{
    "uniprot_canonical_ac": "A0A0G2K171-1",
    "uniprot_ac": "A0A0G2K171",
    "uniprot_id": "A0A0G2K171_RAT",
    "mass": {
        "chemical_mass": 54769.0,
        "monoisotopic_mass": 54769.0
    },
    "refseq": {},
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        {
            "name": "Slc19a3",
            "resource": "UniProtKB",
            "type": "recommended",
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    ],
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            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A0G2K171"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0050659",
            "recommended_name": {
                "id": "DOID:0050659",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050659",
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                "description": "A basal ganglia disease that is characterized by recurrent subacute encephalopathy, has_symptom confusion, has_symptom seizure, has_symptom ataxia, has_symptom dystonia, has_symptom supranuclear facial palsy, has_symptom external ophthalmoplegia, and has_symptom dysphagia."
            },
            "synonyms": [
                {
                    "id": "MONDO:0011841",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011841",
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                    "description": ""
                },
                {
                    "id": "MONDO:0011841",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011841",
                    "name": "BBGD",
                    "description": ""
                },
                {
                    "id": "MONDO:0011841",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011841",
                    "name": "BTBGD",
                    "description": ""
                },
                {
                    "id": "MONDO:0011841",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011841",
                    "name": "biotin-thiamine-responsive basal ganglia disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0011841",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011841",
                    "name": "thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)",
                    "description": ""
                },
                {
                    "id": "MONDO:0011841",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011841",
                    "name": "thiamine-responsive encephalopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0011841",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011841",
                    "name": "THMD2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011841",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011841",
                    "name": "basal ganglia disease, biotin-responsive",
                    "description": ""
                },
                {
                    "id": "MONDO:0011841",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011841",
                    "name": "encephalopathy, thiamine-responsive",
                    "description": ""
                },
                {
                    "id": "MONDO:0011841",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011841",
                    "name": "thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive type)",
                    "description": ""
                },
                {
                    "id": "MIM:607483",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/607483",
                    "name": "Thiamine metabolism dysfunction syndrome 2, biotin- or thiamine-responsive type",
                    "description": "Thiamine metabolism dysfunction syndrome 2, biotin- or thiamine-responsive type"
                }
            ],
            "evidence": [
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                    "id": "0050659",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050659"
                }
            ]
        },
        {
            "disease_id": "DOID:784",
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                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:784",
                "name": "chronic kidney disease",
                "description": "A kidney failure that is characterized by the gradual loss of kidney function."
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            "synonyms": [
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                    "id": "DOID:784",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:784",
                    "name": "CKD",
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                },
                {
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:784",
                    "name": "CRF",
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                },
                {
                    "id": "DOID:784",
                    "resource": "Disease Ontology",
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                    "name": "chronic kidney failure",
                    "description": ""
                },
                {
                    "id": "DOID:784",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:784",
                    "name": "chronic renal disease",
                    "description": ""
                },
                {
                    "id": "DOID:784",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:784",
                    "name": "chronic renal failure syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:784",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:784",
                    "name": "renal failure - chronic",
                    "description": ""
                }
            ],
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                    "id": "784",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:784"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
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            "name": "Rattus norvegicus",
            "taxid": 10116,
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                    "url": "https://www.uniprot.org/uniprot/A0A0G2K171"
                }
            ],
            "common_name": "Rat"
        }
    ],
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            "url": "https://www.uniprot.org/uniprot/A0A0G2K171",
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        }
    ],
    "crossref": [
        {
            "id": "ENSRNOG00000057256",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000057256",
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            ]
        },
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            "url": "https://www.ebi.ac.uk/interpro/entry/IPR002666",
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            "categories": [
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            ]
        },
        {
            "id": "IPR036259",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR036259",
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            "categories": [
                "Protein Classification"
            ]
        },
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            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:316559",
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        },
        {
            "id": "DIWACYA",
            "url": "https://omabrowser.org/oma/group/DIWACYA/",
            "database": "OMA",
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                "Protein Classification"
            ]
        },
        {
            "id": "51626at2759",
            "url": "http://www.orthodb.org/?query=51626at2759",
            "database": "OrthoDB",
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                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10686",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10686",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10686:SF37",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10686:SF37",
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                "Protein Classification"
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        },
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            "id": "PF01770",
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            ]
        },
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            "id": "1311413",
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            ]
        },
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            "id": "A0A0G2K171",
            "url": "https://www.uniprot.org/uniprot/A0A0G2K171",
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        },
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            ]
        }
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    },
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            "isoform_ac": "A0A0G2K171-1",
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                "length": 485,
                "header": "tr|A0A0G2K171-1|A0A0G2K171_RAT Isoform 1 of Solute carrier family 19 member 3  OS=Rattus norvegicus OX=10116 GN=Slc19a3 PE=3 SV=2 CANONICAL=A0A0G2K171-1"
            },
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                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000083667.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000083667.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000071722.2",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000071722.2"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
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        {
            "id": "rno:316559",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:316559",
            "resource": "KEGG Pathway"
        },
        {
            "id": "R-RNO-196819",
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            "resource": "Reactome",
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                "name": "Cellular Component",
                "total": 1,
                "go_terms": [
                    {
                        "name": "plasma membrane",
                        "id": "GO:0005886",
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                        "name": "transmembrane transport",
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                        ],
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                    },
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                        "name": "thiamine transmembrane transporter activity",
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