Interaction with its ligand, integrin alpha2/beta1, is required for the anti-angiogenic properties. Evokes a reduction in phosphorylation of receptor tyrosine kinases via alpha2/beta1 integrin-mediated activation of the tyrosine phosphatase, PTPN6., [UniProtKB, UniProtKB]; Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components., [UniProtKB, UniProtKB]; Data confirmed aquaporin-4 and laminin-alpha1 induction in cMVs., [RefSeq, PubMed]; Has anti-angiogenic properties that require binding of calcium ions for full activity., [UniProtKB, UniProtKB]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0043208 glycosphingolipid binding;GO:0046872 metal ion binding;GO:0048018 receptor ligand activity;GO:0005201 extracellular matrix structural constituent",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005796 Golgi lumen;GO:0005911 cell-cell junction;GO:0016020 membrane;GO:0031012 extracellular matrix",
        "go_biological_process": "GO:1904395 positive regulation of skeletal muscle acetylcholine-gated channel clustering;GO:0001525 angiogenesis;GO:0007155 cell adhesion;GO:0007166 cell surface receptor signaling pathway;GO:0030155 regulation of cell adhesion",
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        ],
        "mass": 29557.0,
        "length": 271,
        "protein_name": "Elastase, neutrophil expressed",
        "gene_name": "Elane",
        "organism": "Rat",
        "refseq_name": "neutrophil elastase precursor",
        "refseq_ac": [
            {
                "id": "NP_001100237",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001100237",
                "type": "external"
            }
        ],
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        "gene_names_refseq": "Ela2; Elane",
        "protein_names_uniprotkb": "Elastase, neutrophil expressed",
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            {
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        "protein_name": "Ferredoxin-2, mitochondrial",
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        "go_molecular_function": "GO:0009055 electron transfer activity;GO:0046872 metal ion binding;GO:0051537 2 iron, 2 sulfur cluster binding",
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        "protein_name": "Cell division cycle 7-related protein kinase",
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        "function": "Cdc7 kinase stimulates Aurora B kinase in M-phase. Publication Status: Online-Only, [RefSeq, PubMed]; Kinase involved in initiation of DNA replication. Phosphorylates critical substrates that regulate the G1/S phase transition and initiation of DNA replication, such as MCM proteins and CLASPIN., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "Small ribosomal subunit protein mS40; 28S ribosomal protein S18-2, mitochondrial; 28S ribosomal protein S18b, mitochondrial",
        "protein_names_refseq": "28S ribosomal protein S18b, mitochondrial; small ribosomal subunit protein mS40",
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        "go_cellular_component": "GO:0005763 mitochondrial small ribosomal subunit;GO:0005739 mitochondrion;GO:0005840 ribosome;GO:1990904 ribonucleoprotein complex",
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        "protein_name": "E3 ubiquitin-protein ligase synoviolin",
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                "id": "NP_001426924",
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        ],
        "gene_names_uniprotkb": "Syvn1",
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        "function": "Endoplasmic reticulum stress induces HRD1 to protect alveolar type II epithelial cells from apoptosis induced by cigarette smoke extract., [RefSeq, PubMed]; Hrd1 might mediate the ubiquitination of IGF-1R through sema3a and then participate in the regulation of cardiomyocyte apoptosis., [RefSeq, PubMed]; SYVN1 attenuates ferroptosis and alleviates spinal cord ischemia-reperfusion injury in rats by regulating the HMGB1/NRF2/HO-1 axis., [RefSeq, PubMed]; The E3 Ubiquitin Ligase SYVN1 Plays an Antiapoptotic Role in Polycystic Ovary Syndrome by Regulating Mitochondrial Fission. Publication Status: Online-Only, [RefSeq, PubMed]",
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            {
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            {
                "id": "3.1.-.-",
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            }
        ],
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        "function": "Catalytic component of the RAG complex, a multiprotein complex that mediates the DNA cleavage phase during V(D)J recombination. V(D)J recombination assembles a diverse repertoire of immunoglobulin and T-cell receptor genes in developing B and T-lymphocytes through rearrangement of different V (variable), in some cases D (diversity), and J (joining) gene segments. In the RAG complex, RAG1 mediates the DNA-binding to the conserved recombination signal sequences (RSS) and catalyzes the DNA cleavage activities by introducing a double-strand break between the RSS and the adjacent coding segment. RAG2 is not a catalytic component but is required for all known catalytic activities. DNA cleavage occurs in 2 steps: a first nick is introduced in the top strand immediately upstream of the heptamer, generating a 3'-hydroxyl group that can attack the phosphodiester bond on the opposite strand in a direct transesterification reaction, thereby creating 4 DNA ends: 2 hairpin coding ends and 2 blunt, 5'-phosphorylated ends., [UniProtKB, UniProtKB]; Rag1-null Dahl SS rats provide evidence that adaptive immune mechanisms contribute to the exacerbation of salt-induced hypertension and renal injury mediated by increased dietary protein intake., [RefSeq, PubMed]; The infiltration of T cells into the kidney following high-salt intake was significantly blunted in the Rag1-null rats, [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005886 plasma membrane;GO:0042734 presynaptic membrane;GO:0016020 membrane;GO:0005829 cytosol",
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            {
                "id": "G3V7G9_RAT",
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        ],
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        "length": 564,
        "protein_name": "Eukaryotic translation initiation factor 3 subunit L",
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        "refseq_ac": [
            {
                "id": "NP_001029306",
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            }
        ],
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        "protein_names_uniprotkb": "Eukaryotic translation initiation factor 3 subunit L; Eukaryotic translation initiation factor 3 subunit 6-interacting protein; Eukaryotic translation initiation factor 3 subunit E-interacting protein; eIF3l",
        "protein_names_refseq": "eukaryotic translation initiation factor 3 subunit L; eukaryotic translation initiation factor 3, subunit 6 interacting protein",
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        "disease": "",
        "pathway": " (rno:300069);  (R-RNO-156827);  (R-RNO-72649);  (R-RNO-72689);  (R-RNO-72695);  (R-RNO-72702)",
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        "function": "Component of the eukaryotic translation initiation factor 3 (eIF-3) complex, which is required for several steps in the initiation of protein synthesis. The eIF-3 complex associates with the 40S ribosome and facilitates the recruitment of eIF-1, eIF-1A, eIF-2:GTP:methionyl-tRNAi and eIF-5 to form the 43S pre-initiation complex (43S PIC). The eIF-3 complex stimulates mRNA recruitment to the 43S PIC and scanning of the mRNA for AUG recognition. The eIF-3 complex is also required for disassembly and recycling of post-termination ribosomal complexes and subsequently prevents premature joining of the 40S and 60S ribosomal subunits prior to initiation. The eIF-3 complex specifically targets and initiates translation of a subset of mRNAs involved in cell proliferation, including cell cycling, differentiation and apoptosis, and uses different modes of RNA stem-loop binding to exert either translational activation or repression., [UniProtKB, HAMAP, UniProtKB]",
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        ],
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            {
                "id": "NP_705888",
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            }
        ],
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        "protein_names_uniprotkb": "NPC intracellular cholesterol transporter 1",
        "protein_names_refseq": "NPC intracellular cholesterol transporter 1 precursor; Niemann-Pick disease, type C1; solute carrier family 66 member 1",
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        "disease": "Niemann-Pick disease type C1 (Disease Ontology:DOID:0070113); Niemann-Pick disease (Disease Ontology:DOID:14504)",
        "pathway": " (rno:266732);  (R-RNO-8964038)",
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        "function": "Here, we identify lamellar inclusions as the subcellular site of lipid accumulation in neurons, we uncover a vicious cycle of cholesterol synthesis and accretion, which may cause gradual neurodegeneration, and we reveal how beta-cyclodextrin, a potential therapeutic drug, reverts these changes. Our study provides new mechanistic insight in NPC disease and uncovers new targets for therapeutic approaches., [RefSeq, PubMed]; Increased exosome secretion in neurons aging in vitro by NPC1-mediated endosomal cholesterol buildup. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_biological_process": "GO:0031579 membrane raft organization;GO:1904036 negative regulation of epithelial cell apoptotic process;GO:0001889 liver development;GO:0006897 endocytosis;GO:0008203 cholesterol metabolic process",
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    },
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            }
        ],
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        "length": 356,
        "protein_name": "Heparan sulfate 2-O-sulfotransferase 1",
        "gene_name": "Hs2st1",
        "organism": "Rat",
        "refseq_name": "heparan sulfate 2-O-sulfotransferase 1",
        "refseq_ac": [
            {
                "id": "NP_001093988",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001093988",
                "type": "external"
            }
        ],
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        "gene_names_refseq": "Hs2st1",
        "protein_names_uniprotkb": "Heparan sulfate 2-O-sulfotransferase 1; 2-O-sulfotransferase; HS 2-O-sulfotransferase; Heparan sulfate 2-sulfotransferase",
        "protein_names_refseq": "heparan sulfate 2-O-sulfotransferase 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:292155);  (R-RNO-2022928)",
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        "function": "Catalyzes the transfer of a sulfo group from 3'-phospho-5'-adenylyl sulfate (PAPS) to the 2-OH position of iduronic acid (IdoA) or glucuronic acid (GlcA) within the heparan sulfate (HS) chain and participates in HS biosynthesis. Required for metanephric development of kidney formation, suggesting that 2-O-sulfation within HS is essential for signaling between ureteric bud and metanephric mesenchyme., [UniProtKB, UniProtKB]; Chromosome 2 Fragment Substitutions in Dahl Salt-Sensitive Rats and RNA Sequencing Identified Enpep and Hs2st1 as Vascular Inflammatory Modulators., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0004394 heparan sulfate 2-sulfotransferase activity",
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    },
    {
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            {
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                "url": "https://www.uniprot.org/uniprot/G3V7N6",
                "type": "external"
            }
        ],
        "mass": 53380.0,
        "length": 473,
        "protein_name": "Leukocyte receptor cluster member 4",
        "gene_name": "Mboat7",
        "organism": "Rat",
        "refseq_name": "lysophospholipid acyltransferase 7",
        "refseq_ac": [
            {
                "id": "NP_001128450",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001128450",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Mboat7",
        "gene_names_refseq": "Leng4; Mboat7l1; Mboat7; RGD1306945",
        "protein_names_uniprotkb": "Leukocyte receptor cluster member 4; Lysophospholipid acyltransferase 7; Membrane-bound O-acyltransferase domain-containing protein 7",
        "protein_names_refseq": "leukocyte receptor cluster (LRC) member 4; lysophospholipid acyltransferase 7; membrane bound O-acyltransferase domain containing 7-like 1; membrane bound O-acyltransferase domain containing 7",
        "tax_id": 10116,
        "disease": "autosomal recessive intellectual developmental disorder 57 (Disease Ontology:DOID:0081219); hydrocephalus (Disease Ontology:DOID:10908)",
        "pathway": " (rno:308309);  (R-RNO-1482922)",
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        "ec_number_list": [
            {
                "id": "2.3.1.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.23",
                "type": "external"
            },
            {
                "id": "2.3.1.n6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.n6",
                "type": "external"
            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.n7",
                "type": "external"
            },
            {
                "id": "2.3.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.-",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0071617 lysophospholipid acyltransferase activity;GO:0008374 O-acyltransferase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0016020 membrane;GO:0005789 endoplasmic reticulum membrane;GO:0044233 mitochondria-associated endoplasmic reticulum membrane contact site",
        "go_biological_process": "GO:0036151 phosphatidylcholine acyl-chain remodeling;GO:0006661 phosphatidylinositol biosynthetic process;GO:0021819 layer formation in cerebral cortex;GO:0021591 ventricular system development;GO:0046488 phosphatidylinositol metabolic process",
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        ],
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        "protein_name": "Alpha-N-acetylneuraminide alpha-2,8-sialyltransferase",
        "gene_name": "St8sia1",
        "organism": "Rat",
        "refseq_name": "alpha-N-acetylneuraminide alpha-2,8-sialyltransferase",
        "refseq_ac": [
            {
                "id": "NP_036945",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_036945",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "St8sia1",
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        "protein_names_uniprotkb": "Alpha-N-acetylneuraminide alpha-2,8-sialyltransferase; 2.4.3.8; Alpha-2,8-sialyltransferase 8A; Ganglioside GD3 synthase; Ganglioside GT3 synthase; Sialyltransferase 8A; Sialyltransferase St8Sia I",
        "protein_names_refseq": "ST8 alpha-N-acetylneuraminate alpha-2,8-sialyltransferase 1; Sialyltransferase 8 (alpha-N-acetylneuraminate: alpha-28-sialytransferase GD3 synthase); Sialyltransferase 8 A (alpha-N-acetylneuraminate: alpha-28-sialytransferase GD3 synthase) GenBank no: U53883; alpha-2, 8-sialytransferase; alpha-2,8-sialyltransferase; alpha-N-acetylneuraminate: alpha-2,8-sialytransferase; alpha-N-acetylneuraminide alpha-2,8-sialyltransferase; sialyltransferase 8 (alpha-2 8-sialytransferase) A",
        "tax_id": 10116,
        "disease": "developmental and epileptic encephalopathy 47 (Disease Ontology:DOID:0080425)",
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        "publication_count": 1,
        "publication_id_list": "15645117",
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        "function": "Alpha2,8-sialyltransferase has roles in cell proliferation and mobility, [RefSeq, PubMed]",
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        ],
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        ],
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        "refseq_name": "interferon-induced transmembrane protein 5",
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            {
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        "tax_id": 10116,
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        "function": "Catalyzes the transfer of a gamma-phosphoryl group from a nucleoside triphosphate, mainly ATP, to a nucleoside diphosphate via a ping-pong mechanism involving a phosphohistidine intermediate, therefore contributing to the nucleoside triphosphate homeostasis. In vitro, can also use other phosphate donors such as UTP and GTP. Independently of its nucleoside diphosphate kinase activity, involved in mitochondrial membrane tethering, a prerequisite for fusion through direct membrane-binding and hexamerization. Involved in DNA repair of both single- and double-stranded breaks by associating with the ribonucleotide reductase (RNR) complex via interaction with the histone acetyltransferase KAT5, facilitating recruitment to DNA damage sites independently of its kinase activity. Inhibits granulocyte differentiation. May be required for ciliary function during renal development., [UniProtKB, UniProtKB]",
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        "function": "Data indicate that the NLR family, pyrin domain containing 3 protein (Nlrp3)/PYD and CARD domain containing protein (ASC)-mediated alveolar macrophage (AM) pyroptosis increased high-mobility group box 1(HMGB1) secretion in cardiopulmonary bypass (CPB)-induced acute lung injury (ALI)., [RefSeq, PubMed]; Exosome miR-223-3p in the bone marrow-derived mesenchymal stem cells alleviates the inflammation and airway remodeling through NLRP3-induced ASC/Caspase-1/GSDMD signaling pathway., [RefSeq, PubMed]",
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        "protein_name": "T-cell differentiation antigen CD6",
        "gene_name": "Cd6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Cd6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "T-cell differentiation antigen CD6",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "carboxypeptidase N deficiency (Disease Ontology:DOID:0111583)",
        "pathway": " (rno:25752)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Cell adhesion molecule that mediates cell-cell contacts and regulates T-cell responses via its interaction with ALCAM/CD166. Contributes to signaling cascades triggered by activation of the TCR/CD3 complex. Functions as a costimulatory molecule; promotes T-cell activation and proliferation. Contributes to the formation and maturation of the immunological synapse. Functions as a calcium-dependent pattern receptor that binds and aggregates both Gram-positive and Gram-negative bacteria. Binds both lipopolysaccharide (LPS) from Gram-negative bacteria and lipoteichoic acid from Gram-positive bacteria. LPS binding leads to the activation of signaling cascades and down-stream MAP kinases. Mediates activation of the inflammatory response and the secretion of pro-inflammatory cytokines in response to LPS., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0005044 scavenger receptor activity;GO:0019901 protein kinase binding;GO:0042802 identical protein binding;GO:0001530 lipopolysaccharide binding;GO:0070891 lipoteichoic acid binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0042101 T cell receptor complex;GO:0001772 immunological synapse",
        "go_biological_process": "GO:0001934 positive regulation of protein phosphorylation;GO:0032496 response to lipopolysaccharide;GO:0007157 heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules;GO:0042102 positive regulation of T cell proliferation;GO:0031663 lipopolysaccharide-mediated signaling pathway",
        "synthesized_glycan_count": 0,
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        "filter_code": "0000000.0000011.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "G3V8Y2-1",
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            {
                "id": "G3V8Y2_RAT",
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                "type": "external"
            }
        ],
        "mass": 122592.0,
        "length": 1116,
        "protein_name": "Leucine-rich repeats and immunoglobulin-like domains 3",
        "gene_name": "Lrig3",
        "organism": "Rat",
        "refseq_name": "leucine-rich repeats and immunoglobulin-like domains protein 3 precursor",
        "refseq_ac": [
            {
                "id": "NP_001419387",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001419387",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Lrig3",
        "gene_names_refseq": "Lrig3; RGD1561255",
        "protein_names_uniprotkb": "Leucine-rich repeats and immunoglobulin-like domains 3",
        "protein_names_refseq": "leucine-rich repeats and immunoglobulin-like domains protein 3 precursor; leucine-rich repeats and immunoglobulin-like domains protein 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:299830)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "31119777",
        "class_list": "",
        "function": "Upregulation of microRNA-196a improves cognitive impairment and alleviates neuronal damage in hippocampus tissues of Alzheimer's disease through downregulating LRIG3 expression., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0032474 otolith morphogenesis",
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        "kg_view_protein": true
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    {
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            {
                "id": "G3V8Y5_RAT",
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                "type": "external"
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        ],
        "mass": 133897.0,
        "length": 1174,
        "protein_name": "DNA-directed RNA polymerase subunit beta",
        "gene_name": "Polr2b",
        "organism": "Rat",
        "refseq_name": "DNA-directed RNA polymerase II subunit RPB2",
        "refseq_ac": [
            {
                "id": "NP_001099472",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099472",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Polr2b",
        "gene_names_refseq": "Polr2b; RpB2",
        "protein_names_uniprotkb": "DNA-directed RNA polymerase subunit beta; 2.7.7.6",
        "protein_names_refseq": "DNA directed RNA polymerase II polypeptide B; DNA-directed RNA polymerase II subunit RPB2; polymerase (RNA) II (DNA directed) polypeptide B, 140kDa; polymerase (RNA) II subunit B",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:289561);  (R-RNO-112382);  (R-RNO-113418);  (R-RNO-5578749);  (R-RNO-674695);  (R-RNO-6781823);  (R-RNO-6782135);  (R-RNO-6782210);  (R-RNO-6796648);  (R-RNO-6803529);  (R-RNO-6807505);  (R-RNO-72086);  (R-RNO-72163);  (R-RNO-72165);  (R-RNO-72203);  (R-RNO-73776);  (R-RNO-73779);  (R-RNO-75953);  (R-RNO-75955);  (R-RNO-76042);  (R-RNO-77075);  (R-RNO-9018519);  (R-RNO-9770562)",
        "pathway_count": 23,
        "publication_count": 1,
        "publication_id_list": "25568312",
        "class_list": "",
        "function": "DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates., [UniProtKB, UniProtKB, UniProtKB]; Data indicate that activation of RNA polymerase II and p70 S6 kinase (P70S6K) are increased in apoptotic neurons, and their inhibition prevents apoptosis., [RefSeq, PubMed]; RNA-dependent RNA polymerase that catalyzes the extension of a non-coding RNA (ncRNA) at the 3'-end using the four ribonucleoside triphosphates as substrates. An internal ncRNA sequence near the 3'-end serves as a template in a single-round Pol II-mediated RNA polymerization reaction. May decrease the stability of ncRNAs that repress Pol II-mediated gene transcription., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": [
            {
                "id": "6.5.1.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.5.1.1",
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            {
                "id": "3.6.4.13",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.32",
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            },
            {
                "id": "3.1.3.16",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.7",
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.6",
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            },
            {
                "id": "5.6.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.3",
                "type": "external"
            },
            {
                "id": "2.7.7.19",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.19",
                "type": "external"
            },
            {
                "id": "5.2.1.8",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.2.1.8",
                "type": "external"
            },
            {
                "id": "2.1.1.348",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.348",
                "type": "external"
            },
            {
                "id": "2.3.2.27",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
                "type": "external"
            },
            {
                "id": "3.1.11.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.11.-",
                "type": "external"
            },
            {
                "id": "2.7.11.22",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.22",
                "type": "external"
            },
            {
                "id": "2.7.11.23",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.23",
                "type": "external"
            },
            {
                "id": "2.7.11.24",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.24",
                "type": "external"
            },
            {
                "id": "3.1.3.53",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.53",
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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": "3.6.4.10",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.4.10",
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            },
            {
                "id": "3.1.27.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.27.-",
                "type": "external"
            },
            {
                "id": "2.7.7.52",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.52",
                "type": "external"
            },
            {
                "id": "5.6.2.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.4",
                "type": "external"
            },
            {
                "id": "3.4.19.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.19.12",
                "type": "external"
            },
            {
                "id": "2.7.1.78",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.78",
                "type": "external"
            },
            {
                "id": "2.1.1.56",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.1.1.56",
                "type": "external"
            },
            {
                "id": "3.1.26.n2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.26.n2",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0003968 RNA-directed RNA polymerase activity;GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0008270 zinc ion binding;GO:0016787 hydrolase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005665 RNA polymerase II, core complex;GO:0000781 chromosome, telomeric region;GO:0000428 DNA-directed RNA polymerase complex",
        "go_biological_process": "GO:0006366 transcription by RNA polymerase II;GO:0006367 transcription initiation at RNA polymerase II promoter;GO:0006368 transcription elongation by RNA polymerase II;GO:0006354 DNA-templated transcription elongation;GO:0006351 DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "G3V8Y5-1",
        "record_type": "protein",
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        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
                "id": "G3V8Z3_RAT",
                "url": "https://www.uniprot.org/uniprot/G3V8Z3",
                "type": "external"
            }
        ],
        "mass": 53259.0,
        "length": 487,
        "protein_name": "G-patch domain and KOW motifs-containing protein",
        "gene_name": "Gpkow",
        "organism": "Rat",
        "refseq_name": "G-patch domain and KOW motifs-containing protein",
        "refseq_ac": [
            {
                "id": "NP_001102851",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001102851",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Gpkow",
        "gene_names_refseq": "Gpkow",
        "protein_names_uniprotkb": "G-patch domain and KOW motifs-containing protein",
        "protein_names_refseq": "G patch domain and KOW motifs-containing protein; G-patch domain and KOW motifs-containing protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:679890);  (R-RNO-72163)",
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        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "RNA-binding protein involved in pre-mRNA splicing., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003723 RNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005681 spliceosomal complex;GO:0071018 U12-type catalytic step 2 spliceosome",
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        "record_id": "G3V8Z3-1",
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        "kg_view_protein": true
    },
    {
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            {
                "id": "G3V901_RAT",
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                "type": "external"
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        ],
        "mass": 86308.0,
        "length": 746,
        "protein_name": "Exostosin-1",
        "gene_name": "Ext1",
        "organism": "Rat",
        "refseq_name": "exostosin-1",
        "refseq_ac": [
            {
                "id": "NP_001124012",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001124012",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ext1",
        "gene_names_refseq": "Ext1",
        "protein_names_uniprotkb": "Exostosin-1; 2.4.1.225; N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase",
        "protein_names_refseq": "exostoses (multiple) 1; exostosin-1",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); hereditary multiple exostoses (Disease Ontology:DOID:206); germ cell cancer (Disease Ontology:DOID:2994); chondrosarcoma (Disease Ontology:DOID:3371)",
        "pathway": " (rno:299907);  (R-RNO-2022928)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22339633",
        "class_list": "",
        "function": "Ext1 gene is involved in heparan sulfate proteoglycans metabolism., [RefSeq, PubMed]; Glycosyltransferase forming with EXT2 the heterodimeric heparan sulfate polymerase which catalyzes the elongation of the heparan sulfate glycan backbone. Glycan backbone extension consists in the alternating transfer of (1->4)-beta-D-GlcA and (1->4)-alpha-D-GlcNAc residues from their respective UDP-sugar donors. Both EXT1 and EXT2 are required for the full activity of the polymerase since EXT1 bears the N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase activity within the complex while EXT2 carries the glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase activity. Heparan sulfate proteoglycans are ubiquitous components of the extracellular matrix and play an important role in tissue homeostasis and signaling., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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            },
            {
                "id": "2.4.1.225",
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            }
        ],
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        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0045202 synapse;GO:0005789 endoplasmic reticulum membrane;GO:0043541 UDP-N-acetylglucosamine transferase complex",
        "go_biological_process": "GO:1904888 cranial skeletal system development;GO:0051923 sulfation;GO:0060429 epithelium development;GO:0043931 ossification involved in bone maturation;GO:0000271 polysaccharide biosynthetic process",
        "synthesized_glycan_count": 0,
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    },
    {
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            {
                "id": "G3V918_RAT",
                "url": "https://www.uniprot.org/uniprot/G3V918",
                "type": "external"
            }
        ],
        "mass": 107580.0,
        "length": 1010,
        "protein_name": "Trifunctional purine biosynthetic protein adenosine-3",
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        "refseq_name": "trifunctional purine biosynthetic protein adenosine-3",
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            {
                "id": "NP_001011899",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001011899",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Gart",
        "gene_names_refseq": "Gart",
        "protein_names_uniprotkb": "Trifunctional purine biosynthetic protein adenosine-3; 5'-phosphoribosylglycinamide transformylase; AIR synthase; AIRS; GAR transformylase; GARS; GART; Glycinamide ribonucleotide synthetase; Phosphoribosyl-aminoimidazole synthetase; Phosphoribosylglycinamide synthetase",
        "protein_names_refseq": "trifunctional purine biosynthetic protein adenosine-3",
        "tax_id": 10116,
        "disease": "Down syndrome (Disease Ontology:DOID:14250)",
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        "publication_id_list": "24709117;29393594",
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            {
                "id": "XP_219296",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
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                "id": "3.6.4.13",
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                "id": "2.7.7.19",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.19",
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                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
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            {
                "id": "2.3.2.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.-",
                "type": "external"
            },
            {
                "id": "2.3.2.25",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.25",
                "type": "external"
            },
            {
                "id": "2.7.7.6",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.6",
                "type": "external"
            },
            {
                "id": "3.1.4.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.4.-",
                "type": "external"
            },
            {
                "id": "3.1.4.35",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.4.35",
                "type": "external"
            },
            {
                "id": "3.1.3.16",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.16",
                "type": "external"
            },
            {
                "id": "3.1.3.53",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.53",
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            },
            {
                "id": "2.7.7.52",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.7.52",
                "type": "external"
            },
            {
                "id": "2.7.1.78",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.1.78",
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            },
            {
                "id": "3.6.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.-",
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            {
                "id": "2.7.11.39",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.39",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003676 nucleic acid binding;GO:0061630 ubiquitin protein ligase activity;GO:0019901 protein kinase binding;GO:0004842 ubiquitin-protein transferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005813 centrosome;GO:0016607 nuclear speck;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0006397 mRNA processing;GO:0016567 protein ubiquitination;GO:0006275 regulation of DNA replication;GO:0006511 ubiquitin-dependent protein catabolic process;GO:0001701 in utero embryonic development",
        "synthesized_glycan_count": 0,
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        "record_id": "G3V953-1",
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    },
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            {
                "id": "G3V970_RAT",
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            }
        ],
        "mass": 32210.0,
        "length": 284,
        "protein_name": "SIX homeobox 1",
        "gene_name": "Six1",
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        "refseq_name": "homeobox protein SIX1",
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            {
                "id": "NP_446211",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_446211",
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            }
        ],
        "gene_names_uniprotkb": "Six1",
        "gene_names_refseq": "Six1",
        "protein_names_uniprotkb": "SIX homeobox 1",
        "protein_names_refseq": "homeobox protein SIX1; sine oculis homeobox homolog 1; sine oculis-related homeobox 1 homolog",
        "tax_id": 10116,
        "disease": "branchiootic syndrome 3 (Disease Ontology:DOID:0061210); autosomal dominant nonsyndromic deafness 23 (Disease Ontology:DOID:0110553); branchiootorenal syndrome (Disease Ontology:DOID:14702); breast cancer (Disease Ontology:DOID:1612); nephroblastoma (Disease Ontology:DOID:2154); neurilemmoma (Disease Ontology:DOID:3192); ovarian carcinoma (Disease Ontology:DOID:4001); hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (rno:114634)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "35180623;37479098",
        "class_list": "",
        "function": "SIX1 attenuates inflammation and rheumatoid arthritis by silencing MyD88-dependent TLR1/2 signaling., [RefSeq, PubMed]; SIX1 induced HULC modulates neuropathic pain and Schwann cell oxidative stress after sciatic nerve injury., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0003700 DNA-binding transcription factor activity;GO:0000976 transcription cis-regulatory region binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0030878 thyroid gland development;GO:0001759 organ induction;GO:0050678 regulation of epithelial cell proliferation;GO:0086100 endothelin receptor signaling pathway;GO:0061055 myotome development",
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        ],
        "mass": 18766.0,
        "length": 166,
        "protein_name": "Gem-associated protein 6",
        "gene_name": "Gemin6",
        "organism": "Rat",
        "refseq_name": "gem-associated protein 6 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001009466",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001009466",
                "type": "external"
            }
        ],
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        "gene_names_refseq": "Gemin6",
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        "protein_names_refseq": "gem-associated protein 6 isoform 1; gem-associated protein 6",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362688);  (R-RNO-191859)",
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        "function": "The SMN complex catalyzes the assembly of small nuclear ribonucleoproteins (snRNPs), the building blocks of the spliceosome, and thereby plays an important role in the splicing of cellular pre-mRNAs. Most spliceosomal snRNPs contain a common set of Sm proteins SNRPB, SNRPD1, SNRPD2, SNRPD3, SNRPE, SNRPF and SNRPG that assemble in a heptameric protein ring on the Sm site of the small nuclear RNA to form the core snRNP (Sm core). In the cytosol, the Sm proteins SNRPD1, SNRPD2, SNRPE, SNRPF and SNRPG are trapped in an inactive 6S pICln-Sm complex by the chaperone CLNS1A that controls the assembly of the core snRNP. To assemble core snRNPs, the SMN complex accepts the trapped 5Sm proteins from CLNS1A forming an intermediate. Binding of snRNA inside 5Sm triggers eviction of the SMN complex, thereby allowing binding of SNRPD3 and SNRPB to complete assembly of the core snRNP., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0016604 nuclear body;GO:0032797 SMN complex",
        "go_biological_process": "GO:0000387 spliceosomal snRNP assembly;GO:0000245 spliceosomal complex assembly",
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                "type": "external"
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        ],
        "mass": 20437.0,
        "length": 175,
        "protein_name": "Bcl-2-related protein A1",
        "gene_name": "Bcl2a1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Bcl2a1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Bcl-2-related protein A1; Hemopoietic-specific early response protein; Protein BFL-1",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "class_list": "",
        "function": "Retards apoptosis induced by IL-3 deprivation. May function in the response of hemopoietic cells to external signals and in maintaining endothelial survival during infection. Can inhibit apoptosis induced by serum starvation in the mammary epithelial cell line HC11., [UniProtKB, UniProtKB]",
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        "function": "Component of the MICOS complex, a large protein complex of the mitochondrial inner membrane that plays crucial roles in the maintenance of crista junctions, inner membrane architecture, and formation of contact sites to the outer membrane., [UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0006631 fatty acid metabolic process;GO:0006974 DNA damage response;GO:0010883 regulation of lipid storage;GO:1902445 regulation of mitochondrial membrane permeability involved in programmed necrotic cell death;GO:0035513 oxidative RNA demethylation",
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        ],
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        "length": 666,
        "protein_name": "Frizzled-3",
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        "organism": "Rat",
        "refseq_name": "frizzled-3 precursor",
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            {
                "id": "NP_703204",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_703204",
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            }
        ],
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        "gene_names_refseq": "Fzd3",
        "protein_names_uniprotkb": "Frizzled-3",
        "protein_names_refseq": "frizzled family receptor 3; frizzled-3 precursor; frizzled-3",
        "tax_id": 10116,
        "disease": "Williams-Beuren syndrome (Disease Ontology:DOID:1928); schizophrenia (Disease Ontology:DOID:5419)",
        "pathway": " (R-RNO-4086398);  (R-RNO-4086400);  (R-RNO-4608870)",
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        "class_list": "",
        "function": "Over-expressed LOC101927196 suppressed oxidative stress levels and neuron cell proliferation in a rat model of autism through disrupting the Wnt signaling pathway by targeting FZD3. Erratum:[Cell Signal. 2019 Dec;64:109396. PMID: 31471214], [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0048787 presynaptic active zone membrane;GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0030424 axon",
        "go_biological_process": "GO:0042472 inner ear morphogenesis;GO:0001764 neuron migration;GO:0001843 neural tube closure;GO:0001942 hair follicle development;GO:0051602 response to electrical stimulus",
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        ],
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            {
                "id": "NP_001395655",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001395655",
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            }
        ],
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