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        "protein_names_uniprotkb": "Ig-like domain-containing protein",
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        "length": 343,
        "protein_name": "Lymphatic vessel endothelial hyaluronic acid receptor 1",
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        "refseq_name": "lymphatic vessel endothelial hyaluronic acid receptor 1",
        "refseq_ac": "NP_001099756",
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        "protein_names_uniprotkb": "Lymphatic vessel endothelial hyaluronic acid receptor 1; Cell surface retention sequence-binding protein 1; Extracellular link domain-containing protein 1",
        "protein_names_refseq": "extra cellular link domain-containing 1; extracellular link domain-containing 1; lymphatic vessel endothelial hyaluronic acid receptor 1",
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        "function": "Different levels of protein for LYVE-1-positive cells may reflect alterations in the functional properties of the blood supply., [RefSeq, PubMed]; Expression of Lyve1 followed the same temporal pattern as hyaluronic acid deposition in a bladder regeneration model., [RefSeq, PubMed]; Immunostaining for the specific lymphatic markers LYVE-1 revealed an extensive lymphatic vessel system in dental tissues. Unexpected cell staining for the above lymphatic markers was found in the pulp of both molars and incisors in rats., [RefSeq, PubMed]; Ligand-specific transporter trafficking between intracellular organelles (TGN) and the plasma membrane. Plays a role in autocrine regulation of cell growth mediated by growth regulators containing cell surface retention sequence binding (CRS). May act as a hyaluronan (HA) transporter, either mediating its uptake for catabolism within lymphatic endothelial cells themselves, or its transport into the lumen of afferent lymphatic vessels for subsequent re-uptake and degradation in lymph nodes. Binds to pericelluar hyaluronan matrices deposited on the surface of leukocytes and facilitates cell adhesion and migration through lymphatic endothelium., [UniProtKB, UniProtKB, UniProtKB]; Upregulation of hyaluronan and its binding receptors CD44 and LYVE-1 are involved in interstitial fibrosis in chronic cyclosporine-induced renal injury., [RefSeq, PubMed]",
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        "refseq_name": "olfactory receptor Olr1485",
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        "gene_names_refseq": "Olr1485; Or1e23",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1485; olfactory receptor Olr1485; olfactory receptor gene Olr1485",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "protein_name": "Olfactory receptor",
        "gene_name": "Or2m13",
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        "refseq_name": "similar to olfactory receptor 1394",
        "refseq_ac": "NP_001396100",
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        "protein_names_refseq": "olfactory receptor 2M3; olfactory receptor 2M5; similar to olfactory receptor 1394",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "record_id": "A0ABK0LFF7-1",
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    {
        "uniprot_canonical_ac": "A0ABK0LFH1-1",
        "uniprot_id": "A0ABK0LFH1_RAT",
        "mass": 34757.0,
        "length": 305,
        "protein_name": "Vomeronasal type-1 receptor",
        "gene_name": "Vom1r27",
        "organism": "Rat",
        "refseq_name": "vomeronasal 1 receptor 27",
        "refseq_ac": "NP_001008952",
        "gene_names_uniprotkb": "Vom1r27",
        "gene_names_refseq": "V1re19; Vom1r27",
        "protein_names_uniprotkb": "Vomeronasal type-1 receptor",
        "protein_names_refseq": "vomernasal 1 receptor Vom1r27; vomeronasal 1 receptor 27; vomeronasal 1 receptor, E19; vomeronasal V1r-type receptor V1re19; vomeronasal type-1 receptor 4",
        "tax_id": 10116,
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        "pathway": " (rno:494297)",
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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_names_uniprotkb": "Disks large homolog 5 N-terminal domain-containing protein",
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        "uniprot_canonical_ac": "A0ABK0LFI7-1",
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        "length": 249,
        "protein_name": "Spindlin family, member 4",
        "gene_name": "Spin4",
        "organism": "Rat",
        "refseq_name": "spindlin-4",
        "refseq_ac": "NP_001388046",
        "gene_names_uniprotkb": "Spin4",
        "gene_names_refseq": "AABR07038930.1; RGD1564004; Spin4",
        "protein_names_uniprotkb": "Spindlin family, member 4",
        "protein_names_refseq": "spindlin-4",
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        "reported_phosphosites": 0,
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        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0000781 chromosome, telomeric region;GO:0030915 Smc5-Smc6 complex",
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        "record_id": "A0ABK0LFN0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFN2-1",
        "uniprot_id": "A0ABK0LFN2_RAT",
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        "length": 61,
        "protein_name": "Keratin associated protein 8-1",
        "gene_name": "Krtap8-1",
        "organism": "Rat",
        "refseq_name": "keratin associated protein 8-1",
        "refseq_ac": "NP_001385928",
        "gene_names_uniprotkb": "Krtap8-1",
        "gene_names_refseq": "Krtap8-1",
        "protein_names_uniprotkb": "Keratin associated protein 8-1",
        "protein_names_refseq": "keratin associated protein 8-1",
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        "biomarker_type": "",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005882 intermediate filament",
        "go_biological_process": "",
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        "record_id": "A0ABK0LFN2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFP2-1",
        "uniprot_id": "A0ABK0LFP2_RAT",
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        "length": 225,
        "protein_name": "Esterase OVCA2",
        "gene_name": "Ovca2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ovca2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Esterase OVCA2; 3.1.1.1; OVCA2 serine hydrolase domain-containing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Miller-Dieker lissencephaly syndrome (Disease Ontology:DOID:0060469); diphthamide deficiency syndrome (Disease Ontology:DOID:0070476); diphthamide deficiency syndrome 1 (Disease Ontology:DOID:0070477); ovarian cancer (Disease Ontology:DOID:2394)",
        "pathway": "",
        "pathway_count": 0,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Exhibits ester hydrolase activity with a strong preference for long-chain alkyl ester substrates and high selectivity against a variety of short, branched, and substituted esters. Is able to hydrolyze ester bonds within a wide range of p-nitrophenyl derivatives (C2-C14) in vitro, with a strong preference toward substrates of >8 carbons., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "ec_number_list": "3.1.1.1;3.1.1.-;3.1.1.67",
        "go_molecular_function": "GO:0106435 carboxylesterase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0032526 response to retinoic acid",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "A0ABK0LFP6-1",
        "uniprot_id": "A0ABK0LFP6_RAT",
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        "length": 211,
        "protein_name": "Paraneoplastic antigen Ma-like N-terminal domain-containing protein",
        "gene_name": "Pnma8c",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Pnma8c",
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        "protein_names_uniprotkb": "Paraneoplastic antigen Ma-like N-terminal domain-containing protein",
        "protein_names_refseq": "",
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        "record_type": "protein"
    },
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        "length": 59,
        "protein_name": "Immunoglobulin V-set domain-containing protein",
        "gene_name": "",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Immunoglobulin V-set domain-containing protein",
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        "go_biological_process": "GO:0002250 adaptive immune response",
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        "record_id": "A0ABK0LFR4-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "A0ABK0LG90-1",
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        "length": 569,
        "protein_name": "Golgi associated kinase 1A",
        "gene_name": "Gask1a",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Gask1a; Fam198a",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Golgi associated kinase 1A",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:316090)",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005576 extracellular region;GO:0005783 endoplasmic reticulum",
        "go_biological_process": "",
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        "record_id": "A0ABK0LG90-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFY7-1",
        "uniprot_id": "A0ABK0LFY7_RAT",
        "mass": 80515.0,
        "length": 718,
        "protein_name": "tRNA (carboxymethyluridine(34)-5-O)-methyltransferase ALKBH8",
        "gene_name": "Alkbh8",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Alkbh8",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "tRNA (carboxymethyluridine(34)-5-O)-methyltransferase ALKBH8; 2.1.1.229; Alkylated DNA repair protein alkB homolog 8; Alpha-ketoglutarate-dependent dioxygenase ALKBH8; S-adenosyl-L-methionine-dependent tRNA methyltransferase ALKBH8",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autosomal recessive intellectual developmental disorder 71 (Disease Ontology:DOID:0081232)",
        "pathway": " (rno:366783)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the methylation of 5-carboxymethyl uridine to 5-methylcarboxymethyl uridine at the wobble position of the anticodon loop in tRNA via its methyltransferase domain. Catalyzes the last step in the formation of 5-methylcarboxymethyl uridine at the wobble position of the anticodon loop in target tRNA. Has a preference for tRNA(Arg) and tRNA(Glu), and does not bind tRNA(Lys). Binds tRNA and catalyzes the iron and alpha-ketoglutarate dependent hydroxylation of 5-methylcarboxymethyl uridine at the wobble position of the anticodon loop in tRNA via its dioxygenase domain, giving rise to 5-(S)-methoxycarbonylhydroxymethyluridine; has a preference for tRNA(Gly). Required for normal survival after DNA damage. May inhibit apoptosis and promote cell survival and angiogenesis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "2.1.1.229",
        "go_molecular_function": "GO:0000049 tRNA binding;GO:0016706 2-oxoglutarate-dependent dioxygenase activity;GO:0106335 tRNA (5-carboxymethyluridine(34)-5-O)-methyltransferase activity;GO:0005506 iron ion binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0043527 tRNA methyltransferase complex",
        "go_biological_process": "GO:0002098 tRNA wobble uridine modification;GO:0030488 tRNA methylation;GO:0006974 DNA damage response;GO:0006400 tRNA modification;GO:0032259 methylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LFY7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LGW0-1",
        "uniprot_id": "A0ABK0LGW0_RAT",
        "mass": 264614.0,
        "length": 2423,
        "protein_name": "histone acetyltransferase",
        "gene_name": "Ep300",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ep300",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "histone acetyltransferase; 2.3.1.48",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "idiopathic pulmonary fibrosis (Disease Ontology:DOID:0050156); cardiomyopathy (Disease Ontology:DOID:0050700); cardiac arrest (Disease Ontology:DOID:0060319); prostate cancer (Disease Ontology:DOID:10283); Alzheimer's disease (Disease Ontology:DOID:10652); hypertension (Disease Ontology:DOID:10763); heart disease (Disease Ontology:DOID:114); alcohol use disorder (Disease Ontology:DOID:1574); Rubinstein-Taybi syndrome (Disease Ontology:DOID:1933); transient cerebral ischemia (Disease Ontology:DOID:224); membranoproliferative glomerulonephritis (Disease Ontology:DOID:2920); glomerulonephritis (Disease Ontology:DOID:2921); breast carcinoma (Disease Ontology:DOID:3459); congenital diaphragmatic hernia (Disease Ontology:DOID:3827); clear cell renal cell carcinoma (Disease Ontology:DOID:4467); congestive heart failure (Disease Ontology:DOID:6000); hepatocellular carcinoma (Disease Ontology:DOID:684); diabetic retinopathy (Disease Ontology:DOID:8947); systemic lupus erythematosus (Disease Ontology:DOID:9074); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (R-RNO-1234158);  (R-RNO-201722);  (R-RNO-3134973);  (R-RNO-3371568);  (R-RNO-3899300);  (R-RNO-5250924);  (R-RNO-5621575);  (R-RNO-5689901);  (R-RNO-6804758);  (R-RNO-6804760);  (R-RNO-6811555);  (R-RNO-8866907);  (R-RNO-8936459);  (R-RNO-8939243);  (R-RNO-8941856);  (R-RNO-8941858);  (R-RNO-8951936);  (R-RNO-9018519);  (R-RNO-9029569);  (R-RNO-933541);  (R-RNO-9617629);  (R-RNO-9701898);  (R-RNO-9759194);  (R-RNO-9841922);  (R-RNO-9856649)",
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        "disease": "visceral heterotaxy (Disease Ontology:DOID:0050545); visceral heterotaxy 1 (Disease Ontology:DOID:0051016); right atrial isomerism (Disease Ontology:DOID:0060856); spina bifida (Disease Ontology:DOID:0080016); X-linked VACTERL association (Disease Ontology:DOID:0111766); Goldenhar syndrome (Disease Ontology:DOID:2907); holoprosencephaly (Disease Ontology:DOID:4621); visceral heterotaxy 5 (Disease Ontology:DOID:758)",
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        "go_molecular_function": "GO:0008013 beta-catenin binding;GO:0003712 transcription coregulator activity;GO:0003713 transcription coactivator activity",
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    },
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        "uniprot_canonical_ac": "A0ABK0LH08-1",
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        "length": 1134,
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        "gene_names_uniprotkb": "Cep126; RGD1563556",
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        "protein_names_uniprotkb": "Centrosomal protein 126",
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    },
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        "protein_names_uniprotkb": "Zinc finger protein 516",
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        "function": "Transcriptional regulator that binds to the promoter and activates the transcription of genes promoting brown adipose tissue (BAT) differentiation. Among brown adipose tissue-specific genes, binds the proximal region of the promoter of the UCP1 gene to activate its transcription and thereby regulate thermogenesis. May also play a role in the cellular response to replication stress., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005634 nucleus",
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        "record_type": "protein"
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        "function": "Component of clathrin-coated vesicles. Component of the aftiphilin/p200/gamma-synergin complex, which plays roles in AP1G1/AP-1-mediated protein trafficking including the trafficking of transferrin from early to recycling endosomes, and the membrane trafficking of furin and the lysosomal enzyme cathepsin D between the trans-Golgi network (TGN) and endosomes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_refseq": "E3 ubiquitin-protein ligase Arkadia isoform X6",
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        "disease": "primary ovarian insufficiency (Disease Ontology:DOID:5426)",
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        "protein_name": "Fibrous sheath-interacting protein 2",
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        "protein_names_uniprotkb": "Fibrous sheath-interacting protein 2",
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        "disease": "spermatogenic failure 34 (Disease Ontology:DOID:0111911)",
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        "go_cellular_component": "GO:0097229 sperm end piece;GO:0097228 sperm principal piece;GO:0097225 sperm midpiece;GO:0120212 sperm head-tail coupling apparatus",
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        "record_type": "protein"
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    {
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        "length": 702,
        "protein_name": "1,4-alpha-glucan-branching enzyme",
        "gene_name": "Gbe1",
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        "refseq_name": "1,4-alpha-glucan-branching enzyme",
        "refseq_ac": "NP_001093972",
        "gene_names_uniprotkb": "Gbe1",
        "gene_names_refseq": "Gbe1",
        "protein_names_uniprotkb": "1,4-alpha-glucan-branching enzyme; 2.4.1.18; Brancher enzyme; Glycogen-branching enzyme",
        "protein_names_refseq": "1,4-alpha-glucan-branching enzyme; glucan (1,4-alpha-), branching enzyme 1",
        "tax_id": 10116,
        "disease": "porphyria (Disease Ontology:DOID:13268); glycogen storage disease IV (Disease Ontology:DOID:2750); pulmonary tuberculosis (Disease Ontology:DOID:2957)",
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        "function": "Glycogen-branching enzyme participates in the glycogen biosynthetic process along with glycogenin and glycogen synthase. Generates alpha-1,6-glucosidic branches from alpha-1,4-linked glucose chains, to increase solubility of the glycogen polymer., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "2.4.1.18;2.4.1.11;2.4.1.186",
        "go_molecular_function": "GO:0004553 hydrolase activity, hydrolyzing O-glycosyl compounds;GO:0003844 1,4-alpha-glucan branching enzyme activity;GO:0043169 cation binding;GO:0030246 carbohydrate binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0005978 glycogen biosynthetic process;GO:0043524 negative regulation of neuron apoptotic process",
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        "record_id": "A0ABK0LHH2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LIB6-1",
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        "length": 1709,
        "protein_name": "Arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 2",
        "gene_name": "Arap2",
        "organism": "Rat",
        "refseq_name": "arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 2 isoform X1",
        "refseq_ac": "XP_038947855",
        "gene_names_uniprotkb": "Arap2",
        "gene_names_refseq": "Arap2; Centd1",
        "protein_names_uniprotkb": "Arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 2; Centaurin-delta-1",
        "protein_names_refseq": "arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 2 isoform X1",
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        "pathway": " (rno:305367);  (R-RNO-8980692);  (R-RNO-9013148);  (R-RNO-9013149);  (R-RNO-9013423)",
        "pathway_count": 5,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Phosphatidylinositol 3,4,5-trisphosphate-dependent GTPase-activating protein that modulates actin cytoskeleton remodeling by regulating ARF and RHO family members. Is activated by phosphatidylinositol 3,4,5-trisphosphate (PtdIns(3,4,5)P3) binding. Can be activated by phosphatidylinositol 3,4-bisphosphate (PtdIns(3,4,5)P2) binding, albeit with lower efficiency., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0005547 phosphatidylinositol-3,4,5-trisphosphate binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0007165 signal transduction;GO:0032956 regulation of actin cytoskeleton organization",
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        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "A0ABK0LHN4-1",
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        "length": 718,
        "protein_name": "Coiled-coil domain containing 170",
        "gene_name": "Ccdc170",
        "organism": "Rat",
        "refseq_name": "coiled-coil domain containing 170 isoform 1",
        "refseq_ac": "NP_001418950",
        "gene_names_uniprotkb": "Ccdc170",
        "gene_names_refseq": "Ccdc170; RGD1310945",
        "protein_names_uniprotkb": "Coiled-coil domain containing 170",
        "protein_names_refseq": "coiled-coil domain containing 170 isoform 1; coiled-coil domain-containing protein 170",
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        "pathway": " (rno:292266)",
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        "go_molecular_function": "GO:0008017 microtubule binding",
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        "record_type": "protein"
    },
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        "length": 280,
        "protein_name": "Lin-28 homolog B",
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        "refseq_name": "protein lin-28 homolog B isoform X1",
        "refseq_ac": "XP_038955078",
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        "gene_names_refseq": "Lin28b",
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        "protein_names_refseq": "protein lin-28 homolog B isoform X1",
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        "go_molecular_function": "GO:0003729 mRNA binding;GO:0008270 zinc ion binding;GO:0003723 RNA binding;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005654 nucleoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0060964 regulation of miRNA-mediated gene silencing;GO:0010608 post-transcriptional regulation of gene expression;GO:0031054 pre-miRNA processing;GO:0010587 miRNA catabolic process;GO:0050779 RNA destabilization",
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        "record_type": "protein"
    },
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        "gene_name": "Chaf1a",
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        "gene_names_uniprotkb": "Chaf1a",
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        "protein_names_uniprotkb": "Chromatin assembly factor 1 subunit A",
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        "tax_id": 10116,
        "disease": "colon cancer (Disease Ontology:DOID:219); high grade glioma (Disease Ontology:DOID:3070); neuroblastoma (Disease Ontology:DOID:769); systemic lupus erythematosus (Disease Ontology:DOID:9074)",
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0070087 chromo shadow domain binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0033186 CAF-1 complex;GO:0005654 nucleoplasm;GO:0000785 chromatin;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0006281 DNA repair;GO:0006260 DNA replication;GO:0006334 nucleosome assembly;GO:0006335 DNA replication-dependent chromatin assembly",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LHP5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LGP3-1",
        "uniprot_id": "A0ABK0LGP3_RAT",
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        "length": 798,
        "protein_name": "Endoglin",
        "gene_name": "Eng",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Eng",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Endoglin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "renal fibrosis (Disease Ontology:DOID:0050855); arteriovenous malformations of the brain (Disease Ontology:DOID:0060688); prostate cancer (Disease Ontology:DOID:10283); lymphoid leukemia (Disease Ontology:DOID:1037); pre-eclampsia (Disease Ontology:DOID:10591); hypertension (Disease Ontology:DOID:10763); intracranial aneurysm (Disease Ontology:DOID:10941); arteriovenous malformation (Disease Ontology:DOID:11294); secondary hyperparathyroidism (Disease Ontology:DOID:12466); hereditary hemorrhagic telangiectasia (Disease Ontology:DOID:1270); cholestasis (Disease Ontology:DOID:13580); breast cancer (Disease Ontology:DOID:1612); coronary artery disease (Disease Ontology:DOID:3393); clear cell renal cell carcinoma (Disease Ontology:DOID:4467); congestive heart failure (Disease Ontology:DOID:6000); hepatocellular carcinoma (Disease Ontology:DOID:684); diabetic retinopathy (Disease Ontology:DOID:8947); multiple myeloma (Disease Ontology:DOID:9538); acute lymphoblastic leukemia (Disease Ontology:DOID:9952)",
        "pathway": " (rno:497010)",
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        "go_molecular_function": "GO:0050431 transforming growth factor beta binding;GO:0015026 coreceptor activity;GO:0030546 signaling receptor activator activity;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005615 extracellular space;GO:0009986 cell surface;GO:0043235 receptor complex;GO:0009897 external side of plasma membrane",
        "go_biological_process": "GO:0007179 transforming growth factor beta receptor signaling pathway;GO:0090092 regulation of transmembrane receptor protein serine/threonine kinase signaling pathway;GO:0001570 vasculogenesis;GO:0017015 regulation of transforming growth factor beta receptor signaling pathway;GO:0071559 response to transforming growth factor beta",
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        "record_id": "A0ABK0LGP3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LGA2-1",
        "uniprot_id": "A0ABK0LGA2_RAT",
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        "length": 509,
        "protein_name": "Hyaluronan and proteoglycan link protein 4",
        "gene_name": "Hapln4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Hapln4; LOC100911378",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Hyaluronan and proteoglycan link protein 4; Brain link protein 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:361129)",
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        "class_list": "",
        "function": "Essential for the proper localization of brevican (BCAN), mainly as a perineuronal nets (PNNs)-type deposition in the brainstem and cerebellum thereby playing a key role in the formation and structural organization of PNNs. Contributes to the formation and transmission of inhibitory GABAergic synapses between Purkinje cells and deep cerebellar nuclei neurons., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005540 hyaluronic acid binding;GO:0150043 structural constituent of synapse-associated extracellular matrix",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0045202 synapse;GO:0072534 perineuronal net;GO:0005576 extracellular region",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0007417 central nervous system development;GO:0001501 skeletal system development;GO:0051932 synaptic transmission, GABAergic;GO:1904862 inhibitory synapse assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LGA2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFY1-1",
        "uniprot_id": "A0ABK0LFY1_RAT",
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        "length": 502,
        "protein_name": "Periodic tryptophan protein 1 homolog",
        "gene_name": "Pwp1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pwp1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Periodic tryptophan protein 1 homolog",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362856)",
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Chromatin-associated factor that regulates transcription. Regulates Pol I-mediated rRNA biogenesis and, probably, Pol III-mediated transcription. Regulates the epigenetic status of rDNA., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:1990889 histone H4K20me3 reader activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005730 nucleolus;GO:0005694 chromosome",
        "go_biological_process": "GO:0006364 rRNA processing;GO:1901838 positive regulation of transcription of nucleolar large rRNA by RNA polymerase I;GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0045892 negative regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LFY1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LG51-1",
        "uniprot_id": "A0ABK0LG51_RAT",
        "mass": 398506.0,
        "length": 3619,
        "protein_name": "Zinc finger homeobox protein 4",
        "gene_name": "Zfhx4",
        "organism": "Rat",
        "refseq_name": "zinc finger homeobox protein 4 isoform 1",
        "refseq_ac": "XP_006232224",
        "gene_names_uniprotkb": "Zfhx4",
        "gene_names_refseq": "RGD1563022; Zfhx4",
        "protein_names_uniprotkb": "Zinc finger homeobox protein 4; Zinc finger homeodomain protein 4",
        "protein_names_refseq": "zinc finger homeobox protein 4 isoform 1; zinc finger homeobox protein 4; zinc finger homeodomain 4",
        "tax_id": 10116,
        "disease": "spinocerebellar ataxia 4 (Disease Ontology:DOID:0050957); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:310250)",
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        "protein_names_uniprotkb": "Basic leucine zipper transcriptional factor ATF-like 2",
        "protein_names_refseq": "basic leucine zipper transcriptional factor ATF-like 2 isoform X1",
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        "protein_name": "Prostate stem cell antigen",
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        "function": "Hypomethylation of PSCA could mediate the effect of di(2-ethylhexyl) phthalate on prostate carcinogenesis in rats., [RefSeq, PubMed]",
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        "record_type": "protein"
    },
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        "protein_name": "Lysophosphatidylglycerol acyltransferase 1",
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        "go_biological_process": "GO:0036152 phosphatidylethanolamine acyl-chain remodeling;GO:0045723 positive regulation of fatty acid biosynthetic process;GO:0019432 triglyceride biosynthetic process;GO:0008654 phospholipid biosynthetic process;GO:0036149 phosphatidylinositol acyl-chain remodeling",
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        "gene_names_uniprotkb": "Sgca",
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        "protein_names_uniprotkb": "Sarcoglycan, alpha",
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    },
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        "protein_name": "Similar to human chromosome 1 open reading frame 216",
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        "protein_names_uniprotkb": "Jade family PHD finger 2",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0140566 histone reader activity;GO:0043997 histone H4K12 acetyltransferase activity;GO:0061630 ubiquitin protein ligase activity;GO:0043995 histone H4K5 acetyltransferase activity",
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        "protein_name": "HEAT repeat-containing protein 5B",
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        "protein_names_refseq": "HEAT repeat-containing protein 5A isoform X2",
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        "function": "Component of clathrin-coated vesicles. Component of the aftiphilin/p200/gamma-synergin complex, which plays roles in AP1G1/AP-1-mediated protein trafficking including the trafficking of transferrin from early to recycling endosomes, and the membrane trafficking of furin and the lysosomal enzyme cathepsin D between the trans-Golgi network (TGN) and endosomes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005829 cytosol;GO:0030136 clathrin-coated vesicle;GO:0030139 endocytic vesicle",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LG84-1",
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        "length": 189,
        "protein_name": "CST complex subunit TEN1",
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        "refseq_name": "CST complex subunit TEN1",
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        "protein_names_uniprotkb": "CST complex subunit TEN1; Protein telomeric pathways with STN1 homolog; Telomere length regulation protein TEN1 homolog",
        "protein_names_refseq": "CST complex subunit TEN1; TEN1 CST complex subunit; TEN1 telomerase capping complex subunit",
        "tax_id": 10116,
        "disease": "dyskeratosis congenita (Disease Ontology:DOID:2729)",
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        "go_cellular_component": "GO:1990879 CST complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0000781 chromosome, telomeric region",
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    {
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        "protein_names_uniprotkb": "Family with sequence similarity 13, member C",
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        "length": 289,
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        "gene_name": "Hvcn1",
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        "gene_names_uniprotkb": "Hvcn1",
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        "protein_names_uniprotkb": "Voltage-gated hydrogen channel 1; Hydrogen voltage-gated channel 1; Voltage sensor domain-only protein",
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        "disease": "middle cerebral artery infarction (Disease Ontology:DOID:3525)",
        "pathway": " (rno:304485);  (R-RNO-1222556);  (R-RNO-1300642);  (R-RNO-6798695)",
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        "refseq_name": "kinesin-like protein KIF7 isoform 1",
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        "protein_names_refseq": "kinesin-like protein KIF7 isoform 1; kinesin-like protein KIF7",
        "tax_id": 10116,
        "disease": "hydrolethalus syndrome (Disease Ontology:DOID:0050779); idiopathic scoliosis (Disease Ontology:DOID:0060250); ciliopathy (Disease Ontology:DOID:0060340); hydrolethalus syndrome 2 (Disease Ontology:DOID:0111356); congenital diaphragmatic hernia (Disease Ontology:DOID:3827); acrocallosal syndrome (Disease Ontology:DOID:9250); cleft lip (Disease Ontology:DOID:9296)",
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        "function": "Decreased Kif7 expression during diaphragmatic development may result in diaphragmatic defects in the nitrofen-induced congenital diaphragmatic hernia model., [RefSeq, PubMed]; Kinesin-7 CENP-E mediates chromosome alignment and spindle assembly checkpoint in meiosis I., [RefSeq, PubMed]",
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        "protein_name": "FERM and PDZ domain containing 3",
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        "refseq_ac": "XP_038956525",
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        "gene_names_refseq": "Frmpd3",
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        "length": 977,
        "protein_name": "Neuronal PAS domain-containing protein 3",
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        "gene_names_uniprotkb": "Npas3",
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        "protein_names_uniprotkb": "Neuronal PAS domain-containing protein 3; Basic-helix-loop-helix-PAS protein MOP6; Member of PAS protein 6",
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        "disease": "cancer (Disease Ontology:DOID:162)",
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        "function": "May play a broad role in neurogenesis. May control regulatory pathways relevant to schizophrenia and to psychotic illness., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0046983 protein dimerization activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0003677 DNA binding;GO:0046982 protein heterodimerization activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription;GO:0001964 startle response;GO:0007626 locomotory behavior",
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    },
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        "length": 404,
        "protein_name": "TERF1 interacting nuclear factor 2",
        "gene_name": "Tinf2",
        "organism": "Rat",
        "refseq_name": "TERF1-interacting nuclear factor 2 isoform X1",
        "refseq_ac": "XP_063130196",
        "gene_names_uniprotkb": "Tinf2",
        "gene_names_refseq": "Tinf2",
        "protein_names_uniprotkb": "TERF1 interacting nuclear factor 2",
        "protein_names_refseq": "TERF1-interacting nuclear factor 2 isoform X1",
        "tax_id": 10116,
        "disease": "autosomal dominant dyskeratosis congenita 3 (Disease Ontology:DOID:0070018); Revesz syndrome (Disease Ontology:DOID:0070026); dyskeratosis congenita (Disease Ontology:DOID:2729)",
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        "go_cellular_component": "GO:0070187 shelterin complex;GO:0010370 perinucleolar chromocenter;GO:0016604 nuclear body;GO:0000783 nuclear telomere cap complex;GO:0000781 chromosome, telomeric region",
        "go_biological_process": "GO:0016233 telomere capping;GO:0032205 negative regulation of telomere maintenance;GO:1904356 regulation of telomere maintenance via telomere lengthening;GO:0050680 negative regulation of epithelial cell proliferation;GO:0032202 telomere assembly",
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    },
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        "protein_names_uniprotkb": "TAP binding protein",
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        "tax_id": 10116,
        "disease": "metabolic dysfunction and alcohol associated liver disease (Disease Ontology:DOID:0070508); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); prostate cancer (Disease Ontology:DOID:10283); Parkinson's disease (Disease Ontology:DOID:14330); alveolar rhabdomyosarcoma (Disease Ontology:DOID:4051); congestive heart failure (Disease Ontology:DOID:6000); severe combined immunodeficiency (Disease Ontology:DOID:627); hepatocellular carcinoma (Disease Ontology:DOID:684)",
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        "go_molecular_function": "GO:0023024 MHC class I protein complex binding;GO:0062061 TAP complex binding;GO:0046978 TAP1 binding;GO:0046979 TAP2 binding;GO:0060090 molecular adaptor activity",
        "go_cellular_component": "GO:0042824 MHC class I peptide loading complex;GO:0000139 Golgi membrane;GO:0005789 endoplasmic reticulum membrane;GO:0061779 Tapasin-ERp57 complex",
        "go_biological_process": "GO:0019885 antigen processing and presentation of endogenous peptide antigen via MHC class I;GO:0002502 peptide antigen assembly with MHC class I protein complex;GO:0050823 peptide antigen stabilization;GO:0006952 defense response;GO:0002479 antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent",
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        "protein_name": "Leucine rich repeat containing 3C",
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        "gene_names_uniprotkb": "Lrrc3c",
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        "protein_names_uniprotkb": "Leucine rich repeat containing 3C",
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        "tax_id": 10116,
        "disease": "allergic asthma (Disease Ontology:DOID:9415)",
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        "go_molecular_function": "GO:0044325 transmembrane transporter binding;GO:0005249 voltage-gated potassium channel activity;GO:0099104 potassium channel activator activity",
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        "length": 323,
        "protein_name": "Serine/threonine-protein phosphatase 2A activator",
        "gene_name": "Ptpa",
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        "refseq_name": "serine/threonine-protein phosphatase 2A activator",
        "refseq_ac": "NP_001102047",
        "gene_names_uniprotkb": "Ptpa",
        "gene_names_refseq": "Ppp2r4; Ptpa",
        "protein_names_uniprotkb": "Serine/threonine-protein phosphatase 2A activator; 5.2.1.8; Phosphotyrosyl phosphatase activator",
        "protein_names_refseq": "protein phosphatase 2 regulatory subunit 4; protein phosphatase 2A activator, regulatory subunit 4; protein phosphatase 2A regulatory subunit 4; protein phosphatase 2A, regulatory subunit B (PR 53); serine/threonine-protein phosphatase 2A activator",
        "tax_id": 10116,
        "disease": "Parkinson's disease 25 (Disease Ontology:DOID:0070486)",
        "pathway": " (rno:362102)",
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        "publication_id_list": "20568963",
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        "function": "PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Protein phosphatase 2A, but not 2B, activity is downregulated following compressive injury of the cerebral cortex., [RefSeq, PubMed]",
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        "ec_number_list": "5.2.1.8",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0000159 protein phosphatase type 2A complex;GO:0005654 nucleoplasm;GO:0005829 cytosol",
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        "hit_score": 0.2,
        "record_id": "A0ABK0LHB2-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "A0ABK0LHI6-1",
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        "length": 251,
        "protein_name": "CD27 antigen",
        "gene_name": "Cd27",
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        "refseq_name": "CD27 antigen precursor",
        "refseq_ac": "NP_001019506",
        "gene_names_uniprotkb": "Cd27",
        "gene_names_refseq": "Cd27; Tnfrsf7",
        "protein_names_uniprotkb": "CD27 antigen; CD27L receptor; T-cell activation antigen CD27; Tumor necrosis factor receptor superfamily member 7",
        "protein_names_refseq": "CD antigen 27; CD27 antigen precursor; CD27 antigen; tumor necrosis factor receptor superfamily, member 7",
        "tax_id": 10116,
        "disease": "lymphoproliferative syndrome 2 (Disease Ontology:DOID:0060708); alcohol-associated liver disease (Disease Ontology:DOID:0070658)",
        "pathway": " (rno:500318)",
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        "function": "Costimulatory immune-checkpoint receptor expressed at the surface of T-cells, NK-cells and B-cells which binds to and is activated by its ligand CD70/CD27L expressed by B-cells. The CD70-CD27 signaling pathway mediates antigen-specific T-cell activation and expansion which in turn provides immune surveillance of B-cells. Mechanistically, CD70 ligation activates the TRAF2-PTPN6 axis that subsequently inhibits LCK phosphorylation to promote phenotypic and transcriptional adaptations of T-cell memory. In addition, activation by CD70 on early progenitor cells provides a negative feedback signal to leukocyte differentiation during immune activation and thus modulates hematopoiesis. Negatively regulates the function of Th2 lymphocytes in the adipose tissue., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "go_molecular_function": "GO:0004888 transmembrane signaling receptor activity;GO:0043027 cysteine-type endopeptidase inhibitor activity involved in apoptotic process",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0009897 external side of plasma membrane",
        "go_biological_process": "GO:0043066 negative regulation of apoptotic process;GO:0045579 positive regulation of B cell differentiation;GO:0045582 positive regulation of T cell differentiation;GO:0006915 apoptotic process;GO:0160162 CD27 signaling pathway",
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        "record_type": "protein"
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        "uniprot_canonical_ac": "A0ABK0LH61-1",
        "uniprot_id": "A0ABK0LH61_RAT",
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        "length": 410,
        "protein_name": "NAD(P)H oxidoreductase RTN4IP1, mitochondrial",
        "gene_name": "Rtn4ip1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rtn4ip1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "NAD(P)H oxidoreductase RTN4IP1, mitochondrial; NOGO-interacting mitochondrial protein; Reticulon-4-interacting protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "optic atrophy 10 (Disease Ontology:DOID:0111434)",
        "pathway": " (rno:309912)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "NAD(P)H oxidoreductase involved in the ubiquinone biosynthetic pathway. Required for the O-methyltransferase activity of COQ3. Able to catalyze the oxidoreduction of 3-demethylubiquinone into 3-demethylubiquinol in vitro. However, it is unclear if 3-demethylubiquinone constitutes a substrate in vivo. May also play a role in the regulation of retinal ganglion cell (RGC) neurite outgrowth, and hence in the development of the inner retina and optic nerve. Appears to be a potent inhibitor of regeneration following spinal cord injury., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0016491 oxidoreductase activity;GO:0008753 NADPH dehydrogenase (quinone) activity;GO:0050136 NADH dehydrogenase (quinone) (non-electrogenic) activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005741 mitochondrial outer membrane;GO:0005759 mitochondrial matrix",
        "go_biological_process": "GO:0006744 ubiquinone biosynthetic process;GO:0050773 regulation of dendrite development",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LH61-1",
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    {
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        "length": 219,
        "protein_name": "Transmembrane protein 213",
        "gene_name": "Tmem213",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tmem213",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transmembrane protein 213",
        "protein_names_refseq": "",
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        "length": 344,
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        "organism": "Rat",
        "refseq_name": "transcription factor JunB",
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        "gene_names_uniprotkb": "Junb; ENSRNOG00000065682",
        "gene_names_refseq": "Junb",
        "protein_names_uniprotkb": "Transcription factor JunB; Transcription factor AP-1 subunit JunB",
        "protein_names_refseq": "Jun-B oncogene; jun B proto-oncogene; transcription factor AP-1 subunit JunB; transcription factor JunB; transcription factor jun-B",
        "tax_id": 10116,
        "disease": "anaplastic large cell lymphoma (Disease Ontology:DOID:0050744); colorectal adenocarcinoma (Disease Ontology:DOID:0050861); tongue squamous cell carcinoma (Disease Ontology:DOID:0050865); oral squamous cell carcinoma (Disease Ontology:DOID:0050866); melanoma (Disease Ontology:DOID:1909); colon cancer (Disease Ontology:DOID:219); gallbladder cancer (Disease Ontology:DOID:3121); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); lung non-small cell carcinoma (Disease Ontology:DOID:3908); renal carcinoma (Disease Ontology:DOID:4451); head and neck squamous cell carcinoma (Disease Ontology:DOID:5520); Hodgkin's lymphoma (Disease Ontology:DOID:8567); systemic lupus erythematosus (Disease Ontology:DOID:9074)",
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        "publication_id_list": "29703907",
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        "function": "Based on these findings, miR-199a-5p induces apoptosis by targeting JunB. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0003690 double-stranded DNA 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_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0090575 RNA polymerase II transcription regulator complex;GO:0035976 transcription factor AP-1 complex",
        "go_biological_process": "GO:0030316 osteoclast differentiation;GO:0033687 osteoblast proliferation;GO:0001570 vasculogenesis;GO:0001701 in utero embryonic development;GO:0045944 positive regulation of transcription by RNA polymerase II",
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        "protein_name": "Eukaryotic translation initiation factor 5B",
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        "gene_name": "H3f3l1",
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        "protein_names_uniprotkb": "Immunoglobulin V-set domain-containing protein",
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        "protein_names_uniprotkb": "Disks large homolog 5 N-terminal domain-containing protein",
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        "length": 338,
        "protein_name": "Mitochondrial amidoxime reducing component 2",
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        "refseq_name": "mitochondrial amidoxime reducing component 2 precursor",
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        "protein_names_refseq": "MOCO sulphurase C-terminal domain containing 2; MOSC domain-containing protein 2, mitochondrial; mitochondrial amidoxime reducing component 2 precursor; moco sulfurase C-terminal domain-containing protein 2; molybdenum cofactor sulfurase C-terminal domain-containing protein 2",
        "tax_id": 10116,
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        "length": 129,
        "protein_name": "NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 4",
        "gene_name": "Ndufb4l3",
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        "refseq_name": "similar to NADH:ubiquinone oxidoreductase B15 subunit",
        "refseq_ac": "NP_001388792",
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        "gene_names_refseq": "Ndufb4l3; RGD1560088",
        "protein_names_uniprotkb": "NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 4; Complex I-B15; NADH-ubiquinone oxidoreductase B15 subunit",
        "protein_names_refseq": "NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 4-like; similar to NADH:ubiquinone oxidoreductase B15 subunit",
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        "function": "Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane",
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    },
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        "length": 149,
        "protein_name": "Atonal bHLH transcription factor 7",
        "gene_name": "Atoh7",
        "organism": "Rat",
        "refseq_name": "transcription factor ATOH7",
        "refseq_ac": "NP_001163953",
        "gene_names_uniprotkb": "Atoh7",
        "gene_names_refseq": "Atoh7",
        "protein_names_uniprotkb": "Atonal bHLH transcription factor 7",
        "protein_names_refseq": "atonal homolog 7; transcription factor ATOH7",
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        "disease": "persistent hyperplastic primary vitreous (Disease Ontology:DOID:0060282)",
        "pathway": " (rno:365564)",
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        "publication_id_list": "25710928;37792226",
        "class_list": "",
        "function": "Atoh7 promotes the differentiation of Muller cells-derived retinal stem cells into retinal ganglion cells in a rat model of glaucoma, thus opening up a new avenue for gene therapy and optic nerve regeneration in glaucoma, [RefSeq, PubMed]; TRIM9 promotes Muller cell-derived retinal stem cells to differentiate into retinal ganglion cells by regulating Atoh7., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0046983 protein dimerization activity;GO:0000976 transcription cis-regulatory region binding;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0030424 axon;GO:0043204 perikaryon",
        "go_biological_process": "GO:0003407 neural retina development;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0030154 cell differentiation;GO:0045944 positive regulation of transcription by RNA polymerase II",
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        "record_id": "A0ABK0LH80-1",
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    {
        "uniprot_canonical_ac": "A0ABK0LH83-1",
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        "length": 433,
        "protein_name": "Ras-related GTP-binding protein",
        "gene_name": "Rragc",
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        "gene_names_uniprotkb": "Rragc",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ras-related GTP-binding protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); follicular lymphoma (Disease Ontology:DOID:0050873); candidiasis (Disease Ontology:DOID:1508)",
        "pathway": " (rno:298514)",
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Guanine nucleotide-binding protein that plays a crucial role in the cellular response to amino acid availability through regulation of the mTORC1 signaling cascade., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "3.6.5.2;3.6.1.1;3.6.5.-;3.6.5.3;2.3.2.27;2.7.11.1;3.6.5.5;3.6.1.5;3.6.1.-;3.6.5.4",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005764 lysosome;GO:0005765 lysosomal membrane",
        "go_biological_process": "GO:1904263 positive regulation of TORC1 signaling;GO:0031669 cellular response to nutrient levels;GO:0072657 protein localization to membrane;GO:0043200 response to amino acid;GO:0032006 regulation of TOR signaling",
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        "protein_name": "DNA-directed RNA polymerase II subunit GRINL1A",
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        "organism": "Rat",
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        "protein_names_uniprotkb": "DNA-directed RNA polymerase II subunit GRINL1A; DNA-directed RNA polymerase II subunit M; Glutamate receptor-like protein 1A",
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        "go_molecular_function": "GO:0003711 transcription elongation factor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000428 DNA-directed RNA polymerase complex",
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        "record_id": "A0ABK0LH87-1",
        "record_type": "protein"
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        "uniprot_canonical_ac": "A0ABK0LH99-1",
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        "length": 143,
        "protein_name": "Ig-like domain-containing protein",
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        "organism": "Rat",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
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        "record_id": "A0ABK0LH99-1",
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    {
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        "protein_name": "LINE-1 retrotransposable element ORF1 protein",
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        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "LINE-1 retrotransposable element ORF1 protein; LINE retrotransposable element 1; LINE1 retrotransposable element 1",
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        "function": "Nucleic acid-binding protein which is essential for retrotransposition of LINE-1 elements in the genome. Functions as a nucleic acid chaperone binding its own transcript and therefore preferentially mobilizing the transcript from which they are encoded., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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    },
    {
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        "protein_name": "Ig-like domain-containing protein",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Tapbpl",
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        "protein_names_uniprotkb": "Tapasin-related protein; TAP-binding protein-like; TAP-binding protein-related protein; Tapasin-like",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
        "publication_count": 0,
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        "function": "",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0019814 immunoglobulin complex",
        "go_biological_process": "GO:0002250 adaptive immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LIG6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LIH8-1",
        "uniprot_id": "A0ABK0LIH8_RAT",
        "mass": 89420.0,
        "length": 855,
        "protein_name": "Zinc finger, X-linked, duplicated A",
        "gene_name": "Zxda",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zxda",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger, X-linked, duplicated A",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Cooperates with CIITA to promote transcription of MHC class I and MHC class II genes., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0008270 zinc ion binding;GO:0070742 C2H2 zinc finger domain binding",
        "go_cellular_component": "",
        "go_biological_process": "GO:0045893 positive regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LIH8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LKZ7-1",
        "uniprot_id": "A0ABK0LKZ7_RAT",
        "mass": 71625.0,
        "length": 635,
        "protein_name": "Elongation factor for RNA polymerase II 2",
        "gene_name": "Ell2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ell2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Elongation factor for RNA polymerase II 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "cancer (Disease Ontology:DOID:162)",
        "pathway": " (rno:309918);  (R-RNO-6807505)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
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        "mined_s_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
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        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0000987 cis-regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0008023 transcription elongation factor complex;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006368 transcription elongation by RNA polymerase II;GO:0032968 positive regulation of transcription elongation by RNA polymerase II;GO:0042795 snRNA transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LKZ7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LIZ5-1",
        "uniprot_id": "A0ABK0LIZ5_RAT",
        "mass": 77818.0,
        "length": 690,
        "protein_name": "F-box/LRR-repeat protein 5",
        "gene_name": "Fbxl5",
        "organism": "Rat",
        "refseq_name": "F-box/LRR-repeat protein 5",
        "refseq_ac": "NP_001388361",
        "gene_names_uniprotkb": "Fbxl5",
        "gene_names_refseq": "Fbxl5",
        "protein_names_uniprotkb": "F-box/LRR-repeat protein 5; F-box and leucine-rich repeat protein 5",
        "protein_names_refseq": "F-box/LRR-repeat protein 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:305424);  (R-RNO-8951664);  (R-RNO-917937);  (R-RNO-983168)",
        "pathway_count": 4,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0051536 iron-sulfur cluster binding;GO:0005506 iron ion binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0048471 perinuclear region of cytoplasm;GO:0019005 SCF ubiquitin ligase complex",
        "go_biological_process": "GO:0006879 intracellular iron ion homeostasis;GO:0030163 protein catabolic process;GO:0016567 protein ubiquitination;GO:0031146 SCF-dependent proteasomal ubiquitin-dependent protein catabolic process;GO:0045732 positive regulation of protein catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LIZ5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LKA1-1",
        "uniprot_id": "A0ABK0LKA1_RAT",
        "mass": 179854.0,
        "length": 1663,
        "protein_name": "Protein scribble homolog",
        "gene_name": "Scrib",
        "organism": "Rat",
        "refseq_name": "protein scribble homolog",
        "refseq_ac": "NP_001178808",
        "gene_names_uniprotkb": "Scrib",
        "gene_names_refseq": "RGD1565055; Scrib",
        "protein_names_uniprotkb": "Protein scribble homolog; Protein LAP4",
        "protein_names_refseq": "protein scribble homolog; scribbled homolog; scribbled planar cell polarity protein",
        "tax_id": 10116,
        "disease": "benign neoplasm (Disease Ontology:DOID:0060072); cancer (Disease Ontology:DOID:162); kidney cancer (Disease Ontology:DOID:263); carcinoma (Disease Ontology:DOID:305)",
        "pathway": " (rno:362938);  (R-RNO-9013406);  (R-RNO-9696264);  (R-RNO-9696270)",
        "pathway_count": 4,
        "publication_count": 3,
        "publication_id_list": "22673903;23973368;25310985",
        "class_list": "",
        "function": "Scrib1 YxxR motif interacts with AP2 to control NMDAR postendocytic traffic, [RefSeq, PubMed]; Scribble complexes with HRas and Rac1 and controls neurite growth in NGF-treated PC12 cells., [RefSeq, PubMed]",
        "predicted_glycosites": 4,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 4,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 4,
        "glyco_site_count": 4,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0019901 protein kinase binding;GO:0035591 signaling adaptor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0005912 adherens junction;GO:0030027 lamellipodium;GO:0098794 postsynapse",
        "go_biological_process": "GO:0030154 cell differentiation;GO:0001843 neural tube closure;GO:0030010 establishment of cell polarity;GO:0035088 establishment or maintenance of apical/basal cell polarity;GO:0098887 neurotransmitter receptor transport, endosome to postsynaptic membrane",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0ABK0LKA1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LJW5-1",
        "uniprot_id": "A0ABK0LJW5_RAT",
        "mass": 72219.0,
        "length": 636,
        "protein_name": "Beta-galactosidase",
        "gene_name": "Glb1l2",
        "organism": "Rat",
        "refseq_name": "beta-galactosidase-1-like protein 2 isoform 1",
        "refseq_ac": "NP_001423487",
        "gene_names_uniprotkb": "Glb1l2",
        "gene_names_refseq": "Glb1l2; RGD1564436",
        "protein_names_uniprotkb": "Beta-galactosidase; 3.2.1.23",
        "protein_names_refseq": "beta-galactosidase-1-like protein 2 isoform 1; beta-galactosidase-1-like protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:503194);  (R-RNO-2022857);  (R-RNO-2024101);  (R-RNO-9840310)",
        "pathway_count": 4,
        "publication_count": 1,
        "publication_id_list": "16641100",
        "class_list": "",
        "function": "Cleaves beta-linked terminal galactosyl residues from gangliosides, glycoproteins, and glycosaminoglycans., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.2.1.23",
        "go_molecular_function": "GO:0004565 beta-galactosidase activity",
        "go_cellular_component": "GO:0005773 vacuole",
        "go_biological_process": "GO:0005975 carbohydrate metabolic process;GO:0019388 galactose catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LJW5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LJG1-1",
        "uniprot_id": "A0ABK0LJG1_RAT",
        "mass": 117994.0,
        "length": 1047,
        "protein_name": "Mannosyltransferase",
        "gene_name": "Alg9; Fdxacb1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Alg9; Fdxacb1; Alg9",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Mannosyltransferase; 2.4.1.-",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "congenital disorder of glycosylation type I (Disease Ontology:DOID:0050570); congenital disorder of glycosylation Il (Disease Ontology:DOID:0080564)",
        "pathway": " (rno:367083);  (R-RNO-446193)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.4.1.-",
        "go_molecular_function": "GO:0016757 glycosyltransferase activity;GO:0000026 alpha-1,2-mannosyltransferase activity;GO:0070042 rRNA (uridine-N3-)-methyltransferase activity;GO:0052918 dol-P-Man:Man(8)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase activity;GO:0052926 dol-P-Man:Man(6)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase activity",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006487 protein N-linked glycosylation;GO:0070475 rRNA base methylation;GO:0006488 dolichol-linked oligosaccharide biosynthetic process",
        "synthesized_glycan_count": 505,
        "hit_score": 0.1,
        "record_id": "A0ABK0LJG1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LK60-1",
        "uniprot_id": "A0ABK0LK60_RAT",
        "mass": 10042.0,
        "length": 93,
        "protein_name": "Secretoglobin, family 3A, member 2",
        "gene_name": "Scgb3a2",
        "organism": "Rat",
        "refseq_name": "secretoglobin family 3A member 2",
        "refseq_ac": "NP_001019454",
        "gene_names_uniprotkb": "Scgb3a2",
        "gene_names_refseq": "Pnsp1; Scgb3a2",
        "protein_names_uniprotkb": "Secretoglobin, family 3A, member 2",
        "protein_names_refseq": "pneumo secretory protein 1; secretoglobin family 3A member 2",
        "tax_id": 10116,
        "disease": "sinusitis (Disease Ontology:DOID:0050127); asthma (Disease Ontology:DOID:2841); lung non-small cell carcinoma (Disease Ontology:DOID:3908); allergic rhinitis (Disease Ontology:DOID:4481); rhinitis (Disease Ontology:DOID:4483)",
        "pathway": " (rno:498854)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
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        "protein_name": "Protein kish",
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        "gene_names_refseq": "Tmem167a",
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        "protein_names_refseq": "protein kish-A; rCG44733-like",
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        "protein_names_uniprotkb": "Similar to human chromosome 15 open reading frame 61",
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        "protein_names_uniprotkb": "Dendrocyte expressed seven transmembrane protein",
        "protein_names_refseq": "dendritic cell-specific transmembrane protein; dendrocyte expressed seven transmembrane protein; transmembrane 7 superfamily member 4",
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        "length": 474,
        "protein_name": "Tumor necrosis factor receptor superfamily member 19L",
        "gene_name": "Relt",
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        "refseq_name": "tumor necrosis factor receptor superfamily member 19L isoform X1",
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        "protein_names_refseq": "tumor necrosis factor receptor superfamily member 19L isoform X1",
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        "disease": "amelogenesis imperfecta type 3C (Disease Ontology:DOID:0111722)",
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        "function": "May play a role in apoptosis. Induces activation of MAPK14/p38 and MAPK8/JNK MAPK cascades, when overexpressed. Involved in dental enamel formation., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005829 cytosol",
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    {
        "uniprot_canonical_ac": "A0ABK0LIN4-1",
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        "length": 1637,
        "protein_name": "Laminin subunit gamma-3",
        "gene_name": "Lamc3",
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        "gene_names_uniprotkb": "Lamc3",
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        "protein_names_uniprotkb": "Laminin subunit gamma-3; Laminin-12 subunit gamma; Laminin-14 subunit gamma; Laminin-15 subunit gamma",
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        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041)",
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        "function": "Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005576 extracellular region;GO:0005604 basement membrane",
        "go_biological_process": "GO:0009887 animal organ morphogenesis;GO:0007411 axon guidance;GO:0009888 tissue development;GO:0000902 cell morphogenesis;GO:0007601 visual perception",
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    {
        "uniprot_canonical_ac": "A0ABK0LKN3-1",
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        "length": 540,
        "protein_name": "Upstream-binding protein 1",
        "gene_name": "Ubp1",
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        "refseq_name": "upstream-binding protein 1",
        "refseq_ac": "NP_001178748",
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        "gene_names_refseq": "RGD1564700; Ubp1",
        "protein_names_uniprotkb": "Upstream-binding protein 1",
        "protein_names_refseq": "upstream binding protein 1 (LBP-1a); upstream-binding protein 1",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0032897 negative regulation of viral transcription;GO:0001525 angiogenesis;GO:0045944 positive regulation of transcription by RNA polymerase II",
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    {
        "uniprot_canonical_ac": "A0ABK0LJ67-1",
        "uniprot_id": "A0ABK0LJ67_RAT",
        "mass": 106125.0,
        "length": 942,
        "protein_name": "Protein O-mannosyl-transferase TMTC1",
        "gene_name": "Tmtc1",
        "organism": "Rat",
        "refseq_name": "transmembrane O-mannosyltransferase targeting cadherins 1 isoform 1",
        "refseq_ac": "NP_001418720",
        "gene_names_uniprotkb": "Tmtc1",
        "gene_names_refseq": "RGD1564868; Tmtc1",
        "protein_names_uniprotkb": "Protein O-mannosyl-transferase TMTC1; 2.4.1.109; Transmembrane O-mannosyltransferase targeting cadherins 1; Transmembrane and tetratricopeptide repeat-containing 1",
        "protein_names_refseq": "transmembrane O-mannosyltransferase targeting cadherins 1 isoform 1; transmembrane and TPR repeat-containing protein 1; transmembrane and tetratricopeptide repeat containing 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Transfers mannosyl residues to the hydroxyl group of serine or threonine residues. The 4 members of the TMTC family are O-mannosyl-transferases dedicated primarily to the cadherin superfamily, each member seems to have a distinct role in decorating the cadherin domains with O-linked mannose glycans at specific regions. Also acts as O-mannosyl-transferase on other proteins such as PDIA3., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004169 dolichyl-phosphate-mannose-protein mannosyltransferase activity;GO:0000030 mannosyltransferase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0016020 membrane",
        "go_biological_process": "GO:0035269 protein O-linked glycosylation via mannose",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LJ67-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LJZ0-1",
        "uniprot_id": "A0ABK0LJZ0_RAT",
        "mass": 49092.0,
        "length": 435,
        "protein_name": "Sister chromatid cohesion protein DCC1",
        "gene_name": "Dscc1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Dscc1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Sister chromatid cohesion protein DCC1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-174411)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0000775 chromosome, centromeric region;GO:0000785 chromatin;GO:0031390 Ctf18 RFC-like complex;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006260 DNA replication;GO:0034088 maintenance of mitotic sister chromatid cohesion;GO:0007064 mitotic sister chromatid cohesion;GO:0006275 regulation of DNA replication;GO:1900264 positive regulation of DNA-directed DNA polymerase activity",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LJZ0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LKQ1-1",
        "uniprot_id": "A0ABK0LKQ1_RAT",
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        "length": 406,
        "protein_name": "Caspase 4",
        "gene_name": "Casp4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Casp4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Caspase 4",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652)",
        "pathway": "",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 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": 1,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004197 cysteine-type endopeptidase activity;GO:0008289 lipid binding;GO:0097110 scaffold protein binding;GO:0001530 lipopolysaccharide binding;GO:0050700 CARD domain binding",
        "go_cellular_component": "GO:0097169 AIM2 inflammasome complex;GO:0072559 NLRP3 inflammasome complex;GO:0072557 IPAF inflammasome complex;GO:0005737 cytoplasm;GO:0005739 mitochondrion",
        "go_biological_process": "GO:0048731 system development;GO:0016485 protein processing;GO:0043065 positive regulation of apoptotic process;GO:0006915 apoptotic process;GO:0050727 regulation of inflammatory response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LKQ1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LIT9-1",
        "uniprot_id": "A0ABK0LIT9_RAT",
        "mass": 149815.0,
        "length": 1308,
        "protein_name": "Lysine-specific demethylase 2B",
        "gene_name": "Kdm2b",
        "organism": "Rat",
        "refseq_name": "lysine-specific demethylase 2B isoform X1",
        "refseq_ac": "XP_063127396",
        "gene_names_uniprotkb": "Kdm2b",
        "gene_names_refseq": "Fbxl10; Kdm2b",
        "protein_names_uniprotkb": "Lysine-specific demethylase 2B; 1.14.11.27; F-box and leucine-rich repeat protein 10; F-box protein FBL10; F-box/LRR-repeat protein 10; JmjC domain-containing histone demethylation protein 1B; [Histone-H3]-lysine-36 demethylase 1B",
        "protein_names_refseq": "lysine-specific demethylase 2B isoform X1",
        "tax_id": 10116,
        "disease": "T-cell non-Hodgkin lymphoma (Disease Ontology:DOID:0081312); pancreatic ductal carcinoma (Disease Ontology:DOID:3587); acute lymphoblastic leukemia (Disease Ontology:DOID:9952)",
        "pathway": " (rno:304495);  (R-RNO-3214842)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Histone demethylase that demethylates 'Lys-4' and 'Lys-36' of histone H3, thereby playing a central role in histone code. Preferentially demethylates trimethylated H3 'Lys-4' and dimethylated H3 'Lys-36' residue while it has weak or no activity for mono- and tri-methylated H3 'Lys-36'. Preferentially binds the transcribed region of ribosomal RNA and represses the transcription of ribosomal RNA genes which inhibits cell growth and proliferation. May also serve as a substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "1.14.11.69;1.14.11.66;1.14.11.27;1.14.11.79",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0019843 rRNA binding;GO:0043565 sequence-specific DNA binding;GO:0140680 histone H3K36me/H3K36me2 demethylase activity",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0005694 chromosome;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0019005 SCF ubiquitin ligase complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0001843 neural tube closure;GO:0048562 embryonic organ morphogenesis;GO:0006338 chromatin remodeling;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LIT9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LIZ3-1",
        "uniprot_id": "A0ABK0LIZ3_RAT",
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        "length": 172,
        "protein_name": "Secretoglobin, family 2B, member 2",
        "gene_name": "Scgb2b2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Scgb2b2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Secretoglobin, family 2B, member 2",
        "protein_names_refseq": "",
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        "go_cellular_component": "GO:0005615 extracellular space",
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        "record_id": "A0ABK0LIZ3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LJL6-1",
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        "length": 368,
        "protein_name": "Single-pass membrane protein with coiled-coil domains 2",
        "gene_name": "Smco2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Smco2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Single-pass membrane protein with coiled-coil domains 2",
        "protein_names_refseq": "",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LJG4-1",
        "uniprot_id": "A0ABK0LJG4_RAT",
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        "length": 700,
        "protein_name": "Terminal nucleotidyltransferase 4B",
        "gene_name": "Tent4b",
        "organism": "Rat",
        "refseq_name": "terminal nucleotidyltransferase 4B isoform 3",
        "refseq_ac": "NP_001401942",
        "gene_names_uniprotkb": "Tent4b",
        "gene_names_refseq": "Papd5; Tent4b",
        "protein_names_uniprotkb": "Terminal nucleotidyltransferase 4B; 2.7.7.19; Non-canonical poly(A) RNA polymerase PAPD5; PAP-associated domain-containing protein 5; Terminal guanylyltransferase; Terminal uridylyltransferase 3; Topoisomerase-related function protein 4-2",
        "protein_names_refseq": "PAP associated domain containing 5; PAP-associated domain-containing protein 5; non-canonical poly(A) RNA polymerase PAPD5; poly(A) RNA polymerase D5, non-canonical; terminal nucleotidyltransferase 4B isoform 3",
        "tax_id": 10116,
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        "pathway": " (rno:307745)",
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        "secondary_ac_list": "",
        "ec_number_list": "2.7.7.19;2.7.7.52",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:1990817 poly(A) RNA polymerase activity;GO:0070034 telomerase RNA binding;GO:0070568 guanylyltransferase activity;GO:0005524 ATP binding",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0031499 TRAMP complex",
        "go_biological_process": "GO:0033500 carbohydrate homeostasis;GO:0032211 negative regulation of telomere maintenance via telomerase;GO:0071044 histone mRNA catabolic process;GO:0031124 mRNA 3'-end processing;GO:1905870 positive regulation of 3'-UTR-mediated mRNA stabilization",
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        "record_id": "A0ABK0LJG4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LKD4-1",
        "uniprot_id": "A0ABK0LKD4_RAT",
        "mass": 172718.0,
        "length": 1556,
        "protein_name": "Protein dispatched homolog 1",
        "gene_name": "Disp1",
        "organism": "Rat",
        "refseq_name": "protein dispatched homolog 1 isoform X1",
        "refseq_ac": "XP_038946501",
        "gene_names_uniprotkb": "Disp1",
        "gene_names_refseq": "Disp1",
        "protein_names_uniprotkb": "Protein dispatched homolog 1",
        "protein_names_refseq": "protein dispatched homolog 1 isoform X1",
        "tax_id": 10116,
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        "pathway": " (rno:289338)",
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        "function": "Functions in hedgehog (Hh) signaling. Regulates the release and extracellular accumulation of cholesterol-modified hedgehog proteins and is hence required for effective production of the Hh signal. Synergizes with SCUBE2 to cause an increase in SHH secretion., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0140104 molecular carrier activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0016323 basolateral plasma membrane",
        "go_biological_process": "GO:0007224 smoothened signaling pathway;GO:0015833 peptide transport;GO:0007368 determination of left/right symmetry;GO:0050708 regulation of protein secretion;GO:0009953 dorsal/ventral pattern formation",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LK58-1",
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        "length": 1260,
        "protein_name": "Codanin 1",
        "gene_name": "Cdan1",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "Cdan1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Codanin 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "congenital dyserythropoietic anemia type I (Disease Ontology:DOID:0111396); congenital dyserythropoietic anemia type Ia (Disease Ontology:DOID:0111398); congenital dyserythropoietic anemia (Disease Ontology:DOID:1338)",
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        "protein_names_refseq": "tudor domain-containing protein 1 isoform 1; tudor domain-containing protein 1",
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        "go_molecular_function": "GO:0008270 zinc ion binding",
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        "go_biological_process": "GO:0030719 P granule organization;GO:0007283 spermatogenesis;GO:0034587 piRNA processing;GO:0007281 germ cell development;GO:0141196 transposable element silencing by piRNA-mediated DNA methylation",
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        "protein_name": "Wee1-like protein kinase",
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        "gene_names_uniprotkb": "Wee2",
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        "protein_names_uniprotkb": "Wee1-like protein kinase; 2.7.10.2",
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        "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0004713 protein tyrosine kinase activity;GO:0004715 non-membrane spanning protein tyrosine kinase activity;GO:0005524 ATP binding",
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        "go_biological_process": "GO:0000278 mitotic cell cycle;GO:0051321 meiotic cell cycle;GO:0060631 regulation of meiosis I;GO:0060283 negative regulation of oocyte development;GO:0007143 female meiotic nuclear division",
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        "protein_name": "Teneurin-4",
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        "gene_names_uniprotkb": "Tenm4; Odz4",
        "gene_names_refseq": "Odz4; Tenm4",
        "protein_names_uniprotkb": "Teneurin-4; Protein Odd Oz/ten-m homolog 4; Tenascin-M4; Teneurin transmembrane protein 4",
        "protein_names_refseq": "teneurin-4 isoform X9",
        "tax_id": 10116,
        "disease": "essential tremor 5 (Disease Ontology:DOID:0111432)",
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        "function": "Involved in neural development, regulating the establishment of proper connectivity within the nervous system. Plays a role in the establishment of the anterior-posterior axis during gastrulation. Regulates the differentiation and cellular process formation of oligodendrocytes and myelination of small-diameter axons in the central nervous system (CNS). Promotes activation of focal adhesion kinase. May function as a cellular signal transducer., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0042803 protein homodimerization activity;GO:0046982 protein heterodimerization activity;GO:0050839 cell adhesion molecule binding;GO:0042802 identical protein binding",
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        "protein_name": "Glycerophosphodiester phosphodiesterase domain containing 4",
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        "refseq_name": "glycerophosphodiester phosphodiesterase domain-containing protein 4 isoform X1",
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        "gene_names_uniprotkb": "Gdpd4",
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        "protein_names_uniprotkb": "Glycerophosphodiester phosphodiesterase domain containing 4",
        "protein_names_refseq": "glycerophosphodiester phosphodiesterase domain-containing protein 4 isoform X1",
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        "go_molecular_function": "GO:0008889 glycerophosphodiester phosphodiesterase activity;GO:0008081 phosphoric diester hydrolase activity",
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        "protein_name": "Armadillo repeat containing 3",
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        "refseq_name": "armadillo repeat-containing protein 3 isoform X1",
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        "go_biological_process": "GO:0030317 flagellated sperm motility;GO:0007286 spermatid development;GO:0034517 ribophagy",
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        "protein_name": "IKAROS family zinc finger 2",
        "gene_name": "Ikzf2",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "Ikzf2",
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        "protein_names_uniprotkb": "IKAROS family zinc finger 2",
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        "tax_id": 10116,
        "disease": "lung non-small cell carcinoma (Disease Ontology:DOID:3908)",
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    },
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        "protein_names_refseq": "meiotic recombination protein REC114 isoform 3; meiotic recombination protein REC114",
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    },
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        "tax_id": 10116,
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        "function": "Cadherins are calcium-dependent cell adhesion proteins., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "IZUMO family member 2",
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        "gene_names_refseq": "Izumo2; RGD1562619",
        "protein_names_uniprotkb": "IZUMO family member 2",
        "protein_names_refseq": "IZUMO family member 2 isoform 1 precursor; izumo sperm-egg fusion protein 2-like; izumo sperm-egg fusion protein 2",
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        "protein_names_refseq": "cation channel sperm-associated auxiliary subunit epsilon; cation channel sperm-associated protein subunit epsilon; catsper channel auxiliary subunit epsilon; uncharacterized protein C1orf101 homolog",
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        "refseq_ac": "NP_001421218",
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        "protein_names_refseq": "probable E3 ubiquitin-protein ligase MID2 isoform 2; probable E3 ubiquitin-protein ligase MID2",
        "tax_id": 10116,
        "disease": "non-syndromic X-linked intellectual disability 101 (Disease Ontology:DOID:0112048)",
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        "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0008017 microtubule binding;GO:0008270 zinc ion binding;GO:0019899 enzyme binding;GO:0042802 identical protein binding",
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        "go_biological_process": "GO:0032897 negative regulation of viral transcription;GO:0044790 suppression of viral release by host;GO:0045087 innate immune response;GO:0043123 positive regulation of canonical NF-kappaB signal transduction;GO:0010508 positive regulation of autophagy",
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        "length": 265,
        "protein_name": "Triosephosphate isomerase",
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        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Tpi1l1; LOC500959",
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        "protein_names_uniprotkb": "Triosephosphate isomerase; 5.3.1.1",
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        "tax_id": 10116,
        "disease": "triosephosphate isomerase deficiency (Disease Ontology:DOID:0050884); neurodegenerative disease (Disease Ontology:DOID:1289); cancer (Disease Ontology:DOID:162); carbohydrate metabolic disorder (Disease Ontology:DOID:2978)",
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        "ec_number_list": "5.3.1.1;4.2.3.3",
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        "go_cellular_component": "GO:0005829 cytosol",
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        "protein_name": "Kelch-like family member 26",
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        "gene_names_uniprotkb": "Klhl26",
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        "protein_names_uniprotkb": "Kelch-like family member 26",
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        "go_molecular_function": "GO:1990756 ubiquitin-like ligase-substrate adaptor activity",
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        "length": 506,
        "protein_name": "Raftlin family member 2",
        "gene_name": "Rftn2",
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        "disease": "ciliopathy (Disease Ontology:DOID:0060340); Leber congenital amaurosis 6 (Disease Ontology:DOID:0110329); cone-rod dystrophy 13 (Disease Ontology:DOID:0111016); retinitis pigmentosa (Disease Ontology:DOID:10584); Leber hereditary optic neuropathy (Disease Ontology:DOID:705)",
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        "gene_names_refseq": "",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Small ribosomal subunit protein uS15; 40S ribosomal protein S13",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "protein_names_uniprotkb": "Mitochondrial import receptor subunit TOM20 homolog; Mitochondrial 20 kDa outer membrane protein; Outer mitochondrial membrane receptor Tom20",
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        "protein_name": "Olfactory receptor",
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        "disease": "Parkinsonism (Disease Ontology:DOID:0080855); graft-versus-host disease (Disease Ontology:DOID:0081267); age related macular degeneration 12 (Disease Ontology:DOID:0110024); otitis media (Disease Ontology:DOID:10754); portal hypertension (Disease Ontology:DOID:10762); sciatic neuropathy (Disease Ontology:DOID:11446); retinal vasculitis (Disease Ontology:DOID:11563); uveitis (Disease Ontology:DOID:13141); cystitis (Disease Ontology:DOID:1679); status epilepticus (Disease Ontology:DOID:1824); transient cerebral ischemia (Disease Ontology:DOID:224); nephrosis (Disease Ontology:DOID:2527); asthma (Disease Ontology:DOID:2841); glomerulonephritis (Disease Ontology:DOID:2921); atopic dermatitis (Disease Ontology:DOID:3310); systemic scleroderma (Disease Ontology:DOID:418); macular degeneration (Disease Ontology:DOID:4448); anti-basement membrane glomerulonephritis (Disease Ontology:DOID:4780); borna disease (Disease Ontology:DOID:5154); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); congestive heart failure (Disease Ontology:DOID:6000); pulmonary hypertension (Disease Ontology:DOID:6432); prion disease (Disease Ontology:DOID:649); psoriasis (Disease Ontology:DOID:8893); hepatopulmonary syndrome (Disease Ontology:DOID:900); systemic lupus erythematosus (Disease Ontology:DOID:9074); pulmonary embolism (Disease Ontology:DOID:9477); obesity (Disease Ontology:DOID:9970)",
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        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "LOC134478836",
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        "refseq_name": "sperm motility kinase 2B-like",
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        "refseq_name": "olfactory receptor Olr984",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0019814 immunoglobulin complex",
        "go_biological_process": "GO:0002250 adaptive immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LL16-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LL22-1",
        "uniprot_id": "A0ABK0LL22_RAT",
        "mass": 8786.0,
        "length": 76,
        "protein_name": "NADH dehydrogenase [ubiquinone] 1 subunit C1, mitochondrial",
        "gene_name": "Ndufc1",
        "organism": "Rat",
        "refseq_name": "NADH dehydrogenase [ubiquinone] 1 subunit C1, mitochondrial",
        "refseq_ac": "NP_001386532",
        "gene_names_uniprotkb": "Ndufc1",
        "gene_names_refseq": "Ndufc1",
        "protein_names_uniprotkb": "NADH dehydrogenase [ubiquinone] 1 subunit C1, mitochondrial; Complex I-KFYI; NADH-ubiquinone oxidoreductase KFYI subunit",
        "protein_names_refseq": "NADH dehydrogenase (ubiquinone) 1, subcomplex unknown, 1; NADH dehydrogenase [ubiquinone] 1 subunit C1, mitochondrial; rCG49984-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0045271 respiratory chain complex I",
        "go_biological_process": "GO:0022904 respiratory electron transport chain",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LL22-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LL33-1",
        "uniprot_id": "A0ABK0LL33_RAT",
        "mass": 35373.0,
        "length": 330,
        "protein_name": "Sperm acrosome associated 6",
        "gene_name": "Spaca6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Spaca6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Sperm acrosome associated 6",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway_count": 0,
        "publication_count": 0,
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        "class_list": "",
        "function": "",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0001669 acrosomal vesicle",
        "go_biological_process": "GO:0035036 sperm-egg recognition;GO:0007342 fusion of sperm to egg plasma membrane involved in single fertilization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LL33-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LL44-1",
        "uniprot_id": "A0ABK0LL44_RAT",
        "mass": 88664.0,
        "length": 807,
        "protein_name": "C3H1-type domain-containing protein",
        "gene_name": "Zc3h11a",
        "organism": "Rat",
        "refseq_name": "zinc finger CCCH domain-containing protein 11A isoform 1",
        "refseq_ac": "NP_001430555",
        "gene_names_uniprotkb": "Zc3h11a",
        "gene_names_refseq": "RGD1308290; Zc3h11a",
        "protein_names_uniprotkb": "C3H1-type domain-containing protein",
        "protein_names_refseq": "zinc finger CCCH domain-containing protein 11A isoform 1; zinc finger CCCH domain-containing protein 11A",
        "tax_id": 10116,
        "disease": "",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0000346 transcription export complex",
        "go_biological_process": "GO:0016973 poly(A)+ mRNA export from nucleus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LL44-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LL50-1",
        "uniprot_id": "A0ABK0LL50_RAT",
        "mass": 19469.0,
        "length": 174,
        "protein_name": "Glycosylphosphatidylinositol anchored molecule like",
        "gene_name": "Gml",
        "organism": "Rat",
        "refseq_name": "glycosyl-phosphatidylinositol-anchored molecule-like protein precursor",
        "refseq_ac": "NP_001411401",
        "gene_names_uniprotkb": "Gml",
        "gene_names_refseq": "Gml",
        "protein_names_uniprotkb": "Glycosylphosphatidylinositol anchored molecule like",
        "protein_names_refseq": "GPI anchored molecule like protein; glycosyl-phosphatidylinositol-anchored molecule-like protein precursor; glycosyl-phosphatidylinositol-anchored molecule-like protein; glycosylphosphatidylinositol anchored molecule like protein; lymphocyte antigen 6K",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
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        "class_list": "",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LL50-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LLW9-1",
        "uniprot_id": "A0ABK0LLW9_RAT",
        "mass": 91955.0,
        "length": 841,
        "protein_name": "OTU domain-containing protein 7B",
        "gene_name": "Otud7b",
        "organism": "Rat",
        "refseq_name": "OTU domain-containing protein 7B",
        "refseq_ac": "NP_001101167",
        "gene_names_uniprotkb": "Otud7b",
        "gene_names_refseq": "Otud7b; RGD1308111",
        "protein_names_uniprotkb": "OTU domain-containing protein 7B; 3.4.19.12; Cellular zinc finger anti-NF-kappa-B protein; Zinc finger A20 domain-containing protein 1; Zinc finger protein Cezanne",
        "protein_names_refseq": "OTU domain containing 7B; OTU domain-containing protein 7B; cellular zinc finger anti-NF-kappaB Cezanne",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:310677);  (R-RNO-5357786);  (R-RNO-5357905);  (R-RNO-5357956);  (R-RNO-5689896)",
        "pathway_count": 5,
        "publication_count": 4,
        "publication_id_list": "22673903;34324860;35523269;38084712",
        "class_list": "",
        "function": "OTUD7B (Cezanne) ameliorates fibrosis after myocardial infarction via FAK-ERK/P38 MAPK signaling pathway., [RefSeq, PubMed]; Ovarian Tumor Domain-Containing 7B Attenuates Pathological Cardiac Hypertrophy by Inhibiting Ubiquitination and Degradation of Kruppel-Like Factor 4., [RefSeq, PubMed]; Transcranial direct-current stimulation protects against cerebral ischemia-reperfusion injury through regulating Cezanne-dependent signaling., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
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        "reported_s_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "3.4.19.12;2.3.2.27;2.7.11.1;2.3.2.31;2.7.11.10;2.7.11.25",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0008234 cysteine-type peptidase activity;GO:0070530 K63-linked polyubiquitin modification-dependent protein binding;GO:0004843 cysteine-type deubiquitinase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001701 in utero embryonic development;GO:0016579 protein deubiquitination;GO:0070536 protein K63-linked deubiquitination;GO:1900181 negative regulation of protein localization to nucleus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "A0ABK0LLW9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LN10-1",
        "uniprot_id": "A0ABK0LN10_RAT",
        "mass": 121792.0,
        "length": 1121,
        "protein_name": "GPI ethanolamine phosphate transferase 3, catalytic subunit",
        "gene_name": "Pigo",
        "organism": "Rat",
        "refseq_name": "GPI ethanolamine phosphate transferase 3 isoform X2",
        "refseq_ac": "XP_233141",
        "gene_names_uniprotkb": "Pigo",
        "gene_names_refseq": "Pigo",
        "protein_names_uniprotkb": "GPI ethanolamine phosphate transferase 3, catalytic subunit; Phosphatidylinositol-glycan biosynthesis class O protein",
        "protein_names_refseq": "GPI ethanolamine phosphate transferase 3 isoform X2",
        "tax_id": 10116,
        "disease": "hyperphosphatasia with impaired intellectual development syndrome 2 (Disease Ontology:DOID:0070434)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalytic subunit of the ethanolamine phosphate transferase 3 complex that transfers an ethanolamine phosphate (EtNP) from a phosphatidylethanolamine (PE) to the 6-OH position of the third alpha-1,2-linked mannose of the a 2-acyl-6-[alpha-D-mannosyl-(1->2)-alpha-D-mannosyl-(1->6)-2-phosphoethanolamine-alpha-D-mannosyl-(1->4)-alpha-D-glucosaminyl]-1-(1-radyl,2-acyl-sn-glycero-3-phospho)-1D-myo-inositol (also termed H6) intermediate to generate a a 2-acyl-6-[6-phosphoethanolamine-alpha-D-mannosyl-(1->2)-alpha-D-mannosyl-(1->6)-2-phosphoethanolamine-alpha-D-mannosyl-(1->4)-alpha-D-glucosaminyl]-1-(1-radyl,2-acyl-sn-glycero-3-phospho)-1D-myo-inositol (also termed H7) and participates in the tenth step of the glycosylphosphatidylinositol-anchor biosynthesis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0051377 mannose-ethanolamine phosphotransferase activity",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006506 GPI anchor biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LN10-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LND7-1",
        "uniprot_id": "A0ABK0LND7_RAT",
        "mass": 121756.0,
        "length": 1111,
        "protein_name": "C2 domain-containing protein 5",
        "gene_name": "C2cd5",
        "organism": "Rat",
        "refseq_name": "C2 domain-containing protein 5 isoform X8",
        "refseq_ac": "XP_038963851",
        "gene_names_uniprotkb": "C2cd5",
        "gene_names_refseq": "C2cd5; RGD1304592",
        "protein_names_uniprotkb": "C2 domain-containing protein 5",
        "protein_names_refseq": "C2 domain-containing protein 5 isoform X8",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Required for insulin-stimulated glucose transport and glucose transporter SLC2A4/GLUT4 translocation from intracellular glucose storage vesicle (GSV) to the plasma membrane (PM) in adipocytes. Binds phospholipid membranes in a calcium-dependent manner and is necessary for the optimal membrane fusion between SLC2A4/GLUT4 GSV and the PM., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
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        "go_biological_process": "GO:0070374 positive regulation of ERK1 and ERK2 cascade;GO:0032755 positive regulation of interleukin-6 production;GO:0002720 positive regulation of cytokine production involved in immune response;GO:0034142 toll-like receptor 4 signaling pathway;GO:0034154 toll-like receptor 7 signaling pathway",
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        "protein_name": "Collagen type XXIV alpha 1 chain",
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        "organism": "Rat",
        "refseq_name": "collagen alpha-1(XXIV) chain isoform X1",
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        "protein_names_refseq": "collagen alpha-1(XXIV) chain isoform X1",
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        "pathway": " (rno:499723);  (R-RNO-1650814);  (R-RNO-2022090);  (R-RNO-8874081);  (R-RNO-8948216)",
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        "protein_names_uniprotkb": "F-box only protein 10",
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        "protein_names_uniprotkb": "Rhomboid-related protein 2; 3.4.21.105",
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        "gene_names_uniprotkb": "Bmp8b; Oxct2b",
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        "protein_names_uniprotkb": "Succinyl-CoA:3-ketoacid-coenzyme A transferase; 2.8.3.5",
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        "function": "Key enzyme for ketone body catabolism. Transfers the CoA moiety from succinate to acetoacetate. Formation of the enzyme-CoA intermediate proceeds via an unstable anhydride species formed between the carboxylate groups of the enzyme and substrate., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "RBR-type E3 ubiquitin transferase",
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        "protein_names_uniprotkb": "RBR-type E3 ubiquitin transferase; 2.3.2.31",
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        "protein_name": "Serpin family A member 5",
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        "gene_names_uniprotkb": "Serpina5",
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        "protein_names_uniprotkb": "Serpin family A member 5",
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        "gene_names_uniprotkb": "Nxpe1; LOC100360202; RGD1566243",
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        "protein_names_uniprotkb": "Neurexophilin and PC-esterase domain family, member 1",
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        "go_molecular_function": "GO:0047186 N-acetylneuraminate 9-O-acetyltransferase activity",
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        "uniprot_canonical_ac": "A0ABK0LNJ4-1",
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        "length": 521,
        "protein_name": "Transmembrane and coiled-coil domain family 3",
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        "gene_names_uniprotkb": "Tmcc3",
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        "protein_names_uniprotkb": "Transmembrane and coiled-coil domain family 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "alcohol-related neurodevelopmental disorder (Disease Ontology:DOID:0050667)",
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        "length": 415,
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        "gene_names_uniprotkb": "Ctns",
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        "protein_names_uniprotkb": "Cystinosin",
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        "disease": "Fanconi syndrome (Disease Ontology:DOID:1062); cystinosis (Disease Ontology:DOID:1064)",
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        "function": "Cystine/H(+) symporter that mediates export of cystine, the oxidized dimer of cysteine, from lysosomes. Plays an important role in melanin synthesis by catalyzing cystine export from melanosomes, possibly by inhibiting pheomelanin synthesis. In addition to cystine export, also acts as a positive regulator of mTORC1 signaling in kidney proximal tubular cells, via interactions with components of the v-ATPase and Ragulator complexes. Also involved in small GTPase-regulated vesicle trafficking and lysosomal localization of LAMP2A, independently of cystine transporter activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "length": 1057,
        "protein_name": "Sin3A associated protein 130",
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        "refseq_ac": "XP_063133456",
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        "gene_names_refseq": "RGD1311657; Sap130",
        "protein_names_uniprotkb": "Sin3A associated protein 130",
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        "disease": "congenital heart disease (Disease Ontology:DOID:1682); hypoplastic left heart syndrome (Disease Ontology:DOID:9955)",
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        "gene_names_uniprotkb": "Ube2e1; LOC100366017",
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        "protein_names_uniprotkb": "E2 ubiquitin-conjugating enzyme; 2.3.2.23",
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        "pathway": " (rno:100366017);  (R-RNO-1169408);  (R-RNO-141430);  (R-RNO-174048);  (R-RNO-174084);  (R-RNO-174154);  (R-RNO-174178);  (R-RNO-174184);  (R-RNO-176407);  (R-RNO-176408);  (R-RNO-176412);  (R-RNO-179409);  (R-RNO-2467813);  (R-RNO-2559582);  (R-RNO-68867);  (R-RNO-69017);  (R-RNO-8866652);  (R-RNO-8866654);  (R-RNO-983168)",
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        "go_biological_process": "GO:0070936 protein K48-linked ubiquitination;GO:0032020 ISG15-protein conjugation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0016567 protein ubiquitination;GO:0000209 protein polyubiquitination",
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    {
        "uniprot_canonical_ac": "A0ABK0LND6-1",
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        "length": 300,
        "protein_name": "Ectodysplasin A2 receptor",
        "gene_name": "Eda2r",
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        "refseq_name": "tumor necrosis factor receptor superfamily member 27",
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        "gene_names_uniprotkb": "Eda2r",
        "gene_names_refseq": "Eda2r; RGD1564025",
        "protein_names_uniprotkb": "Ectodysplasin A2 receptor",
        "protein_names_refseq": "tumor necrosis factor receptor superfamily member 27",
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        "record_id": "A0ABK0LND6-1",
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    {
        "uniprot_canonical_ac": "A0ABK0LMY4-1",
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        "length": 1624,
        "protein_name": "Pappalysin-1",
        "gene_name": "Pappa",
        "organism": "Rat",
        "refseq_name": "pappalysin-1 precursor",
        "refseq_ac": "NP_001388248",
        "gene_names_uniprotkb": "Pappa; Pappa1",
        "gene_names_refseq": "Pappa1; Pappa",
        "protein_names_uniprotkb": "Pappalysin-1; 3.4.24.79; Insulin-like growth factor-dependent IGF-binding protein 4 protease; Pregnancy-associated plasma protein A",
        "protein_names_refseq": "pappalysin-1 precursor; pappalysin; pregnancy-associated plasma protein A",
        "tax_id": 10116,
        "disease": "hypertension (Disease Ontology:DOID:10763); arteriosclerosis (Disease Ontology:DOID:2349); coronary artery disease (Disease Ontology:DOID:3393); carotid artery disease (Disease Ontology:DOID:3407); myocardial infarction (Disease Ontology:DOID:5844); degenerative disc disease (Disease Ontology:DOID:90); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": " (R-RNO-381426)",
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        "publication_id_list": "23169786;27537370;34906040;39244846",
        "class_list": "",
        "function": "Differential effects of chronic (transgenic) and transient (endogenous) PAPP-A expression on neointimal formation following vascular injury that may be due in part to the differential impact on IGF-I signaling., [RefSeq, PubMed]; IGFBP-4 Proteolysis by PAPP-A in a Primary Culture of Rat Neonatal Cardiomyocytes under Normal and Hypertrophic Conditions., [RefSeq, PubMed]; Pappa has been shown to positively regulate the IGF signaling pathway, which is required for proper mammary gland/breast development and is of increasing interest in breast cancer pathogenesis. Mcs5c-mediated regulation of Pappa appears to occur through age-dependent and mammary gland-specific chromatin looping, as well as genotype-dependent CpG island shore methylation Publication Status: Online-Only, [RefSeq, PubMed]; Specific cleavage of IGFBP-4 by papp-a in nervous tissue., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0008237 metallopeptidase activity;GO:0004222 metalloendopeptidase activity;GO:0046872 metal ion binding;GO:0004175 endopeptidase activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005576 extracellular region",
        "go_biological_process": "GO:0006508 proteolysis;GO:0007166 cell surface receptor signaling pathway;GO:0007565 female pregnancy;GO:0030163 protein catabolic process;GO:0032354 response to follicle-stimulating hormone",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "A0ABK0LMY4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LLS5-1",
        "uniprot_id": "A0ABK0LLS5_RAT",
        "mass": 35860.0,
        "length": 325,
        "protein_name": "Probable E3 SUMO-protein ligase RNF212",
        "gene_name": "Rnf212",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rnf212",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Probable E3 SUMO-protein ligase RNF212; Probable E3 SUMO-protein transferase RNF212; RING finger protein 212",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "spermatogenic failure (Disease Ontology:DOID:0111910); spermatogenic failure 62 (Disease Ontology:DOID:0112351)",
        "pathway": " (rno:689721)",
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        "class_list": "",
        "function": "SUMO E3 ligase that acts as a regulator of crossing-over during meiosis: required to couple chromosome synapsis to the formation of crossover-specific recombination complexes. Localizes to recombination sites and stabilizes meiosis-specific recombination factors, such as MutS-gamma complex proteins (MSH4 and MSH5) and TEX11. May mediate sumoylation of target proteins MSH4 and/or MSH5, leading to enhance their binding to recombination sites. Acts as a limiting factor for crossover designation and/or reinforcement and plays an antagonist role with CCNB1IP1/HEI10 in the regulation of meiotic recombination., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0019789 SUMO transferase activity",
        "go_cellular_component": "GO:0000795 synaptonemal complex",
        "go_biological_process": "GO:0007129 homologous chromosome pairing at meiosis;GO:0007131 reciprocal meiotic recombination;GO:0006311 meiotic gene conversion;GO:0051026 chiasma assembly",
        "synthesized_glycan_count": 0,
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        "record_type": "protein"
    },
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        "length": 1304,
        "protein_name": "Zinc finger protein 541",
        "gene_name": "Zfp541",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp541",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 541",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003714 transcription corepressor activity",
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        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007283 spermatogenesis;GO:0030154 cell differentiation;GO:0045892 negative regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LNF8-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "A0ABK0LLW4-1",
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        "length": 1009,
        "protein_name": "Probable RNA-binding protein 19",
        "gene_name": "Rbm19",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rbm19",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Probable RNA-binding protein 19; RNA-binding motif protein 19",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "class_list": "",
        "function": "Plays a role in embryo pre-implantation development., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "record_id": "A0ABK0LLW4-1",
        "record_type": "protein"
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        "protein_name": "Mesenteric estrogen-dependent adipogenesis",
        "gene_name": "Medag",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Medag",
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        "protein_names_uniprotkb": "Mesenteric estrogen-dependent adipogenesis",
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        "protein_name": "Collagen type VIII alpha 2 chain",
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        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Col8a2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Collagen type VIII alpha 2 chain",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "posterior polymorphous corneal dystrophy 2 (Disease Ontology:DOID:0110856); Fuchs' endothelial dystrophy (Disease Ontology:DOID:11555)",
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        "protein_name": "Protein phosphatase 1, regulatory subunit 13B",
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        "refseq_ac": "XP_038968346",
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        "gene_names_refseq": "Ppp1r13b",
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        "protein_names_refseq": "apoptosis-stimulating of p53 protein 1 isoform X2",
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        "refseq_name": "nucleolar protein 4-like isoform X1",
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        "gene_names_refseq": "Nol4l",
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        "protein_names_refseq": "nucleolar protein 4-like isoform X1",
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    {
        "uniprot_canonical_ac": "A0ABK0LL59-1",
        "uniprot_id": "A0ABK0LL59_RAT",
        "mass": 53127.0,
        "length": 475,
        "protein_name": "M-phase inducer phosphatase",
        "gene_name": "Cdc25c",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cdc25c",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "M-phase inducer phosphatase; 3.1.3.48",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "endometrial hyperplasia (Disease Ontology:DOID:0080365); prostate cancer (Disease Ontology:DOID:10283); endometrial cancer (Disease Ontology:DOID:1380); breast cancer (Disease Ontology:DOID:1612); vulva squamous cell carcinoma (Disease Ontology:DOID:2101); cervical cancer (Disease Ontology:DOID:4362)",
        "pathway": " (rno:307511);  (R-RNO-156711);  (R-RNO-176187);  (R-RNO-5625740);  (R-RNO-6804115);  (R-RNO-69273);  (R-RNO-75035)",
        "pathway_count": 7,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Functions as a dosage-dependent inducer in mitotic control. Tyrosine protein phosphatase required for progression of the cell cycle. When phosphorylated, highly effective in activating G2 cells into prophase. Directly dephosphorylates CDK1 and activates its kinase activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Tyrosine protein phosphatase which functions as a dosage-dependent inducer of mitotic progression., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_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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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 6,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.1.3.48;2.7.10.1;3.1.3.16;3.1.3.2;3.1.3.21;3.1.3.18;3.1.3.67;3.1.3.-;3.1.3.27;3.1.3.5;2.7.11.22;2.7.11.23;2.7.11.21;2.7.11.13;2.7.11.17;2.7.11.1;2.4.99.18",
        "go_molecular_function": "GO:0004725 protein tyrosine phosphatase activity;GO:0019901 protein kinase binding;GO:0050699 WW domain binding;GO:0120283 protein serine/threonine kinase binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005758 mitochondrial intermembrane space;GO:0016607 nuclear speck;GO:0048471 perinuclear region of cytoplasm",
        "go_biological_process": "GO:0010971 positive regulation of G2/M transition of mitotic cell cycle;GO:0051301 cell division;GO:0000086 G2/M transition of mitotic cell cycle;GO:0110032 positive regulation of G2/MI transition of meiotic cell cycle;GO:0007283 spermatogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LL59-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LLF4-1",
        "uniprot_id": "A0ABK0LLF4_RAT",
        "mass": 153383.0,
        "length": 1406,
        "protein_name": "PAS domain-containing serine/threonine-protein kinase",
        "gene_name": "Pask",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pask",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "PAS domain-containing serine/threonine-protein kinase; 2.7.11.1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:301617)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Serine/threonine-protein kinase involved in energy homeostasis and protein translation. Phosphorylates EEF1A1, GYS1, PDX1 and RPS6. Probably plays a role under changing environmental conditions (oxygen, glucose, nutrition), rather than under standard conditions. Acts as a sensor involved in energy homeostasis: regulates glycogen synthase synthesis by mediating phosphorylation of GYS1, leading to GYS1 inactivation. May be involved in glucose-stimulated insulin production in pancreas and regulation of glucagon secretion by glucose in alpha cells; however such data require additional evidences. May play a role in regulation of protein translation by phosphorylating EEF1A1, leading to increase translation efficiency. May also participate in respiratory regulation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 2,
        "predicted_c_glycosites": 0,
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        "reported_mutagensis": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 2,
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        "secondary_ac_list": "",
        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0008289 lipid binding;GO:0035091 phosphatidylinositol binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0035556 intracellular signal transduction;GO:0045719 negative regulation of glycogen biosynthetic process;GO:0006468 protein phosphorylation;GO:0097009 energy homeostasis;GO:0046777 protein autophosphorylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LLF4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LM52-1",
        "uniprot_id": "A0ABK0LM52_RAT",
        "mass": 57736.0,
        "length": 513,
        "protein_name": "T-complex protein 10b",
        "gene_name": "Tcp10b",
        "organism": "Rat",
        "refseq_name": "T-complex protein 10A homolog 2 isoform X2",
        "refseq_ac": "XP_017444582",
        "gene_names_uniprotkb": "Tcp10b",
        "gene_names_refseq": "Tcp10b",
        "protein_names_uniprotkb": "T-complex protein 10b",
        "protein_names_refseq": "T-complex protein 10A homolog 2 isoform X2",
        "tax_id": 10116,
        "disease": "primary autosomal recessive microcephaly 6 (Disease Ontology:DOID:0070290); microcephaly (Disease Ontology:DOID:10907)",
        "pathway": " (rno:308169)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
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        "ec_number_list": "",
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        "go_cellular_component": "",
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        "record_id": "A0ABK0LM52-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LLD5-1",
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        "length": 515,
        "protein_name": "Major facilitator superfamily domain containing 4B2",
        "gene_name": "Mfsd4b2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mfsd4b2; RGD1304770",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Major facilitator superfamily domain containing 4B2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:309810)",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0022857 transmembrane transporter activity",
        "go_cellular_component": "GO:0016020 membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LLD5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LM30-1",
        "uniprot_id": "A0ABK0LM30_RAT",
        "mass": 130414.0,
        "length": 1188,
        "protein_name": "Laminin subunit gamma-2",
        "gene_name": "Lamc2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Lamc2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Laminin subunit gamma-2; Epiligrin subunit gamma; Kalinin subunit gamma; Kalinin/nicein/epiligrin 100 kDa subunit; Laminin B2t chain; Laminin-5 subunit gamma; Nicein subunit gamma",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); junctional epidermolysis bullosa Herlitz type (Disease Ontology:DOID:0060737); junctional epidermolysis bullosa non-Herlitz type (Disease Ontology:DOID:0060738); junctional epidermolysis bullosa (Disease Ontology:DOID:3209); lung squamous cell carcinoma (Disease Ontology:DOID:3907); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung small cell carcinoma (Disease Ontology:DOID:5409)",
        "pathway": " (rno:192362)",
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        "class_list": "",
        "function": "",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008201 heparin binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005938 cell cortex;GO:0048471 perinuclear region of cytoplasm;GO:0005604 basement membrane;GO:0005607 laminin-2 complex",
        "go_biological_process": "GO:0008284 positive regulation of cell population proliferation;GO:0030335 positive regulation of cell migration;GO:0009887 animal organ morphogenesis;GO:0007411 axon guidance;GO:0009888 tissue development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LM30-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LLE3-1",
        "uniprot_id": "A0ABK0LLE3_RAT",
        "mass": 50022.0,
        "length": 446,
        "protein_name": "Tubulin alpha chain",
        "gene_name": "Tubal3",
        "organism": "Rat",
        "refseq_name": "tubulin alpha chain-like 3",
        "refseq_ac": "NP_001427053",
        "gene_names_uniprotkb": "Tubal3",
        "gene_names_refseq": "Tubal3",
        "protein_names_uniprotkb": "Tubulin alpha chain",
        "protein_names_refseq": "tubulin alpha chain-like 3",
        "tax_id": 10116,
        "disease": "lissencephaly (Disease Ontology:DOID:0050453); polymicrogyria (Disease Ontology:DOID:0080918); lissencephaly 3 (Disease Ontology:DOID:0112232); microlissencephaly (Disease Ontology:DOID:0112234)",
        "pathway": " (R-RNO-190840);  (R-RNO-2132295);  (R-RNO-2467813);  (R-RNO-2500257);  (R-RNO-3371497);  (R-RNO-380320);  (R-RNO-437239);  (R-RNO-5620920);  (R-RNO-5626467);  (R-RNO-5663220);  (R-RNO-6807878);  (R-RNO-6811434);  (R-RNO-6811436);  (R-RNO-68877);  (R-RNO-8852276);  (R-RNO-8955332);  (R-RNO-9646399);  (R-RNO-9648025);  (R-RNO-9668328);  (R-RNO-983189);  (R-RNO-9833482)",
        "pathway_count": 21,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms. Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "3.6.5.2;3.6.1.1;3.6.5.-;3.6.5.3;2.3.2.27;2.7.11.1;3.6.5.5;3.6.1.5;3.6.1.-;3.6.5.4",
        "go_molecular_function": "GO:0005200 structural constituent of cytoskeleton;GO:0005525 GTP binding;GO:0016787 hydrolase activity;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005874 microtubule",
        "go_biological_process": "GO:0000278 mitotic cell cycle;GO:0000226 microtubule cytoskeleton organization;GO:0007017 microtubule-based process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LLE3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LM80-1",
        "uniprot_id": "A0ABK0LM80_RAT",
        "mass": 18106.0,
        "length": 166,
        "protein_name": "LIM domain transcription factor LMO4",
        "gene_name": "Lmo4",
        "organism": "Rat",
        "refseq_name": "LIM domain transcription factor LMO4 isoform X1",
        "refseq_ac": "XP_063138297",
        "gene_names_uniprotkb": "Lmo4",
        "gene_names_refseq": "Lmo4",
        "protein_names_uniprotkb": "LIM domain transcription factor LMO4; Breast tumor autoantigen; LIM domain only protein 4",
        "protein_names_refseq": "LIM domain transcription factor LMO4 isoform X1",
        "tax_id": 10116,
        "disease": "anencephaly (Disease Ontology:DOID:0060668)",
        "pathway": " (rno:362051)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Transcription cofactor. Plays a role in establishing motor neuron identity, in concert with MNX1, acting, at least in part, to disrupt LDB1-LHX3 complexes thereby negatively modulating interneuron genes in motor neurons., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0003712 transcription coregulator activity;GO:0003714 transcription corepressor activity;GO:0140297 DNA-binding transcription factor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0031252 cell leading edge;GO:0090575 RNA polymerase II transcription regulator complex",
        "go_biological_process": "GO:0050793 regulation of developmental process;GO:0006351 DNA-templated transcription;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0009888 tissue development;GO:0021520 spinal cord motor neuron cell fate specification",
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        "length": 211,
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Nrtn",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Neurturin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Hirschsprung's disease (Disease Ontology:DOID:10487)",
        "pathway": " (rno:84423);  (R-RNO-5673001);  (R-RNO-8853659)",
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        "function": "Growth factor that supports the survival of sympathetic neurons in culture. May regulate the development and maintenance of the CNS. Involved in the development of the neural crest. Might control the size of non-neuronal cell population such as haemopoietic cells. Acts by binding to its coreceptor, GFRA2, leading to autophosphorylation and activation of the RET receptor. Heparan sulfate-binding is required for signaling., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0030971 receptor tyrosine kinase binding;GO:0008083 growth factor activity;GO:0030116 glial cell-derived neurotrophic factor receptor binding;GO:1904399 heparan sulfate binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005576 extracellular region;GO:0030424 axon",
        "go_biological_process": "GO:0035860 glial cell-derived neurotrophic factor receptor signaling pathway;GO:0031175 neuron projection development;GO:0048731 system development;GO:0007169 cell surface receptor protein tyrosine kinase signaling pathway;GO:0001755 neural crest cell migration",
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        "length": 959,
        "protein_name": "Oxysterol-binding protein",
        "gene_name": "Osbpl6",
        "organism": "Rat",
        "refseq_name": "oxysterol-binding protein-related protein 6 isoform a",
        "refseq_ac": "NP_001418626",
        "gene_names_uniprotkb": "Osbpl6",
        "gene_names_refseq": "Osbpl6",
        "protein_names_uniprotkb": "Oxysterol-binding protein",
        "protein_names_refseq": "oxysterol-binding protein-related protein 6 isoform a; oxysterol-binding protein-related protein 6",
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        "go_biological_process": "GO:0006869 lipid transport;GO:0006699 bile acid biosynthetic process;GO:0032374 regulation of cholesterol transport",
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        "protein_name": "Pleckstrin homology and RhoGEF domain containing G3",
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        "gene_names_uniprotkb": "Plekhg3",
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        "protein_names_uniprotkb": "Pleckstrin homology and RhoGEF domain containing G3",
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        "pathway": " (R-RNO-8980692);  (R-RNO-9013148);  (R-RNO-9013149);  (R-RNO-9013406);  (R-RNO-9013408)",
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        "go_molecular_function": "GO:0005085 guanyl-nucleotide exchange factor activity;GO:0031267 small GTPase binding;GO:0003779 actin binding",
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        "record_type": "protein"
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        "length": 1207,
        "protein_name": "Fibronectin type III domain-containing protein 3B",
        "gene_name": "Fndc3b",
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        "refseq_name": "fibronectin type III domain-containing protein 3B",
        "refseq_ac": "NP_001178633",
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        "gene_names_refseq": "Fndc3b; RGD1311673",
        "protein_names_uniprotkb": "Fibronectin type III domain-containing protein 3B; Factor for adipocyte differentiation 104; HCV NS5A-binding protein 37",
        "protein_names_refseq": "fibronectin type III domain-containing protein 3B",
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        "record_id": "A0ABK0LL52-1",
        "record_type": "protein"
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        "uniprot_id": "A0ABK0LN35_RAT",
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        "length": 572,
        "protein_name": "Multidrug and toxin extrusion protein",
        "gene_name": "Slc47a2",
        "organism": "Rat",
        "refseq_name": "multidrug and toxin extrusion protein 2",
        "refseq_ac": "NP_001178849",
        "gene_names_uniprotkb": "Slc47a2",
        "gene_names_refseq": "RGD1562382; Slc47a2",
        "protein_names_uniprotkb": "Multidrug and toxin extrusion protein",
        "protein_names_refseq": "multidrug and toxin extrusion protein 2; solute carrier family 47 (multidrug and toxin extrusion), member 2",
        "tax_id": 10116,
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        "pathway": " (rno:497921)",
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        "go_molecular_function": "GO:0042910 xenobiotic transmembrane transporter activity;GO:0022857 transmembrane transporter activity;GO:0015297 antiporter activity;GO:0140968 polyspecific organic cation:proton antiporter activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0005886 plasma membrane",
        "go_biological_process": "GO:1990961 xenobiotic detoxification by transmembrane export across the plasma membrane;GO:0015695 organic cation transport",
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        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0ABK0LMR7-1",
        "uniprot_id": "A0ABK0LMR7_RAT",
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        "length": 785,
        "protein_name": "Phosphoinositide phospholipase C",
        "gene_name": "Plcd3",
        "organism": "Rat",
        "refseq_name": "1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3",
        "refseq_ac": "NP_001099315",
        "gene_names_uniprotkb": "Plcd3",
        "gene_names_refseq": "Plcd3",
        "protein_names_uniprotkb": "Phosphoinositide phospholipase C; 3.1.4.11",
        "protein_names_refseq": "1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3",
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        "disease": "",
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        "function": "Hydrolyzes the phosphatidylinositol 4,5-bisphosphate (PIP2) to generate 2 second messenger molecules diacylglycerol (DAG) and inositol 1,4,5-trisphosphate (IP3). DAG mediates the activation of protein kinase C (PKC), while IP3 releases Ca(2+) from intracellular stores. Essential for trophoblast and placental development. May participate in cytokinesis by hydrolyzing PIP2 at the cleavage furrow. Regulates neurite outgrowth through the inhibition of RhoA/Rho kinase signaling., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Results indicate that PLCdelta1 and PLCdelta3 are required for cardiomyocyte survival and normal cardiac function. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "ec_number_list": "3.1.4.11",
        "go_molecular_function": "GO:0004435 phosphatidylinositol-4,5-bisphosphate phospholipase C activity;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0032154 cleavage furrow",
        "go_biological_process": "GO:0035556 intracellular signal transduction;GO:0016042 lipid catabolic process;GO:0001525 angiogenesis;GO:0042127 regulation of cell population proliferation;GO:0060716 labyrinthine layer blood vessel development",
        "synthesized_glycan_count": 0,
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        "length": 308,
        "protein_name": "Cyclin B1 interacting protein 1",
        "gene_name": "Ccnb1ip1",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase CCNB1IP1 isoform X1",
        "refseq_ac": "XP_038949511",
        "gene_names_uniprotkb": "Ccnb1ip1",
        "gene_names_refseq": "Ccnb1ip1",
        "protein_names_uniprotkb": "Cyclin B1 interacting protein 1",
        "protein_names_refseq": "E3 ubiquitin-protein ligase CCNB1IP1 isoform X1",
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        "protein_names_uniprotkb": "Pre-mRNA-splicing factor CWC22 homolog; Nucampholin homolog",
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        "protein_name": "non-specific serine/threonine protein kinase",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Modulator of apoptosis 1",
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        "publication_id_list": "",
        "class_list": "",
        "function": "May play a role in sperm motility, especially in the regulation of flagellar function., [UniProtKB, UniProtKB]",
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding",
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    },
    {
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        "length": 307,
        "protein_name": "Olfactory receptor family 12 subfamily J member 3",
        "gene_name": "Or12j3",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr297",
        "refseq_ac": "NP_001000234",
        "gene_names_uniprotkb": "Or12j3",
        "gene_names_refseq": "Olr297; Or12j3",
        "protein_names_uniprotkb": "Olfactory receptor family 12 subfamily J member 3",
        "protein_names_refseq": "olfactory receptor 297; olfactory receptor Olr297; olfactory receptor gene Olr297",
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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]; Possible taste receptor., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LNM5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LNM7-1",
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        "length": 317,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or13c3c",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr847",
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        "gene_names_uniprotkb": "Or13c3c",
        "gene_names_refseq": "Olr847; Or13c3c; ratchr5-70187780-70186827_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 13C3-like; olfactory receptor 847; olfactory receptor Olr847; olfactory receptor gene Olr847",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:298045)",
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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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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LNM7-1",
        "record_type": "protein"
    },
    {
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        "length": 135,
        "protein_name": "Ig-like domain-containing protein",
        "gene_name": "",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "reported_c_glycosites_with_glycan": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0019814 immunoglobulin complex",
        "go_biological_process": "GO:0002250 adaptive immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LNM9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LP56-1",
        "uniprot_id": "A0ABK0LP56_RAT",
        "mass": 195686.0,
        "length": 1729,
        "protein_name": "LIM domain 7",
        "gene_name": "Lmo7",
        "organism": "Rat",
        "refseq_name": "LIM domain only protein 7 isoform 1",
        "refseq_ac": "NP_001001515",
        "gene_names_uniprotkb": "Lmo7",
        "gene_names_refseq": "Lmo7",
        "protein_names_uniprotkb": "LIM domain 7",
        "protein_names_refseq": "LIM domain only 7; LIM domain only protein 7 isoform 1; LIM domain only protein 7; TGF-beta induced protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-8951664);  (R-RNO-983168)",
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        "publication_count": 4,
        "publication_id_list": "15140894;16641100;22673903;26370512",
        "class_list": "",
        "function": "JNK-dependent LMO7b phosphorylation is required for hypercapnia-mediated Na,K-ATPase endocytosis., [RefSeq, PubMed]; LMO7 is an afadin- and alpha-actinin-binding protein that connects the nectin-afadin and E-cadherin-catenin systems through alpha-actinin., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0042805 actinin binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005635 nuclear envelope;GO:0005737 cytoplasm;GO:0009986 cell surface;GO:0005912 adherens junction",
        "go_biological_process": "GO:0030155 regulation of cell adhesion;GO:0023051 regulation of signaling;GO:0010604 positive regulation of macromolecule metabolic process;GO:0080090 regulation of primary metabolic process;GO:0045944 positive regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "A0ABK0LP56-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LNT5-1",
        "uniprot_id": "A0ABK0LNT5_RAT",
        "mass": 80726.0,
        "length": 786,
        "protein_name": "POU domain protein",
        "gene_name": "Pou2f2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pou2f2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "POU domain protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "immune system disease (Disease Ontology:DOID:2914)",
        "pathway": " (R-RNO-6807505)",
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        "class_list": "",
        "function": "Transcription factor that binds to the octamer motif (5'-ATTTGCAT-3') and activates the promoters of the genes for some small nuclear RNAs (snRNA) and of genes such as those for histone H2B and immunoglobulins. Modulates transcription transactivation by NR3C1, AR and PGR., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0003700 DNA-binding transcription factor activity;GO:0019904 protein domain specific binding;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0002335 mature B cell differentiation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription;GO:0032755 positive regulation of interleukin-6 production",
        "synthesized_glycan_count": 0,
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        "record_id": "A0ABK0LNT5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LPW7-1",
        "uniprot_id": "A0ABK0LPW7_RAT",
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        "length": 379,
        "protein_name": "Brain expressed, associated with NEDD4, 1",
        "gene_name": "Bean1",
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        "protein_names_uniprotkb": "Brain expressed, associated with NEDD4, 1",
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        "tax_id": 10116,
        "disease": "spinocerebellar ataxia 31 (Disease Ontology:DOID:0050980)",
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    {
        "uniprot_canonical_ac": "A0ABK0LQZ5-1",
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        "length": 761,
        "protein_name": "Centrosomal protein kizuna",
        "gene_name": "Kiz",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Kiz; Plk1s1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Centrosomal protein kizuna; Polo-like kinase 1 substrate 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa 69 (Disease Ontology:DOID:0110410)",
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        "function": "Centrosomal protein required for establishing a robust mitotic centrosome architecture that can endure the forces that converge on the centrosomes during spindle formation. Required for stabilizing the expanded pericentriolar material around the centriole., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "refseq_name": "GPI ethanolamine phosphate transferase 1 isoform X2",
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        "function": "Ethanolamine phosphate transferase involved in glycosylphosphatidylinositol-anchor biosynthesis. Transfers ethanolamine phosphate to the first alpha-1,4-linked mannose of the glycosylphosphatidylinositol precursor of GPI-anchor., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "DENN domain containing 1A",
        "protein_names_refseq": "DENN domain-containing protein 1A isoform X8",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005681 spliceosomal complex;GO:0034693 U11/U12 snRNP;GO:0005689 U12-type spliceosomal complex",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LNS5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LR08-1",
        "uniprot_id": "A0ABK0LR08_RAT",
        "mass": 102325.0,
        "length": 908,
        "protein_name": "Flap endonuclease GEN homolog 1",
        "gene_name": "Gen1",
        "organism": "Rat",
        "refseq_name": "flap endonuclease GEN homolog 1 isoform X2",
        "refseq_ac": "XP_038967872",
        "gene_names_uniprotkb": "Gen1",
        "gene_names_refseq": "Gen1; RGD1559792",
        "protein_names_uniprotkb": "Flap endonuclease GEN homolog 1",
        "protein_names_refseq": "flap endonuclease GEN homolog 1 isoform X2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:298884);  (R-RNO-5693568)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0000400 four-way junction DNA binding;GO:0017108 5'-flap endonuclease activity;GO:0000287 magnesium ion binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005813 centrosome",
        "go_biological_process": "GO:0010824 regulation of centrosome duplication;GO:0000724 double-strand break repair via homologous recombination;GO:0031297 replication fork processing;GO:0090267 positive regulation of mitotic cell cycle spindle assembly checkpoint;GO:0071139 resolution of DNA recombination intermediates",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LR08-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LPT0-1",
        "uniprot_id": "A0ABK0LPT0_RAT",
        "mass": 40277.0,
        "length": 365,
        "protein_name": "Solute carrier family 35 member C1",
        "gene_name": "Slc35c1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Slc35c1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Solute carrier family 35 member C1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "congenital disorder of glycosylation type II (Disease Ontology:DOID:0050571); congenital disorder of glycosylation type IIc (Disease Ontology:DOID:0070255)",
        "pathway": " (rno:311204);  (R-RNO-6787639);  (R-RNO-727802)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Putative transporter., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0015297 antiporter activity;GO:0005457 GDP-fucose transmembrane transporter activity",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0016020 membrane;GO:0000139 Golgi membrane",
        "go_biological_process": "GO:0036085 GDP-fucose import into Golgi lumen;GO:0042351 'de novo' GDP-L-fucose biosynthetic process;GO:0042352 GDP-L-fucose salvage;GO:0009247 glycolipid biosynthetic process;GO:0045746 negative regulation of Notch signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LPT0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LQM7-1",
        "uniprot_id": "A0ABK0LQM7_RAT",
        "mass": 25881.0,
        "length": 238,
        "protein_name": "Glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1",
        "gene_name": "Gpihbp1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Gpihbp1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "familial GPIHBP1 deficiency (Disease Ontology:DOID:0111420)",
        "pathway": " (rno:300027);  (R-RNO-163125);  (R-RNO-8963889);  (R-RNO-8963901);  (R-RNO-975634)",
        "pathway_count": 5,
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        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0035473 lipase binding;GO:0035478 chylomicron binding;GO:0008035 high-density lipoprotein particle binding;GO:0060230 lipoprotein lipase activator activity;GO:0071813 lipoprotein particle binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0016323 basolateral plasma membrane;GO:0009897 external side of plasma membrane;GO:0016324 apical plasma membrane",
        "go_biological_process": "GO:0070328 triglyceride homeostasis;GO:0006869 lipid transport;GO:0006886 intracellular protein transport;GO:0042632 cholesterol homeostasis;GO:0050821 protein stabilization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LQM7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LPF7-1",
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        "length": 203,
        "protein_name": "Heat shock protein family B (small) member 9",
        "gene_name": "Hspb9",
        "organism": "Rat",
        "refseq_name": "heat shock protein beta-9",
        "refseq_ac": "NP_001102305",
        "gene_names_uniprotkb": "Hspb9",
        "gene_names_refseq": "Hspb9",
        "protein_names_uniprotkb": "Heat shock protein family B (small) member 9",
        "protein_names_refseq": "heat shock protein beta-9; heat shock protein, alpha-crystallin-related, B9",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363681)",
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        "go_biological_process": "",
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        "hit_score": 0.2,
        "record_id": "A0ABK0LPF7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LNU8-1",
        "uniprot_id": "A0ABK0LNU8_RAT",
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        "length": 187,
        "protein_name": "Testis expressed 12",
        "gene_name": "Tex12",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tex12",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Testis expressed 12",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:690393)",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0000801 central element;GO:0005694 chromosome;GO:0000795 synaptonemal complex",
        "go_biological_process": "GO:0007130 synaptonemal complex assembly;GO:0000711 meiotic DNA repair synthesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LNU8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LNW8-1",
        "uniprot_id": "A0ABK0LNW8_RAT",
        "mass": 43827.0,
        "length": 384,
        "protein_name": "Lysophosphatidic acid phosphatase type 6",
        "gene_name": "Acp6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Acp6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Lysophosphatidic acid phosphatase type 6; 3.1.3.2; Acid phosphatase 6, lysophosphatidic",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295305);  (R-RNO-1483166)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Hydrolyzes lysophosphatidic acid (LPA) containing a medium length fatty acid chain to the corresponding monoacylglycerol. Has highest activity with lysophosphatidic acid containing myristate (C14:0), monounsaturated oleate (C18:1) or palmitate (C16:0), and lower activity with C18:0 and C6:0 lysophosphatidic acid., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "3.1.3.2;3.1.3.4;3.6.1.75;3.1.3.1;3.1.3.48;3.1.3.-;3.1.3.106;3.9.1.1;3.1.3.5;3.3.2.10;3.1.3.76",
        "go_molecular_function": "GO:0052642 lysophosphatidic acid phosphatase activity;GO:0003993 acid phosphatase activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005737 cytoplasm",
        "go_biological_process": "GO:2001311 lysobisphosphatidic acid metabolic process;GO:0002244 hematopoietic progenitor cell differentiation;GO:0006644 phospholipid metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LNW8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LQY8-1",
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        "length": 619,
        "protein_name": "E3 ubiquitin-protein ligase",
        "gene_name": "Dtx4",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase DTX4 isoform 1",
        "refseq_ac": "NP_001388322",
        "gene_names_uniprotkb": "Dtx4",
        "gene_names_refseq": "Dtx4; LRRGT00037",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase; 2.3.2.27",
        "protein_names_refseq": "E3 ubiquitin-protein ligase DTX4 isoform 1; E3 ubiquitin-protein ligase DTX4; deltex 4 homolog; deltex 4, E3 ubiquitin ligase; deltex homolog 4; protein deltex-4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:293774);  (R-RNO-2122948);  (R-RNO-3134975);  (R-RNO-3270619)",
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        "secondary_ac_list": "",
        "ec_number_list": "2.3.2.26;2.3.2.27;2.7.11.1",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005813 centrosome",
        "go_biological_process": "GO:0007219 Notch signaling pathway;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0016567 protein ubiquitination;GO:0010498 proteasomal protein catabolic process;GO:0070936 protein K48-linked ubiquitination",
        "synthesized_glycan_count": 0,
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        "record_id": "A0ABK0LQY8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LNP9-1",
        "uniprot_id": "A0ABK0LNP9_RAT",
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        "length": 513,
        "protein_name": "SERTA domain containing 4",
        "gene_name": "Sertad4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Sertad4",
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        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005765 lysosomal membrane;GO:0031901 early endosome membrane;GO:0034451 centriolar satellite;GO:0016020 membrane",
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        "gene_names_uniprotkb": "Fblim1",
        "gene_names_refseq": "Cal; Fblim1; Hnrnpl; hnRNP L",
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        "protein_names_refseq": "cyclic AMP-responsive element-binding protein 5 isoform X2",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0042802 identical protein 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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        "protein_names_uniprotkb": "Large ribosomal subunit protein mL48; 39S ribosomal protein L48, mitochondrial",
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        "length": 442,
        "protein_name": "Protein Wnt",
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        "protein_names_uniprotkb": "Protein Wnt",
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        "function": "Ligand for members of the frizzled family of seven transmembrane receptors., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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    {
        "uniprot_canonical_ac": "A0ABK0LNP5-1",
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        "length": 1144,
        "protein_name": "Calcium voltage-gated channel auxiliary subunit alpha2delta 4",
        "gene_name": "Cacna2d4",
        "organism": "Rat",
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        "refseq_ac": "NP_001178680",
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        "gene_names_refseq": "Cacna2d4; RGD1562038",
        "protein_names_uniprotkb": "Calcium voltage-gated channel auxiliary subunit alpha2delta 4",
        "protein_names_refseq": "calcium channel, voltage-dependent, alpha 2/delta subunit 4; voltage-dependent calcium channel subunit alpha-2/delta-4",
        "tax_id": 10116,
        "disease": "nicotine dependence (Disease Ontology:DOID:0050742); retinal cone dystrophy 4 (Disease Ontology:DOID:0081023); heart conduction disease (Disease Ontology:DOID:10273)",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0005245 voltage-gated calcium channel activity",
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        "record_id": "A0ABK0LNP5-1",
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    {
        "uniprot_canonical_ac": "A0ABK0LP46-1",
        "uniprot_id": "A0ABK0LP46_RAT",
        "mass": 56858.0,
        "length": 530,
        "protein_name": "T-box transcription factor 1",
        "gene_name": "Tbx1",
        "organism": "Rat",
        "refseq_name": "T-box transcription factor TBX1 isoform 1",
        "refseq_ac": "NP_001402633",
        "gene_names_uniprotkb": "Tbx1",
        "gene_names_refseq": "T-box 1; Tbx1",
        "protein_names_uniprotkb": "T-box transcription factor 1",
        "protein_names_refseq": "T-box transcription factor TBX1 isoform 1; T-box transcription factor TBX1",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); chromosome 22q11.2 deletion syndrome, distal (Disease Ontology:DOID:0060413); sensorineural hearing loss (Disease Ontology:DOID:10003); otitis media (Disease Ontology:DOID:10754); DiGeorge syndrome (Disease Ontology:DOID:11198); hypoparathyroidism (Disease Ontology:DOID:11199); velocardiofacial syndrome (Disease Ontology:DOID:12583); ventricular septal defect (Disease Ontology:DOID:1657); congenital heart disease (Disease Ontology:DOID:1682); epilepsy (Disease Ontology:DOID:1826); acute kidney failure (Disease Ontology:DOID:3021); tetralogy of Fallot (Disease Ontology:DOID:6419); acute myocardial infarction (Disease Ontology:DOID:9408)",
        "pathway": " (rno:360737)",
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        "publication_id_list": "31982878;37227215",
        "class_list": "",
        "function": "Brachyury positively regulates extracellular matrix synthesis via directly promoting aggrecan transcription in nucleus pulposus., [RefSeq, PubMed]; MiR-144 acts as a proliferation inhibitor in cardiomyocytes via the TBX1/JAK2/STAT1 axis, [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "go_cellular_component": "GO:0005634 nucleus;GO:0000785 chromatin",
        "go_biological_process": "GO:0030878 thyroid gland development;GO:0001708 cell fate specification;GO:0048752 semicircular canal morphogenesis;GO:2001054 negative regulation of mesenchymal cell apoptotic process;GO:0060017 parathyroid gland development",
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        "hit_score": 0.3,
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    },
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        "protein_name": "Pleckstrin homology and RhoGEF domain containing G6",
        "gene_name": "Plekhg6",
        "organism": "Rat",
        "refseq_name": "pleckstrin homology domain-containing family G member 6",
        "refseq_ac": "NP_001414672",
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        "gene_names_refseq": "Plekhg6",
        "protein_names_uniprotkb": "Pleckstrin homology and RhoGEF domain containing G6",
        "protein_names_refseq": "pleckstrin homology domain containing, family G (with RhoGef domain) member 6; pleckstrin homology domain-containing family G member 6",
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        "disease": "cystic fibrosis (Disease Ontology:DOID:1485)",
        "pathway": " (rno:100362241);  (R-RNO-8980692);  (R-RNO-9013149)",
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        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0005085 guanyl-nucleotide exchange factor activity",
        "go_cellular_component": "GO:0030054 cell junction",
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        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LR97-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LQ26-1",
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        "length": 431,
        "protein_name": "Paired box 2",
        "gene_name": "Pax2",
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        "gene_names_uniprotkb": "Pax2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Paired box 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "renal coloboma syndrome (Disease Ontology:DOID:0090006); focal segmental glomerulosclerosis 7 (Disease Ontology:DOID:0111132); coloboma (Disease Ontology:DOID:12270); nephroblastoma (Disease Ontology:DOID:2154); renal Wilms' tumor (Disease Ontology:DOID:5176); chronic kidney disease (Disease Ontology:DOID:784)",
        "pathway": " (rno:293992)",
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        "go_molecular_function": "GO:0003677 DNA 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:0000987 cis-regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005815 microtubule organizing center;GO:0034451 centriolar satellite;GO:0032993 protein-DNA complex;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0072307 regulation of metanephric nephron tubule epithelial cell differentiation;GO:0007501 mesodermal cell fate specification;GO:0021633 optic nerve structural organization;GO:0039003 pronephric field specification;GO:0061360 optic chiasma development",
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        "record_id": "A0ABK0LQ26-1",
        "record_type": "protein"
    },
    {
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        "length": 732,
        "protein_name": "TIR domain-containing adapter molecule 1",
        "gene_name": "Ticam1",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Ticam1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "TIR domain-containing adapter molecule 1; TICAM-1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "brain disease (Disease Ontology:DOID:936)",
        "pathway": " (rno:363328);  (R-RNO-140534);  (R-RNO-166166);  (R-RNO-2562578);  (R-RNO-936964);  (R-RNO-937041);  (R-RNO-937072);  (R-RNO-975163);  (R-RNO-9824878)",
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        "function": "Involved in innate immunity against invading pathogens. Adapter used by TLR3, TLR4 (through TICAM2) and TLR5 to mediate NF-kappa-B and interferon-regulatory factor (IRF) activation, and to induce apoptosis. Ligand binding to these receptors results in TRIF recruitment through its TIR domain. Distinct protein-interaction motifs allow recruitment of the effector proteins TBK1, TRAF6 and RIPK1, which in turn, lead to the activation of transcription factors IRF3 and IRF7, NF-kappa-B and FADD respectively. Phosphorylation by TBK1 on the pLxIS motif leads to recruitment and subsequent activation of the transcription factor IRF3 to induce expression of type I interferon and exert a potent immunity against invading pathogens. Component of a multi-helicase-TICAM1 complex that acts as a cytoplasmic sensor of viral double-stranded RNA (dsRNA) and plays a role in the activation of a cascade of antiviral responses including the induction of pro-inflammatory cytokines., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0035591 signaling adaptor activity;GO:0060090 molecular adaptor activity;GO:0019901 protein kinase binding",
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        "protein_name": "Actin-related protein 8",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Actr8",
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        "protein_names_uniprotkb": "Actin-related protein 8",
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        "pathway": " (R-RNO-5689603);  (R-RNO-5696394)",
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        "function": "Plays an important role in the functional organization of mitotic chromosomes. Exhibits low basal ATPase activity, and unable to polymerize., [UniProtKB, UniProtKB, UniProtKB]; Proposed core component of the chromatin remodeling INO80 complex which is involved in transcriptional regulation, DNA replication and probably DNA repair. Required for the recruitment of INO80 (and probably the INO80 complex) to sites of DNA damage Strongly prefer nucleosomes and H3-H4 tetramers over H2A-H2B dimers, suggesting it may act as a nucleosome recognition module within the complex., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003729 mRNA binding",
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    },
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        "length": 392,
        "protein_name": "Estrogen-induced osteoclastogenesis regulator 1",
        "gene_name": "Eeig1",
        "organism": "Rat",
        "refseq_name": "early estrogen-induced gene 1 protein",
        "refseq_ac": "NP_001386512",
        "gene_names_uniprotkb": "Eeig1; Fam102a; LOC687750",
        "gene_names_refseq": "Eeig1; Fam102a",
        "protein_names_uniprotkb": "Estrogen-induced osteoclastogenesis regulator 1",
        "protein_names_refseq": "early estrogen-induced gene 1 protein; family with sequence similarity 102, member A",
        "tax_id": 10116,
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        "pathway": " (rno:687750)",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0045121 membrane raft",
        "go_biological_process": "GO:0045672 positive regulation of osteoclast differentiation",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LPZ9-1",
        "record_type": "protein"
    },
    {
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        "length": 478,
        "protein_name": "Iroquois homeobox 2",
        "gene_name": "Irx2",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Irx2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Iroquois homeobox 2",
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        "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0043565 sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0030182 neuron differentiation;GO:0048468 cell development;GO:0048513 animal organ development;GO:0072086 specification of loop of Henle identity",
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        "record_id": "A0ABK0LNN7-1",
        "record_type": "protein"
    },
    {
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        "uniprot_id": "A0ABK0LPG5_RAT",
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        "length": 497,
        "protein_name": "Solute carrier family 2, facilitated glucose transporter member 6",
        "gene_name": "Slc2a6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Slc2a6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Solute carrier family 2, facilitated glucose transporter member 6; Glucose transporter type 6",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:296600)",
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        "class_list": "",
        "function": "Probable sugar transporter that acts as a regulator of glycolysis in macrophages. Does not transport glucose., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "protein_names_refseq": "serine-protein kinase ATM isoform X1",
        "tax_id": 10116,
        "disease": "female breast cancer (Disease Ontology:DOID:0050671); oral squamous cell carcinoma (Disease Ontology:DOID:0050866); lymphoma (Disease Ontology:DOID:0060058); pre-malignant neoplasm (Disease Ontology:DOID:0060071); stomach cancer (Disease Ontology:DOID:10534); Alzheimer's disease (Disease Ontology:DOID:10652); leukemia (Disease Ontology:DOID:1240); ataxia telangiectasia (Disease Ontology:DOID:12704); endometrial cancer (Disease Ontology:DOID:1380); Parkinson's disease (Disease Ontology:DOID:14330); disease of cellular proliferation (Disease Ontology:DOID:14566); breast cancer (Disease Ontology:DOID:1612); cancer (Disease Ontology:DOID:162); pancreatic cancer (Disease Ontology:DOID:1793); status epilepticus (Disease Ontology:DOID:1824); breast carcinoma (Disease Ontology:DOID:3459); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); lung squamous cell carcinoma (Disease Ontology:DOID:3907); lung non-small cell carcinoma (Disease Ontology:DOID:3908); papillary thyroid carcinoma (Disease Ontology:DOID:3969); infertility (Disease Ontology:DOID:5223); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); lung small cell carcinoma (Disease Ontology:DOID:5409); prostate carcinoma in situ (Disease Ontology:DOID:8634); colorectal cancer (Disease Ontology:DOID:9256); nasopharynx carcinoma (Disease Ontology:DOID:9261); oral mucosa leukoplakia (Disease Ontology:DOID:9655); senile cataract (Disease Ontology:DOID:9669)",
        "pathway": " (rno:300711);  (R-RNO-2559586);  (R-RNO-349425);  (R-RNO-5685938);  (R-RNO-5685942);  (R-RNO-5693537);  (R-RNO-5693548);  (R-RNO-5693565);  (R-RNO-5693568);  (R-RNO-5693571);  (R-RNO-5693579);  (R-RNO-5693607);  (R-RNO-5693616);  (R-RNO-6803204);  (R-RNO-6803207);  (R-RNO-6804756);  (R-RNO-6804757);  (R-RNO-6804760);  (R-RNO-69473);  (R-RNO-69541);  (R-RNO-9664873)",
        "pathway_count": 21,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Serine/threonine protein kinase which activates checkpoint signaling upon double strand breaks (DSBs), apoptosis and genotoxic stresses such as ionizing ultraviolet A light (UVA), thereby acting as a DNA damage sensor. Recognizes the substrate consensus sequence [ST]-Q. Phosphorylates 'Ser-139' of histone variant H2AX at double strand breaks (DSBs), thereby regulating DNA damage response mechanism. Also plays a role in pre-B cell allelic exclusion, a process leading to expression of a single immunoglobulin heavy chain allele to enforce clonality and monospecific recognition by the B-cell antigen receptor (BCR) expressed on individual B-lymphocytes. After the introduction of DNA breaks by the RAG complex on one immunoglobulin allele, acts by mediating a repositioning of the second allele to pericentromeric heterochromatin, preventing accessibility to the RAG complex and recombination of the second allele. Also involved in signal transduction and cell cycle control. May function as a tumor suppressor. Necessary for activation of ABL1 and SAPK. Phosphorylates DYRK2, CHEK2, p53/TP53, FANCD2, NFKBIA, BRCA1, CTIP, nibrin (NBN), TERF1, RAD9, UBQLN4 and DCLRE1C. May play a role in vesicle and/or protein transport. Could play a role in T-cell development, gonad and neurological function. Binds DNA ends. Plays a role in replication-dependent histone mRNA degradation. Phosphorylation of DYRK2 in nucleus in response to genotoxic stress prevents its MDM2-mediated ubiquitination and subsequent proteasome degradation. Phosphorylates ATF2 which stimulates its function in DNA damage response. Phosphorylates ERCC6 which is essential for its chromatin remodeling activity at DNA double-strand breaks., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 3,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 3,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 28,
        "glyco_site_count": 3,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "5.6.2.3;2.7.11.1;2.3.2.27;2.7.12.1;2.3.2.26;3.1.3.48;2.7.1.153;2.7.1.137;2.7.7.7;3.1.-.-;1.14.11.69;1.14.11.66;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;3.4.19.-;2.7.11.34;2.7.10.2;3.4.19.12;5.6.2.4;2.7.1.150;2.7.11.13;5.6.2.1;2.1.1.357;4.1.1.32;3.1.11.-;2.7.11.19;2.7.2.3;2.7.11.11;3.1.3.16;2.7.11.31;2.3.2.-;2.7.11.4;2.3.1.48;2.7.13.3;2.7.4.18;3.1.24.-;3.1.22.-;2.7.11.39;3.6.4.-;2.4.99.18;2.3.1.-;2.3.2.23;6.5.1.1;3.6.-.-;2.7.11.10",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0004672 protein kinase activity;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005782 peroxisomal matrix;GO:0005813 centrosome",
        "go_biological_process": "GO:0010557 positive regulation of macromolecule biosynthetic process;GO:0010506 regulation of autophagy;GO:0043065 positive regulation of apoptotic process;GO:0000723 telomere maintenance;GO:0006302 double-strand break repair",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LQX5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LNS6-1",
        "uniprot_id": "A0ABK0LNS6_RAT",
        "mass": 73377.0,
        "length": 642,
        "protein_name": "Coiled-coil domain containing 96",
        "gene_name": "Cfap184",
        "organism": "Rat",
        "refseq_name": "coiled-coil domain-containing protein 96",
        "refseq_ac": "NP_001419724",
        "gene_names_uniprotkb": "Cfap184; Ccdc96",
        "gene_names_refseq": "Ccdc96; Cfap184; RGD1305153",
        "protein_names_uniprotkb": "Coiled-coil domain containing 96",
        "protein_names_refseq": "coiled-coil domain containing 96; coiled-coil domain-containing protein 96",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005930 axoneme;GO:0036064 ciliary basal body;GO:0005929 cilium",
        "go_biological_process": "GO:0060271 cilium assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LNS6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LNX9-1",
        "uniprot_id": "A0ABK0LNX9_RAT",
        "mass": 47878.0,
        "length": 423,
        "protein_name": "Alpha-galactosidase",
        "gene_name": "Gla",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Gla",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Alpha-galactosidase; 3.2.1.-",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Fabry disease (Disease Ontology:DOID:14499); lysosomal storage disease (Disease Ontology:DOID:3211)",
        "pathway": " (rno:363494);  (R-RNO-6798695);  (R-RNO-9840310)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the hydrolysis of glycosphingolipids and participates in their degradation in the lysosome., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 2,
        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "1.11.2.2;3.4.21.4;3.4.16.-;3.2.1.-;5.3.4.1;1.1.1.205;3.2.1.23;5.3.99.3;1.11.1.27;3.1.1.4;2.3.1.23;3.2.1.17;3.2.1.31;3.5.3.1;2.7.11.13;2.3.3.8;3.2.1.51;3.4.21.20;1.6.2.2;3.5.3.15;3.5.1.26;3.6.4.6;3.1.6.12;2.4.1.1;2.7.11.24;3.1.27.-;3.4.14.1;3.1.6.4;3.1.6.8;1.6.5.5;3.6.1.-;2.7.10.2;3.4.19.9;3.1.3.16;3.2.1.52;6.3.4.21;3.4.14.2",
        "go_molecular_function": "GO:0004557 alpha-galactosidase activity;GO:0005102 signaling receptor binding;GO:0016787 hydrolase activity;GO:0042803 protein homodimerization activity;GO:0003824 catalytic activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005737 cytoplasm;GO:0016020 membrane;GO:0005764 lysosome;GO:0005615 extracellular space",
        "go_biological_process": "GO:0009311 oligosaccharide metabolic process;GO:0016139 glycoside catabolic process;GO:0046479 glycosphingolipid catabolic process;GO:0090325 regulation of locomotion involved in locomotory behavior;GO:0030168 platelet activation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LNX9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LNR1-1",
        "uniprot_id": "A0ABK0LNR1_RAT",
        "mass": 72842.0,
        "length": 629,
        "protein_name": "Zinc finger protein",
        "gene_name": "Prdm5",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Prdm5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein; 2.1.1.-",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "brittle cornea syndrome 2 (Disease Ontology:DOID:0080729)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000976 transcription cis-regulatory region binding;GO:0008168 methyltransferase activity;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:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0016604 nuclear body",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006325 chromatin organization;GO:0032259 methylation;GO:0006357 regulation of transcription by RNA polymerase II;GO:0000122 negative regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LNR1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LNX0-1",
        "uniprot_id": "A0ABK0LNX0_RAT",
        "mass": 143416.0,
        "length": 1293,
        "protein_name": "Alpha-kinase 1",
        "gene_name": "Alpk1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Alpk1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Alpha-kinase 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-445989);  (R-RNO-9645460)",
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        "publication_count": 0,
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        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0048029 monosaccharide binding",
        "go_cellular_component": "GO:0005929 cilium;GO:0000922 spindle pole;GO:0005813 centrosome;GO:0005829 cytosol;GO:0036064 ciliary basal body",
        "go_biological_process": "GO:0045087 innate immune response;GO:0002753 cytoplasmic pattern recognition receptor signaling pathway;GO:0009617 response to bacterium;GO:0043123 positive regulation of canonical NF-kappaB signal transduction;GO:0060271 cilium assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LNX0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LPS1-1",
        "uniprot_id": "A0ABK0LPS1_RAT",
        "mass": 93454.0,
        "length": 853,
        "protein_name": "ADAM metallopeptidase domain 9",
        "gene_name": "Adam9",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Adam9",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "ADAM metallopeptidase domain 9",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "cone-rod dystrophy 9 (Disease Ontology:DOID:0111020); Alzheimer's disease (Disease Ontology:DOID:10652); pancreatic cancer (Disease Ontology:DOID:1793); status epilepticus (Disease Ontology:DOID:1824); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); pancreatic ductal carcinoma (Disease Ontology:DOID:3587); cervix uteri carcinoma in situ (Disease Ontology:DOID:8991)",
        "pathway": " (rno:290834)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "38843836",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 1,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 1,
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        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 7,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004222 metalloendopeptidase activity;GO:0005178 integrin binding;GO:0008237 metallopeptidase activity;GO:0017124 SH3 domain binding;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0016323 basolateral plasma membrane",
        "go_biological_process": "GO:0006509 membrane protein ectodomain proteolysis;GO:0007155 cell adhesion;GO:0016477 cell migration;GO:0016485 protein processing;GO:0030335 positive regulation of cell migration",
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        "hit_score": 0.4,
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        "record_type": "protein"
    },
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        "length": 319,
        "protein_name": "Membrane spanning 4-domains A6A",
        "gene_name": "Ms4a6a",
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        "gene_names_uniprotkb": "Ms4a6a; Ms4a11",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Membrane spanning 4-domains A6A",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:361735)",
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        "reported_mutagensis": 0,
        "reported_glycation": 0,
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        "missing_score": 10000,
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        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005802 trans-Golgi network;GO:0016020 membrane",
        "go_biological_process": "GO:0007166 cell surface receptor signaling pathway",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LPT8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LPH6-1",
        "uniprot_id": "A0ABK0LPH6_RAT",
        "mass": 552568.0,
        "length": 4875,
        "protein_name": "Ryanodine receptor 3",
        "gene_name": "Ryr3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ryr3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ryanodine receptor 3; Brain ryanodine receptor-calcium release channel; Brain-type ryanodine receptor; Type 3 ryanodine receptor",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "congenital myopathy 20 (Disease Ontology:DOID:0081352); pre-eclampsia (Disease Ontology:DOID:10591); gestational diabetes (Disease Ontology:DOID:11714); pulmonary hypertension (Disease Ontology:DOID:6432); hepatocellular carcinoma (Disease Ontology:DOID:684)",
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        "class_list": "",
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 5,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.7.11.1",
        "go_molecular_function": "GO:0005516 calmodulin binding;GO:0005509 calcium ion binding;GO:0005219 ryanodine-sensitive calcium-release channel activity;GO:0015278 intracellularly gated calcium channel activity;GO:0048763 calcium-induced calcium release activity",
        "go_cellular_component": "GO:0033017 sarcoplasmic reticulum membrane;GO:0032991 protein-containing complex;GO:0048471 perinuclear region of cytoplasm;GO:0009898 cytoplasmic side of plasma membrane;GO:0030314 junctional membrane complex",
        "go_biological_process": "GO:0006874 intracellular calcium ion homeostasis;GO:0001666 response to hypoxia;GO:0006816 calcium ion transport;GO:0006941 striated muscle contraction;GO:0051481 negative regulation of cytosolic calcium ion concentration",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LPH6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LQ42-1",
        "uniprot_id": "A0ABK0LQ42_RAT",
        "mass": 82137.0,
        "length": 727,
        "protein_name": "Zinc finger protein 235",
        "gene_name": "Znf235",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Znf235",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 235",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:102548230)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO: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:0003677 DNA binding",
        "go_cellular_component": "GO:0031981 nuclear lumen;GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LQ42-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7F2B3-1",
        "uniprot_id": "F7F2B3_RAT",
        "mass": 39386.0,
        "length": 367,
        "protein_name": "Cd68 molecule",
        "gene_name": "Cd68",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cd68",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Cd68 molecule",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "adult T-cell leukemia/lymphoma (Disease Ontology:DOID:0050523); metabolic dysfunction and alcohol associated liver disease (Disease Ontology:DOID:0070508); metabolic dysfunction-associated steatohepatitis (Disease Ontology:DOID:0080547); endometriosis of pelvic peritoneum (Disease Ontology:DOID:11429); primary biliary cholangitis (Disease Ontology:DOID:12236); diverticulitis of colon (Disease Ontology:DOID:13254); hepatitis B (Disease Ontology:DOID:2043); Epstein-Barr virus infectious disease (Disease Ontology:DOID:2938); severe acute respiratory syndrome (Disease Ontology:DOID:2945); Merkel cell carcinoma (Disease Ontology:DOID:3965); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); acquired immunodeficiency syndrome (Disease Ontology:DOID:635); hepatocellular carcinoma (Disease Ontology:DOID:684); Hodgkin's lymphoma (Disease Ontology:DOID:8567)",
        "pathway": " (rno:287435);  (R-RNO-6798695)",
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        "function": "Could play a role in phagocytic activities of tissue macrophages, both in intracellular lysosomal metabolism and extracellular cell-cell and cell-pathogen interactions. Binds to tissue- and organ-specific lectins or selectins, allowing homing of macrophage subsets to particular sites. Rapid recirculation of CD68 from endosomes and lysosomes to the plasma membrane may allow macrophages to crawl over selectin-bearing substrates or other cells., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005765 lysosomal membrane;GO:0031902 late endosome membrane;GO:0010008 endosome membrane;GO:0005764 lysosome",
        "go_biological_process": "GO:0072594 establishment of protein localization to organelle;GO:0045471 response to ethanol;GO:0002437 inflammatory response to antigenic stimulus;GO:0071222 cellular response to lipopolysaccharide;GO:0031669 cellular response to nutrient levels",
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        "record_id": "F7F2B3-1",
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        "uniprot_canonical_ac": "A0ABK0LQL4-1",
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        "length": 206,
        "protein_name": "Nuclear nucleic acid-binding protein C1D",
        "gene_name": "C1d",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "C1d",
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        "protein_names_uniprotkb": "Nuclear nucleic acid-binding protein C1D",
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        "tax_id": 10116,
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        "function": "Plays a role in the recruitment of the exosome to pre-rRNA to mediate the 3'-5' end processing of the 5.8S rRNA., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003723 RNA binding;GO:0003714 transcription corepressor activity;GO:0016922 nuclear receptor binding",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005654 nucleoplasm;GO:0017053 transcription repressor complex",
        "go_biological_process": "GO:0006364 rRNA processing;GO:0045892 negative regulation of DNA-templated transcription;GO:0000460 maturation of 5.8S rRNA",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LQL4-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "F7F1S0-1",
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        "length": 840,
        "protein_name": "DLG associated protein 5",
        "gene_name": "Dlgap5",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Dlgap5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "DLG associated protein 5",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:289997)",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol;GO:0031616 spindle pole centrosome;GO:0072686 mitotic spindle",
        "go_biological_process": "GO:0023052 signaling",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7F1S0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LQ73-1",
        "uniprot_id": "A0ABK0LQ73_RAT",
        "mass": 22437.0,
        "length": 207,
        "protein_name": "Armadillo repeat containing 7",
        "gene_name": "Armc7",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Armc7",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Armadillo repeat containing 7",
        "protein_names_refseq": "",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005829 cytosol;GO:0071018 U12-type catalytic step 2 spliceosome",
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        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LQ73-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LQS8-1",
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        "mass": 43696.0,
        "length": 395,
        "protein_name": "Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6",
        "gene_name": "St6galnac6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "St6galnac6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6; GalNAc alpha-2,6-sialyltransferase VI; ST6GalNAc VI; Sialyltransferase 7F",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "publication_count": 0,
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        "predicted_glycosites": 1,
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        "length": 431,
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        "refseq_name": "interleukin-20 receptor subunit beta isoform X1",
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        "protein_names_refseq": "interleukin-20 receptor subunit beta isoform X1",
        "tax_id": 10116,
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        "pathway": " (rno:501043);  (R-RNO-5684996);  (R-RNO-8854691)",
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        "protein_name": "Zinc finger protein 81",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 81",
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        "protein_name": "Pleckstrin homology domain containing A2",
        "gene_name": "Plekha2",
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        "protein_names_uniprotkb": "Pleckstrin homology domain containing A2",
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        "length": 453,
        "protein_name": "F-box/LRR-repeat protein 20",
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        "refseq_ac": "XP_017453008",
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        "gene_names_refseq": "Fbl2; Fbxl20; Fbxl2",
        "protein_names_uniprotkb": "F-box/LRR-repeat protein 20; F-box and leucine-rich repeat protein 20; F-box/LRR-repeat protein 2-like",
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        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0045202 synapse;GO:0098793 presynapse;GO:0098685 Schaffer collateral - CA1 synapse",
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    {
        "uniprot_canonical_ac": "A0ABK0LQ59-1",
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        "length": 897,
        "protein_name": "Zinc finger, X-linked, duplicated B",
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        "length": 489,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "Smok2bl",
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        "gene_names_uniprotkb": "Smok2bl; Smok4al",
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        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
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        "disease": "small cell carcinoma (Disease Ontology:DOID:0050685); polycystic ovary syndrome (Disease Ontology:DOID:11612); arteriosclerosis (Disease Ontology:DOID:2349); osteoarthritis (Disease Ontology:DOID:8398); type 1 diabetes mellitus (Disease Ontology:DOID:9744)",
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        "protein_names_uniprotkb": "Protein SHQ1 homolog",
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        "function": "Required for the quantitative accumulation of H/ACA ribonucleoproteins (RNPs), including telomerase, probably through the stabilization of DKC1, from the time of its synthesis until its association with NOP10, NHP2, and NAF1 at the nascent H/ACA RNA., [UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "Protein phosphatase 2, regulatory subunit B'', beta",
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        "protein_names_uniprotkb": "Ribosomal protein L10e/L16 domain-containing protein",
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        "protein_name": "Polycomb group RING finger protein 2",
        "gene_name": "LOC103692755",
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        "refseq_name": "polycomb group RING finger protein 2-like",
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        "gene_names_uniprotkb": "LOC103692755",
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        "protein_names_uniprotkb": "Polycomb group RING finger protein 2; DNA-binding protein Mel-18; RING finger protein 110; Zinc finger protein 144",
        "protein_names_refseq": "polycomb group RING finger protein 2-like",
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        "function": "Transcriptional repressor. Binds specifically to the DNA sequence 5'-GACTNGACT-3'. Has tumor suppressor activity. May play a role in control of cell proliferation and/or neural cell development. Regulates proliferation of early T progenitor cells by maintaining expression of HES1. Also plays a role in antero-posterior specification of the axial skeleton and negative regulation of the self-renewal activity of hematopoietic stem cells. Component of a Polycomb group (PcG) multiprotein PRC1-like complex, a complex class required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development. PcG PRC1 complex acts via chromatin remodeling and modification of histones; it mediates monoubiquitination of histone H2A 'Lys-119', rendering chromatin heritably changed in its expressibility. Within the PRC1-like complex, regulates RNF2 ubiquitin ligase activity., [UniProtKB, UniProtKB]",
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        "record_type": "protein"
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        "protein_name": "Olfactory receptor",
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        "protein_names_uniprotkb": "Olfactory receptor",
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        "protein_names_uniprotkb": "Protein phosphatase 1 regulatory subunit 14",
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        "protein_names_uniprotkb": "LysM and putative peptidoglycan-binding domain-containing protein 1",
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        "reported_snv": 0,
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        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0061651 Atg12 conjugating enzyme activity;GO:0019777 Atg12 transferase activity;GO:0019787 ubiquitin-like protein transferase activity",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0000045 autophagosome assembly;GO:0015031 protein transport;GO:0000423 mitophagy;GO:0032446 protein modification by small protein conjugation;GO:0006914 autophagy",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LRX5-1",
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        "length": 1475,
        "protein_name": "Probable ATP-dependent DNA helicase HFM1",
        "gene_name": "Hfm1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Hfm1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Probable ATP-dependent DNA helicase HFM1; 5.6.2.4; DNA 3'-5' helicase HFM1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "primary ovarian insufficiency 9 (Disease Ontology:DOID:0080866)",
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        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Required for crossover formation and complete synapsis of homologous chromosomes during meiosis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;5.6.2.4;3.6.5.-;5.6.2.-;3.1.-.-;2.7.7.7;2.7.7.49;3.1.13.1;4.2.99.18;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;2.7.4.3;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
        "go_molecular_function": "GO:0043138 3'-5' DNA helicase activity;GO:0005524 ATP binding;GO:0016787 hydrolase activity;GO:0003676 nucleic acid binding;GO:0003678 DNA helicase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0051321 meiotic cell cycle;GO:0000712 resolution of meiotic recombination intermediates",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LRX5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LTU5-1",
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        "length": 469,
        "protein_name": "DNA repair protein RAD51 homolog 2",
        "gene_name": "Rad51b",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rad51b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "DNA repair protein RAD51 homolog 2; RAD51 homolog B; RAD51-like protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500679);  (R-RNO-5685942);  (R-RNO-5693537);  (R-RNO-5693568);  (R-RNO-5693579);  (R-RNO-5693616);  (R-RNO-983231)",
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        "class_list": "",
        "function": "Involved in the homologous recombination repair (HRR) pathway of double-stranded DNA breaks arising during DNA replication or induced by DNA-damaging agents. May promote the assembly of presynaptic RAD51 nucleoprotein filaments. Binds single-stranded DNA and double-stranded DNA and has DNA-dependent ATPase activity. Part of the RAD51 paralog protein complex BCDX2 which acts in the BRCA1-BRCA2-dependent HR pathway. Upon DNA damage, BCDX2 acts downstream of BRCA2 recruitment and upstream of RAD51 recruitment. BCDX2 binds predominantly to the intersection of the four duplex arms of the Holliday junction and to junction of replication forks. The BCDX2 complex was originally reported to bind single-stranded DNA, single-stranded gaps in duplex DNA and specifically to nicks in duplex DNA. The BCDX2 subcomplex RAD51B:RAD51C exhibits single-stranded DNA-dependent ATPase activity suggesting an involvement in early stages of the HR pathway., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0005524 ATP binding;GO:0140664 ATP-dependent DNA damage sensor activity;GO:0003690 double-stranded DNA binding;GO:0003697 single-stranded DNA binding",
        "go_cellular_component": "GO:0033063 Rad51B-Rad51C-Rad51D-XRCC2 complex;GO:0005657 replication fork",
        "go_biological_process": "GO:0000724 double-strand break repair via homologous recombination;GO:0001701 in utero embryonic development;GO:0008284 positive regulation of cell population proliferation;GO:0010971 positive regulation of G2/M transition of mitotic cell cycle;GO:0001832 blastocyst growth",
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        "record_type": "protein"
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    {
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        "protein_name": "Switch-associated protein 70",
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        "refseq_name": "switch-associated protein 70",
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        "gene_names_uniprotkb": "Swap70",
        "gene_names_refseq": "Swap70",
        "protein_names_uniprotkb": "Switch-associated protein 70",
        "protein_names_refseq": "SWA-70 protein; SWAP complex protein; SWAP switching B-cell complex 70; SWAP-70 protein; switch-associated protein 70",
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        "disease": "",
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        "function": "Phosphatidylinositol 3,4,5-trisphosphate-dependent guanine nucleotide exchange factor (GEF) which, independently of RAS, transduces signals from tyrosine kinase receptors to RAC. It also mediates signaling of membrane ruffling. Regulates the actin cytoskeleton as an effector or adapter protein in response to agonist stimulated phosphatidylinositol (3,4)-bisphosphate production and cell protrusion., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "record_type": "protein"
    },
    {
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        "length": 2921,
        "protein_name": "Pericentrin",
        "gene_name": "Pcnt",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pcnt; LOC309692",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Pericentrin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "microcephalic osteodysplastic primordial dwarfism type II (Disease Ontology:DOID:0060609); Down syndrome (Disease Ontology:DOID:14250)",
        "pathway": " (R-RNO-2565942);  (R-RNO-380259);  (R-RNO-380270);  (R-RNO-380284);  (R-RNO-380320);  (R-RNO-5620912);  (R-RNO-8854518);  (R-RNO-9646399)",
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        "go_molecular_function": "GO:0060090 molecular adaptor activity",
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        "record_type": "protein"
    },
    {
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        "protein_name": "Glypican 5",
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        "protein_names_uniprotkb": "Glypican 5",
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        "pathway": " (R-RNO-1971475);  (R-RNO-2022928);  (R-RNO-2024096);  (R-RNO-5362798);  (R-RNO-975634);  (R-RNO-9769739)",
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        "go_cellular_component": "GO:0005886 plasma membrane;GO:0031012 extracellular matrix;GO:0098552 side of membrane;GO:0009986 cell surface",
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    },
    {
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        "gene_names_uniprotkb": "Gm6569",
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        "protein_names_uniprotkb": "Predicted gene 6569",
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        "gene_names_uniprotkb": "Purg",
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        "protein_names_uniprotkb": "Purine-rich element binding protein G",
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        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0032422 purine-rich negative regulatory element binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0045202 synapse",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LUE9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LRG3-1",
        "uniprot_id": "A0ABK0LRG3_RAT",
        "mass": 17063.0,
        "length": 152,
        "protein_name": "Protein ripply3",
        "gene_name": "Ripply3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ripply3; Dscr6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein ripply3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:288239)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
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        "reported_phosphosites": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0009880 embryonic pattern specification;GO:0007507 heart development;GO:0008285 negative regulation of cell population proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LRG3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LTJ9-1",
        "uniprot_id": "A0ABK0LTJ9_RAT",
        "mass": 54835.0,
        "length": 505,
        "protein_name": "Sialidase-4",
        "gene_name": "Neu4",
        "organism": "Rat",
        "refseq_name": "sialidase-4 isoform X1",
        "refseq_ac": "XP_008765598",
        "gene_names_uniprotkb": "Neu4",
        "gene_names_refseq": "Neu4",
        "protein_names_uniprotkb": "Sialidase-4; 3.2.1.18; N-acetyl-alpha-neuraminidase 4",
        "protein_names_refseq": "sialidase-4 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:316642);  (R-RNO-4085001);  (R-RNO-9840310)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Exo-alpha-sialidase that catalyzes the hydrolytic cleavage of the terminal sialic acid (N-acetylneuraminic acid, Neu5Ac) of a glycan moiety in the catabolism of glycolipids, glycoproteins and oligosacharides. Efficiently hydrolyzes gangliosides including alpha-(2->3)-sialylated GD1a and GM3 and alpha-(2->8)-sialylated GD3. Hydrolyzes poly-alpha-(2->8)-sialylated neural cell adhesion molecule NCAM1 likely at growth cones, suppressing neurite outgrowth in hippocampal neurons. May desialylate sialyl Lewis A and X antigens at the cell surface, down-regulating these glycan epitopes recognized by SELE/E selectin in the initiation of cell adhesion and extravasation. Has sialidase activity toward mucin, fetuin and sialyllactose., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.4.16.-;3.2.1.18;3.2.1.23",
        "go_molecular_function": "GO:0004308 exo-alpha-sialidase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005741 mitochondrial outer membrane;GO:0005743 mitochondrial inner membrane;GO:0005886 plasma membrane;GO:0016020 membrane",
        "go_biological_process": "GO:0006689 ganglioside catabolic process;GO:0009313 oligosaccharide catabolic process;GO:0006516 glycoprotein catabolic process;GO:0010977 negative regulation of neuron projection development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LTJ9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LS36-1",
        "uniprot_id": "A0ABK0LS36_RAT",
        "mass": 58190.0,
        "length": 520,
        "protein_name": "EGF-like-domain, multiple 6",
        "gene_name": "Egfl6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Egfl6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "EGF-like-domain, multiple 6",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:317470)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "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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        "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:0005509 calcium ion binding",
        "go_cellular_component": "GO:0016020 membrane;GO:0031012 extracellular matrix;GO:0005604 basement membrane",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0030154 cell differentiation;GO:0030198 extracellular matrix organization;GO:0010811 positive regulation of cell-substrate adhesion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LS36-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LTI9-1",
        "uniprot_id": "A0ABK0LTI9_RAT",
        "mass": 26107.0,
        "length": 232,
        "protein_name": "Forkhead box protein G1",
        "gene_name": "Foxl3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Foxl3; LOC680273",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Forkhead box protein G1; Brain factor 1; Forkhead-related protein FKHL1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Transcription repression factor which plays an important role in the establishment of the regional subdivision of the developing brain and in the development of the telencephalon., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0003700 DNA-binding transcription factor activity;GO:0043565 sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0030154 cell differentiation;GO:0009653 anatomical structure morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LTI9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LSC4-1",
        "uniprot_id": "A0ABK0LSC4_RAT",
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        "length": 301,
        "protein_name": "E3 ubiquitin-protein ligase ZNRF1",
        "gene_name": "Znrf2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Znrf2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase ZNRF1; 2.3.2.27; Nerve injury-induced gene 283 protein; RING-type E3 ubiquitin transferase ZNRF1; Zinc/RING finger protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362367);  (R-RNO-983168)",
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        "ec_number_list": "2.3.2.26;2.3.2.32;2.3.2.31;2.3.2.23;2.3.2.27;2.3.2.34;2.3.2.24;2.3.2.-;2.3.2.25",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity",
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        "go_biological_process": "GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0070936 protein K48-linked ubiquitination;GO:0160177 positive regulation of autophagosome-lysosome fusion",
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        "hit_score": 0.2,
        "record_id": "A0ABK0LSC4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LTB3-1",
        "uniprot_id": "A0ABK0LTB3_RAT",
        "mass": 31198.0,
        "length": 273,
        "protein_name": "Transmembrane protein 182",
        "gene_name": "Tmem182",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tmem182",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transmembrane protein 182",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:501129)",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007517 muscle organ development;GO:1901740 negative regulation of myoblast fusion;GO:0045662 negative regulation of myoblast differentiation;GO:0014908 myotube differentiation involved in skeletal muscle regeneration;GO:0014906 myotube cell development involved in skeletal muscle regeneration",
        "synthesized_glycan_count": 0,
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        "record_id": "A0ABK0LTB3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LTS4-1",
        "uniprot_id": "A0ABK0LTS4_RAT",
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        "length": 275,
        "protein_name": "Ciliary microtubule associated protein 1C",
        "gene_name": "Cimap1c",
        "organism": "Rat",
        "refseq_name": "protein CIMAP1C isoform 1",
        "refseq_ac": "NP_001101621",
        "gene_names_uniprotkb": "Cimap1c; Odf3l1",
        "gene_names_refseq": "Cimap1c; Odf3l1; RGD1304976",
        "protein_names_uniprotkb": "Ciliary microtubule associated protein 1C",
        "protein_names_refseq": "outer dense fiber of sperm tails 3-like 1; outer dense fiber protein 3-like protein 1; protein CIMAP1C isoform 1",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005856 cytoskeleton",
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        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LTS4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LRK7-1",
        "uniprot_id": "A0ABK0LRK7_RAT",
        "mass": 35187.0,
        "length": 318,
        "protein_name": "Sarcoglycan, delta",
        "gene_name": "Sgcd",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Sgcd",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Sarcoglycan, delta",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); autosomal recessive limb-girdle muscular dystrophy type 2F (Disease Ontology:DOID:0110280); dilated cardiomyopathy 1L (Disease Ontology:DOID:0110436); muscular dystrophy (Disease Ontology:DOID:9884)",
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        "protein_names_uniprotkb": "NIPA magnesium transporter 1",
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        "tax_id": 10116,
        "disease": "hereditary spastic paraplegia 6 (Disease Ontology:DOID:0110811); hereditary spastic paraplegia (Disease Ontology:DOID:2476)",
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        "protein_names_refseq": "family with sequence similarity 154, member A; rCG55202-like; stabilizer of axonemal microtubules 1",
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        "protein_names_uniprotkb": "Zinc finger protein 780B",
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        "function": "May have a role during differentiation processes., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Endosomal transmembrane epsin interactor 2",
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        "protein_names_uniprotkb": "Endosomal transmembrane epsin interactor 2",
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        "length": 676,
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        "refseq_name": "folylpolyglutamate synthase, mitochondrial isoform X2",
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        "gene_names_refseq": "Fpgs",
        "protein_names_uniprotkb": "tetrahydrofolate synthase; 6.3.2.17; Folylpoly-gamma-glutamate synthetase; Tetrahydrofolylpolyglutamate synthase",
        "protein_names_refseq": "folylpolyglutamate synthase, mitochondrial isoform X2",
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        "function": "Catalyzes conversion of folates to polyglutamate derivatives allowing concentration of folate compounds in the cell and the intracellular retention of these cofactors, which are important substrates for most of the folate-dependent enzymes that are involved in one-carbon transfer reactions involved in purine, pyrimidine and amino acid synthesis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_refseq": "ectonucleoside triphosphate diphosphohydrolase 4 isoform 1",
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        "protein_name": "Meiotic double-stranded break formation protein 1",
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        "protein_names_uniprotkb": "Meiotic double-stranded break formation protein 1",
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        "disease": "gestational trophoblastic neoplasm (Disease Ontology:DOID:3590)",
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        "protein_names_uniprotkb": "Mediator of RNA polymerase II transcription subunit 26; Cofactor required for Sp1 transcriptional activation subunit 7; Mediator complex subunit 26",
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        "protein_names_uniprotkb": "MAP3K7 C-terminal like",
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        "gene_names_refseq": "Lrrc58; RGD1307440",
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        "protein_names_refseq": "leucine-rich repeat-containing protein 58",
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    },
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        "protein_name": "Coiled-coil domain containing 66",
        "gene_name": "Ccdc66",
        "organism": "Rat",
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        "protein_names_uniprotkb": "Coiled-coil domain containing 66",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa (Disease Ontology:DOID:10584)",
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        "go_molecular_function": "GO:0008017 microtubule binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity",
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        "go_biological_process": "GO:0060271 cilium assembly;GO:1902850 microtubule cytoskeleton organization involved in mitosis;GO:0090307 mitotic spindle assembly;GO:0001895 retina homeostasis;GO:0007020 microtubule nucleation",
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    },
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        "protein_name": "B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB",
        "gene_name": "Bdp1",
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        "gene_names_uniprotkb": "Bdp1",
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        "protein_names_uniprotkb": "B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB",
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        "disease": "autosomal recessive nonsyndromic deafness 112 (Disease Ontology:DOID:0111637)",
        "pathway": " (R-RNO-76061);  (R-RNO-76066);  (R-RNO-76071)",
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        "hit_score": 0.2,
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LSF8-1",
        "uniprot_id": "A0ABK0LSF8_RAT",
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        "length": 254,
        "protein_name": "Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase",
        "gene_name": "Hacd2",
        "organism": "Rat",
        "refseq_name": "very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2",
        "refseq_ac": "NP_001389032",
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        "gene_names_refseq": "Hacd2; Ptplb",
        "protein_names_uniprotkb": "Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase; 4.2.1.134",
        "protein_names_refseq": "protein tyrosine phosphatase-like (proline instead of catalytic arginine), member b; protein-tyrosine phosphatase-like member B; very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2-like; very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2; very-long-chain (3R)-3-hydroxyacyl-[acyl-carrier protein] dehydratase 2-like",
        "tax_id": 10116,
        "disease": "cancer (Disease Ontology:DOID:162)",
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        "function": "Catalyzes the third of the four reactions of the long-chain fatty acids elongation cycle. This endoplasmic reticulum-bound enzymatic process, allows the addition of two carbons to the chain of long- and very long-chain fatty acids/VLCFAs per cycle. This enzyme catalyzes the dehydration of the 3-hydroxyacyl-CoA intermediate into trans-2,3-enoyl-CoA, within each cycle of fatty acid elongation. Thereby, it participates to the production of VLCFAs of different chain lengths that are involved in multiple biological processes as precursors of membrane lipids and lipid mediators., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0030148 sphingolipid biosynthetic process;GO:0030497 fatty acid elongation;GO:0042761 very long-chain fatty acid biosynthetic process;GO:0006633 fatty acid biosynthetic process",
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        "record_id": "A0ABK0LSF8-1",
        "record_type": "protein"
    },
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        "length": 899,
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        "protein_names_uniprotkb": "Scm polycomb group protein like 2",
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        "go_molecular_function": "GO:0003682 chromatin binding;GO:0042393 histone binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000785 chromatin;GO:0031519 PcG protein complex;GO:0001741 XY body",
        "go_biological_process": "GO:0045892 negative regulation of DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0006915 apoptotic process;GO:0008104 intracellular protein localization;GO:0009653 anatomical structure morphogenesis",
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        "record_id": "A0ABK0LRY6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LT85-1",
        "uniprot_id": "A0ABK0LT85_RAT",
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        "length": 454,
        "protein_name": "Calreticulin",
        "gene_name": "Calr4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Calr4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Calreticulin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Parkinson's disease (Disease Ontology:DOID:14330)",
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        "class_list": "",
        "function": "Calcium-binding chaperone that promotes folding, oligomeric assembly and quality control in the endoplasmic reticulum (ER) via the calreticulin/calnexin cycle. This lectin interacts transiently with almost all of the monoglucosylated glycoproteins that are synthesized in the ER. Interacts with the DNA-binding domain of NR3C1 and mediates its nuclear export. Involved in maternal gene expression regulation. May participate in oocyte maturation via the regulation of calcium homeostasis. Present in the cortical granules of non-activated oocytes, is exocytosed during the cortical reaction in response to oocyte activation and might participate in the block to polyspermy., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0051082 unfolded protein binding;GO:0005509 calcium ion binding;GO:0003729 mRNA binding;GO:0030246 carbohydrate binding",
        "go_cellular_component": "GO:0005788 endoplasmic reticulum lumen;GO:0005789 endoplasmic reticulum membrane;GO:0009986 cell surface;GO:0033018 sarcoplasmic reticulum lumen;GO:0060473 cortical granule",
        "go_biological_process": "GO:0006457 protein folding;GO:0036503 ERAD pathway",
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        "record_id": "A0ABK0LT85-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LU03-1",
        "uniprot_id": "A0ABK0LU03_RAT",
        "mass": 99652.0,
        "length": 929,
        "protein_name": "GLIS family zinc finger 3",
        "gene_name": "Glis3",
        "organism": "Rat",
        "refseq_name": "GLIS family zinc finger 3 isoform 1",
        "refseq_ac": "NP_001419411",
        "gene_names_uniprotkb": "Glis3",
        "gene_names_refseq": "Glis3; RGD1565505",
        "protein_names_uniprotkb": "GLIS family zinc finger 3",
        "protein_names_refseq": "GLIS family zinc finger 3 isoform 1; zinc finger protein GLIS3",
        "tax_id": 10116,
        "disease": "neonatal diabetes mellitus with congenital hypothyroidism (Disease Ontology:DOID:0060638); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
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        "publication_count": 3,
        "publication_id_list": "26147758;28911974;38652652",
        "class_list": "",
        "function": "Downregulation of Glis3 in INS1 cells exposed to chronically elevated glucose contributes to glucotoxicity-associated beta cell dysfunction., [RefSeq, PubMed]; GLIS3 controls the expression of genes involved in autophagy.  Glis3 sequence polymorphisms in the diabetic GK rat alter beta-cell function and modify neurogenesis in hippocampus neurons., [RefSeq, PubMed]; It may play a role in a number of physiological processes controlled by Glis3. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006366 transcription by RNA polymerase II",
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        "record_id": "A0ABK0LU03-1",
        "record_type": "protein"
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    {
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        "length": 362,
        "protein_name": "Transmembrane protein 116",
        "gene_name": "Tmem116",
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        "gene_names_uniprotkb": "Tmem116",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transmembrane protein 116",
        "protein_names_refseq": "",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity",
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    {
        "uniprot_canonical_ac": "A0ABK0LU98-1",
        "uniprot_id": "A0ABK0LU98_RAT",
        "mass": 30645.0,
        "length": 307,
        "protein_name": "Heterogeneous nuclear ribonucleoprotein A0",
        "gene_name": "Hnrnpa0",
        "organism": "Rat",
        "refseq_name": "heterogeneous nuclear ribonucleoprotein A0",
        "refseq_ac": "NP_001387712",
        "gene_names_uniprotkb": "Hnrnpa0",
        "gene_names_refseq": "Hnrnpa0; Hnrpa0; RGD1563684",
        "protein_names_uniprotkb": "Heterogeneous nuclear ribonucleoprotein A0",
        "protein_names_refseq": "heterogeneous nuclear ribonucleoprotein A0",
        "tax_id": 10116,
        "disease": "gastric adenocarcinoma (Disease Ontology:DOID:3717)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "34502162",
        "class_list": "",
        "function": "mRNA-binding component of ribonucleosomes. Specifically binds AU-rich element (ARE)-containing mRNAs. Involved in post-transcriptional regulation of cytokines mRNAs., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 1,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 1,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 1,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 1,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003729 mRNA binding;GO:0019901 protein kinase binding;GO:0035925 mRNA 3'-UTR AU-rich region binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0045202 synapse",
        "go_biological_process": "GO:0070935 3'-UTR-mediated mRNA stabilization;GO:0006954 inflammatory response;GO:0032496 response to lipopolysaccharide",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0ABK0LU98-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LTG6-1",
        "uniprot_id": "A0ABK0LTG6_RAT",
        "mass": 48894.0,
        "length": 442,
        "protein_name": "Radical S-adenosyl methionine domain-containing protein",
        "gene_name": "Rsad1",
        "organism": "Rat",
        "refseq_name": "radical S-adenosyl methionine domain-containing protein 1, mitochondrial",
        "refseq_ac": "NP_001258140",
        "gene_names_uniprotkb": "Rsad1",
        "gene_names_refseq": "Rsad1",
        "protein_names_uniprotkb": "Radical S-adenosyl methionine domain-containing protein",
        "protein_names_refseq": "radical S-adenosyl methionine domain-containing protein 1, mitochondrial",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:688146)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be a heme chaperone, appears to bind heme. Homologous bacterial proteins do not have oxygen-independent coproporphyrinogen-III oxidase activity. Binds 1 [4Fe-4S] cluster. The cluster is coordinated with 3 cysteines and an exchangeable S-adenosyl-L-methionine., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0051539 4 iron, 4 sulfur cluster binding;GO:0020037 heme binding;GO:0004109 coproporphyrinogen oxidase activity;GO:0003824 catalytic activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion",
        "go_biological_process": "GO:0006779 porphyrin-containing compound biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LTG6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LU34-1",
        "uniprot_id": "A0ABK0LU34_RAT",
        "mass": 35937.0,
        "length": 312,
        "protein_name": "Derlin",
        "gene_name": "Derl1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Derl1; LOC120094610",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Derlin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362912)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Functional component of endoplasmic reticulum-associated degradation (ERAD) for misfolded lumenal proteins. May act by forming a channel that allows the retrotranslocation of misfolded proteins into the cytosol where they are ubiquitinated and degraded by the proteasome., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005047 signal recognition particle binding;GO:0002020 protease binding;GO:0042802 identical protein binding;GO:0051117 ATPase binding;GO:0031625 ubiquitin protein ligase binding",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0036502 Derlin-1-VIMP complex;GO:0005769 early endosome;GO:0005783 endoplasmic reticulum;GO:0016020 membrane",
        "go_biological_process": "GO:0010498 proteasomal protein catabolic process;GO:0033554 cellular response to stress;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0031398 positive regulation of protein ubiquitination;GO:0030968 endoplasmic reticulum unfolded protein response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LU34-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LTW0-1",
        "uniprot_id": "A0ABK0LTW0_RAT",
        "mass": 58156.0,
        "length": 494,
        "protein_name": "Zinc finger protein 950 like 4",
        "gene_name": "Zfp950l4",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 431-like",
        "refseq_ac": "XP_017445584",
        "gene_names_uniprotkb": "Zfp950l4; LOC100912683",
        "gene_names_refseq": "Zfp950l4",
        "protein_names_uniprotkb": "Zinc finger protein 950 like 4",
        "protein_names_refseq": "zinc finger protein 431-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100912683)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO: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_biological_process": "GO:0006355 regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LTW0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LS22-1",
        "uniprot_id": "A0ABK0LS22_RAT",
        "mass": 20003.0,
        "length": 176,
        "protein_name": "Coiled-coil domain containing 182",
        "gene_name": "Ccdc182",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ccdc182",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Coiled-coil domain containing 182",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:689962)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "GO:0008585 female gonad development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LS22-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LSK9-1",
        "uniprot_id": "A0ABK0LSK9_RAT",
        "mass": 68147.0,
        "length": 614,
        "protein_name": "Hyaluronan and proteoglycan link protein 3",
        "gene_name": "Hapln3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Hapln3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Hyaluronan and proteoglycan link protein 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May function in hyaluronic acid binding., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005540 hyaluronic acid binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0045202 synapse;GO:0072534 perineuronal net;GO:0005576 extracellular region",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0007417 central nervous system development;GO:0001501 skeletal system development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LSK9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LU39-1",
        "uniprot_id": "A0ABK0LU39_RAT",
        "mass": 29376.0,
        "length": 261,
        "protein_name": "COMM domain-containing protein 1",
        "gene_name": "Commd1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Commd1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "COMM domain-containing protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0019871 sodium channel inhibitor activity;GO:0005546 phosphatidylinositol-4,5-bisphosphate binding;GO:0005547 phosphatidylinositol-3,4,5-trisphosphate binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005768 endosome;GO:0005769 early endosome",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0055070 copper ion homeostasis;GO:0097006 regulation of plasma lipoprotein particle levels;GO:1902072 negative regulation of hypoxia-inducible factor-1alpha signaling pathway;GO:1904109 positive regulation of cholesterol import",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LU39-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LRM4-1",
        "uniprot_id": "A0ABK0LRM4_RAT",
        "mass": 52732.0,
        "length": 478,
        "protein_name": "Serine hydroxymethyltransferase",
        "gene_name": "Shmt1",
        "organism": "Rat",
        "refseq_name": "serine hydroxymethyltransferase, cytosolic",
        "refseq_ac": "NP_001400080",
        "gene_names_uniprotkb": "Shmt1",
        "gene_names_refseq": "LRRGT00032; Shmt1; Shmt; mShmt",
        "protein_names_uniprotkb": "Serine hydroxymethyltransferase; 2.1.2.1",
        "protein_names_refseq": "serine hydroxymethyltransferase 1 (soluble); serine hydroxymethyltransferase, cytosolic",
        "tax_id": 10116,
        "disease": "alcohol use disorder (Disease Ontology:DOID:1574); breast cancer (Disease Ontology:DOID:1612); cancer (Disease Ontology:DOID:162); ovarian cancer (Disease Ontology:DOID:2394); amino acid metabolic disorder (Disease Ontology:DOID:9252)",
        "pathway": " (rno:287379);  (R-RNO-196757);  (R-RNO-71262)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "36735737",
        "class_list": "",
        "function": "Identification of AGXT2, SHMT1, and ACO2 as important biomarkers of acute kidney injury by WGCNA. Publication Status: Online-Only, [RefSeq, PubMed]; Interconversion of serine and glycine., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
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