{
    "uniprot_canonical_ac": "A0A0G2JTY3-1",
    "uniprot_ac": "A0A0G2JTY3",
    "uniprot_id": "A0A0G2JTY3_RAT",
    "mass": {
        "chemical_mass": 48894.0,
        "monoisotopic_mass": 48894.0
    },
    "refseq": {},
    "gene_names": [
        {
            "name": "Slc37a4",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3",
            "id": "A0A0G2JTY3"
        }
    ],
    "protein_names": [
        {
            "name": "Solute carrier family 37 member 4",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A0G2JTY3"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0050571",
            "recommended_name": {
                "id": "DOID:0050571",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050571",
                "name": "congenital disorder of glycosylation type II",
                "description": "A congenital disorder of glycosylation that involves malfunctioning trimming or processing of the protein-bound oligosaccharide chain."
            },
            "synonyms": [
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "MGAT2-congenital disorder of glycosylation",
                    "description": "MGAT2-CDG is a form of congenital disorders of N-linked glycosylation characterized by facial dysmorphism (large, posteriorly rotated ears with prominent antihelices, convex nasal ridge, open mouth, large and crowded teeth), stereotypic hand movements, seizures, and varying degrees of developmental delay. A bleeding tendency is also observed and this results from diminished platelet aggregation. The disease is caused by loss-of-function mutations in the gene MGAT2 (14q21)."
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "CDG syndrome type IIa",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "CDG-IIa",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "CDG2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "MGAT2-CDG",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "N-acetylglucosaminyltransferase 2 deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "carbohydrate deficient glycoprotein syndrome type IIa",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "congenital disorder of glycosylation type 2a",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "congenital disorder of glycosylation type IIa",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "Alkuraya syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "CDG 2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "CDG IIa",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "CDGS2",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "MGAT2-CDG (CDG-IIa)",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "carbohydrate-deficient glycoprotein syndrome type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "carbohydrate-deficient glycoprotein syndrome, type II",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "carbohydrate-deficient glycoprotein syndrome, type II, formerly",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "carbohydrate-deficient glycoprotein syndrome, type II, formerly; CDGS2, formerly",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "congenital disorder of glycosylation, type IIa",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "intellectual disability, Growth retardation, prominent columella, and open mouth",
                    "description": ""
                },
                {
                    "id": "MONDO:0008908",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008908",
                    "name": "mental retardation, Growth retardation, prominent columella, and open mouth",
                    "description": ""
                },
                {
                    "id": "MIM:212066",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/212066",
                    "name": "Congenital disorder of glycosylation 2A",
                    "description": "Congenital disorder of glycosylation 2A"
                }
            ],
            "evidence": [
                {
                    "id": "0050571",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050571"
                }
            ]
        },
        {
            "disease_id": "DOID:0081330",
            "recommended_name": {
                "id": "DOID:0081330",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0081330",
                "name": "glycogen storage disease Ib",
                "description": "A glycogen storage disease I that has_material_basis_in homozygous or compound heterozygous mutation in the G6PT1 gene (SLC37A4), which encodes glucose-6-phosphate translocase, on chromosome 11q23."
            },
            "synonyms": [
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease Ib",
                    "description": "A type of glycogenosis due to G6P deficiency."
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "G6P deficiency type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "G6P translocase deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "G6PT deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD Ib",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD due to G6P deficiency type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD due to G6PT deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD type 1 non a",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD type 1b",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD1B",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSDIb",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glucose-6-phosphate transport defect",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease Ib",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease Ic",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease due to G6P deficiency type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease type 1b",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease type I non-a",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease type Ic",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogenosis due to glucose-6-phosphatase deficiency type 1B",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogenosis due to glucose-6-phosphatase transport defect type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogenosis type 1b",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogenosis type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD Ic",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD1C",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "Gsd1C",
                    "description": ""
                },
                {
                    "id": "MIM:232220",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/232220",
                    "name": "Glycogen storage disease 1B",
                    "description": "Glycogen storage disease 1B"
                }
            ],
            "evidence": [
                {
                    "id": "0081330",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0081330"
                }
            ]
        },
        {
            "disease_id": "DOID:0081331",
            "recommended_name": {
                "id": "DOID:0081331",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0081331",
                "name": "glycogen storage disease Ic",
                "description": "A glycogen storage disease I that has_material_basis_in homozygous or compound heterozygous mutation in the G6PT1 gene (SLC37A4), which encodes glucose-6-phosphate translocase, on chromosome 11q23. G6PT1 is also the site of the defect in glycogen storage disease Ib."
            },
            "synonyms": [
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease Ib",
                    "description": "A type of glycogenosis due to G6P deficiency."
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "G6P deficiency type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "G6P translocase deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "G6PT deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD Ib",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD due to G6P deficiency type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD due to G6PT deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD type 1 non a",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD type 1b",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD1B",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSDIb",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glucose-6-phosphate transport defect",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease Ib",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease Ic",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease due to G6P deficiency type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease type 1b",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease type I non-a",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogen storage disease type Ic",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogenosis due to glucose-6-phosphatase deficiency type 1B",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogenosis due to glucose-6-phosphatase transport defect type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogenosis type 1b",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "glycogenosis type IB",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD Ic",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "GSD1C",
                    "description": ""
                },
                {
                    "id": "MONDO:0009288",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009288",
                    "name": "Gsd1C",
                    "description": ""
                },
                {
                    "id": "MIM:232240",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/232240",
                    "name": "Glycogen storage disease 1C",
                    "description": "Glycogen storage disease 1C"
                }
            ],
            "evidence": [
                {
                    "id": "0081331",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0081331"
                }
            ]
        },
        {
            "disease_id": "DOID:2749",
            "recommended_name": {
                "id": "DOID:2749",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2749",
                "name": "glycogen storage disease Ia",
                "description": "A glycogen storage disease I that has_material_basis_in homozygous or compound heterozygous mutation in the G6PC gene, which encodes glucose-6-phosphatase (G6Pase), on chromosome 17q21."
            },
            "synonyms": [
                {
                    "id": "MONDO:0009287",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
                    "name": "glycogen storage disease due to glucose-6-phosphatase deficiency type IA",
                    "description": "Glycogenosis due to glucose-6-phosphatase deficiency (G6P) type a, or glycogen storage disease (GSD) type 1a, is a type of glycogenosis due to G6P deficiency."
                },
                {
                    "id": "MONDO:0009287",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
                    "name": "G6P deficiency type 1a",
                    "description": ""
                },
                {
                    "id": "MONDO:0009287",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
                    "name": "G6PC glycogen storage disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0009287",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
                    "name": "GSD due to G6P deficiency type 1a",
                    "description": ""
                },
                {
                    "id": "MONDO:0009287",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
                    "name": "GSD due to G6P deficiency type Ia",
                    "description": ""
                },
                {
                    "id": "MONDO:0009287",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
                    "name": "GSD type 1a",
                    "description": ""
                },
                {
                    "id": "MONDO:0009287",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
                    "name": "GSDIa",
                    "description": ""
                },
                {
                    "id": "MONDO:0009287",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
                    "name": "glycogen storage disease caused by mutation in G6PC",
                    "description": ""
                },
                {
                    "id": "MONDO:0009287",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
                    "name": "glycogen storage disease due to G6P deficiency type Ia",
                    "description": ""
                },
                {
                    "id": "MONDO:0009287",
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                {
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                {
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                {
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                },
                {
                    "id": "MONDO:0009287",
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                },
                {
                    "id": "MONDO:0009287",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
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                },
                {
                    "id": "MONDO:0009287",
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                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
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                },
                {
                    "id": "MONDO:0009287",
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                {
                    "id": "MONDO:0009287",
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                {
                    "id": "MONDO:0009287",
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                },
                {
                    "id": "MONDO:0009287",
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                {
                    "id": "MONDO:0009287",
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                {
                    "id": "MONDO:0009287",
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                    "url": "https://monarchinitiative.org/disease/MONDO:0009287",
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                },
                {
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                {
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            "id": "PF07690",
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    },
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            "isoform_ac": "A0A0G2JTY3-1",
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                "length": 455,
                "header": "tr|A0A0G2JTY3-1|A0A0G2JTY3_RAT Isoform 1 of Solute carrier family 37 member 4  OS=Rattus norvegicus OX=10116 GN=Slc37a4 PE=1 SV=2 CANONICAL=A0A0G2JTY3-1"
            },
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                "start_pos": 44728789,
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                        "id": "ENSRNOT00000089763.2",
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                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000068889.2",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000068889.2"
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                ]
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        },
        {
            "isoform_ac": "F7EWB7-1",
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                "length": 434,
                "header": "tr|F7EWB7-1|F7EWB7_RAT Computationally mapped isoform of Solute carrier family 37 member 4  OS=Rattus norvegicus OX=10116 GN=Slc37a4 PE=1 SV=1 CANONICAL=A0A0G2JTY3-1"
            },
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                "start_pos": 44728789,
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                "evidence": [
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                        "id": "ENSRNOT00000015810.6",
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                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000015810.4",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000015810.4"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "R-RNO-70263",
            "name": "Gluconeogenesis",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-70263",
            "resource": "Reactome",
            "description": "Gluconeogenesis"
        }
    ],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Biological Process",
                "total": 20,
                "go_terms": [
                    {
                        "name": "myeloid progenitor cell differentiation",
                        "id": "GO:0002318",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002318",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "triglyceride metabolic process",
                        "id": "GO:0006641",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006641",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to nutrient",
                        "id": "GO:0007584",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007584",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "glycogen metabolic process",
                        "id": "GO:0005977",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005977",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "intracellular calcium ion homeostasis",
                        "id": "GO:0006874",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006874",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to organic cyclic compound",
                        "id": "GO:0014070",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0014070",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of catalytic activity",
                        "id": "GO:0043085",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043085",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "gluconeogenesis",
                        "id": "GO:0006094",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006094",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "glucose homeostasis",
                        "id": "GO:0042593",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042593",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cholesterol homeostasis",
                        "id": "GO:0042632",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042632",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to glucose",
                        "id": "GO:0009749",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009749",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "steroid metabolic process",
                        "id": "GO:0008202",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008202",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "neutrophil homeostasis",
                        "id": "GO:0001780",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001780",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "glucose-6-phosphate transport",
                        "id": "GO:0015760",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015760",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "neutrophil chemotaxis",
                        "id": "GO:0030593",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030593",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "respiratory burst",
                        "id": "GO:0045730",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045730",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "lactate metabolic process",
                        "id": "GO:0006089",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006089",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "negative regulation of chemokine production",
                        "id": "GO:0032682",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032682",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "post-embryonic hemopoiesis",
                        "id": "GO:0035166",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035166",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "phosphate ion transmembrane transport",
                        "id": "GO:0035435",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035435",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JTY3",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JTY3"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 1,
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