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            {
                "id": "NP_001099277",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001099277",
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            }
        ],
        "gene_names_uniprotkb": "Mnt",
        "gene_names_refseq": "Mnt",
        "protein_names_uniprotkb": "Max-binding protein MNT; Myc antagonist MNT; Protein ROX",
        "protein_names_refseq": "MNT, MAX dimerization protein; max binding protein; max-binding protein MNT",
        "tax_id": 10116,
        "disease": "Miller-Dieker lissencephaly syndrome (Disease Ontology:DOID:0060469)",
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        "publication_id_list": "23535568",
        "class_list": "",
        "function": "Binds DNA as a heterodimer with MAX and represses transcription. Binds to the canonical E box sequence 5'-CACGTG-3' and, with higher affinity, to 5'-CACGCG-3'., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; These data identify Mnt as a previously unrecognized negative regulator of pathological vascular remodeling., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0046983 protein dimerization activity;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0070443 Mad-Max complex",
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    },
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        ],
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        "protein_name": "NF-kappa-B-repressing factor",
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            {
                "id": "NP_001389153",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001389153",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Nkrf",
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        "function": "Enhances the ATPase activity of DHX15 by acting like a brace that tethers mobile sections of DHX15 together, stabilizing a functional conformation with high RNA affinity of DHX15. Involved in the constitutive silencing of the interferon beta promoter, independently of the virus-induced signals, and in the inhibition of the basal and cytokine-induced iNOS promoter activity. Also involved in the regulation of IL-8 transcription. May also act as a DNA-binding transcription regulator: interacts with a specific negative regulatory element (NRE) 5'-AATTCCTCTGA-3' to mediate transcriptional repression of certain NK-kappa-B responsive genes., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0001671 ATPase activator activity;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus",
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    },
    {
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            {
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        ],
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        "protein_name": "Methyl-CpG-binding domain protein 5",
        "gene_name": "Mbd5",
        "organism": "Rat",
        "refseq_name": "methyl-CpG-binding domain protein 5 isoform X1",
        "refseq_ac": [
            {
                "id": "XP_056841390",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_056841390",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Mbd5",
        "gene_names_refseq": "Mbd5",
        "protein_names_uniprotkb": "Methyl-CpG-binding domain protein 5; Methyl-CpG-binding protein MBD5",
        "protein_names_refseq": "methyl-CpG-binding domain protein 5 isoform X1",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); autosomal dominant intellectual developmental disorder (Disease Ontology:DOID:0060307); autosomal dominant intellectual developmental disorder 1 (Disease Ontology:DOID:0070031)",
        "pathway": " (rno:311026);  (R-RNO-5689603)",
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        "function": "Non-catalytic component of the polycomb repressive deubiquitinase (PR-DUB) complex, a complex that specifically mediates deubiquitination of histone H2A monoubiquitinated at 'Lys-120' (H2AK119ub1). Important for stability of PR-DUB components and stimulating its ubiquitinase activity. As part of the PR-DUB complex, associates with chromatin enriched in histone marks H3K4me1, H3K4me3, and H3K27Ac, but not in H3K27me3. The PR-DUB complex is an epigenetic regulator of gene expression, including genes involved in cell growth and survivability. MBD5 and MBD6 containing complexes associate with distinct chromatin regions enriched in genes involved in different pathways. Heterochromatin recruitment is not mediated by DNA methylation. The PR-DUB complex is an epigenetic regulator of gene expression, including genes involved in development, cell communication, signaling, cell proliferation and cell viability., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003682 chromatin binding",
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        "go_biological_process": "GO:0060399 positive regulation of growth hormone receptor signaling pathway;GO:0007399 nervous system development;GO:0040014 regulation of multicellular organism growth;GO:0042593 glucose homeostasis;GO:0050795 regulation of behavior",
        "synthesized_glycan_count": 0,
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        "kg_view_protein": true
    },
    {
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            {
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        ],
        "mass": 149536.0,
        "length": 1332,
        "protein_name": "FA complementation group I",
        "gene_name": "Fanci",
        "organism": "Rat",
        "refseq_name": "Fanconi anemia group I protein",
        "refseq_ac": [
            {
                "id": "NP_001414599",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414599",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Fanci",
        "gene_names_refseq": "Fanci",
        "protein_names_uniprotkb": "FA complementation group I",
        "protein_names_refseq": "Fanconi anemia group I protein; Fanconi anemia, complementation group I",
        "tax_id": 10116,
        "disease": "female breast cancer (Disease Ontology:DOID:0050671); tongue squamous cell carcinoma (Disease Ontology:DOID:0050865); Fanconi anemia complementation group I (Disease Ontology:DOID:0111091); Fanconi anemia (Disease Ontology:DOID:13636)",
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    {
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            {
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        ],
        "mass": 35025.0,
        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or14j3",
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        "gene_names_uniprotkb": "Or14j3; LOC100365012",
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        "protein_names_uniprotkb": "Olfactory receptor",
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        "tax_id": 10116,
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        "pathway": " (rno:309578);  (rno:406014)",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
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    {
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            {
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        ],
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        "protein_name": "A disintegrin and metalloproteinase with thrombospondin motifs 18",
        "gene_name": "Adamts18",
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        "refseq_name": "A disintegrin and metalloproteinase with thrombospondin motifs 18 precursor",
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            {
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001178873",
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            }
        ],
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        "gene_names_refseq": "Adamts18; RGD1560118",
        "protein_names_uniprotkb": "A disintegrin and metalloproteinase with thrombospondin motifs 18",
        "protein_names_refseq": "A disintegrin and metalloproteinase with thrombospondin motifs 18 precursor; A disintegrin and metalloproteinase with thrombospondin motifs 18; a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 18",
        "tax_id": 10116,
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        "function": "The progression of obstructive renal fibrosis in rats is regulated by ADAMTS18 gene methylation in the embryonic kidney through the AKT/Notch pathway., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0004222 metalloendopeptidase activity;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0031012 extracellular matrix",
        "go_biological_process": "GO:0006508 proteolysis;GO:0030198 extracellular matrix organization;GO:0090331 negative regulation of platelet aggregation;GO:0001654 eye development",
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    {
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        ],
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        "protein_name": "Olfactory receptor",
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        "refseq_name": "olfactory receptor Olr1452",
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            {
                "id": "NP_001000773",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000773",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Or2t44b",
        "gene_names_refseq": "Olr1452; Or2t44b",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1452; olfactory receptor Olr1452; olfactory receptor gene Olr1452",
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            }
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        "function": "Promotes the growth of epithelial cells. May stimulate the phosphorylation of EGFR and mitogen-activated protein kinases., [UniProtKB, UniProtKB]",
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            {
                "id": "NP_001128333",
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        ],
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                "id": "NP_001258141",
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        "function": "Autophagy factor required for autophagosome formation and mitophagy. Target of the TOR kinase signaling pathway that regulates autophagy through the control of the phosphorylation status of ATG13 and ULK1, and the regulation of the ATG13-ULK1-RB1CC1 complex. Through its regulation of ULK1 activity, plays a role in the regulation of the kinase activity of mTORC1 and cell proliferation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Circulating Exosomal miR-1-3p from Rats with Myocardial Infarction Plays a Protective Effect on Contrast-Induced Nephropathy via Targeting ATG13 and activating the AKT Signaling Pathway. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "protein_name": "Transcription initiation factor IIE subunit beta",
        "gene_name": "Gtf2e2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Gtf2e2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transcription initiation factor IIE subunit beta",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "nonphotosensitive trichothiodystrophy 6 (Disease Ontology:DOID:0111872)",
        "pathway": " (rno:306516);  (R-RNO-674695);  (R-RNO-6807505);  (R-RNO-73776);  (R-RNO-73779);  (R-RNO-75953);  (R-RNO-76042)",
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        "class_list": "",
        "function": "Recruits TFIIH to the initiation complex and stimulates the RNA polymerase II C-terminal domain kinase and DNA-dependent ATPase activities of TFIIH. Both TFIIH and TFIIE are required for promoter clearance by RNA polymerase., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0016251 RNA polymerase II general transcription initiation factor activity",
        "go_cellular_component": "GO:0005673 transcription factor TFIIE complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005669 transcription factor TFIID complex",
        "go_biological_process": "GO:0006366 transcription by RNA polymerase II;GO:0006367 transcription initiation at RNA polymerase II promoter;GO:0051123 RNA polymerase II preinitiation complex assembly",
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    },
    {
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            {
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        ],
        "mass": 240518.0,
        "length": 2121,
        "protein_name": "Polycystin family receptor for egg jelly",
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            {
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            }
        ],
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        "gene_names_refseq": "Pkdrej",
        "protein_names_uniprotkb": "Polycystin family receptor for egg jelly; PKD and REJ homolog; Polycystic kidney disease and receptor for egg jelly-related protein",
        "protein_names_refseq": "polycystic kidney disease (polycystin) and REJ homolog (sperm receptor for egg jelly homolog, sea urchin); polycystic kidney disease and receptor for egg jelly-related protein; polycystin (PKD) family receptor for egg jelly; polycystin family receptor for egg jelly precursor",
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        "publication_id_list": "29393594",
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        "function": "Testis-specific protein that controls sperm transport and the timing of zona pellucida-evoked exocytosis of the sperm acrosome., [UniProtKB, UniProtKB]",
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        ],
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        ],
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        "go_cellular_component": "GO:0005634 nucleus",
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            {
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        "protein_names_uniprotkb": "Protocadherin Fat 4; FAT tumor suppressor homolog 4; Fat-like cadherin protein FAT-J",
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        ],
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        "go_molecular_function": "GO:0004222 metalloendopeptidase activity",
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        "go_biological_process": "GO:0006508 proteolysis;GO:0007155 cell adhesion;GO:0007339 binding of sperm to zona pellucida;GO:0008584 male gonad development",
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        "protein_name": "FRAS1-related extracellular matrix protein 2",
        "gene_name": "Frem2",
        "organism": "Rat",
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        "protein_names_uniprotkb": "FRAS1-related extracellular matrix protein 2; ECM3 homolog",
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        "tax_id": 10116,
        "disease": "Fraser syndrome (Disease Ontology:DOID:0090001); Fraser syndrome 2 (Disease Ontology:DOID:0111407); isolated cryptophthalmia (Disease Ontology:DOID:0111717)",
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        "function": "Extracellular matrix protein required for maintenance of the integrity of the skin epithelium and for maintenance of renal epithelia. Required for epidermal adhesion. Involved in the development of eyelids and the anterior segment of the eyeballs., [UniProtKB, UniProtKB]",
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        "function": "Part of the spliceosome which catalyzes two sequential transesterification reactions, first the excision of the non-coding intron from pre-mRNA and then the ligation of the coding exons to form the mature mRNA. Plays a role in stabilizing the structure of the spliceosome catalytic core and docking of the branch helix into the active site, producing 5'-exon and lariat intron-3'-intermediates. May protect cells from TP53-dependent apoptosis upon dsDNA break damage through association with PRP19-CD5L complex., [UniProtKB, HAMAP]",
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        "function": "A shedding soluble form of interleukin-17 receptor D exacerbates collagen-induced arthritis through facilitating TNF-alpha-dependent receptor clustering., [RefSeq, PubMed]; Results suggest an involvement of Sef during the nerve regeneration process, possibly by fine-tuning the effects of FGF signaling, [RefSeq, PubMed]; The IL-17RD.TNFR2 complex in activation of NF-kappaB may explain the role of TNFR2 in inflammatory diseases including nephritis., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0030368 interleukin-17 receptor activity",
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        "protein_name": "Olfactory receptor",
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            {
                "id": "NP_001000250",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000250",
                "type": "external"
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
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        "protein_name": "Junctophilin",
        "gene_name": "Ap1g2",
        "organism": "Rat",
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        "protein_names_uniprotkb": "Junctophilin",
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        "tax_id": 10116,
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        "function": "Junctophilins contribute to the formation of junctional membrane complexes (JMCs) which link the plasma membrane with the endoplasmic or sarcoplasmic reticulum in excitable cells. Provides a structural foundation for functional cross-talk between the cell surface and intracellular calcium release channels. JPH4 is brain-specific and appears to have an active role in certain neurons involved in motor coordination and memory., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0035615 clathrin adaptor activity",
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        "protein_name": "Extracellular leucine-rich repeat and fibronectin type III domain containing 2",
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        "protein_names_uniprotkb": "Extracellular leucine-rich repeat and fibronectin type III domain containing 2",
        "protein_names_refseq": "extracellular leucine-rich repeat and fibronectin type III containing 2; extracellular leucine-rich repeat and fibronectin type III domain containing 2 precursor; extracellular leucine-rich repeat and fibronectin type III domain containing 2, pseudogene 1; protein phosphatase 1 regulatory subunit 29-like",
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        "go_molecular_function": "GO:0004864 protein phosphatase inhibitor activity;GO:0038023 signaling receptor activity",
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    {
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        ],
        "mass": 142998.0,
        "length": 1283,
        "protein_name": "RNA helicase Mov10l1",
        "gene_name": "Mov10l1",
        "organism": "Rat",
        "refseq_name": "RNA helicase Mov10l1",
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            {
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        "gene_names_uniprotkb": "Mov10l1",
        "gene_names_refseq": "Mov10l1",
        "protein_names_uniprotkb": "RNA helicase Mov10l1; 3.6.4.13",
        "protein_names_refseq": "Moloney leukemia virus 10-like 1; Mov10 RISC complex RNA helicase like 1; Mov10 like RISC complex RNA helicase 1; Mov10l1, Moloney leukemia virus 10-like 1, homolog; RNA helicase Mov10l1",
        "tax_id": 10116,
        "disease": "spermatogenic failure 73 (Disease Ontology:DOID:0070572); primary ovarian insufficiency (Disease Ontology:DOID:5426)",
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        "function": "ATP-dependent RNA helicase required during spermatogenesis to repress transposable elements and prevent their mobilization, which is essential for germline integrity. Acts via the piRNA metabolic process, which mediates the repression of transposable elements during meiosis by forming complexes composed of piRNAs and Piwi proteins and governs the methylation and subsequent repression of transposons. Involved in the primary piRNA metabolic process. Specifically binds to piRNA precursors and promotes the generation of intermediate piRNA processing fragments that are subsequently loaded to Piwi proteins. Acts via its ATP-dependent RNA helicase activity: displays 5'-3' RNA unwinding activity and probably mediates unwinding and funneling of single-stranded piRNA precursor transcripts to the endonuclease that catalyzes the first cleavage step of piRNA processing to generate piRNA intermediate fragments that are subsequently loaded to Piwi proteins., [UniProtKB, UniProtKB]",
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        "biomarker_type": "",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0042802 identical protein binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0042127 regulation of cell population proliferation;GO:0045944 positive regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
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        "kg_view_protein": true
    },
    {
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            {
                "id": "D3ZJE0_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZJE0",
                "type": "external"
            }
        ],
        "mass": 73420.0,
        "length": 650,
        "protein_name": "alpha-1,2-Mannosidase",
        "gene_name": "Edem1",
        "organism": "Rat",
        "refseq_name": "ER degradation-enhancing alpha-mannosidase-like protein 1",
        "refseq_ac": [
            {
                "id": "NP_001292208",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001292208",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Edem1",
        "gene_names_refseq": "Edem1; RGD1563633",
        "protein_names_uniprotkb": "alpha-1,2-Mannosidase; 3.2.1.-",
        "protein_names_refseq": "ER degradation enhancer, mannosidase alpha-like 1; ER degradation-enhancing alpha-mannosidase-like 1; ER degradation-enhancing alpha-mannosidase-like protein 1",
        "tax_id": 10116,
        "disease": "cystic fibrosis (Disease Ontology:DOID:1485)",
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        "publication_id_list": "17360537",
        "class_list": "",
        "function": "Extracts misfolded glycoproteins, but not glycoproteins undergoing productive folding, from the calnexin cycle. It is directly involved in endoplasmic reticulum-associated degradation (ERAD) and targets misfolded glycoproteins for degradation in an N-glycan-independent manner, probably by forming a complex with SEL1L. It has low mannosidase activity, catalyzing mannose trimming from Man8GlcNAc2 to Man7GlcNAc2., [UniProtKB, UniProtKB]; The endoplasmic reticulum quality control vesicular transport pathway using EDEM1 does not involve the COPII exit sites, [RefSeq, PubMed]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0051787 misfolded protein binding;GO:0004571 mannosyl-oligosaccharide 1,2-alpha-mannosidase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane;GO:0044322 endoplasmic reticulum quality control compartment",
        "go_biological_process": "GO:0005975 carbohydrate metabolic process;GO:0006511 ubiquitin-dependent protein catabolic process;GO:0036503 ERAD pathway;GO:1904380 endoplasmic reticulum mannose trimming;GO:1904154 positive regulation of retrograde protein transport, ER to cytosol",
        "synthesized_glycan_count": 0,
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZJM7-1",
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            {
                "id": "D3ZJM7_RAT",
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                "type": "external"
            }
        ],
        "mass": 92371.0,
        "length": 836,
        "protein_name": "Microcephalin",
        "gene_name": "Mcph1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Mcph1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Microcephalin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "oral squamous cell carcinoma (Disease Ontology:DOID:0050866); primary autosomal recessive microcephaly 1 (Disease Ontology:DOID:0070285); autosomal recessive primary microcephaly (Disease Ontology:DOID:0070296); microcephaly (Disease Ontology:DOID:10907); endometrial cancer (Disease Ontology:DOID:1380); breast cancer (Disease Ontology:DOID:1612); renal carcinoma (Disease Ontology:DOID:4451)",
        "pathway": " (R-RNO-2299718)",
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Implicated in chromosome condensation and DNA damage induced cellular responses. May play a role in neurogenesis and regulation of the size of the cerebral cortex., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "go_molecular_function": "GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005813 centrosome",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0000278 mitotic cell cycle;GO:0021987 cerebral cortex development;GO:0050727 regulation of inflammatory response;GO:0060348 bone development",
        "synthesized_glycan_count": 0,
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        "filter_code": "0000000.0000111.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "D3ZJU0-1",
        "uniprot_id": [
            {
                "id": "D3ZJU0_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZJU0",
                "type": "external"
            }
        ],
        "mass": 195057.0,
        "length": 1826,
        "protein_name": "AT-rich interactive domain-containing protein 2",
        "gene_name": "Arid2",
        "organism": "Rat",
        "refseq_name": "AT-rich interactive domain-containing protein 2",
        "refseq_ac": [
            {
                "id": "NP_001419436",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001419436",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Arid2",
        "gene_names_refseq": "Arid2",
        "protein_names_uniprotkb": "AT-rich interactive domain-containing protein 2; BRG1-associated factor 200; Zinc finger protein with activation potential; Zipzap/p200",
        "protein_names_refseq": "AT rich interactive domain 2 (Arid-rfx like); AT-rich interactive domain-containing protein 2",
        "tax_id": 10116,
        "disease": "oral squamous cell carcinoma (Disease Ontology:DOID:0050866); Coffin-Siris syndrome 6 (Disease Ontology:DOID:0080297); alcohol use disorder (Disease Ontology:DOID:1574); hepatocellular carcinoma (Disease Ontology:DOID:684); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:366980)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Required for the stability of the SWI/SNF chromatin remodeling complex SWI/SNF-B (PBAF). May be involved in targeting the complex to different genes. May be involved in regulating transcriptional activation of cardiac genes., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0016514 SWI/SNF complex;GO:0035060 brahma complex",
        "go_biological_process": "GO:0072359 circulatory system development;GO:0006338 chromatin remodeling;GO:0006351 DNA-templated transcription;GO:0008285 negative regulation of cell population proliferation;GO:0006355 regulation of DNA-templated transcription",
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    },
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            {
                "id": "D3ZKC9_RAT",
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                "type": "external"
            }
        ],
        "mass": 215857.0,
        "length": 1931,
        "protein_name": "Vir like m6A methyltransferase associated",
        "gene_name": "Virma",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Virma; RGD1559904",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Vir like m6A methyltransferase associated",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:313061)",
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        "go_cellular_component": "GO:0036396 RNA N6-methyladenosine methyltransferase complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0016607 nuclear speck",
        "go_biological_process": "GO:0006397 mRNA processing;GO:0008380 RNA splicing",
        "synthesized_glycan_count": 0,
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        "record_id": "D3ZKC9-1",
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    },
    {
        "uniprot_canonical_ac": "D3ZKE0-1",
        "uniprot_id": [
            {
                "id": "D3ZKE0_RAT",
                "url": "https://www.uniprot.org/uniprot/D3ZKE0",
                "type": "external"
            }
        ],
        "mass": 140017.0,
        "length": 1228,
        "protein_name": "N-acetylglucosamine-1-phosphotransferase subunits alpha/beta",
        "gene_name": "Gnptab",
        "organism": "Rat",
        "refseq_name": "N-acetylglucosamine-1-phosphotransferase subunits alpha/beta",
        "refseq_ac": [
            {
                "id": "NP_001414087",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414087",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Gnptab",
        "gene_names_refseq": "Gnptab; RGD1564821",
        "protein_names_uniprotkb": "N-acetylglucosamine-1-phosphotransferase subunits alpha/beta; 2.7.8.17; GlcNAc-1-phosphotransferase subunits alpha/beta; Stealth protein GNPTAB; UDP-N-acetylglucosamine-1-phosphotransferase subunits alpha/beta",
        "protein_names_refseq": "N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits; N-acetylglucosamine-1-phosphotransferase subunits alpha/beta",
        "tax_id": 10116,
        "disease": "mucolipidosis II alpha/beta (Disease Ontology:DOID:0080070); mucolipidosis III alpha/beta (Disease Ontology:DOID:0080071); mucolipidosis (Disease Ontology:DOID:0080488); congenital heart disease (Disease Ontology:DOID:1682)",
        "pathway": " (rno:362865)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the formation of mannose 6-phosphate (M6P) markers on high mannose type oligosaccharides in the Golgi apparatus. M6P residues are required to bind to the M6P receptors (MPR), which mediate the vesicular transport of lysosomal enzymes to the endosomal/prelysosomal compartment., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "secondary_ac_list": "",
        "ec_number_list": [
            {
                "id": "2.7.8.17",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.8.17",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0003976 UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase activity;GO:0005509 calcium ion binding;GO:0016772 transferase activity, transferring phosphorus-containing groups",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus;GO:0070622 UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase complex;GO:0012505 endomembrane system",
        "go_biological_process": "GO:0007040 lysosome organization;GO:0009306 protein secretion;GO:0016256 N-glycan processing to lysosome;GO:0046835 carbohydrate phosphorylation;GO:0033299 secretion of lysosomal enzymes",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZKE0-1",
        "record_type": "protein",
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        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
                "id": "D3ZKQ1_RAT",
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                "type": "external"
            }
        ],
        "mass": 35165.0,
        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5w14",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr581",
        "refseq_ac": [
            {
                "id": "NP_001000663",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000663",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Or5w14",
        "gene_names_refseq": "Olr581; Or5w14",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 581; olfactory receptor Olr581; olfactory receptor gene Olr581",
        "tax_id": 10116,
        "disease": "",
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        "publication_id_list": "29393594",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "function": "2-oxoglutarate dehydrogenase (E1-like) component of the 2-oxoglutarate dehydrogenase multienzyme complex (OGDHC) which mediates the decarboxylation of alpha-ketoglutarate in the tricarboxylic acid cycle (PubMed:18783430). The OGDHC complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) while reducing NAD(+) to NADH (PubMed:18783430). The OGDHC complex is mainly active in the mitochondrion (PubMed:18783430). Involved in the inhibition of cell proliferation and in apoptosis (By similarity)., [UniProtKB, UniProtKB, PubMed, UniProtKB, UniProtKB]; In contrast to the heart complex, where only the known OGDH was determined, the band corresponding to the brain OGDH component was found to also include the novel 2-oxoglutarate dehydrogenase-like (OGDHL) protein., [RefSeq, PubMed]; Oxoglutarate dehydrogenase and mitochondrial nitric-oxide synthase require calcium under hypoxic conditions, [RefSeq, PubMed]",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:1.2.4.2",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0030976 thiamine pyrophosphate binding;GO:0004591 oxoglutarate dehydrogenase (succinyl-transferring) activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix;GO:0045252 oxoglutarate dehydrogenase complex",
        "go_biological_process": "GO:0006099 tricarboxylic acid cycle;GO:0006103 2-oxoglutarate metabolic process;GO:0006096 glycolytic process",
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        "hit_score": 0.3,
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        "kg_view_protein": true
    },
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        ],
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        "length": 1209,
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        "refseq_name": "",
        "refseq_ac": [],
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Exportin-5; Ran-binding protein 21",
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        "tax_id": 10116,
        "disease": "breast cancer (Disease Ontology:DOID:1612); transitional cell carcinoma (Disease Ontology:DOID:2671); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung small cell carcinoma (Disease Ontology:DOID:5409); primary ovarian insufficiency (Disease Ontology:DOID:5426); hepatocellular carcinoma (Disease Ontology:DOID:684); colorectal cancer (Disease Ontology:DOID:9256); multiple myeloma (Disease Ontology:DOID:9538)",
        "pathway": "",
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        "function": "Mediates the nuclear export of micro-RNA precursors, which form short hairpins. Also mediates the nuclear export of synthetic short hairpin RNAs used for RNA interference. In some circumstances can also mediate the nuclear export of deacylated and aminoacylated tRNAs. Specifically recognizes dsRNAs that lack a 5'-overhang in a sequence-independent manner, have only a short 3'-overhang, and that have a double-stranded length of at least 15 base-pairs. Binding is dependent on Ran-GTP., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:1905172 RISC complex binding;GO:0003729 mRNA binding;GO:0000049 tRNA binding;GO:0031267 small GTPase binding;GO:0070883 pre-miRNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0016442 RISC complex",
        "go_biological_process": "GO:0006611 protein export from nucleus;GO:0035281 pre-miRNA export from nucleus;GO:0006405 RNA export from nucleus",
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        ],
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "protein_name": "RecQ-like DNA helicase BLM",
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        "pathway": " (R-RNO-174414);  (R-RNO-174437);  (R-RNO-3108214);  (R-RNO-5685938);  (R-RNO-5685942);  (R-RNO-5693537);  (R-RNO-5693568);  (R-RNO-5693579);  (R-RNO-5693607);  (R-RNO-5693616);  (R-RNO-6804756);  (R-RNO-69473)",
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        "protein_name": "Eomesodermin",
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        "refseq_name": "eomesodermin homolog",
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                "id": "NP_001414322",
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        "protein_name": "Protein phosphatase 2C-like domain containing 1",
        "gene_name": "Pp2d1",
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        "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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        "go_biological_process": "GO:0032869 cellular response to insulin stimulus;GO:0006695 cholesterol biosynthetic process;GO:0032933 SREBP signaling pathway;GO:0036316 SREBP-SCAP complex retention in endoplasmic reticulum",
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            {
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        "ec_number_list": [
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.53",
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            },
            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.52",
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            },
            {
                "id": "3.1.3.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.-",
                "type": "external"
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.27",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.22",
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        "function": "Catalyzes the initial reaction in O-linked oligosaccharide biosynthesis, the transfer of an N-acetyl-D-galactosamine residue to a serine or threonine residue on the protein receptor. Although it displays a much weaker activity toward all substrates tested compared to GALNT2, it is able to transfer up to seven GalNAc residues to the Muc5AC peptide, suggesting that it can fill vicinal Thr/Ser residues in cooperation with other GALNT proteins. Prefers Muc1a as substrate., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.4.1.41",
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            }
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        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus;GO:0030133 transport vesicle",
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        "protein_names_refseq": "AT rich interactive domain 1A (SWI-like); AT rich interactive domain 1A (Swi1 like); AT-rich interactive domain-containing protein 1A isoform 1; AT-rich interactive domain-containing protein 1A",
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        "disease": "ovarian clear cell carcinoma (Disease Ontology:DOID:0050934); Coffin-Siris syndrome 1 (Disease Ontology:DOID:0070042); Coffin-Siris syndrome 2 (Disease Ontology:DOID:0070044); stomach cancer (Disease Ontology:DOID:10534); pre-eclampsia (Disease Ontology:DOID:10591); alcohol use disorder (Disease Ontology:DOID:1574); breast cancer (Disease Ontology:DOID:1612); cancer (Disease Ontology:DOID:162); Coffin-Siris syndrome (Disease Ontology:DOID:1925); colon cancer (Disease Ontology:DOID:219); endometrial adenocarcinoma (Disease Ontology:DOID:2870); gastric adenocarcinoma (Disease Ontology:DOID:3717); lung non-small cell carcinoma (Disease Ontology:DOID:3908); esophagus adenocarcinoma (Disease Ontology:DOID:4914); Klatskin's tumor (Disease Ontology:DOID:4927); intrahepatic cholangiocarcinoma (Disease Ontology:DOID:4928); hepatocellular carcinoma (Disease Ontology:DOID:684); neuroblastoma (Disease Ontology:DOID:769); colorectal cancer (Disease Ontology:DOID:9256); nasopharynx carcinoma (Disease Ontology:DOID:9261)",
        "pathway": " (rno:297867);  (R-RNO-3214858);  (R-RNO-8939243);  (R-RNO-9933937);  (R-RNO-9933946);  (R-RNO-9934037)",
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        "protein_name": "Ubiquitin thioesterase ZRANB1",
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        "tax_id": 10116,
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        "pathway": " (rno:100360606);  (R-RNO-195253);  (R-RNO-5689896)",
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        "function": "Ubiquitin thioesterase, which specifically hydrolyzes 'Lys-29'-linked and 'Lys-33'-linked diubiquitin. Also cleaves 'Lys-63'-linked chains, but with 40-fold less efficiency compared to 'Lys-29'-linked ones. Positive regulator of the Wnt signaling pathway that deubiquitinates APC protein, a negative regulator of Wnt-mediated transcription. Acts as a regulator of autophagy by mediating deubiquitination of PIK3C3/VPS34, thereby promoting autophagosome maturation. Plays a role in the regulation of cell morphology and cytoskeletal organization. Required in the stress fiber dynamics and cell migration., [UniProtKB, UniProtKB]",
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        "function": "These results bring evidence that endogenous VASH-1 isoforms p36 and p42 are key actors of physiological and pathological muscle angio-adaptation., [RefSeq, PubMed]; Vasohibin has an activity to prevent neointimal formation by inhibiting adventitial angiogenesis [vasohibin], [RefSeq, PubMed]; Vasohibin inhibition improves myocardial relaxation in a rat model of heart failure with preserved ejection fraction., [RefSeq, PubMed]",
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        "function": "Essential for sustained cell growth, maintenance of chromosomal stability, and ATR-dependent checkpoint activation upon DNA damage. Has a weak ATPase activity required for binding to chromatin. Participates in the recruitment of the 9-1-1 (RAD1-RAD9-HUS1) complex and RHNO1 onto chromatin, and in CHEK1 activation. Involved in homologous recombination by mediating recruitment of the MRN complex to DNA damage sites. May also serve as a sensor of DNA replication progression., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Ribonuclease 3",
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        "gene_names_refseq": "Drosha; Etohi2; RGD1307626; Rn3; Rnasen",
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        "protein_names_refseq": "drosha, ribonuclease type III; ethanol induced 2; ribonuclease 3; ribonuclease III, nuclear; ribonuclease type III, nuclear",
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        "function": "Ribonuclease III double-stranded (ds) RNA-specific endoribonuclease that is involved in the initial step of microRNA (miRNA) biogenesis. Component of the microprocessor complex that is required to process primary miRNA transcripts (pri-miRNAs) to release precursor miRNA (pre-miRNA) in the nucleus. Within the microprocessor complex, DROSHA cleaves the 3' and 5' strands of a stem-loop in pri-miRNAs (processing center 11 bp from the dsRNA-ssRNA junction) to release hairpin-shaped pre-miRNAs that are subsequently cut by the cytoplasmic DICER to generate mature miRNAs. Involved also in pre-rRNA processing. Cleaves double-strand RNA and does not cleave single-strand RNA. Involved in the formation of GW bodies. Plays a role in growth homeostasis in response to autophagy in motor neurons., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; The 24-h pattern of dgcr8, drosha, and dicer expression in the rat suprachiasmatic nuclei and peripheral tissues and its modulation by angiotensin II., [RefSeq, PubMed]",
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        "protein_name": "KLF transcription factor 11",
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                "id": "NP_001032431",
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        "protein_names_uniprotkb": "KLF transcription factor 11",
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        "disease": "maturity-onset diabetes of the young type 7 (Disease Ontology:DOID:0111106); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
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        "function": "An important role for KLF11 in the regulation of INS transcription via the novel c.-331 KLF site., [RefSeq, PubMed]; In hypoxia/reoxygenation injury of rat cardiomyocytes, inhibition of KLF11 by siRNA suppressed apoptosis, the activity of caspase3, the expression of cleaved-caspase3 and cytochrome C in the cytoplasm and the damage of mitochondrial membrane.  KLF11 knockdown elevated the expression of p-JAK2 and p-STAT3. KLF11 silencing protects against H/R injury by activating the JAK2/STAT3 signaling pathway ., [RefSeq, PubMed]; Kruppel-like factor 11 protein is up-regulated following chronic exposure to stress or ethanol in a region-specific manner and may contribute to pro-apoptotic signaling in ethanol-treated rats., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0000976 transcription cis-regulatory region binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:1990859 cellular response to endothelin;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0008285 negative regulation of cell population proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "E9PTS6-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "E9PTX9-1",
        "uniprot_id": [
            {
                "id": "E9PTX9_RAT",
                "url": "https://www.uniprot.org/uniprot/E9PTX9",
                "type": "external"
            }
        ],
        "mass": 130367.0,
        "length": 1203,
        "protein_name": "Solute carrier family 12 member 2",
        "gene_name": "Slc12a2",
        "organism": "Rat",
        "refseq_name": "solute carrier family 12 member 2",
        "refseq_ac": [
            {
                "id": "NP_113986",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_113986",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Slc12a2",
        "gene_names_refseq": "Bsc2; Nkcc1; Slc12a2",
        "protein_names_uniprotkb": "Solute carrier family 12 member 2",
        "protein_names_refseq": "solute carrier family 12 (sodium/potassium/chloride transporter), member 2; solute carrier family 12 (sodium/potassium/chloride transporters), member 2; solute carrier family 12 member 2",
        "tax_id": 10116,
        "disease": "autosomal dominant nonsyndromic deafness 78 (Disease Ontology:DOID:0112159); sensorineural hearing loss (Disease Ontology:DOID:10003); hypertension (Disease Ontology:DOID:10763); epilepsy (Disease Ontology:DOID:1826); transient cerebral ischemia (Disease Ontology:DOID:224); middle cerebral artery infarction (Disease Ontology:DOID:3525)",
        "pathway": " (rno:83629);  (R-RNO-426117)",
        "pathway_count": 2,
        "publication_count": 6,
        "publication_id_list": "22673903;35729645;37328833;37458846;37830575;38160798",
        "class_list": "",
        "function": "Age-appropriate potassium clearance from perinatal cerebrospinal fluid depends on choroid plexus NKCC1. Publication Status: Online-Only, [RefSeq, PubMed]; DNA demethylation in the hypothalamus promotes transcription of Agtr1a and Slc12a2 and hypertension development., [RefSeq, PubMed]; Dietary Na[+] depletion up-regulates NKCC1 expression and enhances electrogenic Cl[-] secretion in rat proximal colon. Publication Status: Online-Only, [RefSeq, PubMed]; NKCC1 and KCC2 Chloride Transporters Have Different Membrane Dynamics on the Surface of Hippocampal Neurons. Publication Status: Online-Only, [RefSeq, PubMed]; NLRP3 inflammasome-mediated choroid plexus hypersecretion contributes to hydrocephalus after intraventricular hemorrhage via phosphorylated NKCC1 channels. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_c_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 6,
        "glyco_site_count": 1,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0019901 protein kinase binding;GO:0051087 protein-folding chaperone binding;GO:0051879 Hsp90 protein binding;GO:0008519 ammonium channel activity;GO:0015079 potassium ion transmembrane transporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane;GO:0043025 neuronal cell body;GO:0016324 apical plasma membrane;GO:0030659 cytoplasmic vesicle membrane",
        "go_biological_process": "GO:1990869 cellular response to chemokine;GO:0030644 intracellular chloride ion homeostasis;GO:0061044 negative regulation of vascular wound healing;GO:0070634 transepithelial ammonium transport;GO:0050910 detection of mechanical stimulus involved in sensory perception of sound",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "E9PTX9-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.010000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "E9PTY0-1",
        "uniprot_id": [
            {
                "id": "E9PTY0_RAT",
                "url": "https://www.uniprot.org/uniprot/E9PTY0",
                "type": "external"
            }
        ],
        "mass": 117502.0,
        "length": 1010,
        "protein_name": "Leucine-rich repeat and coiled-coil domain-containing protein 1",
        "gene_name": "Lrrcc1",
        "organism": "Rat",
        "refseq_name": "leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X1",
        "refseq_ac": [
            {
                "id": "XP_038957738",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_038957738",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Lrrcc1",
        "gene_names_refseq": "Lrrcc1; Sap2",
        "protein_names_uniprotkb": "Leucine-rich repeat and coiled-coil domain-containing protein 1",
        "protein_names_refseq": "leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Required for the organization of the mitotic spindle. Maintains the structural integrity of centrosomes during mitosis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
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        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005813 centrosome;GO:0005814 centriole",
        "go_biological_process": "GO:0051301 cell division",
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        "hit_score": 0.2,
        "record_id": "E9PTY0-1",
        "record_type": "protein",
        "filter_code": "0000000.0000100.010000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "E9PTZ1-1",
        "uniprot_id": [
            {
                "id": "E9PTZ1_RAT",
                "url": "https://www.uniprot.org/uniprot/E9PTZ1",
                "type": "external"
            }
        ],
        "mass": 110354.0,
        "length": 1033,
        "protein_name": "Platelet endothelial aggregation receptor 1",
        "gene_name": "Pear1",
        "organism": "Rat",
        "refseq_name": "platelet endothelial aggregation receptor 1 isoform X2",
        "refseq_ac": [
            {
                "id": "XP_038957982",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_038957982",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Pear1",
        "gene_names_refseq": "Pear1; RGD1305653",
        "protein_names_uniprotkb": "Platelet endothelial aggregation receptor 1; Multiple epidermal growth factor-like domains protein 12",
        "protein_names_refseq": "platelet endothelial aggregation receptor 1 isoform X2",
        "tax_id": 10116,
        "disease": "neurodegenerative disease (Disease Ontology:DOID:1289); myopathy (Disease Ontology:DOID:423)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Required for SVEP1-mediated platelet activation, via its interaction with SVEP1 and subsequent activation of AKT/mTOR signaling. May be involved in the early stages of hematopoiesis., [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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        "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,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0001891 phagocytic cup;GO:0005886 plasma membrane;GO:0016020 membrane;GO:0030027 lamellipodium",
        "go_biological_process": "GO:0070527 platelet aggregation;GO:0043491 phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0010572 positive regulation of platelet activation;GO:0043654 recognition of apoptotic cell",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "E9PTZ1-1",
        "record_type": "protein",
        "filter_code": "0000000.0000010.010000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "E9PTZ7-1",
        "uniprot_id": [
            {
                "id": "E9PTZ7_RAT",
                "url": "https://www.uniprot.org/uniprot/E9PTZ7",
                "type": "external"
            }
        ],
        "mass": 39731.0,
        "length": 350,
        "protein_name": "RT1 class Ia, locus A2",
        "gene_name": "Rt1-ec3",
        "organism": "Rat",
        "refseq_name": "RT1 class Ia, locus A2 isoform X6",
        "refseq_ac": [
            {
                "id": "XP_017457034",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_017457034",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Rt1-ec3; ENSRNOG00000069480; RT1-A2",
        "gene_names_refseq": "RT1-A2n; RT1-A2; RT1.A2(N); RT1A-2",
        "protein_names_uniprotkb": "RT1 class Ia, locus A2",
        "protein_names_refseq": "RT1 class Ia, locus A2 isoform X6",
        "tax_id": 10116,
        "disease": "Stevens-Johnson syndrome (Disease Ontology:DOID:0050426); colitis (Disease Ontology:DOID:0060180); Cytomegalovirus retinitis (Disease Ontology:DOID:0080160); COVID-19 (Disease Ontology:DOID:0080600); ankylosing spondylitis 1 (Disease Ontology:DOID:0080603); erythema nodosum (Disease Ontology:DOID:0080750); occupational asthma (Disease Ontology:DOID:0080820); birdshot chorioretinopathy (Disease Ontology:DOID:0111079); psoriasis 1 (Disease Ontology:DOID:0111286); sensorineural hearing loss (Disease Ontology:DOID:10003); spondyloarthropathy (Disease Ontology:DOID:1123); trachoma (Disease Ontology:DOID:11265); sarcoidosis (Disease Ontology:DOID:11335); retinal vasculitis (Disease Ontology:DOID:11563); otosclerosis (Disease Ontology:DOID:12185); Graves' disease (Disease Ontology:DOID:12361); respiratory syncytial virus infectious disease (Disease Ontology:DOID:1273); retinopathy of prematurity (Disease Ontology:DOID:13025); uveitis (Disease Ontology:DOID:13141); Behcet's disease (Disease Ontology:DOID:13241); anterior uveitis (Disease Ontology:DOID:1407); cystic fibrosis (Disease Ontology:DOID:1485); hepatitis C (Disease Ontology:DOID:1883); Takayasu's arteritis (Disease Ontology:DOID:2508); synovitis (Disease Ontology:DOID:2703); dermatitis (Disease Ontology:DOID:2723); asthma (Disease Ontology:DOID:2841); severe acute respiratory syndrome (Disease Ontology:DOID:2945); cerebral infarction (Disease Ontology:DOID:3526); acute retinal necrosis syndrome (Disease Ontology:DOID:3611); thrombophlebitis (Disease Ontology:DOID:3875); tuberculosis (Disease Ontology:DOID:399); cervical cancer (Disease Ontology:DOID:4362); allergic rhinitis (Disease Ontology:DOID:4481); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); uveal melanoma (Disease Ontology:DOID:6039); reactive arthritis (Disease Ontology:DOID:6196); myositis (Disease Ontology:DOID:633); ankylosing spondylitis (Disease Ontology:DOID:7147); diabetic retinopathy (Disease Ontology:DOID:8947); allergic asthma (Disease Ontology:DOID:9415); Meniere's disease (Disease Ontology:DOID:9849); alopecia (Disease Ontology:DOID:987); mitral valve prolapse (Disease Ontology:DOID:988)",
        "pathway": " (R-RNO-1236974);  (R-RNO-1236977);  (R-RNO-198933);  (R-RNO-6798695);  (R-RNO-983170)",
        "pathway_count": 5,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in the presentation of foreign antigens to the immune system., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 44,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0046703 natural killer cell lectin-like receptor binding;GO:0005102 signaling receptor binding;GO:0030881 beta-2-microglobulin binding;GO:0042605 peptide antigen binding;GO:0042608 T cell receptor binding",
        "go_cellular_component": "GO:0032398 MHC class Ib protein complex;GO:0005615 extracellular space;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0009897 external side of plasma membrane",
        "go_biological_process": "GO:0002476 antigen processing and presentation of endogenous peptide antigen via MHC class Ib;GO:0002715 regulation of natural killer cell mediated immunity;GO:0002717 positive regulation of natural killer cell mediated immunity;GO:0032736 positive regulation of interleukin-13 production;GO:0032759 positive regulation of TRAIL production",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "E9PTZ7-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "F1LM38-1",
        "uniprot_id": [
            {
                "id": "F1LM38_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LM38",
                "type": "external"
            }
        ],
        "mass": 64688.0,
        "length": 613,
        "protein_name": "KH homology domain-containing protein 4",
        "gene_name": "Khdc4",
        "organism": "Rat",
        "refseq_name": "KH homology domain-containing protein 4",
        "refseq_ac": [
            {
                "id": "NP_001386167",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001386167",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Khdc4; RGD1565775",
        "gene_names_refseq": "Blom7; Khdc4; RGD1565775",
        "protein_names_uniprotkb": "KH homology domain-containing protein 4; Brings lots of money 7; Pre-mRNA Splicing factor protein khdc4",
        "protein_names_refseq": "KH homology domain-containing protein 4; nuclear ribonucleoprotein K homology domain protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:361980)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "RNA-binding protein involved in pre-mRNA splicing. Interacts with the PRP19C/Prp19 complex/NTC/Nineteen complex which is part of the spliceosome. Involved in regulating splice site selection. Binds preferentially RNA with A/C rich sequences and poly-C stretches., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003723 RNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005681 spliceosomal complex",
        "go_biological_process": "GO:0006376 mRNA splice site recognition",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1LM38-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "F1LM66-1",
        "uniprot_id": [
            {
                "id": "F1LM66_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LM66",
                "type": "external"
            }
        ],
        "mass": 109102.0,
        "length": 969,
        "protein_name": "116 kDa U5 small nuclear ribonucleoprotein component",
        "gene_name": "Eftud2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Eftud2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "116 kDa U5 small nuclear ribonucleoprotein component; U5 snRNP-specific protein, 116 kDa",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "mandibulofacial dysostosis, Guion-Almeida type (Disease Ontology:DOID:0080196); esophageal atresia (Disease Ontology:DOID:10485); microcephaly (Disease Ontology:DOID:10907); hepatitis B (Disease Ontology:DOID:2043); Treacher Collins syndrome (Disease Ontology:DOID:2908); hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (rno:287739);  (R-RNO-72163);  (R-RNO-72165)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Required for pre-mRNA splicing as component of the spliceosome, including pre-catalytic, catalytic and post-catalytic spliceosomal complexes. Component of the U5 snRNP and the U4/U6-U5 tri-snRNP complex, a building block of the spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0030623 U5 snRNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0016607 nuclear speck;GO:0005681 spliceosomal complex",
        "go_biological_process": "GO:0071466 cellular response to xenobiotic stimulus;GO:0042220 response to cocaine;GO:0000398 mRNA splicing, via spliceosome",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F1LM66-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.010000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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            {
                "id": "F1LMA5_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LMA5",
                "type": "external"
            }
        ],
        "mass": 32360.0,
        "length": 284,
        "protein_name": "Friend virus susceptibility 1",
        "gene_name": "Fv1",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein C19orf48 homolog",
        "refseq_ac": [
            {
                "id": "NP_001014040",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001014040",
                "type": "external"
            }
        ],
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        "gene_names_refseq": "Fv1; RGD1309326",
        "protein_names_uniprotkb": "Friend virus susceptibility 1",
        "protein_names_refseq": "uncharacterized protein C19orf48 homolog",
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        "go_cellular_component": "GO:0005794 Golgi apparatus",
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    },
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                "id": "F1LMC1_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LMC1",
                "type": "external"
            }
        ],
        "mass": 61011.0,
        "length": 575,
        "protein_name": "WT1 interacting protein",
        "gene_name": "Wtip",
        "organism": "Rat",
        "refseq_name": "",
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        "protein_names_uniprotkb": "WT1 interacting protein",
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        "pathway": " (rno:361552);  (R-RNO-1234176)",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0003714 transcription corepressor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005912 adherens junction;GO:0000932 P-body;GO:0005667 transcription regulator complex;GO:0070161 anchoring junction",
        "go_biological_process": "GO:0001666 response to hypoxia;GO:0006355 regulation of DNA-templated transcription;GO:0007010 cytoskeleton organization;GO:0035278 miRNA-mediated gene silencing by inhibition of translation;GO:0035195 miRNA-mediated post-transcriptional gene silencing",
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        "record_type": "protein",
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        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "P0DSP1-1",
        "uniprot_id": [
            {
                "id": "SORL_RAT",
                "url": "https://www.uniprot.org/uniprot/P0DSP1",
                "type": "external"
            }
        ],
        "mass": 247316.0,
        "length": 2215,
        "protein_name": "Sortilin-related receptor",
        "gene_name": "Sorl1",
        "organism": "Rat",
        "refseq_name": "sortilin-related receptor precursor",
        "refseq_ac": [
            {
                "id": "NP_445971",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_445971",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Sorl1",
        "gene_names_refseq": "Lr11; RGD619914; SorLA; Sorl1",
        "protein_names_uniprotkb": "Sortilin-related receptor; LDLR relative with 11 ligand-binding repeats; LR11; Low-density lipoprotein receptor relative with 11 ligand-binding repeats; SorLA; Sorting protein-related receptor containing LDLR class A repeats",
        "protein_names_refseq": "LDLR relative with 11 ligand-binding repeats; low-density lipoprotein receptor relative with 11 ligand-binding repeats; sortilin-related receptor precursor; sortilin-related receptor, LDLR class A repeats-containing; sortilin-related receptor-like; sorting protein-related receptor containing LDLR class A repeats",
        "tax_id": 10116,
        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652)",
        "pathway": " (rno:300652)",
        "pathway_count": 1,
        "publication_count": 8,
        "publication_id_list": "17332490;18683930;21994944;23333276;25967121;29393594;30625365;9510025",
        "class_list": "",
        "function": "Sorting receptor that directs several proteins to their correct location within the cell. Along with AP-1 complex, involved Golgi apparatus - endosome sorting. Sorting receptor for APP, regulating its intracellular trafficking and processing into amyloidogenic-beta peptides. Retains APP in the trans-Golgi network, hence preventing its transit through late endosomes where amyloid beta peptides Abeta40 and Abeta42 are generated. May also sort newly produced amyloid-beta peptides to lysosomes for catabolism. Does not affect APP trafficking from the endoplasmic reticulum to Golgi compartments. Sorting receptor for the BDNF receptor NTRK2/TRKB that facilitates NTRK2 trafficking between synaptic plasma membranes, postsynaptic densities and cell soma, hence positively regulates BDNF signaling by controlling the intracellular location of its receptor (By similarity). Sorting receptor for GDNF that promotes GDNF regulated, but not constitutive secretion (PubMed:21994944). Sorting receptor for the GDNF-GFRA1 complex, directing it from the cell surface to endosomes. GDNF is then targeted to lysosomes and degraded, while its receptor GFRA1 recycles back to the cell membrane, resulting in a GDNF clearance pathway. The SORL1-GFRA1 complex further targets RET for endocytosis, but not for degradation, affecting GDNF-induced neurotrophic activities (PubMed:23333276). Sorting receptor for ERBB2/HER2. Regulates ERBB2 subcellular distribution by promoting its recycling after internalization from endosomes back to the plasma membrane, hence stimulating phosphoinositide 3-kinase (PI3K)-dependent ERBB2 signaling (By similarity). Sorting receptor for lipoprotein lipase LPL. Promotes LPL localization to endosomes and later to the lysosomes, leading to degradation of newly synthesized LPL. Potential sorting receptor for APOA5, inducing APOA5 internalization to early endosomes, then to late endosomes, wherefrom a portion is sent to lysosomes and degradation, another portion is sorted to the trans-Golgi network. Sorting receptor for the insulin receptor INSR. Promotes recycling of internalized INSR via the Golgi apparatus back to the cell surface, thereby preventing lysosomal INSR catabolism, increasing INSR cell surface expression and strengthening insulin signal reception in adipose tissue. Does not affect INSR internalization (By similarity). Plays a role in renal ion homeostasis, controlling the phospho-regulation of SLC12A1/NKCC2 by STK39/SPAK kinase and PPP3CB/calcineurin A beta phosphatase, possibly through intracellular sorting of STK39 and PPP3CB (PubMed:25967121). Stimulates, via the N-terminal ectodomain, the proliferation and migration of smooth muscle cells, possibly by increasing cell surface expression of the urokinase receptor uPAR/PLAUR. This may promote extracellular matrix proteolysis and hence facilitate cell migration. By acting on the migration of intimal smooth muscle cells, may accelerate intimal thickening following vascular injury (By similarity). Stimulates proliferation and migration monocytes/macrophages. Through its action on intimal smooth muscle cells and macrophages, may accelerate intimal thickening and macrophage foam cell formation in the process of atherosclerosis (By similarity). Regulates hypoxia-enhanced adhesion of hematopoietic stem and progenitor cells to the bone marrow stromal cells via a PLAUR-mediated pathway. This function is mediated by the N-terminal ectodomain (By similarity). Metabolic regulator, which functions to maintain the adequate balance between lipid storage and oxidation in response to changing environmental conditions, such as temperature and diet. The N-terminal ectodomain negatively regulates adipose tissue energy expenditure, acting through the inhibition the BMP/Smad pathway (By similarity). Sorting receptor that may regulate signaling by the heterodimeric neurotrophic cytokine CLCF1-CRLF1 bound to the CNTFR receptor by promoting the endocytosis of the tripartite complex CLCF1-CRLF1-CNTFR and lysosomal degradation. Might regulate IL6 signaling, decreasing cis signaling, while up-regulating trans signaling (By similarity)., [UniProtKB, PubMed, UniProtKB, PubMed, UniProtKB, PubMed]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0004888 transmembrane signaling receptor activity;GO:0001540 amyloid-beta binding;GO:0031267 small GTPase binding;GO:0030169 low-density lipoprotein particle binding;GO:0019828 aspartic-type endopeptidase inhibitor activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005615 extracellular space;GO:0005641 nuclear envelope lumen;GO:0005768 endosome;GO:0005769 early endosome",
        "go_biological_process": "GO:0001960 negative regulation of cytokine-mediated signaling pathway;GO:1902966 positive regulation of protein localization to early endosome;GO:1904179 positive regulation of adipose tissue development;GO:0045053 protein retention in Golgi apparatus;GO:0007218 neuropeptide signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 1.1,
        "record_id": "P0DSP1-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.010000.000000000000001000.0100000011001.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZZZ4-1",
        "uniprot_id": [
            {
                "id": "A0A8I5ZZZ4_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A8I5ZZZ4",
                "type": "external"
            }
        ],
        "mass": 35099.0,
        "length": 321,
        "protein_name": "RAD52 motif-containing protein 1",
        "gene_name": "Rdm1",
        "organism": "Rat",
        "refseq_name": "RAD52 motif-containing protein 1 isoform X1",
        "refseq_ac": [
            {
                "id": "XP_063124815",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_063124815",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Rdm1",
        "gene_names_refseq": "Rad52b; Rdm1",
        "protein_names_uniprotkb": "RAD52 motif-containing protein 1",
        "protein_names_refseq": "RAD52 motif-containing protein 1 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:287726)",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003723 RNA binding",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0006310 DNA recombination;GO:0006302 double-strand break repair",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZZZ4-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
                "id": "A0A8I6A742_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A8I6A742",
                "type": "external"
            }
        ],
        "mass": 44859.0,
        "length": 384,
        "protein_name": "Ceramide synthase 6",
        "gene_name": "Cers6",
        "organism": "Rat",
        "refseq_name": "ceramide synthase 6 isoform 2",
        "refseq_ac": [
            {
                "id": "NP_001386292",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001386292",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Cers6",
        "gene_names_refseq": "Cers6; Lass6; RGD1561599",
        "protein_names_uniprotkb": "Ceramide synthase 6",
        "protein_names_refseq": "LAG1 homolog, ceramide synthase 6; LAG1 longevity assurance homolog 6; ceramide synthase 6 isoform 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:366065);  (R-RNO-1660661)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "21148554",
        "class_list": "",
        "function": "A novel role for CerS6 in the regulation of both mitochondrial Ca(2+) homeostasis and calpain, which appears to be important in OL apoptosis during brain development., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0050291 sphingosine N-acyltransferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005789 endoplasmic reticulum membrane;GO:0005783 endoplasmic reticulum",
        "go_biological_process": "GO:0046513 ceramide biosynthetic process;GO:0030148 sphingolipid biosynthetic process;GO:0014003 oligodendrocyte development;GO:1900143 positive regulation of oligodendrocyte apoptotic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I6A742-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005694 chromosome",
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        ],
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        ],
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        ],
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            {
                "id": "NP_001419037",
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        ],
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        "protein_names_uniprotkb": "Regulator of DNA class I crossover intermediates 1",
        "protein_names_refseq": "regulator of DNA class I crossover intermediates 1 isoform 1; uncharacterized protein C12orf40 homolog",
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            {
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        "function": "Dioxygenase that catalyzes the conversion of the modified genomic base 5-methylcytosine (5mC) into 5-hydroxymethylcytosine (5hmC) and plays a key role in epigenetic chromatin reprogramming during embryonic development., [UniProtKB, UniProtKB, UniProtKB]",
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            {
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        "disease": "inflammatory bowel disease (Disease Ontology:DOID:0050589); diffuse large B-cell lymphoma (Disease Ontology:DOID:0050745); peripheral artery disease (Disease Ontology:DOID:0050830); non-arteritic anterior ischemic optic neuropathy (Disease Ontology:DOID:0050864); oral squamous cell carcinoma (Disease Ontology:DOID:0050866); coarctation of the aorta (Disease Ontology:DOID:0051054); stroke (Disease Ontology:DOID:0051061); dextro-looped transposition of the great arteries (Disease Ontology:DOID:0060770); myeloid neoplasm (Disease Ontology:DOID:0070004); spina bifida (Disease Ontology:DOID:0080016); neural tube defect (Disease Ontology:DOID:0080074); hepatic veno-occlusive disease (Disease Ontology:DOID:0080177); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); graft-versus-host disease (Disease Ontology:DOID:0081267); thrombophilia due to thrombin defect (Disease Ontology:DOID:0111907); migraine with aura (Disease Ontology:DOID:10024); open-angle glaucoma (Disease Ontology:DOID:1067); kidney failure (Disease Ontology:DOID:1074); Kuhnt-Junius degeneration (Disease Ontology:DOID:10873); sickle cell anemia (Disease Ontology:DOID:10923); attention deficit hyperactivity disorder (Disease Ontology:DOID:1094); urinary bladder cancer (Disease Ontology:DOID:11054); Budd-Chiari syndrome (Disease Ontology:DOID:11512); nephrosclerosis (Disease Ontology:DOID:11664); portal vein thrombosis (Disease Ontology:DOID:11695); factor VIII deficiency (Disease Ontology:DOID:12134); male infertility (Disease Ontology:DOID:12336); Graves' disease (Disease Ontology:DOID:12361); cardiovascular system disease (Disease Ontology:DOID:1287); carotid stenosis (Disease Ontology:DOID:13001); angle-closure glaucoma (Disease Ontology:DOID:13550); alcoholic liver cirrhosis (Disease Ontology:DOID:14018); Down syndrome (Disease Ontology:DOID:14250); hypothyroidism (Disease Ontology:DOID:1459); thrombocytopenia (Disease Ontology:DOID:1588); retinal vein occlusion (Disease Ontology:DOID:1727); squamous cell carcinoma (Disease Ontology:DOID:1749); pancreatic cancer (Disease Ontology:DOID:1793); atherosclerosis (Disease Ontology:DOID:1936); rectal benign neoplasm (Disease Ontology:DOID:1984); hepatitis B (Disease Ontology:DOID:2043); nephroblastoma (Disease Ontology:DOID:2154); anemia (Disease Ontology:DOID:2355); renal artery disease (Disease Ontology:DOID:2388); thrombophilia (Disease Ontology:DOID:2452); transitional cell carcinoma (Disease Ontology:DOID:2671); asthma (Disease Ontology:DOID:2841); glomerulonephritis (Disease Ontology:DOID:2921); familial Mediterranean fever (Disease Ontology:DOID:2987); lipid metabolism disorder (Disease Ontology:DOID:3146); ischemia (Disease Ontology:DOID:326); amyotrophic lateral sclerosis (Disease Ontology:DOID:332); osteosarcoma (Disease Ontology:DOID:3347); coronary artery disease (Disease Ontology:DOID:3393); cerebral infarction (Disease Ontology:DOID:3526); cervical cancer (Disease Ontology:DOID:4362); renal cell carcinoma (Disease Ontology:DOID:4450); clear cell renal cell carcinoma (Disease Ontology:DOID:4467); cholangiocarcinoma (Disease Ontology:DOID:4947); liver cirrhosis (Disease Ontology:DOID:5082); lung small cell carcinoma (Disease Ontology:DOID:5409); schizophrenia (Disease Ontology:DOID:5419); eye disease (Disease Ontology:DOID:5614); myocardial infarction (Disease Ontology:DOID:5844); mitral valve disease (Disease Ontology:DOID:61); migraine (Disease Ontology:DOID:6364); tetralogy of Fallot (Disease Ontology:DOID:6419); hepatocellular carcinoma (Disease Ontology:DOID:684); ankylosing spondylitis (Disease Ontology:DOID:7147); rheumatoid arthritis (Disease Ontology:DOID:7148); abdominal aortic aneurysm (Disease Ontology:DOID:7693); end stage renal disease (Disease Ontology:DOID:783); chronic kidney disease (Disease Ontology:DOID:784); hyperthyroidism (Disease Ontology:DOID:7998); cataract (Disease Ontology:DOID:83); chronic myeloid leukemia (Disease Ontology:DOID:8552); smallpox (Disease Ontology:DOID:8736); diabetic retinopathy (Disease Ontology:DOID:8947); acute myeloid leukemia (Disease Ontology:DOID:9119); liver benign neoplasm (Disease Ontology:DOID:916); hyperhomocysteinemia (Disease Ontology:DOID:9279); cleft lip (Disease Ontology:DOID:9296); type 2 diabetes mellitus (Disease Ontology:DOID:9352); hypopituitarism (Disease Ontology:DOID:9406); steatotic liver disease (Disease Ontology:DOID:9452); multiple myeloma (Disease Ontology:DOID:9538); aphthous stomatitis (Disease Ontology:DOID:9663); type 1 diabetes mellitus (Disease Ontology:DOID:9744); Meniere's disease (Disease Ontology:DOID:9849); acute lymphoblastic leukemia (Disease Ontology:DOID:9952)",
        "pathway": " (rno:362657);  (R-RNO-196757)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
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        "function": "Catalyzes the conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate, a cosubstrate for homocysteine remethylation to methionine. Represents a key regulatory connection between the folate and methionine cycles., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "ec_number_list": [
            {
                "id": "1.5.1.53",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.5.1.53",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0106313 methylenetetrahydrofolate reductase (NADPH) activity;GO:0050660 flavin adenine dinucleotide binding;GO:0044877 protein-containing complex binding;GO:0004489 methylenetetrahydrofolate reductase [NAD(P)H] activity;GO:0050661 NADP binding",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0035999 tetrahydrofolate interconversion;GO:0006555 methionine metabolic process;GO:0001666 response to hypoxia;GO:0001843 neural tube closure;GO:0070555 response to interleukin-1",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6A4C5-1",
        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZN22-1",
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            {
                "id": "A0A8I5ZN22_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A8I5ZN22",
                "type": "external"
            }
        ],
        "mass": 61774.0,
        "length": 574,
        "protein_name": "E3 ubiquitin-protein ligase NEURL1",
        "gene_name": "Neurl1",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase NEURL1 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001388553",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001388553",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Neurl1; Neurl1a; Neurl",
        "gene_names_refseq": "Neurl1a; Neurl1; Neurl",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase NEURL1; 2.3.2.27; Neuralized-like protein 1A; RING-type E3 ubiquitin transferase NEURL1",
        "protein_names_refseq": "E3 ubiquitin-protein ligase NEURL1 isoform 1; E3 ubiquitin-protein ligase NEURL1; neuralized homolog 1A; neuralized-like homolog; neuralized-like protein 1A",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:309459)",
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        "publication_id_list": "27780737;31068605",
        "class_list": "",
        "function": "Endogenous NEURL1 mRNAs with both longer and shorter 3'UTRs are enriched in the neurites of cultured rat primary hippocampal neurons. Both NEURL1 3'UTRs can mediate transport of reporter mRNAs into dendrites in primary hippocampal neurons., [RefSeq, PubMed]; Neuralized family member NEURL1 is a ubiquitin ligase for the cGMP-specific phosphodiesterase 9A. Publication Status: Online-Only, [RefSeq, PubMed]; Plays a role in hippocampal-dependent synaptic plasticity, learning and memory. Involved in the formation of spines and functional synaptic contacts by modulating the translational activity of the cytoplasmic polyadenylation element-binding protein CPEB3. Promotes ubiquitination of CPEB3, and hence induces CPEB3-dependent mRNA translation activation of glutamate receptor GRIA1 and GRIA2. Can function as an E3 ubiquitin-protein ligase to activate monoubiquitination of JAG1 (in vitro), thereby regulating the Notch pathway. Acts as a tumor suppressor; inhibits malignant cell transformation of medulloblastoma (MB) cells by inhibiting the Notch signaling pathway., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity;GO:0004842 ubiquitin-protein transferase activity;GO:0045182 translation regulator activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0014069 postsynaptic density;GO:0030425 dendrite;GO:0043204 perikaryon;GO:0048471 perinuclear region of cytoplasm",
        "go_biological_process": "GO:0006417 regulation of translation;GO:0007219 Notch signaling pathway;GO:0023051 regulation of signaling;GO:0010646 regulation of cell communication;GO:0008285 negative regulation of cell population proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "A0A8I5ZN22-1",
        "record_type": "protein",
        "filter_code": "0000000.0000101.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
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            {
                "id": "A0A8I6A0N0_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A8I6A0N0",
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            }
        ],
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        "length": 525,
        "protein_name": "Cytidine and dCMP deaminase domain-containing protein 1",
        "gene_name": "Cdadc1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Cdadc1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Cytidine and dCMP deaminase domain-containing protein 1; 3.5.4.5; Cytidine deaminase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the deamination of cytidine and deoxycytidine into uridine and deoxyuridine, respectively. May play an important role in testicular development and spermatogenesis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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            {
                "id": "3.5.4.5",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.5.4.5",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0004126 cytidine deaminase activity;GO:0008270 zinc ion binding;GO:0004132 dCMP deaminase activity;GO:0061676 importin-alpha family protein binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005634 nucleus",
        "go_biological_process": "GO:0070383 DNA cytosine deamination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6A0N0-1",
        "record_type": "protein",
        "filter_code": "0000000.0000000.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZT44-1",
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            {
                "id": "A0A8I5ZT44_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A8I5ZT44",
                "type": "external"
            }
        ],
        "mass": 29352.0,
        "length": 257,
        "protein_name": "TLC domain containing 3A",
        "gene_name": "Tlcd3a",
        "organism": "Rat",
        "refseq_name": "TLC domain-containing protein 3A",
        "refseq_ac": [
            {
                "id": "NP_001385940",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001385940",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Tlcd3a",
        "gene_names_refseq": "Fam57a; RGD1307493; Tlcd3a",
        "protein_names_uniprotkb": "TLC domain containing 3A",
        "protein_names_refseq": "TLC domain-containing protein 3A; family with sequence similarity 57, member A; protein FAM57A",
        "tax_id": 10116,
        "disease": "chromosome 16p11.2 deletion syndrome, 593-kb (Disease Ontology:DOID:0070515)",
        "pathway": " (rno:100360533)",
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        "go_cellular_component": "GO:0016020 membrane;GO:0005783 endoplasmic reticulum;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0055088 lipid homeostasis",
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        "hit_score": 0.1,
        "record_id": "A0A8I5ZT44-1",
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    {
        "uniprot_canonical_ac": "M0RBE8-1",
        "uniprot_id": [
            {
                "id": "M0RBE8_RAT",
                "url": "https://www.uniprot.org/uniprot/M0RBE8",
                "type": "external"
            }
        ],
        "mass": 53247.0,
        "length": 504,
        "protein_name": "Actin nucleation-promoting factor WAS",
        "gene_name": "Was",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Was",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Actin nucleation-promoting factor WAS",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "X-linked severe congenital neutropenia (Disease Ontology:DOID:0112128); thrombocytopenia (Disease Ontology:DOID:1588); IgA glomerulonephritis (Disease Ontology:DOID:2986); Wiskott-Aldrich syndrome (Disease Ontology:DOID:9169)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Effector protein for Rho-type GTPases that regulates actin filament reorganization via its interaction with the Arp2/3 complex. Important for efficient actin polymerization. Possible regulator of lymphocyte and platelet function. Mediates actin filament reorganization and the formation of actin pedestals upon infection by pathogenic bacteria. In addition to its role in the cytoplasmic cytoskeleton, also promotes actin polymerization in the nucleus, thereby regulating gene transcription and repair of damaged DNA. Promotes homologous recombination (HR) repair in response to DNA damage by promoting nuclear actin polymerization, leading to drive motility of double-strand breaks (DSBs)., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 3,
        "predicted_n_glycosites": 0,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0003779 actin binding;GO:0017124 SH3 domain binding;GO:0019901 protein kinase binding;GO:0042802 identical protein binding;GO:0031267 small GTPase binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005856 cytoskeleton;GO:0005829 cytosol;GO:0005884 actin filament;GO:0005911 cell-cell junction",
        "go_biological_process": "GO:0007015 actin filament organization;GO:0008064 regulation of actin polymerization or depolymerization;GO:0006955 immune response;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0042110 T cell activation",
        "synthesized_glycan_count": 0,
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        "record_id": "M0RBE8-1",
        "record_type": "protein",
        "filter_code": "0000000.0000110.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "F1M4W7-1",
        "uniprot_id": [
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                "id": "F1M4W7_RAT",
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                "type": "external"
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        ],
        "mass": 82877.0,
        "length": 717,
        "protein_name": "Cleavage stimulation factor subunit 3",
        "gene_name": "Cstf3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
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    {
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            {
                "id": "MRP4_RAT",
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        ],
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        "protein_name": "ATP-binding cassette subfamily C member 4",
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        "refseq_name": "ATP-binding cassette subfamily C member 4",
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            {
                "id": "NP_596902",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_596902",
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        ],
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        "protein_names_refseq": "ABC-tranporter; ATP-binding cassette protein C4; ATP-binding cassette subfamily C member 4; ATP-binding cassette, sub-family C (CFTR/MRP), member 4; ATP-binding cassette, subfamily C (CFTR/MRP), member 4; multidrug resistance-associated protein 4",
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        "disease": "cholestasis (Disease Ontology:DOID:13580); extrahepatic cholestasis (Disease Ontology:DOID:13619); cystic fibrosis (Disease Ontology:DOID:1485); primary ovarian insufficiency (Disease Ontology:DOID:5426)",
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        "function": "ATP-dependent transporter of the ATP-binding cassette (ABC) family that actively extrudes physiological compounds and xenobiotics from cells (By similarity). Transports a range of endogenous molecules that have a key role in cellular communication and signaling, including cyclic nucleotides such as cyclic AMP (cAMP) and cyclic GMP (cGMP), bile acids, steroid conjugates, urate, and prostaglandins (By similarity). Mediates the ATP-dependent efflux of glutathione conjugates such as leukotriene C4 (LTC4) and leukotriene B4 (LTB4) too. The presence of GSH is necessary for the ATP-dependent transport of LTB4, whereas GSH is not required for the transport of LTC4 (By similarity). Mediates the cotransport of bile acids with reduced glutathione (GSH) (By similarity). Transports a wide range of drugs and their metabolites, including anticancer, antiviral and antibiotic molecules (By similarity). Confers resistance to anticancer agents such as methotrexate (By similarity)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Inflammation-Induced Attenuation of Prostaglandin D2 Elimination across Rat Blood-Brain Barrier: Involvement of the Downregulation of Organic Anion Transporter 3 and Multidrug Resistance-Associated Protein 4., [RefSeq, PubMed]; MRP4 can mediate the efflux of reduced glutatione from hepatocytes into blood by cotransport with monoanionic bile salts., [RefSeq, PubMed]; Obstructive cholestasis results in progressive up-regulation of Mrp4 protein in liver but down-regulation in kidney. The absence of corresponding changes in Mrp4 mRNA suggests posttranscriptional mechanisms as predominant regulators of Mrp4 expression., [RefSeq, PubMed]; The Daily Expression of ABCC4 at the BCSFB Affects the Transport of Its Substrate Methotrexate. Publication Status: Online-Only, [RefSeq, PubMed]; These data suggest that inhibition of MRP4 significantly alleviates sepsis-induced acute lung injury in rats. Erratum:[Int Immunopharmacol. 2023 Sep;122:110699. doi: 10.1016/j.intimp.2023.110699. PMID: 37500384], [RefSeq, PubMed]",
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        "predicted_n_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "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": "Q6QMG6",
        "ec_number_list": [
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                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.1.5",
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                "id": "7.6.2.2",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.6.2.2",
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                "id": "7.6.2.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:7.6.2.3",
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                "id": "3.1.-.-",
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                "id": "7.6.2.-",
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                "id": "7.2.2.-",
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            {
                "id": "3.1.3.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.3.1",
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            {
                "id": "3.9.1.1",
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                "id": "6.1.1.12",
                "url": "https://www.rhea-db.org/rhea/?query=ec:6.1.1.12",
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                "id": "3.6.1.-",
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                "id": "1.11.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.11.1.-",
                "type": "external"
            },
            {
                "id": "1.8.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.8.-.-",
                "type": "external"
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            {
                "id": "3.1.4.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.4.-",
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            {
                "id": "1.8.5.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.8.5.1",
                "type": "external"
            },
            {
                "id": "3.4.24.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.24.-",
                "type": "external"
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            {
                "id": "3.6.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.-.-",
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                "id": "3.4.21.53",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.4.21.53",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:5.6.2.5",
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        ],
        "go_molecular_function": "GO:0042910 xenobiotic transmembrane transporter activity;GO:0005524 ATP binding;GO:0022857 transmembrane transporter activity;GO:0042626 ATPase-coupled transmembrane transporter activity;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0016323 basolateral plasma membrane;GO:0016324 apical plasma membrane;GO:0031088 platelet dense granule membrane",
        "go_biological_process": "GO:0055085 transmembrane transport;GO:0015721 bile acid and bile salt transport;GO:0048661 positive regulation of smooth muscle cell proliferation;GO:0060271 cilium assembly;GO:0009410 response to xenobiotic stimulus",
        "synthesized_glycan_count": 0,
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        "kg_view_protein": true
    },
    {
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            {
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        ],
        "mass": 72534.0,
        "length": 652,
        "protein_name": "Amyloid beta precursor like protein 1",
        "gene_name": "Aplp1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Aplp1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Amyloid beta precursor like protein 1; Amyloid beta (A4) precursor-like protein 1; Amyloid-like protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Alzheimer's disease 1 (Disease Ontology:DOID:0080348); Alzheimer's disease (Disease Ontology:DOID:10652)",
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        "pathway_count": 0,
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        "class_list": "",
        "function": "May play a role in postsynaptic function. The C-terminal gamma-secretase processed fragment, ALID1, activates transcription activation through APBB1 (Fe65) binding. Couples to JIP signal transduction through C-terminal binding. May interact with cellular G-protein signaling pathways. Can regulate neurite outgrowth through binding to components of the extracellular matrix such as heparin and collagen I., [UniProtKB, UniProtKB]; The gamma-CTF peptide, C30, is a potent enhancer of neuronal apoptosis., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 4,
        "predicted_n_glycosites": 0,
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        "ec_number_list": [],
        "go_molecular_function": "GO:0008201 heparin binding;GO:0042802 identical protein binding;GO:0046914 transition metal ion binding;GO:0031694 alpha-2A adrenergic receptor binding;GO:0031696 alpha-2C adrenergic receptor binding",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0016020 membrane;GO:0048471 perinuclear region of cytoplasm",
        "go_biological_process": "GO:0006417 regulation of translation;GO:0030198 extracellular matrix organization;GO:0030900 forebrain development;GO:0071874 cellular response to norepinephrine stimulus;GO:0106072 negative regulation of adenylate cyclase-activating G protein-coupled receptor signaling pathway",
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        "kg_view_protein": true
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        "length": 524,
        "protein_name": "Butyrophilin, subfamily 1, member A1",
        "gene_name": "Btn1a1",
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            {
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            }
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        "protein_names_refseq": "butyrophilin subfamily 1 member A1 precursor",
        "tax_id": 10116,
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        "class_list": "",
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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:0005102 signaling receptor binding",
        "go_cellular_component": "GO:0009897 external side of plasma membrane;GO:0016020 membrane",
        "go_biological_process": "GO:0050852 T cell receptor signaling pathway;GO:0001817 regulation of cytokine production",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1LRV5-1",
        "record_type": "protein",
        "filter_code": "0000000.0000001.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
            {
                "id": "F1LSL7_RAT",
                "url": "https://www.uniprot.org/uniprot/F1LSL7",
                "type": "external"
            }
        ],
        "mass": 49444.0,
        "length": 443,
        "protein_name": "KLF transcription factor 5",
        "gene_name": "Klf5",
        "organism": "Rat",
        "refseq_name": "Krueppel-like factor 5",
        "refseq_ac": [
            {
                "id": "NP_445846",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_445846",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Klf5",
        "gene_names_refseq": "Bteb2; IKLF; Klf5; bteb2",
        "protein_names_uniprotkb": "KLF transcription factor 5",
        "protein_names_refseq": "Krueppel-like factor 5; Kruppel-like factor 5 (intestinal); basic transcription element binding protein 2; basic transcription element binding protein BTEB2",
        "tax_id": 10116,
        "disease": "metabolic dysfunction and alcohol associated liver disease (Disease Ontology:DOID:0070508); intracranial aneurysm (Disease Ontology:DOID:10941); transient cerebral ischemia (Disease Ontology:DOID:224)",
        "pathway": " (rno:84410)",
        "pathway_count": 1,
        "publication_count": 3,
        "publication_id_list": "29211809;30322616;36135378",
        "class_list": "",
        "function": "Demonstrated that RSV activated klf5 phosphorylation by inhibiting PI3K/PKD1/Akt pathway, and then attenuated the interaction of klf5 with c-Myc Publication Status: Online-Only, [RefSeq, PubMed]; Inhibiting Intestinal Kruppel-Like Factor 5 Impairs the Beneficial Role of Renal Denervation in Gut Microbiota in Rats with Heart Failure., [RefSeq, PubMed]; MiR-448-3p affects macrophage infiltration during intracranial aneurysm formation by regulating KLF5 expression., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "secondary_ac_list": "",
        "ec_number_list": [],
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0043403 skeletal muscle tissue regeneration;GO:0014816 skeletal muscle satellite cell differentiation;GO:1990859 cellular response to endothelin;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001525 angiogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "F1LSL7-1",
        "record_type": "protein",
        "filter_code": "0000000.0000111.100000.000000000000001000.0000000001000.001.00000",
        "kg_view_protein": true
    },
    {
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        "uniprot_id": [
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                "url": "https://www.uniprot.org/uniprot/F1LTR7",
                "type": "external"
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        ],
        "mass": 24690.0,
        "length": 223,
        "protein_name": "Natural cytotoxicity triggering receptor 2 like 1",
        "gene_name": "Ncr2l1",
        "organism": "Rat",
        "refseq_name": "triggering receptor expressed on myeloid cells 1-like isoform X1",
        "refseq_ac": [
            {
                "id": "XP_006244556",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006244556",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Ncr2l1; LOC680920",
        "gene_names_refseq": "Ncr2l1",
        "protein_names_uniprotkb": "Natural cytotoxicity triggering receptor 2 like 1",
        "protein_names_refseq": "triggering receptor expressed on myeloid cells 1-like isoform X1",
        "tax_id": 10116,
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        ],
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        ],
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        "protein_name": "EMILIN-2",
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        "refseq_name": "SLIT-ROBO Rho GTPase-activating protein 1",
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        "protein_names_uniprotkb": "SLIT-ROBO Rho GTPase-activating protein 1; Rho GTPase-activating protein 13",
        "protein_names_refseq": "SLIT-ROBO Rho GTPase-activating protein 1",
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        "disease": "focal segmental glomerulosclerosis (Disease Ontology:DOID:1312); papillary thyroid carcinoma (Disease Ontology:DOID:3969)",
        "pathway": " (rno:314903);  (R-RNO-8980692);  (R-RNO-9013148);  (R-RNO-9013149)",
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        "protein_names_refseq": "signal peptide, CUB and EGF-like domain-containing protein 1 precursor; signal peptide, CUB and EGF-like domain-containing protein 1; signal peptide, CUB domain, EGF-like 1",
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        "function": "A pronounced rise in SCUBE-1 levels was determined with 6-hour acute mesenteric ischemia in rats., [RefSeq, PubMed]; Could function as an adhesive molecule and its matrix bound and soluble fragments may play a critical role in vascular biology., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Scube1 encodes a novel stromal molecule that is involved in prostate development and tumorigenesis., [RefSeq, PubMed]",
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        "disease": "exudative vitreoretinopathy (Disease Ontology:DOID:0050535); nonsyndromic deafness (Disease Ontology:DOID:0050563); osteoporosis-pseudoglioma syndrome (Disease Ontology:DOID:0060849); polycystic liver disease 4 (Disease Ontology:DOID:0060977); polycystic liver disease 1 (Disease Ontology:DOID:0060980); Worth syndrome (Disease Ontology:DOID:0080037); autosomal dominant osteopetrosis 1 (Disease Ontology:DOID:0110937); exudative vitreoretinopathy 4 (Disease Ontology:DOID:0111411); osteonecrosis (Disease Ontology:DOID:10159); microphthalmia (Disease Ontology:DOID:10629); osteoporosis (Disease Ontology:DOID:11476); idiopathic juvenile osteoporosis (Disease Ontology:DOID:12559); heart valve disease (Disease Ontology:DOID:4079); autosomal dominant polycystic kidney disease (Disease Ontology:DOID:898); tendinitis (Disease Ontology:DOID:971); neovascular inflammatory vitreoretinopathy (Disease Ontology:DOID:9719)",
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        "function": "Component of the Wnt-Fzd-LRP5-LRP6 complex that triggers beta-catenin signaling through inducing aggregation of receptor-ligand complexes into ribosome-sized signalosomes., [UniProtKB, UniProtKB]; LRP5 Regulates HIF-1alpha Stability via Interaction with PHD2 in Ischemic Myocardium. Publication Status: Online-Only, [RefSeq, PubMed]; Low-Density Lipoprotein Receptor-Related Protein 5-Deficient Rats Have Reduced Bone Mass and Abnormal Development of the Retinal Vasculature., [RefSeq, PubMed]; Structure and function of the retina of low-density lipoprotein receptor-related protein 5 (Lrp5)-deficient rats., [RefSeq, PubMed]",
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        "disease": "childhood-onset asthma (Disease Ontology:DOID:0080815)",
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        "function": "Gene regulation, via an alternative splicing mechanism, affects not only the tissue-specificity of Sema 3D expression, but also the distance over which it can act., [RefSeq, PubMed]; Sema3D may regulate the axonal navigation of the large diameter DRG neurons., [RefSeq, PubMed]",
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            {
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                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001162591",
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        "tax_id": 10116,
        "disease": "stomach cancer (Disease Ontology:DOID:10534); acute myeloid leukemia (Disease Ontology:DOID:9119)",
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        ],
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        "protein_name": "G protein-coupled receptor 55",
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        "function": "Contribution of G Protein-Coupled Receptor 55 to Periaqueductal Gray-Mediated Antinociception in the Inflammatory Pain., [RefSeq, PubMed]; GPR55 activation prevents amphetamine-induced conditioned place preference and decrease the amphetamine-stimulated inflammatory response in the ventral hippocampus in male rats., [RefSeq, PubMed]; GPR55 is expressed in glutamate neurons and functionally modulates drug taking and seeking in rats and mice. Publication Status: Online-Only, [RefSeq, PubMed]; Presynaptic nigral GPR55 receptors stimulate [(3) H]-GABA release through [(3) H]-cAMP production and PKA activation and promote motor behavior., [RefSeq, PubMed]; Prominent expression of GPR55 in decidual cells suggests a role in mediating cannabinoid signalling during fetoplacental development, [RefSeq, PubMed]; The effect of intra-striatal administration of GPR55 agonist (LPI) and antagonist (ML193) on sensorimotor and motor functions in a Parkinson's disease rat model., [RefSeq, PubMed]",
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        "ec_number_list": [
            {
                "id": "2.4.1.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.4.1.-",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0050510 N-acetylgalactosaminyl-proteoglycan 3-beta-glucuronosyltransferase activity;GO:0047238 glucuronosyl-N-acetylgalactosaminyl-proteoglycan 4-beta-N-acetylgalactosaminyltransferase activity",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0032580 Golgi cisterna membrane",
        "go_biological_process": "GO:0050650 chondroitin sulfate proteoglycan biosynthetic process",
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    },
    {
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            {
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            }
        ],
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        "length": 1031,
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        "organism": "Rat",
        "refseq_name": "MMS19 nucleotide excision repair protein homolog",
        "refseq_ac": [
            {
                "id": "NP_001258525",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001258525",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Mms19; Mms19l",
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        "protein_names_refseq": "MMS19 homolog, cytosolic iron-sulfur assembly component; MMS19 nucleotide excision repair homolog; MMS19 nucleotide excision repair protein homolog; MMS19 nucleotide excision repair-like; MMS19-like (MET18 homolog, S. cerevisiae); incisor protein",
        "tax_id": 10116,
        "disease": "",
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        "publication_id_list": "22673903;29393594",
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        "go_cellular_component": "GO:0097361 cytosolic [4Fe-4S] assembly targeting complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005819 spindle",
        "go_biological_process": "GO:0016226 iron-sulfur cluster assembly;GO:0006281 DNA repair;GO:0051604 protein maturation",
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            }
        ],
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    },
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        ],
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        ],
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        ],
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        "function": "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, UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0061617 MICOS complex;GO:0000139 Golgi membrane;GO:0005576 extracellular region;GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane",
        "go_biological_process": "GO:0042407 cristae formation",
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        "kg_view_protein": true
    },
    {
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        ],
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        ],
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        "protein_name": "T cell receptor alpha variable 6-1",
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        "protein_names_uniprotkb": "T cell receptor alpha variable 6-1",
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        "go_cellular_component": "GO:0042101 T cell receptor complex;GO:0019814 immunoglobulin complex",
        "go_biological_process": "GO:0002250 adaptive immune response",
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        "record_id": "M0R7S3-1",
        "record_type": "protein",
        "filter_code": "0000000.0000000.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
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            {
                "id": "M0R7S5_RAT",
                "url": "https://www.uniprot.org/uniprot/M0R7S5",
                "type": "external"
            }
        ],
        "mass": 150887.0,
        "length": 1490,
        "protein_name": "Perilipin-4",
        "gene_name": "Plin4",
        "organism": "Rat",
        "refseq_name": "perilipin 4 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001418257",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001418257",
                "type": "external"
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        ],
        "gene_names_uniprotkb": "Plin4",
        "gene_names_refseq": "Plin4",
        "protein_names_uniprotkb": "Perilipin-4; Adipocyte protein S3-12",
        "protein_names_refseq": "perilipin 4 isoform 1",
        "tax_id": 10116,
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        "pathway": " (rno:363331)",
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        "publication_id_list": "28657654;34502162",
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        "function": "May play a role in triacylglycerol packaging into adipocytes. May function as a coat protein involved in the biogenesis of lipid droplets., [UniProtKB, UniProtKB]",
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            {
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        "protein_names_refseq": "vomernasal 1 receptor Vom1r62; vomeronasal 1 receptor 62; vomeronasal 1 receptor, K2; vomeronasal V1r-type receptor V1rk2; vomeronasal type-1 receptor 4",
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        "function": "Putative pheromone receptor implicated in the regulation of social as well as reproductive behavior., [UniProtKB, UniProtKB]",
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        "protein_name": "Interferon, alpha 1",
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        "protein_name": "Olfactory receptor",
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        "protein_name": "Acyl-CoA thioesterase 3",
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        "function": "Chronic unpredictable stress (CUS) reduced phoenixin expression, induced abnormal sperm and testis morphology in male rats., [RefSeq, PubMed]; Component of the MITRAC (mitochondrial translation regulation assembly intermediate of cytochrome c oxidase complex) complex, that regulates cytochrome c oxidase assembly (By similarity). Promotes the progression of complex assembly after the association of Mt-Co1/Cox11 with Cox4I1 and Cox6c (By similarity). Chaperone-like assembly factor required to stabilize newly synthesized Mt-Co1/Cox1 and to prevent its premature turnover (By similarity)., [UniProtKB, UniProtKB]; Modulatory effect of olanzapine on SMIM20/phoenixin, NPQ/spexin and NUCB2/nesfatin-1 gene expressions in the rat brainstem., [RefSeq, PubMed]; Peptide involved in a broad spectrum of regulatory functions (PubMed:27440717, PubMed:28844870, PubMed:28965207, PubMed:29364701, PubMed:30609107). Is a ligand for GPR173 (PubMed:27440717). As part of the reproductive cycle, it regulates gonadotropin-releasing hormone (GnRH) signaling in the hypothalamus and pituitary gland which augments the release of luteinizing hormone (PubMed:22963497, PubMed:27440717). More specifically, it regulates the expression of transcription factors CEBPB and POU2F1/OCT1 through the cAMP-PKA signaling pathway, which subsequently regulate the expression of GNRHR and KISS1 (By similarity). Plays a protective role in memory retention through activation of GNRHR (By similarity). Regulates the secretion of AVP by hypothalamic neurons (PubMed:29364701). Plays a role in the transduction of the itch sensation (By similarity). Induces anxiolytic effects, reducing behavior associated with anxiety (By similarity). Regulates food intake as well as satiation and satiety by increasing NUCB2 expression in neurons (PubMed:28844870, PubMed:30930149). In the ovary, it regulates follicular growth by stimulating granulosa cell proliferation by increasing the expression of GPR173, CREB1, CYP19A1, KITLG, FSHR, and LHCGR (By similarity). It also increases the production of estradiol (E2) (By similarity). In the heart, it regulates contractility and relaxation by activating the AKT1-NOS3 and MAPK1-MAPK3 signaling pathways (PubMed:28965207). It also plays a cardioprotective role during ischemia, where it activates the SAFE and RISK pathways (PubMed:28965207). Stimulates the proliferation and differentiation of preadipocytes (PubMed:30251651). In pancreatic islet cells, it induces proliferation of islet cells as well as the production of INS1 and INS2 through activation of the MAPK1-MAPK3 signaling pathways (PubMed:31422055)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, UniProtKB, PubMed, PubMed, PubMed, PubMed, UniProtKB]; Phoenixin induced a significant enhancement in plasma FSH, LH and testosterone without inducing any alteration in plasma GnRH in the rats., [RefSeq, PubMed]; Phoenixin may represent a new class of hypothalamically-derived pituitary priming factors that sensitize the pituitary to the action of other releasing factors., [RefSeq, PubMed]; Restraint stress affects circulating NUCB2/nesfatin-1 and phoenixin levels in male rats., [RefSeq, PubMed]",
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    },
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            {
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        ],
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        "gene_name": "Rapgef6",
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        "refseq_ac": [
            {
                "id": "XP_006246339",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006246339",
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            }
        ],
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        "protein_names_refseq": "rap guanine nucleotide exchange factor 6 isoform X2",
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        "go_biological_process": "GO:0032486 Rap protein signal transduction;GO:0031175 neuron projection development;GO:0007265 Ras protein signal transduction;GO:1903698 positive regulation of microvillus assembly;GO:0007264 small GTPase-mediated signal transduction",
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    },
    {
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein Hook homolog 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Emery-Dreifuss muscular dystrophy (Disease Ontology:DOID:11726)",
        "pathway": " (rno:306548)",
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        ],
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        "go_cellular_component": "GO:0005829 cytosol",
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            {
                "id": "NP_001258262",
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            }
        ],
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        "go_molecular_function": "GO:1990050 phosphatidic acid transfer activity",
        "go_cellular_component": "GO:0005758 mitochondrial intermembrane space",
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    },
    {
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            {
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                "type": "external"
            }
        ],
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        "protein_name": "Rab11 family-interacting protein 2",
        "gene_name": "Rab11fip2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Rab11fip2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Rab11 family-interacting protein 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "function": "A Rab11 effector binding preferentially phosphatidylinositol 3,4,5-trisphosphate (PtdInsP3) and phosphatidic acid (PA) and acting in the regulation of the transport of vesicles from the endosomal recycling compartment (ERC) to the plasma membrane. Involved in insulin granule exocytosis. Also involved in receptor-mediated endocytosis and membrane trafficking of recycling endosomes, probably originating from clathrin-coated vesicles. Required in a complex with MYO5B and RAB11 for the transport of NPC1L1 to the plasma membrane. Also acts as a regulator of cell polarity. Plays an essential role in phagocytosis through a mechanism involving TICAM2, RAC1 and CDC42 Rho GTPases for controlling actin-dynamics., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0031267 small GTPase binding;GO:0019901 protein kinase binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0055038 recycling endosome membrane;GO:0001891 phagocytic cup;GO:0005768 endosome",
        "go_biological_process": "GO:0015031 protein transport;GO:0016192 vesicle-mediated transport;GO:0007154 cell communication;GO:0023052 signaling;GO:0035669 TRAM-dependent toll-like receptor 4 signaling pathway",
        "synthesized_glycan_count": 0,
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    },
    {
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        ],
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        "protein_name": "Sad1 and UNC84 domain containing 1",
        "gene_name": "Get4; Sun1",
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        "refseq_name": "SUN domain-containing protein 1 isoform X1",
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        ],
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        "go_molecular_function": "GO:0004535 poly(A)-specific ribonuclease activity;GO:0001222 transcription corepressor binding",
        "go_cellular_component": "GO:0030015 CCR4-NOT core complex;GO:0005737 cytoplasm;GO:0000932 P-body;GO:0030014 CCR4-NOT complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:2000036 regulation of stem cell population maintenance;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001829 trophectodermal cell differentiation",
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        "kg_view_protein": true
    },
    {
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            {
                "id": "A0A8I6A4F2_RAT",
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                "type": "external"
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        ],
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        "protein_name": "Integrator complex subunit 9",
        "gene_name": "Ints9",
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        "gene_names_refseq": "",
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        "function": "Component of the integrator complex, a multiprotein complex that terminates RNA polymerase II (Pol II) transcription in the promoter-proximal region of genes. The integrator complex provides a quality checkpoint during transcription elongation by driving premature transcription termination of transcripts that are unfavorably configured for transcriptional elongation: the complex terminates transcription by (1) catalyzing dephosphorylation of the C-terminal domain (CTD) of Pol II subunit POLR2A/RPB1 and SUPT5H/SPT5, (2) degrading the exiting nascent RNA transcript via endonuclease activity and (3) promoting the release of Pol II from bound DNA. The integrator complex is also involved in terminating the synthesis of non-coding Pol II transcripts, such as enhancer RNAs (eRNAs), small nuclear RNAs (snRNAs), telomerase RNAs and long non-coding RNAs (lncRNAs). Mediates recruitment of cytoplasmic dynein to the nuclear envelope, probably as component of the integrator complex., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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    {
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        ],
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        "function": "Lipid transporter involved in lipid countertransport between the endoplasmic reticulum and the plasma membrane: specifically exchanges phosphatidylserine with phosphatidylinositol 4-phosphate (PI4P), delivering phosphatidylserine to the plasma membrane in exchange for PI4P, which is degraded by the SAC1/SACM1L phosphatase in the endoplasmic reticulum. Binds phosphatidylserine and PI4P in a mutually exclusive manner. May cooperate with NPC1 to mediate the exit of cholesterol from endosomes/lysosomes. Binds 25-hydroxycholesterol and cholesterol., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0015485 cholesterol binding;GO:0008289 lipid binding;GO:0070273 phosphatidylinositol-4-phosphate binding;GO:0001786 phosphatidylserine binding;GO:0140343 phosphatidylserine transfer activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0016020 membrane;GO:0005789 endoplasmic reticulum membrane;GO:0140268 endoplasmic reticulum-plasma membrane contact site;GO:1990351 transporter complex",
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                "id": "3.6.5.-",
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                "id": "3.1.-.-",
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                "id": "3.6.1.-",
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        "go_biological_process": "GO:0045087 innate immune response;GO:0051607 defense response to virus;GO:0002753 cytoplasmic pattern recognition receptor signaling pathway;GO:0140374 antiviral innate immune response;GO:0071360 cellular response to exogenous dsRNA",
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        ],
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        "disease": "orotic aciduria (Disease Ontology:DOID:0050833); developmental and epileptic encephalopathy 50 (Disease Ontology:DOID:0080419); rhabdomyosarcoma (Disease Ontology:DOID:3247); renal cell carcinoma (Disease Ontology:DOID:4450); hepatocellular carcinoma (Disease Ontology:DOID:684); carbamoyl phosphate synthetase I deficiency disease (Disease Ontology:DOID:9280)",
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        "protein_name": "E3 ubiquitin-protein ligase",
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        "function": "Ubiquitin ligase protein which is a component of the N-end rule pathway. Recognizes and binds to proteins bearing specific N-terminal residues that are destabilizing according to the N-end rule, leading to their ubiquitination and subsequent degradation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "WD repeat-containing protein 11; Bromodomain and WD repeat-containing protein 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autosomal recessive intellectual developmental disorder (Disease Ontology:DOID:0060308); ciliopathy (Disease Ontology:DOID:0060340); hypogonadotropic hypogonadism 14 with or without anosmia (Disease Ontology:DOID:0090087); Kallmann syndrome (Disease Ontology:DOID:3614)",
        "pathway": " (rno:309016);  (R-RNO-9013407)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Involved in the Hedgehog (Hh) signaling pathway, is essential for normal ciliogenesis. Regulates the proteolytic processing of GLI3 and cooperates with the transcription factor EMX1 in the induction of downstream Hh pathway gene expression and gonadotropin-releasing hormone production. WDR11 complex facilitates the tethering of Adaptor protein-1 complex (AP-1)-derived vesicles. WDR11 complex acts together with TBC1D23 to facilitate the golgin-mediated capture of vesicles generated using AP-1., [UniProtKB, 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_cellular_component": "GO:0005737 cytoplasm;GO:0005634 nucleus;GO:0005829 cytosol;GO:0005929 cilium;GO:0031410 cytoplasmic vesicle",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0007507 heart development;GO:0035264 multicellular organism growth;GO:0060271 cilium assembly;GO:0008589 regulation of smoothened signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
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        "kg_view_protein": true
    },
    {
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            {
                "id": "A0A8I5ZJ94_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A8I5ZJ94",
                "type": "external"
            }
        ],
        "mass": 209489.0,
        "length": 1908,
        "protein_name": "Ankyrin-1",
        "gene_name": "Ank1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Ank1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ankyrin-1; Erythrocyte ankyrin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "hereditary spherocytosis type 1 (Disease Ontology:DOID:0110916); malaria (Disease Ontology:DOID:12365); hereditary spherocytosis (Disease Ontology:DOID:12971); transient cerebral ischemia (Disease Ontology:DOID:224); anemia (Disease Ontology:DOID:2355)",
        "pathway": " (rno:306570);  (R-RNO-445095);  (R-RNO-447043);  (R-RNO-6807878)",
        "pathway_count": 4,
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        "function": "Component of the ankyrin-1 complex, a multiprotein complex involved in the stability and shape of the erythrocyte membrane. Attaches integral membrane proteins to cytoskeletal elements; binds to the erythrocyte membrane protein band 4.2, to Na-K ATPase, to the lymphocyte membrane protein GP85, and to the cytoskeletal proteins fodrin, tubulin, vimentin and desmin. Erythrocyte ankyrins also link spectrin (beta chain) to the cytoplasmic domain of the erythrocytes anion exchange protein; they retain most or all of these binding functions., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0019899 enzyme binding;GO:0051117 ATPase binding;GO:0044325 transmembrane transporter binding;GO:0030507 spectrin binding;GO:0008093 cytoskeletal anchor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0045211 postsynaptic membrane",
        "go_biological_process": "GO:0007165 signal transduction;GO:0055085 transmembrane transport;GO:0072659 protein localization to plasma membrane;GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport;GO:0006779 porphyrin-containing compound biosynthetic process",
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    },
    {
        "uniprot_canonical_ac": "A0A8I5ZQZ7-1",
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            {
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        ],
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        "protein_name": "Zinc finger protein 655",
        "gene_name": "Zfp655",
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        "refseq_name": "zinc finger protein 655 isoform 1",
        "refseq_ac": [
            {
                "id": "NP_001424414",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001424414",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Zfp655",
        "gene_names_refseq": "RGD1309158; Zfp655; Znf655",
        "protein_names_uniprotkb": "Zinc finger protein 655",
        "protein_names_refseq": "vav-1 interacting Kruppel-like protein; zinc finger protein 205-like; zinc finger protein 655 isoform 1",
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        "function": "Probable transcription factor., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005886 plasma membrane",
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    },
    {
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            {
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            }
        ],
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        "length": 395,
        "protein_name": "Sulfotransferase",
        "gene_name": "Chst6",
        "organism": "Rat",
        "refseq_name": "carbohydrate sulfotransferase 5 isoform 2",
        "refseq_ac": [
            {
                "id": "NP_001424557",
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                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Chst6; Chst5",
        "gene_names_refseq": "Chst5; Chst6; RGD1561144",
        "protein_names_uniprotkb": "Sulfotransferase; 2.8.2.-",
        "protein_names_refseq": "carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 5; carbohydrate sulfotransferase 5 isoform 2; carbohydrate sulfotransferase 5",
        "tax_id": 10116,
        "disease": "macular corneal dystrophy (Disease Ontology:DOID:2565)",
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            {
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            },
            {
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            }
        ],
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        ],
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        "protein_name": "Myocardin related transcription factor A",
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        "organism": "Rat",
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        "gene_names_uniprotkb": "Mrtfa; Mkl1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Myocardin related transcription factor A",
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        "tax_id": 10116,
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        "pathway": " (R-RNO-3899300);  (R-RNO-5663220)",
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        ],
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        "gene_name": "Carmil1",
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        "refseq_ac": [
            {
                "id": "XP_063132488",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_063132488",
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        ],
        "gene_names_uniprotkb": "Carmil1",
        "gene_names_refseq": "Carmil1; Lrrc16a; Lrrc16",
        "protein_names_uniprotkb": "Capping protein regulator and myosin 1 linker 1",
        "protein_names_refseq": "F-actin-uncapping protein LRRC16A isoform X2",
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        "protein_name": "SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1",
        "gene_name": "Smarcc1",
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        "refseq_name": "SWI/SNF complex subunit SMARCC1",
        "refseq_ac": [
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        "mass": 60981.0,
        "length": 551,
        "protein_name": "Steroid transmembrane transporter SLC22A24",
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            {
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        "protein_names_uniprotkb": "Steroid transmembrane transporter SLC22A24; Organic anion transporter 5; Solute carrier family 22 member 24; rOat5",
        "protein_names_refseq": "organic anion transporter 5; solute carrier family 22 (organic anion transporter), member 19; solute carrier family 22 (organic anion transporter), member 9; solute carrier family 22 (organic anion/cation transporter), member 9; solute carrier family 22 member 10; solute carrier family 22, member 24; steroid transmembrane transporter SLC22A24",
        "tax_id": 10116,
        "disease": "mismatch repair cancer syndrome (Disease Ontology:DOID:0112182); Lynch syndrome (Disease Ontology:DOID:3883)",
        "pathway": " (rno:286961)",
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        "publication_id_list": "15068970;16079298;18796410;20865662;24199190;26269671;31553721;32497308",
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        "function": "An increased expression of Oat5 in renal homogenates, in apical membranes, and in its urinary excretion was observed in rats with vascular calcification., [RefSeq, PubMed]; Cholestasis induced by common bile duct ligation in the rat induces upregulation of Oat5 in kidneys., [RefSeq, PubMed]; Highly expressed in kidney. Motive forces behind Oat5 function, which provide insight into its membrane localization, need to be further resolved., [RefSeq, PubMed]; ROat5 is renal organic anion/dicarboxylates exchanger and, under physiological conditions, may function as an apical reabsorptive pathway, [RefSeq, PubMed]; Renal expression of Oat5 in rats (and mice) exhibits zonal and sex differences, [RefSeq, PubMed]; Renal transmembrane organic anion/dicarboxylate exchanger that participates in the reabsorption of conjugated steroids, as well as bile acids, driven by an outward gradient of dicarboxylates such as glutarate or succinate (PubMed:16079298). Transports estrone 3-sulfate and estradiol-17-glucuronide (17beta-estradiol 17-O-(beta-D-glucuronate)), but not androstanediol glucuronide (5alpha-androstane-3alpha,17beta-diol 3-O-(beta-D-glucuronate)), nor taurocholate (PubMed:31553721). Prefers sulfate conjugates of steroids rather than glucuronide conjugates (PubMed:16079298)., [UniProtKB, PubMed, PubMed]; Urinary excretion of Oat5 might be an early indicator of renal dysfunction, [RefSeq, PubMed]; Utility of urinary organic anion transporter 5 as an early biomarker of obstructive nephropathy., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0022857 transmembrane transporter activity;GO:0019534 toxin transmembrane transporter activity",
        "go_cellular_component": "GO:0016324 apical plasma membrane",
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            {
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        "pathway": " (rno:289014);  (R-RNO-171007);  (R-RNO-199920);  (R-RNO-2142691);  (R-RNO-2559580);  (R-RNO-3371453);  (R-RNO-4420097);  (R-RNO-450302);  (R-RNO-450385);  (R-RNO-450513);  (R-RNO-5357905)",
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        "function": "Is suggested that renal protective effect may be related to MAPKAPK-2 activation in the reduction of renal ischemia-reperfusion injury by ischemic postconditioning, [RefSeq, PubMed]; MK2 small interfering RNA delivery arrests lipopolysaccharide-induced inflammatory bone loss, decreases inflammatory infiltrate, and decreases osteoclastogenesis., [RefSeq, PubMed]",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.31",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.18",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.24.-",
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        ],
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006468 protein phosphorylation;GO:0006954 inflammatory response;GO:0032496 response to lipopolysaccharide;GO:0035556 intracellular signal transduction;GO:0048255 mRNA stabilization",
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    },
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        "protein_name": "Ubiquitin C-terminal hydrolase PSMD14",
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        "refseq_name": "26S proteasome non-ATPase regulatory subunit 14",
        "refseq_ac": [
            {
                "id": "NP_001020860",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001020860",
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        "protein_names_refseq": "26S proteasome non-ATPase regulatory subunit 14; proteasome (prosome, macropain) 26S subunit, non-ATPase, 14",
        "tax_id": 10116,
        "disease": "alcohol-associated liver disease (Disease Ontology:DOID:0070658)",
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        "function": "Males and females differ in the regulation and engagement of, but not requirement for, protein degradation in the amygdala during fear memory formation., [RefSeq, PubMed]; Translocation from synapse to the nucleus is involved in regulation of Tbr-1 function in postnatal and adult brains, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_cellular_component": "GO:0031597 cytosolic proteasome complex;GO:0022624 proteasome accessory complex;GO:0005654 nucleoplasm;GO:0000502 proteasome complex;GO:0008541 proteasome regulatory particle, lid subcomplex",
        "go_biological_process": "GO:0006508 proteolysis;GO:0045471 response to ethanol;GO:0070536 protein K63-linked deubiquitination;GO:0016241 regulation of macroautophagy;GO:0006303 double-strand break repair via nonhomologous end joining",
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        ],
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        ],
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        ],
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            {
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        "go_cellular_component": "GO:0005634 nucleus;GO:0000785 chromatin",
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        "protein_names_uniprotkb": "Small ribosomal subunit protein uS9; 40S ribosomal protein S16",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0000781 chromosome, telomeric region;GO:0005819 spindle;GO:0035861 site of double-strand break;GO:0005654 nucleoplasm",
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        ],
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            {
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Phospholipid-transporting ATPase",
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            {
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            }
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        "disease": "X-linked congenital hemolytic anemia (Disease Ontology:DOID:0111846)",
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            {
                "id": "XP_038968572",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_038968572",
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        ],
        "gene_names_uniprotkb": "Rbm25l1; Rbm25; Rbm25l1",
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        "protein_names_refseq": "RNA-binding protein 25 isoform X1",
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        "pathway": " (rno:497865);  (R-RNO-9770562)",
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        ],
        "mass": 266986.0,
        "length": 2439,
        "protein_name": "SEH1-like nucleoporin",
        "gene_name": "Cep192; Seh1l",
        "organism": "Rat",
        "refseq_name": "centrosomal protein of 192 kDa isoform X3",
        "refseq_ac": [
            {
                "id": "XP_063133382",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_063133382",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Cep192; Seh1l; Seh1l",
        "gene_names_refseq": "Cep192; Da1-6; Seh1l",
        "protein_names_uniprotkb": "SEH1-like nucleoporin",
        "protein_names_refseq": "centrosomal protein of 192 kDa isoform X3",
        "tax_id": 10116,
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        "pathway": " (R-RNO-2565942);  (R-RNO-380259);  (R-RNO-380270);  (R-RNO-380284);  (R-RNO-380320);  (R-RNO-5620912);  (R-RNO-8854518)",
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        "function": "As a component of the GATOR2 complex, functions as an activator of the amino acid-sensing branch of the mTORC1 signaling pathway. The GATOR2 complex indirectly activates mTORC1 through the inhibition of the GATOR1 subcomplex. GATOR2 probably acts as an E3 ubiquitin-protein ligase toward GATOR1. In the presence of abundant amino acids, the GATOR2 complex mediates ubiquitination of the NPRL2 core component of the GATOR1 complex, leading to GATOR1 inactivation. In the absence of amino acids, GATOR2 is inhibited, activating the GATOR1 complex. Within the GATOR2 complex, SEC13 and SEH1L are required to stabilize the complex., [UniProtKB, UniProtKB, UniProtKB]; Component of the Nup107-160 subcomplex of the nuclear pore complex (NPC). The Nup107-160 subcomplex is required for the assembly of a functional NPC. The Nup107-160 subcomplex is also required for normal kinetochore microtubule attachment, mitotic progression and chromosome segregation. This subunit plays a role in recruitment of the Nup107-160 subcomplex to the kinetochore., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005198 structural molecule activity;GO:0019902 phosphatase binding",
        "go_cellular_component": "GO:0031080 nuclear pore outer ring;GO:0005635 nuclear envelope;GO:0005765 lysosomal membrane;GO:0000776 kinetochore;GO:0061700 GATOR2 complex",
        "go_biological_process": "GO:1904263 positive regulation of TORC1 signaling;GO:0051315 attachment of mitotic spindle microtubules to kinetochore;GO:0006999 nuclear pore organization;GO:0015031 protein transport;GO:0050830 defense response to Gram-positive bacterium",
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        "record_id": "A0A8I6A567-1",
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        ],
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        "protein_name": "Olfactory receptor family 2 subfamily AG member 19",
        "gene_name": "Or2ag19b",
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            {
                "id": "NP_001000197",
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        ],
        "gene_names_uniprotkb": "Or2ag19b; Or2ag19",
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        "protein_names_uniprotkb": "Olfactory receptor family 2 subfamily AG member 19",
        "protein_names_refseq": "olfactory receptor 214; olfactory receptor Olr214; olfactory receptor gene Olr214",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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                "id": "XP_038935037",
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        "length": 568,
        "protein_name": "Zinc finger protein 950 like 16",
        "gene_name": "Zfp950l16",
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        "gene_names_uniprotkb": "Zfp950l16; LOC102549410",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 950 like 16",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
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        "tax_id": 10116,
        "disease": "Stevens-Johnson syndrome (Disease Ontology:DOID:0050426); colitis (Disease Ontology:DOID:0060180); Cytomegalovirus retinitis (Disease Ontology:DOID:0080160); COVID-19 (Disease Ontology:DOID:0080600); ankylosing spondylitis 1 (Disease Ontology:DOID:0080603); erythema nodosum (Disease Ontology:DOID:0080750); occupational asthma (Disease Ontology:DOID:0080820); graft-versus-host disease (Disease Ontology:DOID:0081267); birdshot chorioretinopathy (Disease Ontology:DOID:0111079); psoriasis 1 (Disease Ontology:DOID:0111286); sensorineural hearing loss (Disease Ontology:DOID:10003); spondyloarthropathy (Disease Ontology:DOID:1123); trachoma (Disease Ontology:DOID:11265); sarcoidosis (Disease Ontology:DOID:11335); retinal vasculitis (Disease Ontology:DOID:11563); otosclerosis (Disease Ontology:DOID:12185); Graves' disease (Disease Ontology:DOID:12361); respiratory syncytial virus infectious disease (Disease Ontology:DOID:1273); retinopathy of prematurity (Disease Ontology:DOID:13025); uveitis (Disease Ontology:DOID:13141); Behcet's disease (Disease Ontology:DOID:13241); anterior uveitis (Disease Ontology:DOID:1407); cystic fibrosis (Disease Ontology:DOID:1485); hepatitis C (Disease Ontology:DOID:1883); Takayasu's arteritis (Disease Ontology:DOID:2508); synovitis (Disease Ontology:DOID:2703); dermatitis (Disease Ontology:DOID:2723); asthma (Disease Ontology:DOID:2841); severe acute respiratory syndrome (Disease Ontology:DOID:2945); cerebral infarction (Disease Ontology:DOID:3526); acute retinal necrosis syndrome (Disease Ontology:DOID:3611); thrombophlebitis (Disease Ontology:DOID:3875); tuberculosis (Disease Ontology:DOID:399); cervical cancer (Disease Ontology:DOID:4362); allergic rhinitis (Disease Ontology:DOID:4481); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); uveal melanoma (Disease Ontology:DOID:6039); reactive arthritis (Disease Ontology:DOID:6196); ankylosing spondylitis (Disease Ontology:DOID:7147); diabetic retinopathy (Disease Ontology:DOID:8947); allergic asthma (Disease Ontology:DOID:9415); Meniere's disease (Disease Ontology:DOID:9849); alopecia (Disease Ontology:DOID:987); mitral valve prolapse (Disease Ontology:DOID:988)",
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        "function": "Involved in the presentation of foreign antigens to the immune system., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0030881 beta-2-microglobulin binding;GO:0044877 protein-containing complex binding;GO:0042277 peptide binding",
        "go_cellular_component": "GO:0030670 phagocytic vesicle membrane;GO:0042612 MHC class I protein complex;GO:0098553 lumenal side of endoplasmic reticulum membrane",
        "go_biological_process": "GO:0002474 antigen processing and presentation of peptide antigen via MHC class I;GO:0001916 positive regulation of T cell mediated cytotoxicity;GO:0045953 negative regulation of natural killer cell mediated cytotoxicity;GO:0002517 T cell tolerance induction;GO:0002657 positive regulation of tolerance induction to nonself antigen",
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    {
        "uniprot_canonical_ac": "A0A8I5ZN27-1",
        "uniprot_id": [
            {
                "id": "CNGB1_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A8I5ZN27",
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            }
        ],
        "mass": 147160.0,
        "length": 1307,
        "protein_name": "Cyclic nucleotide-gated channel beta-1",
        "gene_name": "Cngb1",
        "organism": "Rat",
        "refseq_name": "cyclic nucleotide-gated channel beta-1 isoform 2",
        "refseq_ac": [
            {
                "id": "NP_001376189",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001376189",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Cngb1; CNCG2; CNCG3L; CNCG4; RCNC2",
        "gene_names_refseq": "CNG-4; CNG4; Cngb1; Gm1959",
        "protein_names_uniprotkb": "Cyclic nucleotide-gated channel beta-1; CNG channel 4; CNG-4; CNG4; Cyclic nucleotide-gated cation channel 4",
        "protein_names_refseq": "CNG channel 4; cyclic nucleotide gated channel beta 1; cyclic nucleotide-gated cation channel 4; cyclic nucleotide-gated cation channel beta-1; cyclic nucleotide-gated channel beta subunit 1; cyclic nucleotide-gated channel beta-1 isoform 2",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa 45 (Disease Ontology:DOID:0110402); retinitis pigmentosa (Disease Ontology:DOID:10584)",
        "pathway": " (rno:83686);  (R-RNO-2485179);  (R-RNO-2514859);  (R-RNO-5620916)",
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        "function": "CNGB1b subunit participates in ligand-gated activation of olfactory CNG channels and, particularly, contributes to rapid termination of odorant signal in an olfactory sensory neuron. Erratum:[Sci Rep. 2018 Jun 28;8:47000. doi: 10.1038/srep47000. PMID: 29952375] Publication Status: Online-Only, [RefSeq, PubMed]; Pore-forming subunit of the olfactory cyclic nucleotide-gated channel. Operates in the cilia of olfactory sensory neurons where chemical stimulation of the odorant is converted to an electrical signal. Mediates odorant-induced cAMP-dependent Ca(2+) influx triggering neuron depolarization. The rise of intracellular Ca(2+) levels potentiates the olfactory response by activating Ca(2+)-dependent Cl(-) channels, but it also serves as a negative feedback signal to desensitize the channel for rapid adaptation to odorants., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed]; Pore-forming subunit of the rod cyclic nucleotide-gated channel. Mediates rod photoresponses at dim light converting transient changes in intracellular cGMP levels into electrical signals. In the dark, cGMP levels are high and keep the channel open enabling a steady inward current carried by Na(+) and Ca(2+) ions that leads to membrane depolarization and neurotransmitter release from synaptic terminals. Upon photon absorption cGMP levels decline leading to channel closure and membrane hyperpolarization that ultimately slows neurotransmitter release and signals the presence of light, the end point of the phototransduction cascade. Conducts cGMP- and cAMP-gated ion currents, with permeability for monovalent and divalent cations. The selectivity for Ca(2+) over Na(+) increases with cGMP concentrations, whereas the selectivity among monovalent ions is independent of the cGMP levels., [UniProtKB, UniProtKB]",
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            {
                "id": "2.7.11.1",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.1",
                "type": "external"
            },
            {
                "id": "1.8.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:1.8.-.-",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0005262 calcium channel activity;GO:0044877 protein-containing complex binding;GO:0005223 intracellularly cGMP-activated cation channel activity;GO:0005272 sodium channel activity;GO:0005222 intracellularly cAMP-activated cation channel activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0043195 terminal bouton;GO:0001750 photoreceptor outer segment;GO:0017071 intracellular cyclic nucleotide activated cation channel complex",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0010628 positive regulation of gene expression;GO:0006816 calcium ion transport;GO:0051480 regulation of cytosolic calcium ion concentration;GO:0051899 membrane depolarization",
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        "kg_view_protein": true
    },
    {
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        ],
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        "length": 124,
        "protein_name": "Immunoglobulin V-set domain-containing protein",
        "gene_name": "ENSRNOG00000066577",
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        "gene_names_uniprotkb": "ENSRNOG00000066577",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Immunoglobulin V-set domain-containing protein",
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        "go_cellular_component": "GO:0019814 immunoglobulin complex",
        "go_biological_process": "GO:0006955 immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZNW0-1",
        "record_type": "protein",
        "filter_code": "0000000.0000000.100000.000000000000001000.0000000000000.000.00000",
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    {
        "uniprot_canonical_ac": "A0A8I5ZRJ5-1",
        "uniprot_id": [
            {
                "id": "A0A8I5ZRJ5_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A8I5ZRJ5",
                "type": "external"
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        ],
        "mass": 25311.0,
        "length": 225,
        "protein_name": "Rho GDP-dissociation inhibitor 3",
        "gene_name": "Arhgdig",
        "organism": "Rat",
        "refseq_name": "rho GDP-dissociation inhibitor 3",
        "refseq_ac": [
            {
                "id": "NP_001101739",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001101739",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Arhgdig",
        "gene_names_refseq": "Arhgdig",
        "protein_names_uniprotkb": "Rho GDP-dissociation inhibitor 3; Rho-GDI gamma",
        "protein_names_refseq": "Rho GDP dissociation inhibitor (GDI) gamma; rho GDP-dissociation inhibitor 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:360500);  (R-RNO-9013026);  (R-RNO-9013148);  (R-RNO-9013407);  (R-RNO-9013408)",
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        "publication_id_list": "20051515;38029612",
        "class_list": "",
        "function": "Corticosterone, via SGK phosphorylation of GDI at Ser-213, increases the formation of GDI-Rab4 complex, facilitating the functional cycle of Rab4 and Rab4-mediated recycling of AMPARs to the synaptic membrane, [RefSeq, PubMed]; Inhibits GDP/GTP exchange reaction of RhoB. Interacts specifically with the GDP- and GTP-bound forms of post-translationally processed Rhob and Rhog proteins, both of which show a growth-regulated expression in mammalian cells. Stimulates the release of the GDP-bound but not the GTP-bound RhoB protein. Also inhibits the GDP/GTP exchange of RhoB but shows less ability to inhibit the dissociation of prebound GTP., [UniProtKB, UniProtKB]; RhoGDI3 at the trans-Golgi network participates in NLRP3 inflammasome activation, VSMC phenotypic modulation, and neointima formation., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0005094 Rho GDP-dissociation inhibitor activity;GO:0005096 GTPase activator activity;GO:0030695 GTPase regulator activity;GO:0005092 GDP-dissociation inhibitor activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0016020 membrane",
        "go_biological_process": "GO:0007266 Rho protein signal transduction;GO:0032880 regulation of protein localization;GO:0001835 blastocyst hatching",
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                "id": "A0A8I5ZRU6_RAT",
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        ],
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        "protein_name": "Serpin family A member 1F like 2",
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        "protein_names_uniprotkb": "Serpin family A member 1F like 2",
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                "type": "external"
            },
            {
                "id": "3.6.5.4",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.6.5.4",
                "type": "external"
            }
        ],
        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005516 calmodulin binding;GO:0005525 GTP binding;GO:0003925 G protein activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007265 Ras protein signal transduction",
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        "hit_score": 0.1,
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        "record_type": "protein",
        "filter_code": "0000000.0000011.100000.000000000000001000.0000000000000.000.00000",
        "kg_view_protein": true
    },
    {
        "uniprot_canonical_ac": "A0A8I6ACT0-1",
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            {
                "id": "A0A8I6ACT0_RAT",
                "url": "https://www.uniprot.org/uniprot/A0A8I6ACT0",
                "type": "external"
            }
        ],
        "mass": 60853.0,
        "length": 573,
        "protein_name": "60 kDa heat shock protein, mitochondrial",
        "gene_name": "Hspd1l1",
        "organism": "Rat",
        "refseq_name": "60 kDa heat shock protein, mitochondrial-like",
        "refseq_ac": [
            {
                "id": "XP_063133708",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_063133708",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Hspd1l1; LOC103694176",
        "gene_names_refseq": "Hspd1l1",
        "protein_names_uniprotkb": "60 kDa heat shock protein, mitochondrial; 5.6.1.7; 60 kDa chaperonin; Chaperonin 60; Heat shock protein 60; Mitochondrial matrix protein P1",
        "protein_names_refseq": "60 kDa heat shock protein, mitochondrial-like",
        "tax_id": 10116,
        "disease": "hypomyelinating leukodystrophy 4 (Disease Ontology:DOID:0060789); hereditary spastic paraplegia 13 (Disease Ontology:DOID:0110766); glucose intolerance (Disease Ontology:DOID:10603); Alzheimer's disease (Disease Ontology:DOID:10652); autistic disorder (Disease Ontology:DOID:12849); Down syndrome (Disease Ontology:DOID:14250); cystic fibrosis (Disease Ontology:DOID:1485); arteriosclerosis (Disease Ontology:DOID:2349); hereditary spastic paraplegia (Disease Ontology:DOID:2476); coronary artery disease (Disease Ontology:DOID:3393); carotid artery disease (Disease Ontology:DOID:3407); systemic juvenile rheumatoid arthritis (Disease Ontology:DOID:676); rheumatoid arthritis (Disease Ontology:DOID:7148); systemic lupus erythematosus (Disease Ontology:DOID:9074); aphthous stomatitis (Disease Ontology:DOID:9663)",
        "pathway": " (rno:103694176)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Chaperonin implicated in mitochondrial protein import and macromolecular assembly. Together with Hsp10, facilitates the correct folding of imported proteins. May also prevent misfolding and promote the refolding and proper assembly of unfolded polypeptides generated under stress conditions in the mitochondrial matrix. The functional units of these chaperonins consist of heptameric rings of the large subunit Hsp60, which function as a back-to-back double ring. In a cyclic reaction, Hsp60 ring complexes bind one unfolded substrate protein per ring, followed by the binding of ATP and association with 2 heptameric rings of the co-chaperonin Hsp10. This leads to sequestration of the substrate protein in the inner cavity of Hsp60 where, for a certain period of time, it can fold undisturbed by other cell components. Synchronous hydrolysis of ATP in all Hsp60 subunits results in the dissociation of the chaperonin rings and the release of ADP and the folded substrate protein., [UniProtKB, UniProtKB]",
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        "ec_number_list": [],
        "go_molecular_function": "GO:0005524 ATP binding;GO:0051087 protein-folding chaperone binding;GO:0140662 ATP-dependent protein folding chaperone",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane;GO:0005759 mitochondrial matrix",
        "go_biological_process": "GO:0032727 positive regulation of interferon-alpha production;GO:0045041 protein import into mitochondrial intermembrane space;GO:0032755 positive regulation of interleukin-6 production;GO:0042110 T cell activation;GO:0006457 protein folding",
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    },
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            {
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            }
        ],
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        "protein_name": "Olfactory receptor",
        "gene_name": "Or2y1c",
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        "refseq_name": "olfactory receptor Olr1394",
        "refseq_ac": [
            {
                "id": "NP_001001091",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001001091",
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            }
        ],
        "gene_names_uniprotkb": "Or2y1c; Or2y1",
        "gene_names_refseq": "Olr1394; Or2y1c",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1394; olfactory receptor Olr1394; olfactory receptor gene Olr1394",
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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_cellular_component": "GO:0005886 plasma membrane",
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    },
    {
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            {
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            }
        ],
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        "protein_name": "Polyamine oxidase",
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        "tax_id": 10116,
        "disease": "lung non-small cell carcinoma (Disease Ontology:DOID:3908)",
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        "go_molecular_function": "GO:0016491 oxidoreductase activity;GO:0046592 polyamine oxidase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005782 peroxisomal matrix",
        "go_biological_process": "GO:0046203 spermidine catabolic process;GO:0006598 polyamine catabolic process;GO:0009446 putrescine biosynthetic process;GO:0009447 putrescine catabolic process;GO:0046208 spermine catabolic process",
        "synthesized_glycan_count": 0,
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            {
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        ],
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        "protein_name": "TNF receptor superfamily member 14",
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        "refseq_name": "tumor necrosis factor receptor superfamily member 14 isoform X4",
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            {
                "id": "XP_006239648",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006239648",
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            }
        ],
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        "protein_names_uniprotkb": "TNF receptor superfamily member 14",
        "protein_names_refseq": "tumor necrosis factor receptor superfamily member 14 isoform X4",
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        "disease": "arteriosclerosis (Disease Ontology:DOID:2349); myocardial infarction (Disease Ontology:DOID:5844)",
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        "go_molecular_function": "GO:0031625 ubiquitin protein ligase binding;GO:0048018 receptor ligand activity;GO:0019955 cytokine binding",
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        "go_biological_process": "GO:0050829 defense response to Gram-negative bacterium;GO:0050830 defense response to Gram-positive bacterium;GO:2000406 positive regulation of T cell migration;GO:0031295 T cell costimulation;GO:0042130 negative regulation of T cell proliferation",
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            {
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        ],
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        "protein_name": "Protein transport protein SEC23",
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        "refseq_name": "protein transport protein Sec23B",
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            {
                "id": "NP_001264164",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001264164",
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            }
        ],
        "gene_names_uniprotkb": "Sec23b",
        "gene_names_refseq": "Sec23b",
        "protein_names_uniprotkb": "Protein transport protein SEC23",
        "protein_names_refseq": "Sec23 homolog B, COPII coat complex component; Sec23 homolog B, coat complex II component; protein transport protein Sec23B",
        "tax_id": 10116,
        "disease": "craniolenticulosutural dysplasia (Disease Ontology:DOID:0070307); Cowden syndrome 7 (Disease Ontology:DOID:0081003); congenital dyserythropoietic anemia type II (Disease Ontology:DOID:0111401); Roberts syndrome (Disease Ontology:DOID:5325)",
        "pathway": " (rno:362226)",
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        "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 for their transport to the Golgi complex., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0005096 GTPase activator activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005789 endoplasmic reticulum membrane;GO:0030127 COPII vesicle coat;GO:0070971 endoplasmic reticulum exit site;GO:0005783 endoplasmic reticulum",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0090114 COPII-coated vesicle budding;GO:0090110 COPII-coated vesicle cargo loading",
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    },
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        ],
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        "protein_name": "Zinc finger protein 729b",
        "gene_name": "Zfp729b",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 729b isoform 1",
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            {
                "id": "NP_001395704",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001395704",
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        ],
        "gene_names_uniprotkb": "Zfp729b",
        "gene_names_refseq": "Zfp729b; Zfp748l1",
        "protein_names_uniprotkb": "Zinc finger protein 729b",
        "protein_names_refseq": "zinc finger protein 728-like; zinc finger protein 729b isoform 1; zinc finger protein 748 like 1",
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            {
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        "protein_names_uniprotkb": "Acylcarnitine hydrolase; 3.1.1.-; 3.1.1.28; ACH M1; Carboxylic ester hydrolase",
        "protein_names_refseq": "acylcarnitine hydrolase precursor; acylcarnitine hydrolase-like; carboxylesterase 2 (intestine, liver); carboxylic ester hydrolase",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100910144);  (rno:171118)",
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        "publication_count": 5,
        "publication_id_list": "12230550;15794950;17392394;17764701;29393594",
        "class_list": "",
        "function": "CES2 isoenzymes shown to be major intestinal esterases in first pass hydrolysis of ester containing drugs., [RefSeq, PubMed]; Comparative analysis of CES1 and CES2 in liver and small intestine of humans, monkeys, dogs, rabbits and rats, [RefSeq, PubMed]; Hydrolase with high activity towards palmitoylcarnitine. Is also active with p-nitrophenylacetate and alpha-naphthylacetate (By similarity). May also hydrolyze retinyl esters (PubMed:12230550)., [UniProtKB, PubMed, UniProtKB]",
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        "missing_score": 10000,
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.88",
                "type": "external"
            },
            {
                "id": "3.1.1.-",
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                "type": "external"
            },
            {
                "id": "3.1.1.28",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.28",
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            },
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.23",
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            },
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                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.1.3",
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            }
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        "go_biological_process": "GO:0001523 retinoid metabolic process",
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            {
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                "id": "3.1.3.16",
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.11.4",
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                "id": "2.3.1.48",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.1.48",
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                "id": "3.1.11.-",
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                "id": "2.7.13.3",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.13.3",
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            },
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                "id": "2.7.4.18",
                "url": "https://www.rhea-db.org/rhea/?query=ec:2.7.4.18",
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                "id": "3.1.24.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.24.-",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016604 nuclear body;GO:0016363 nuclear matrix;GO:0005694 chromosome;GO:0005634 nucleus",
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        "go_molecular_function": "GO:0051377 mannose-ethanolamine phosphotransferase activity",
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        "function": "Maintains stem cell potency. Increases STAT3 phosphorylation and controls ERK phosphorylation. May act as a scaffold, increasing STAT3 recruitment onto endosomes., [UniProtKB, UniProtKB]",
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            {
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            }
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        "protein_names_uniprotkb": "TATA box-binding protein-like 1; TATA box-binding protein-related factor 2; TBP-like factor; TBP-related protein",
        "protein_names_refseq": "TATA box-binding protein-like 1; TATA box-binding protein-like protein 1; TBP-like 1",
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        "function": "Part of a specialized transcription system that mediates the transcription of most ribosomal proteins through the 5'-TCT-3' motif which is a core promoter element at these genes. Seems to also mediate the transcription of NF1. Does not bind the TATA box., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; These findings have indicated that overproduction of reactive oxygen species after testicular torsion-detorsion can damage testicular spermatogenesis by downregulation of TRF2 expression., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005672 transcription factor TFIIA complex",
        "go_biological_process": "GO:0006352 DNA-templated transcription initiation;GO:0007283 spermatogenesis;GO:0001675 acrosome assembly;GO:0007289 spermatid nucleus differentiation;GO:0006235 dTTP biosynthetic process",
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            },
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                "id": "3.6.-.-",
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            },
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                "id": "3.1.-.-",
                "url": "https://www.rhea-db.org/rhea/?query=ec:3.1.-.-",
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            }
        ],
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            {
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        "gene_names_uniprotkb": "Tmprss11c; Tmprss11b",
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        "protein_names_refseq": "airway trypsin-like 3; transmembrane protease, serine 11C isoform 1",
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        ],
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        "protein_name": "Dedicator of cytokinesis protein 4",
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        "function": "A new function of the Rac activator Dock4 in dendritic morphogenesis in hippocampal neurons, [RefSeq, PubMed]; Direct targeting of DOCK4 by miRNA-181d in oxygen-glucose deprivation/reoxygenation-mediated neuronal injury. Publication Status: Online-Only, [RefSeq, PubMed]; Dock4 is highly concentrated in dendritic spines and implicated in spine formation via interaction with the actin-binding protein cortactin., [RefSeq, PubMed]; Functions as a guanine nucleotide exchange factor (GEF) that promotes the exchange of GDP to GTP, converting inactive GDP-bound small GTPases into their active GTP-bound form. Involved in regulation of adherens junction between cells. Plays a role in cell migration., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Has a higher guanine nucleotide exchange factor activity compared to other isoforms., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "disease": "autosomal dominant nonsyndromic deafness 67 (Disease Ontology:DOID:0110588); status epilepticus (Disease Ontology:DOID:1824)",
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        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0043005 neuron projection;GO:0035145 exon-exon junction complex",
        "go_biological_process": "GO:0045727 positive regulation of translation;GO:2000623 negative regulation of nuclear-transcribed mRNA catabolic process, nonsense-mediated decay;GO:1905746 positive regulation of mRNA cis splicing, via spliceosome",
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    },
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            {
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        ],
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        "protein_names_uniprotkb": "Low-density lipoprotein receptor-related protein 10",
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        "mass": 51679.0,
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        "refseq_name": "interferon gamma receptor 1 precursor",
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            {
                "id": "NP_446235",
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        ],
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        "go_biological_process": "GO:0001774 microglial cell activation;GO:0010628 positive regulation of gene expression;GO:0048143 astrocyte activation;GO:0051607 defense response to virus;GO:1902004 positive regulation of amyloid-beta formation",
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        "protein_name": "Zinc finger and BTB domain-containing protein 17",
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        "protein_names_refseq": "zinc finger and BTB domain-containing protein 17 isoform a; zinc finger and BTB domain-containing protein 17; zinc finger protein 100",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0032993 protein-DNA complex;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0008285 negative regulation of cell population proliferation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0002682 regulation of immune system process",
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        ],
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        "protein_name": "Protein PIGBOS1",
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        "refseq_name": "protein PIGBOS1",
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            {
                "id": "NP_001295361",
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        ],
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        "protein_names_uniprotkb": "Protein PIGBOS1; PIGB opposite strand protein 1 homolog",
        "protein_names_refseq": "PIGB opposite strand protein 1 homolog; protein PIGBOS1",
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        "go_cellular_component": "GO:0005741 mitochondrial outer membrane",
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        ],
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        "length": 548,
        "protein_name": "Intercellular adhesion molecule 1",
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            {
                "id": "NP_067705",
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        "gene_names_uniprotkb": "Tcam1; Tcam1p",
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        "disease": "dilated cardiomyopathy (Disease Ontology:DOID:12930)",
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        "function": "Cell adhesion molecule that functions as a receptor ligand of the signaling receptor ITGAL:ITGB2/LFA-1 (lymphocyte-function associated (LFA) molecule 1) ensuring leukocyte cell-cell adhesion, by providing a calibrated system to namely adjust T-cell killing to the antigen stimulation strength. Also functions as a ligand receptor of the signaling receptor ITGAM:ITGB2/MAC-1 ensuring adhesion between stimulated neutrophils and stimulated endothelial cells. During leukocyte trans-endothelial migration, ICAM1 engagement promotes the assembly of endothelial apical cups through ARHGEF26/SGEF and RHOG activation. Promotes cell aggregation in epithelial cells through interaction with MUC1., [UniProtKB, UniProtKB]",
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        "protein_name": "Olfactory receptor",
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        "refseq_name": "olfactory receptor Olr442",
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            {
                "id": "NP_001000284",
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        ],
        "gene_names_uniprotkb": "Or5ak25",
        "gene_names_refseq": "Olr442; Or5ak25; TB 567; ratchr3-68554730-68553783_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 442; olfactory receptor Olr442; olfactory receptor gene Olr442; taste bud receptor protein TB 567",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        ],
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        "length": 311,
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        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr416",
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            {
                "id": "NP_001000387",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001000387",
                "type": "external"
            }
        ],
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        "gene_names_refseq": "Olr416; Or1n1b; TB 334",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 416; olfactory receptor Olr416; olfactory receptor gene Olr416; taste bud receptor protein TB 334",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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                "id": "NP_997670",
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            }
        ],
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        "disease": "T-cell non-Hodgkin lymphoma (Disease Ontology:DOID:0081312)",
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        "publication_id_list": "27890615",
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        "function": "Analysis of consensus EGR-binding elements (EBEs) showed that the immediate early response 3 gene (IER3) is a novel transcriptional target gene of EGR2 as confirmed by the luciferase assay, electrophoretic mobility-shift assay (EMSA), chromatin immunoprecipitation (ChIP), and western blot analysis., [RefSeq, PubMed]",
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                "id": "FCG3A_RAT",
                "url": "https://www.uniprot.org/uniprot/Q6XPU4",
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        ],
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        "protein_name": "Low affinity immunoglobulin gamma Fc region receptor III-A",
        "gene_name": "Fcgr3a",
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        "refseq_name": "low affinity immunoglobulin gamma Fc region receptor III-A precursor",
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            {
                "id": "NP_997486",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_997486",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Fcgr3a; Fcgr4",
        "gene_names_refseq": "CD16-2; Fcgr3a; Fcgr4",
        "protein_names_uniprotkb": "Low affinity immunoglobulin gamma Fc region receptor III-A; CD16-2; FcgammaRIV; IgG Fc receptor III-A",
        "protein_names_refseq": "Fc fragment of IgG intermediate affinity IV receptor; Fc fragment of IgG receptor IIIa; Fc fragment of IgG, low affinity IIIa, receptor for (CD16); Fc gamma receptor IIIa; IgG Fc receptor III-A; fcgammaRIV; low affinity immunoglobulin gamma Fc region receptor III-A precursor; low affinity immunoglobulin gamma Fc region receptor III-A; transmembrane receptor FcgammaRIII-X",
        "tax_id": 10116,
        "disease": "myelodysplastic syndrome (Disease Ontology:DOID:0050908); lymphoplasmacytic lymphoma (Disease Ontology:DOID:0060901); lupus nephritis (Disease Ontology:DOID:0080162); graft-versus-host disease (Disease Ontology:DOID:0081267); immunodeficiency 20 (Disease Ontology:DOID:0111941); allergic disease (Disease Ontology:DOID:1205); Behcet's disease (Disease Ontology:DOID:13241); temporal arteritis (Disease Ontology:DOID:13375); polyneuropathy (Disease Ontology:DOID:1389); thrombocytopenia due to platelet alloimmunization (Disease Ontology:DOID:1587); epilepsy (Disease Ontology:DOID:1826); multiple sclerosis (Disease Ontology:DOID:2377); asthma (Disease Ontology:DOID:2841); IgA glomerulonephritis (Disease Ontology:DOID:2986); coronary artery disease (Disease Ontology:DOID:3393); allergic rhinitis (Disease Ontology:DOID:4481); anti-basement membrane glomerulonephritis (Disease Ontology:DOID:4780); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); pneumonia (Disease Ontology:DOID:552); lymphopenia (Disease Ontology:DOID:614); myositis (Disease Ontology:DOID:633); ankylosing spondylitis (Disease Ontology:DOID:7147); rheumatoid arthritis (Disease Ontology:DOID:7148); arthritis (Disease Ontology:DOID:848); Crohn's disease (Disease Ontology:DOID:8778); autoimmune thrombocytopenic purpura (Disease Ontology:DOID:8924); systemic lupus erythematosus (Disease Ontology:DOID:9074)",
        "pathway": " (rno:304966);  (R-RNO-163125);  (R-RNO-6798695)",
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        "function": "Receptor for the invariable Fc fragment of immunoglobulin gamma (IgG). Binds with intermediate affinity to both IgG2a and IgG2b. Can bind to IgG2a and IgG2b monomers. Does not display binding to IgG1 or IgG3 (By similarity). Recognizes neutralizing virus-specific IgGs displayed on the cell surface of infected cells and triggers antibody-dependent cellular cytotoxicity (ADCC). Confers protection to lethal influenza virus infection (By similarity). On splenic dendritic cells, uptakes antigen immune complexes and efficiently divert them into MHC class I and II antigen presentation pathways to provide for superior priming of CD4-positive and CD8-positive T cell immune responses (By similarity). Mediates neutrophil activation by IgG complexes redundantly with FCGR2A (By similarity). Plays a role in promoting bone resorption by enhancing osteoclast differentiation following binding to IgG2a (By similarity). Also acts as a receptor for the Fc region of immunoglobulin epsilon (IgE). Binds with low affinity to both the a and b allotypes of IgE. Has also been shown to bind to IgE allotype a only but not to allotype b. Binds aggregated IgE but not the monomeric form and bound monomeric IgG is readily displaced by IgE complexes. Binding to IgE promotes macrophage-mediated phagocytosis, antigen presentation to T cells, production of pro-inflammatory cytokines and the late phase of cutaneous allergic reactions (By similarity). Mediates enhanced ADCC in response to afucosylated IgGs (PubMed:34485821)., [UniProtKB, PubMed, UniProtKB]",
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        "secondary_ac_list": "A0A0B4J2J1",
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        "go_molecular_function": "GO:0019767 IgE receptor activity;GO:0019863 IgE binding;GO:0019864 IgG binding;GO:0019770 IgG receptor activity;GO:0019772 low-affinity IgG receptor activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0009897 external side of plasma membrane;GO:0033001 Fc-gamma receptor III complex",
        "go_biological_process": "GO:0038094 Fc-gamma receptor signaling pathway;GO:0002468 dendritic cell antigen processing and presentation;GO:0007166 cell surface receptor signaling pathway;GO:0019722 calcium-mediated signaling;GO:0045780 positive regulation of bone resorption",
        "synthesized_glycan_count": 0,
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        "record_id": "Q6XPU4-1",
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    },
    {
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        ],
        "mass": 106033.0,
        "length": 986,
        "protein_name": "DNA damage inducible 1 homolog 2",
        "gene_name": "Ddi2",
        "organism": "Rat",
        "refseq_name": "protein DDI1 homolog 2 isoform X1",
        "refseq_ac": [
            {
                "id": "XP_006239367",
                "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006239367",
                "type": "external"
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        ],
        "gene_names_uniprotkb": "Ddi2",
        "gene_names_refseq": "Ddi2; RGD1311815",
        "protein_names_uniprotkb": "DNA damage inducible 1 homolog 2",
        "protein_names_refseq": "protein DDI1 homolog 2 isoform X1",
        "tax_id": 10116,
        "disease": "obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:313668)",
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0043130 ubiquitin binding;GO:0004190 aspartic-type endopeptidase activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0015031 protein transport;GO:0016485 protein processing;GO:0031647 regulation of protein stability;GO:0010498 proteasomal protein catabolic process;GO:0097752 regulation of DNA stability",
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    {
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        ],
        "mass": 35874.0,
        "length": 327,
        "protein_name": "Potassium channel tetramerization domain containing 12",
        "gene_name": "Kctd12",
        "organism": "Rat",
        "refseq_name": "BTB/POZ domain-containing protein KCTD12",
        "refseq_ac": [
            {
                "id": "NP_001386444",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001386444",
                "type": "external"
            }
        ],
        "gene_names_uniprotkb": "Kctd12",
        "gene_names_refseq": "Kctd12",
        "protein_names_uniprotkb": "Potassium channel tetramerization domain containing 12",
        "protein_names_refseq": "BTB/POZ domain-containing protein KCTD12; potassium channel tetramerisation domain containing 12",
        "tax_id": 10116,
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        "pathway_count": 0,
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        "publication_id_list": "27073217",
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        "function": "Auxiliary subunit of GABA-B receptors that determine the pharmacology and kinetics of the receptor response. Increases agonist potency and markedly alter the G-protein signaling of the receptors by accelerating onset and promoting desensitization., [UniProtKB, UniProtKB]; Study highlights that GABABRs differentially control cholecystokinin-expressing interneuron subtypes, and the kinetics and desensitization of GABABR-mediated currents are modulated by KCTD12 proteins, [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity;GO:0042802 identical protein binding;GO:0099579 G protein-coupled neurotransmitter receptor activity involved in regulation of postsynaptic membrane potential;GO:0150047 G protein-coupled neurotransmitter receptor activity involved in regulation of presynaptic membrane potential",
        "go_cellular_component": "GO:0098982 GABA-ergic synapse;GO:0048787 presynaptic active zone membrane;GO:0043235 receptor complex;GO:0045211 postsynaptic membrane;GO:0042734 presynaptic membrane",
        "go_biological_process": "GO:0051260 protein homooligomerization;GO:0008277 regulation of G protein-coupled receptor signaling pathway",
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        ],
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        "protein_name": "Glycolipid transfer protein domain containing 2",
        "gene_name": "Gltpd2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": [],
        "gene_names_uniprotkb": "Gltpd2",
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        "refseq_name": "serine/arginine-rich splicing factor 3",
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            {
                "id": "NP_001041372",
                "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001041372",
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            }
        ],
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        "gene_names_refseq": "Sfrs3; Srsf3",
        "protein_names_uniprotkb": "Serine/arginine-rich splicing factor 3; Pre-mRNA-splicing factor SRP20; Splicing factor, arginine/serine-rich 3",
        "protein_names_refseq": "serine/arginine-rich splicing factor 3; splicing factor, arginine/serine-rich 3 (SRp20)",
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        "disease": "ovary epithelial cancer (Disease Ontology:DOID:2152); bipolar disorder (Disease Ontology:DOID:3312)",
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        ],
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        "protein_name": "F-BAR and double SH3 domains protein 2",
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            {
                "id": "NP_001382671",
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        "function": "Adapter protein that plays a role in endocytosis via clathrin-coated pits. Contributes to the internalization of cell surface receptors, such as integrin ITGB1 and transferrin receptor. Promotes endocytosis of EGFR in cancer cells, and thereby contributes to the down-regulation of EGFR signaling. Recruited to clathrin-coated pits during a mid-to-late stage of assembly, where it is required for normal progress from U-shaped intermediate stage pits to terminal, omega-shaped pits. Binds to membranes enriched in phosphatidylinositol 3,4-bisphosphate or phosphatidylinositol 3,4,5-trisphosphate. When bound to membranes, promotes actin polymerization via its interaction with WAS and/or WASL which leads to the activation of the Arp2/3 complex. Does not promote actin polymerisation in the absence of membranes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        ],
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        "protein_name": "DEP domain-containing mTOR-interacting protein",
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            {
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        "function": "Low DEPTOR expression is associated with glomerular mesangial cell hypertrophy., [RefSeq, PubMed]; Mechanistically, DEPTOR inhibited both mTOR Complex 1 (mTORC1) and 2 (mTORC2) activities in PA cells. In addition, DEPTOR expression level was increased to suppress mTOR kinase activity via decreasing E3 ubiquitin ligase, betaTrCP1, in response to CAB., [RefSeq, PubMed]; Negative regulator of the mTORC1 and mTORC2 complexes: inhibits the protein kinase activity of MTOR, thereby inactivating both complexes. DEPTOR inhibits mTORC1 and mTORC2 to induce autophagy. In contrast to AKT1S1/PRAS40, only partially inhibits mTORC1 activity., [UniProtKB, UniProtKB]; Results illustrate the presence of DEPTOR in the rat brain and suggest a role for DEPTOR in the hypothalamic regulation of energy balance, which further supports the role of mTOR in energy homeostasis, [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005765 lysosomal membrane",
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        ],
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        "protein_name": "Eukaryotic translation initiation factor 3 subunit K",
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            {
                "id": "NP_001385632",
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        ],
        "gene_names_uniprotkb": "Eif3k; EIF3K; EIF3S12",
        "gene_names_refseq": "Eif3k; Eif3s12; PLAC-24",
        "protein_names_uniprotkb": "Eukaryotic translation initiation factor 3 subunit K; Eukaryotic translation initiation factor 3 subunit 12; eIF-3 p25; eIF3k",
        "protein_names_refseq": "eukaryotic translation initiation factor 3 subunit K; eukaryotic translation initiation factor 3, subunit 12",
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        "disease": "",
        "pathway": " (rno:292762);  (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, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Identification of a novel 24-kDa protein (Plac-24) that binds directly to dynein intermediate chain., [RefSeq, PubMed]; These observations suggest that PLAC-24 may play a role in the transport and the stabilisation of newly synthesised 5-HT(7) receptor towards the plasma membrane., [RefSeq, PubMed]",
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        "go_biological_process": "GO:0006446 regulation of translational initiation;GO:0001732 formation of cytoplasmic translation initiation complex;GO:0006413 translational initiation",
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        ],
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        "protein_name": "MDS1 and EVI1 complex locus",
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        "pathway": " (R-RNO-3214841);  (R-RNO-8943724)",
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            },
            {
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            {
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                "url": "https://www.rhea-db.org/rhea/?query=ec:2.3.2.27",
                "type": "external"
            }
        ],
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        "go_cellular_component": "GO:0005634 nucleus;GO:0016607 nuclear speck;GO:0000118 histone deacetylase complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0045892 negative regulation of DNA-templated transcription;GO:0098727 maintenance of cell number;GO:0001701 in utero embryonic development;GO:0006954 inflammatory response",
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        ],
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        "length": 835,
        "protein_name": "BCL11 transcription factor A",
        "gene_name": "Bcl11a",
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        ],
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        ],
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            {
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        ],
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        "protein_names_refseq": "jumonji C domain containing histone demethylase 1; lysine (K)-specific demethylase 7A; lysine demethylase 7A; lysine-specific demethylase 7A",
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