{
    "uniprot_canonical_ac": "A0A0G2K7F0-1",
    "uniprot_ac": "A0A0G2K7F0",
    "uniprot_id": "A0A0G2K7F0_RAT",
    "mass": {
        "chemical_mass": 225106.0,
        "monoisotopic_mass": 225106.0
    },
    "refseq": {},
    "gene_names": [
        {
            "name": "Fancm",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0",
            "id": "A0A0G2K7F0"
        }
    ],
    "protein_names": [
        {
            "name": "FA complementation group M",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0#names_and_taxonomy",
            "id": "A0A0G2K7F0"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0050865",
            "recommended_name": {
                "id": "DOID:0050865",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050865",
                "name": "tongue squamous cell carcinoma",
                "description": "A head and neck squamous cell carcinoma that is located_in the tongue."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "0050865",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050865"
                }
            ]
        },
        {
            "disease_id": "DOID:0111916",
            "recommended_name": {
                "id": "DOID:0111916",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0111916",
                "name": "spermatogenic failure 28",
                "description": "A spermatogenic failure characterized by nonobstructive azoospermia and a Sertoli cell-only phenotype in testes that has_material_basis_in homozygous or compound heterozygous mutation in FANCM on chromosome 14q21.2."
            },
            "synonyms": [
                {
                    "id": "DOID:0111916",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111916",
                    "name": "SPGF28",
                    "description": ""
                },
                {
                    "id": "MONDO:0054732",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0054732",
                    "name": "spermatogenic failure 28",
                    "description": ""
                },
                {
                    "id": "MONDO:0054732",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0054732",
                    "name": "spermatogenic failure 28; SPGF28",
                    "description": ""
                },
                {
                    "id": "MONDO:0054732",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0054732",
                    "name": "SPGF28",
                    "description": ""
                },
                {
                    "id": "MIM:618086",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/618086",
                    "name": "Spermatogenic failure 28",
                    "description": "Spermatogenic failure 28"
                }
            ],
            "evidence": [
                {
                    "id": "0111916",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111916"
                }
            ]
        },
        {
            "disease_id": "DOID:5426",
            "recommended_name": {
                "id": "DOID:5426",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:5426",
                "name": "premature ovarian failure",
                "description": "An ovarian disease where ovaries do not produce estrogen despite high levels of circulating gonadotropins in women under 40."
            },
            "synonyms": [
                {
                    "id": "DOID:5426",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5426",
                    "name": "hypergonadotropic hypogonadism",
                    "description": ""
                },
                {
                    "id": "DOID:5426",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5426",
                    "name": "premature menopause",
                    "description": ""
                },
                {
                    "id": "DOID:5426",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5426",
                    "name": "premature ovarian insufficiency",
                    "description": ""
                },
                {
                    "id": "DOID:5426",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5426",
                    "name": "primary ovarian insufficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0012689",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012689",
                    "name": "premature ovarian failure 5",
                    "description": "Any primary ovarian failure in which the cause of the disease is a mutation in the NOBOX gene."
                },
                {
                    "id": "MONDO:0012689",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012689",
                    "name": "NOBOX primary ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0012689",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012689",
                    "name": "premature ovarian failure 5; Pof5",
                    "description": ""
                },
                {
                    "id": "MONDO:0012689",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012689",
                    "name": "primary ovarian failure caused by mutation in NOBOX",
                    "description": ""
                },
                {
                    "id": "MONDO:0012689",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012689",
                    "name": "Pof5",
                    "description": ""
                },
                {
                    "id": "MONDO:0012689",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012689",
                    "name": "premature ovarian failure 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0012689",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012689",
                    "name": "premature ovarian failure type 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0010373",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010373",
                    "name": "premature ovarian failure 2B",
                    "description": "Any primary ovarian failure in which the cause of the disease is a mutation in the POF1B gene."
                },
                {
                    "id": "MONDO:0010373",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010373",
                    "name": "premature ovarian failure 2B; POF2B",
                    "description": ""
                },
                {
                    "id": "MONDO:0010373",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010373",
                    "name": "premature ovarian failure type 2B",
                    "description": ""
                },
                {
                    "id": "MONDO:0010373",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010373",
                    "name": "POF2B",
                    "description": ""
                },
                {
                    "id": "MONDO:0010373",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010373",
                    "name": "POF1B primary ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0010373",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010373",
                    "name": "premature ovarian failure 2B",
                    "description": ""
                },
                {
                    "id": "MONDO:0010373",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010373",
                    "name": "primary ovarian failure caused by mutation in POF1B",
                    "description": ""
                },
                {
                    "id": "MONDO:0014322",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014322",
                    "name": "premature ovarian failure 9",
                    "description": "Any primary ovarian failure in which the cause of the disease is a mutation in the HFM1 gene."
                },
                {
                    "id": "MONDO:0014322",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014322",
                    "name": "premature ovarian failure 9; Pof9",
                    "description": ""
                },
                {
                    "id": "MONDO:0014322",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014322",
                    "name": "HFM1 primary ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0014322",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014322",
                    "name": "Pof9",
                    "description": ""
                },
                {
                    "id": "MONDO:0014322",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014322",
                    "name": "premature ovarian failure 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0014322",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014322",
                    "name": "primary ovarian failure caused by mutation in HFM1",
                    "description": ""
                },
                {
                    "id": "MONDO:0014322",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014322",
                    "name": "premature ovarian failure type 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0014321",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014321",
                    "name": "premature ovarian failure 8",
                    "description": "Any primary ovarian failure in which the cause of the disease is a mutation in the STAG3 gene."
                },
                {
                    "id": "MONDO:0014321",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014321",
                    "name": "premature ovarian failure 8; POF8",
                    "description": ""
                },
                {
                    "id": "MONDO:0014321",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014321",
                    "name": "STAG3 primary ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0014321",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014321",
                    "name": "POF8",
                    "description": ""
                },
                {
                    "id": "MONDO:0014321",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014321",
                    "name": "premature ovarian failure 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0014321",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014321",
                    "name": "premature ovarian failure type 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0014321",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014321",
                    "name": "primary ovarian failure caused by mutation in STAG3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "premature ovarian failure 2A",
                    "description": "Any primary ovarian failure in which the cause of the disease is a mutation in the DIAPH2 gene."
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "primary ovarian failure caused by mutation in DIAPH2",
                    "description": ""
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "premature ovarian failure 2A; POF2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "premature ovarian failure type 2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "DIAPH2 primary ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "POF2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0010350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010350",
                    "name": "premature ovarian failure 2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "premature ovarian failure 1",
                    "description": "Any primary ovarian failure in which the cause of the disease is a mutation in the FMR1 gene."
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "premature ovarian failure type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "FMR1-related premature ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "familial premature ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "fragile X-associated primary ovarian insufficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "idiopathic familial premature ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "ovarian failure, premature",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "primary ovarian failure caused by mutation in FMR1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "premature ovarian failure, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "hypergonadotropic ovarian failure, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "Pof1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "FMR1-related primary ovarian insufficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "premature ovarian failure 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "premature ovarian failure 1; Pof1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010706",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010706",
                    "name": "FMR1 primary ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0013065",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013065",
                    "name": "premature ovarian failure 7",
                    "description": "Any primary ovarian failure in which the cause of the disease is a mutation in the NR5A1 gene."
                },
                {
                    "id": "MONDO:0013065",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013065",
                    "name": "Pof7",
                    "description": ""
                },
                {
                    "id": "MONDO:0013065",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013065",
                    "name": "premature ovarian failure 7",
                    "description": ""
                },
                {
                    "id": "MONDO:0013065",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013065",
                    "name": "premature ovarian failure type 7",
                    "description": ""
                },
                {
                    "id": "MONDO:0013065",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013065",
                    "name": "NR5A1 primary ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0013065",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013065",
                    "name": "adrenal insufficiency, Nr5A1-related",
                    "description": ""
                },
                {
                    "id": "MONDO:0013065",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013065",
                    "name": "premature ovarian failure 7; Pof7",
                    "description": ""
                },
                {
                    "id": "MONDO:0013065",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013065",
                    "name": "primary ovarian failure caused by mutation in NR5A1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012169",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012169",
                    "name": "premature ovarian failure 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012169",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012169",
                    "name": "premature ovarian failure type 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012169",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012169",
                    "name": "premature ovarian failure 3; Pof3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012169",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012169",
                    "name": "Pof3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012169",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012169",
                    "name": "premature ovarian failure 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012861",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012861",
                    "name": "premature ovarian failure 6",
                    "description": "Any primary ovarian failure in which the cause of the disease is a mutation in the FIGLA gene."
                },
                {
                    "id": "MONDO:0012861",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012861",
                    "name": "premature ovarian failure type 6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012861",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012861",
                    "name": "FIGLA primary ovarian failure",
                    "description": ""
                },
                {
                    "id": "MONDO:0012861",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012861",
                    "name": "primary ovarian failure caused by mutation in FIGLA",
                    "description": ""
                },
                {
                    "id": "MONDO:0012861",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012861",
                    "name": "premature ovarian failure 6; Pof6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012861",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012861",
                    "name": "Pof6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012861",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012861",
                    "name": "premature ovarian failure 6",
                    "description": ""
                },
                {
                    "id": "MIM:611548",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/611548",
                    "name": "Premature ovarian failure 5",
                    "description": "Premature ovarian failure 5"
                },
                {
                    "id": "MIM:300604",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/300604",
                    "name": "Premature ovarian failure 2B",
                    "description": "Premature ovarian failure 2B"
                },
                {
                    "id": "MIM:615724",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/615724",
                    "name": "Premature ovarian failure 9",
                    "description": "Premature ovarian failure 9"
                },
                {
                    "id": "MIM:615723",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/615723",
                    "name": "Premature ovarian failure 8",
                    "description": "Premature ovarian failure 8"
                },
                {
                    "id": "MIM:300511",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/300511",
                    "name": "Premature ovarian failure 2A",
                    "description": "Premature ovarian failure 2A"
                },
                {
                    "id": "MIM:311360",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/311360",
                    "name": "Premature ovarian failure 1",
                    "description": "Premature ovarian failure 1"
                },
                {
                    "id": "MIM:612964",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/612964",
                    "name": "Premature ovarian failure 7",
                    "description": "Premature ovarian failure 7"
                },
                {
                    "id": "MIM:608996",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/608996",
                    "name": "Premature ovarian failure 3",
                    "description": "Premature ovarian failure 3"
                },
                {
                    "id": "MIM:612310",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/612310",
                    "name": "Premature ovarian failure 6",
                    "description": "Premature ovarian failure 6"
                }
            ],
            "evidence": [
                {
                    "id": "5426",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:5426"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0G2K7F0",
                    "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "gene": [
        {
            "name": "Fancm",
            "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0",
            "locus": {
                "chromosome": "6",
                "start_pos": 86823684,
                "end_pos": 86876633,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSRNOG00000056721",
                        "url": "https://www.ensembl.org/id/ENSRNOG00000056721"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "ENSRNOG00000056721",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000056721",
            "database": "Bgee"
        },
        {
            "id": "cd18033",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd18033",
            "database": "CDD"
        },
        {
            "id": "IPR001650",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001650",
            "database": "InterPro"
        },
        {
            "id": "IPR006166",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR006166",
            "database": "InterPro"
        },
        {
            "id": "IPR006935",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR006935",
            "database": "InterPro"
        },
        {
            "id": "IPR010994",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR010994",
            "database": "InterPro"
        },
        {
            "id": "IPR011335",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR011335",
            "database": "InterPro"
        },
        {
            "id": "IPR014001",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR014001",
            "database": "InterPro"
        },
        {
            "id": "IPR027417",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR027417",
            "database": "InterPro"
        },
        {
            "id": "IPR031879",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR031879",
            "database": "InterPro"
        },
        {
            "id": "IPR039686",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR039686",
            "database": "InterPro"
        },
        {
            "id": "IPR044749",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR044749",
            "database": "InterPro"
        },
        {
            "id": "EQPWDRE",
            "url": "https://omabrowser.org/oma/group/EQPWDRE/",
            "database": "OMA"
        },
        {
            "id": "PTHR14025:SF20",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR14025:SF20",
            "database": "PANTHER"
        },
        {
            "id": "PF00271",
            "url": "http://pfam.xfam.org/family/PF00271",
            "database": "Pfam"
        },
        {
            "id": "PF02732",
            "url": "http://pfam.xfam.org/family/PF02732",
            "database": "Pfam"
        },
        {
            "id": "PF04851",
            "url": "http://pfam.xfam.org/family/PF04851",
            "database": "Pfam"
        },
        {
            "id": "PF16783",
            "url": "http://pfam.xfam.org/family/PF16783",
            "database": "Pfam"
        },
        {
            "id": "R-RNO-6783310",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-6783310",
            "database": "Reactome"
        },
        {
            "id": "1307897",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1307897",
            "database": "RGD"
        },
        {
            "id": "A0A0G2K7F0",
            "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0",
            "database": "UniProtKB"
        },
        {
            "id": "A0A0G2K7F0-1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0-1",
            "database": "UniProtKB"
        },
        {
            "id": "A0A1W2Q6G5",
            "url": "https://www.uniprot.org/uniprot/A0A1W2Q6G5",
            "database": "UniProtKB"
        },
        {
            "id": "A0A1W2Q6G5-1",
            "url": "https://www.uniprot.org/uniprot/A0A1W2Q6G5-1",
            "database": "UniProtKB"
        }
    ],
    "sequence": {
        "sequence": "MSGRQRTLFQTWGPSLVRGAGAPGCGQPRSPAVTESLPEEDDEVLLVAAYEAEQQLDPGDGGFCAAAGALWIYPTNCPVRDYQLDISRTALFCNTLVCLPTGLGKTFIAAVVMYNFYRWFPSGKVVFMAPTKPLVTQQMEACFHVMGIPQSHMAEMTGSTQAVNRKEIWSSRRVLFLTPQVMVNDLTRGAVPAAHVKCLVVDEAHKALGNYAYCQVVRELVKYTNHFRILALSATPGSDIKAVQQVITNLLIEKIELRSEDSPDILPYSHERRVEKLVVPLGEELGAIQKTYVQILETFASSLIKRNILMKRDIPNLTKYQIILARDQFRKNPSPNIVGVQQGIIEGELAICISLYHGYELLQQLGMRSLYFFLSGIMDGTKGMTRVKTELSRNEDFTKLYSHLQSVFAHVRDAAAASEASAFQKGNKEKKFVYSHPKLKKLEEVILEHFKSWNAKNTTEKKCQESRVMIFSSFRDSVEEIAEMLSQHQPGVRVMTFVGHASGKNTKGYTQKEQLRVVRQFRDGGYNTLVSTCVGEEGLDIGEVDLIICFDAQKSPIRLIQRMGRTGRRRQGRIVVILAEGREERTYNQSQSNKKNIYKAISGNRQVLRLYQGSPRMVPDKINPELHKMFITHGVYESEKARSVQRKSFSSRSGIKAGNSNKDGLLSEEEFNLWNRLYRLGDSDTVKGVALPRSHFLSLQEDRVAQEPTTGIHQLSLSEWSLWQDHPLPTHQVEHSDRCHHFISIMRMIEGMRHEEDECSYELKIKPFLQMEDVYSKYNAPRNGYKNVASVTRIAPKKSSFRPSVDAGGSLSVTESEEGCADTVEQMDSEWTKITSLREKATTVGKGQTREQTDDDHDDADSSDSDRNSPADVVSRVPPSGERVADVGGIPILGAVTEDDSHTGTLLMECQVTEKSLARYSLDSGYSSFSDDKSLSSHLFLPLEEELYTERAAELFYRCQPMTEEVLANVEKFLSHSPPSLSGLSDVEYAVTQGFELDNESCLPYPEREHSPKPGSPYPEREHSPKPASLALYTAVNSQSNLELNSAKHTNPPSEKDCLPATTHNNIPDQPSFCDSDSETHNIKNQNLVSNSYGQIQVNLENNLVDENSHDDSEPPVLFTDEDESLLLFEDDLKNIEDGTEELNGVGLPPLDRISQPLCVSDKTLISEMPPVSHFLISDELLDDDSEPEDQIICDTKCWEGVEGRDEEIKTEGQPFDCSADLFSVTFDLGFCSSGSDDENPARASDRSSTLGTAEVPGRHSDKEVKDASHASGPLGGTISPIPSEKMPWSPCAQSKECAPFHSALSLPVRERAMSTPLSKAHRSSKTGAHVLKTLDSTKEKAGGQGFKVTLNPRFDNLGFSVEETKSSDQLSVYQSPRCPKVEHLTSESEDDVFLKKTRKPKGNVLKSPEDQKNNEVDSPIHVVKKSRVLRSELSSSDDESENFHRPCPKLEYFKDRNRNTRKGSKAQKKRIHMKALARGFLDEEAEVSGEDADCVSSDEGDDSENEKDSSLLDFVNDRTQLSQAINDSEMRAIYMKSVRSPLMSTKYKMVREKHNSMNIFSQIPEQDENYLEDSFCVAEEESCRSQSSEEEIFVDFNLTKDSFTDEDIRYKTRHAVKLKQMNKKQNCTRSRKKLSRIILPDSDSSEEENTANGREDPSAGGHAADKHTQQGQLWASGPSGSVQPKVLCNPAGNQSSGQRLQVLPNIMDAVPGALNVRAQSHNQTKSTSPPCASVESRKECGNRPVQLKVGDQDTSAAPCSASLLPDAEVLIAPRHPREGNRACILVDSREITTGLEVISSLRTVHGLQVEICPLNGCDYIVSNRMVVERKSQSEMLSNTAKNKFIEQIQRLQSMFQRICVIVEKDREKAGDISKMFRRTKCYDSLLTALVGAGIRILFSSGQEETAGLIKELSLVEQRKNAGIHIPAVLDTGTCEALQFYLSIPGVSYVTALNMCHQFSSVKKMVNSSPEEISTCAQVTHQKAEEIYKYIHYTFDMQMLPNDLTQERQKSETCSTL",
        "length": 2017,
        "header": "tr|A0A0G2K7F0-1|A0A0G2K7F0_RAT Isoform 1 of FA complementation group M  OS=Rattus norvegicus OX=10116 GN=Fancm PE=3 SV=1 CANONICAL=A0A0G2K7F0-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A0G2K7F0-1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0#A0A0G2K7F0-1",
            "sequence": {
                "sequence": "MSGRQRTLFQTWGPSLVRGAGAPGCGQPRSPAVTESLPEEDDEVLLVAAYEAEQQLDPGDGGFCAAAGALWIYPTNCPVRDYQLDISRTALFCNTLVCLPTGLGKTFIAAVVMYNFYRWFPSGKVVFMAPTKPLVTQQMEACFHVMGIPQSHMAEMTGSTQAVNRKEIWSSRRVLFLTPQVMVNDLTRGAVPAAHVKCLVVDEAHKALGNYAYCQVVRELVKYTNHFRILALSATPGSDIKAVQQVITNLLIEKIELRSEDSPDILPYSHERRVEKLVVPLGEELGAIQKTYVQILETFASSLIKRNILMKRDIPNLTKYQIILARDQFRKNPSPNIVGVQQGIIEGELAICISLYHGYELLQQLGMRSLYFFLSGIMDGTKGMTRVKTELSRNEDFTKLYSHLQSVFAHVRDAAAASEASAFQKGNKEKKFVYSHPKLKKLEEVILEHFKSWNAKNTTEKKCQESRVMIFSSFRDSVEEIAEMLSQHQPGVRVMTFVGHASGKNTKGYTQKEQLRVVRQFRDGGYNTLVSTCVGEEGLDIGEVDLIICFDAQKSPIRLIQRMGRTGRRRQGRIVVILAEGREERTYNQSQSNKKNIYKAISGNRQVLRLYQGSPRMVPDKINPELHKMFITHGVYESEKARSVQRKSFSSRSGIKAGNSNKDGLLSEEEFNLWNRLYRLGDSDTVKGVALPRSHFLSLQEDRVAQEPTTGIHQLSLSEWSLWQDHPLPTHQVEHSDRCHHFISIMRMIEGMRHEEDECSYELKIKPFLQMEDVYSKYNAPRNGYKNVASVTRIAPKKSSFRPSVDAGGSLSVTESEEGCADTVEQMDSEWTKITSLREKATTVGKGQTREQTDDDHDDADSSDSDRNSPADVVSRVPPSGERVADVGGIPILGAVTEDDSHTGTLLMECQVTEKSLARYSLDSGYSSFSDDKSLSSHLFLPLEEELYTERAAELFYRCQPMTEEVLANVEKFLSHSPPSLSGLSDVEYAVTQGFELDNESCLPYPEREHSPKPGSPYPEREHSPKPASLALYTAVNSQSNLELNSAKHTNPPSEKDCLPATTHNNIPDQPSFCDSDSETHNIKNQNLVSNSYGQIQVNLENNLVDENSHDDSEPPVLFTDEDESLLLFEDDLKNIEDGTEELNGVGLPPLDRISQPLCVSDKTLISEMPPVSHFLISDELLDDDSEPEDQIICDTKCWEGVEGRDEEIKTEGQPFDCSADLFSVTFDLGFCSSGSDDENPARASDRSSTLGTAEVPGRHSDKEVKDASHASGPLGGTISPIPSEKMPWSPCAQSKECAPFHSALSLPVRERAMSTPLSKAHRSSKTGAHVLKTLDSTKEKAGGQGFKVTLNPRFDNLGFSVEETKSSDQLSVYQSPRCPKVEHLTSESEDDVFLKKTRKPKGNVLKSPEDQKNNEVDSPIHVVKKSRVLRSELSSSDDESENFHRPCPKLEYFKDRNRNTRKGSKAQKKRIHMKALARGFLDEEAEVSGEDADCVSSDEGDDSENEKDSSLLDFVNDRTQLSQAINDSEMRAIYMKSVRSPLMSTKYKMVREKHNSMNIFSQIPEQDENYLEDSFCVAEEESCRSQSSEEEIFVDFNLTKDSFTDEDIRYKTRHAVKLKQMNKKQNCTRSRKKLSRIILPDSDSSEEENTANGREDPSAGGHAADKHTQQGQLWASGPSGSVQPKVLCNPAGNQSSGQRLQVLPNIMDAVPGALNVRAQSHNQTKSTSPPCASVESRKECGNRPVQLKVGDQDTSAAPCSASLLPDAEVLIAPRHPREGNRACILVDSREITTGLEVISSLRTVHGLQVEICPLNGCDYIVSNRMVVERKSQSEMLSNTAKNKFIEQIQRLQSMFQRICVIVEKDREKAGDISKMFRRTKCYDSLLTALVGAGIRILFSSGQEETAGLIKELSLVEQRKNAGIHIPAVLDTGTCEALQFYLSIPGVSYVTALNMCHQFSSVKKMVNSSPEEISTCAQVTHQKAEEIYKYIHYTFDMQMLPNDLTQERQKSETCSTL",
                "length": 2017,
                "header": "tr|A0A0G2K7F0-1|A0A0G2K7F0_RAT Isoform 1 of FA complementation group M  OS=Rattus norvegicus OX=10116 GN=Fancm PE=3 SV=1 CANONICAL=A0A0G2K7F0-1"
            },
            "locus": {
                "chromosome": "6",
                "start_pos": 83179791,
                "end_pos": 83127167,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000086081.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000086081.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000074177.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000074177.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A1W2Q6G5-1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0#A0A1W2Q6G5-1",
            "sequence": {
                "sequence": "MGSRGFLDEEAEVSGEDADCVSSDEGDDSENEKDSSLLDFVNDRTQLSQAINDSEMRAIYMKSVRSPLMSTKYKMVREKHNSMNIFSQIPEQDENYLEDSFCVAEEESCRSQSSEEEIFVDFNLTKDSFTDEDIRYKTRHAVKLKQMNKKQNCTRSRKKLSRIILPDSDSSEEENTANGREDPSAGGHAADKHTQQGQLWASGPSGSVQPKVLCNPAGNQSSGQRLQVLPNIMDAVPGALNVRAQSHNQTKSTSPPCASVESRKECGNRPVQLKVGDQDTSAAPCSASLLPDAEVLIAPRHPREGNRACILVDSREITTGLEVISSLRTVHGLQVEICPLNGCDYIVSNRMVVERKSQSEMLSNTAKNKFIEQIQRLQSMFQRICVIVEKDREKAGDISKMFRRTKCYDSLLTALVGAGIRILFSSGQEETAGLIKELSLVEQRKNAGIHIPAVLDTGTCEALQFYLSIPGVSYVTALNMCHQFSSVKKMVNRKRQPAERFLCVYSFKADRSALDK",
                "length": 516,
                "header": "tr|A0A1W2Q6G5-1|A0A1W2Q6G5_RAT Computationally mapped isoform of FA complementation group M  OS=Rattus norvegicus OX=10116 GN=Fancm PE=4 SV=2 CANONICAL=A0A0G2K7F0-1"
            },
            "locus": {
                "chromosome": "6",
                "start_pos": 83177096,
                "end_pos": 83166147,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000093492.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000093492.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000076245.2",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000076245.2"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "R-RNO-6783310",
            "name": "Fanconi Anemia Pathway",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-6783310",
            "resource": "Reactome",
            "description": "Fanconi Anemia Pathway"
        }
    ],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Biological Process",
                "total": 6,
                "go_terms": [
                    {
                        "name": "resolution of meiotic recombination intermediates",
                        "id": "GO:0000712",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000712",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "interstrand cross-link repair",
                        "id": "GO:0036297",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036297",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "replication fork processing",
                        "id": "GO:0031297",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031297",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of protein monoubiquitination",
                        "id": "GO:1902527",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1902527",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "replication fork reversal",
                        "id": "GO:0071932",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071932",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": "21873635"
                    },
                    {
                        "name": "double-strand break repair via synthesis-dependent strand annealing",
                        "id": "GO:0045003",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045003",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": "21873635"
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 7,
                "go_terms": [
                    {
                        "name": "3'-5' DNA helicase activity",
                        "id": "GO:0043138",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043138",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "DNA binding",
                        "id": "GO:0003677",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "chromatin binding",
                        "id": "GO:0003682",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003682",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "nuclease activity",
                        "id": "GO:0004518",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004518",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "ATP binding",
                        "id": "GO:0005524",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "four-way junction DNA binding",
                        "id": "GO:0000400",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000400",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": "21873635"
                    },
                    {
                        "name": "four-way junction helicase activity",
                        "id": "GO:0009378",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009378",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": "21873635"
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 4,
                "go_terms": [
                    {
                        "name": "Fanconi anaemia nuclear complex",
                        "id": "GO:0043240",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043240",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "FANCM-MHF complex",
                        "id": "GO:0071821",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071821",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "chromatin",
                        "id": "GO:0000785",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000785",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "nucleoplasm",
                        "id": "GO:0005654",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2K7F0",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2K7F0"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
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    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "synthesized_glycans": [],
    "cluster_types": [
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            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
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    ]
}