{
    "uniprot_canonical_ac": "A0A0G2JYV2-1",
    "uniprot_ac": "A0A0G2JYV2",
    "uniprot_id": "A0A0G2JYV2_RAT",
    "mass": {
        "chemical_mass": 165060.0,
        "monoisotopic_mass": 165060.0
    },
    "refseq": {},
    "gene_names": [
        {
            "name": "Cpsf1",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JYV2",
            "id": "A0A0G2JYV2"
        }
    ],
    "protein_names": [
        {
            "name": "Cleavage and polyadenylation specific factor 1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A0G2JYV2"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:11830",
            "recommended_name": {
                "id": "DOID:11830",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:11830",
                "name": "myopia",
                "description": "A refractive error characterized by the inability to see farther objects clearly."
            },
            "synonyms": [
                {
                    "id": "DOID:11830",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11830",
                    "name": "near vision",
                    "description": ""
                },
                {
                    "id": "DOID:11830",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11830",
                    "name": "near-sightedness",
                    "description": ""
                },
                {
                    "id": "DOID:11830",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11830",
                    "name": "short-sightedness",
                    "description": ""
                },
                {
                    "id": "MONDO:0012229",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012229",
                    "name": "myopia 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012229",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012229",
                    "name": "MYP9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012229",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012229",
                    "name": "myopia 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012230",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012230",
                    "name": "myopia 10",
                    "description": ""
                },
                {
                    "id": "MONDO:0012230",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012230",
                    "name": "MYP10",
                    "description": ""
                },
                {
                    "id": "MONDO:0012230",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012230",
                    "name": "myopia 10",
                    "description": ""
                },
                {
                    "id": "MONDO:0012227",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012227",
                    "name": "myopia 7",
                    "description": ""
                },
                {
                    "id": "MONDO:0012227",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012227",
                    "name": "MYP7",
                    "description": ""
                },
                {
                    "id": "MONDO:0012227",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012227",
                    "name": "myopia 7",
                    "description": ""
                },
                {
                    "id": "MONDO:0013506",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013506",
                    "name": "schizophrenia 16",
                    "description": "A schizophrenia that has material basis in a mutation on chromosome 7q36.3."
                },
                {
                    "id": "MONDO:0013506",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013506",
                    "name": "SCZD16",
                    "description": ""
                },
                {
                    "id": "MONDO:0013506",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013506",
                    "name": "schizophrenia 16",
                    "description": ""
                },
                {
                    "id": "MONDO:0013506",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013506",
                    "name": "schizophrenia type 16",
                    "description": ""
                },
                {
                    "id": "MONDO:0013506",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013506",
                    "name": "chromosome 7Q36.3 Duplication syndrome, 362-Kb",
                    "description": ""
                },
                {
                    "id": "MONDO:0013506",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013506",
                    "name": "schizophrenia susceptibility locus, chromosome 7Q36.3-related",
                    "description": ""
                },
                {
                    "id": "MONDO:0010685",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010685",
                    "name": "myopia 1, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010685",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010685",
                    "name": "MYP1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010685",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010685",
                    "name": "myopia 1, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010685",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010685",
                    "name": "myopia-1, X-linked recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0012995",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012995",
                    "name": "myopia 15, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0012995",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012995",
                    "name": "MYP15",
                    "description": ""
                },
                {
                    "id": "MONDO:0012995",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012995",
                    "name": "myopia 15, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0013604",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013604",
                    "name": "myopia 21, autosomal dominant",
                    "description": "Any myopia (disease) in which the cause of the disease is a mutation in the ZNF644 gene."
                },
                {
                    "id": "MONDO:0013604",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013604",
                    "name": "ZNF644 myopia (disease)",
                    "description": ""
                },
                {
                    "id": "MONDO:0013604",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013604",
                    "name": "myopia (disease) caused by mutation in ZNF644",
                    "description": ""
                },
                {
                    "id": "MONDO:0013604",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013604",
                    "name": "myopia 21, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0013604",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013604",
                    "name": "MYP21",
                    "description": ""
                },
                {
                    "id": "MONDO:0014177",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014177",
                    "name": "myopia 22, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0014177",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014177",
                    "name": "myopia 22, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0014177",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014177",
                    "name": "MYP22",
                    "description": ""
                },
                {
                    "id": "MONDO:0009713",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009713",
                    "name": "myopia 18, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0009713",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009713",
                    "name": "MYP18",
                    "description": ""
                },
                {
                    "id": "MONDO:0009713",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009713",
                    "name": "myopia 18, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0014411",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014411",
                    "name": "myopia 24, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0014411",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014411",
                    "name": "myopia 24, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0014411",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014411",
                    "name": "MYP24",
                    "description": ""
                },
                {
                    "id": "MONDO:0012228",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012228",
                    "name": "myopia 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0012228",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012228",
                    "name": "MYP8",
                    "description": ""
                },
                {
                    "id": "MONDO:0012228",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012228",
                    "name": "myopia 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0014183",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014183",
                    "name": "myopia 23, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0014183",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014183",
                    "name": "myopia 23, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0014183",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014183",
                    "name": "MYP23",
                    "description": ""
                },
                {
                    "id": "MONDO:0011300",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011300",
                    "name": "myopia 3, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0011300",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011300",
                    "name": "MYP3",
                    "description": ""
                },
                {
                    "id": "MONDO:0011300",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011300",
                    "name": "myopia 3, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0011300",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011300",
                    "name": "myopia-3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012154",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012154",
                    "name": "myopia 6",
                    "description": "Any myopia in which the cause of the disease is a mutation in the SCO2 gene."
                },
                {
                    "id": "MONDO:0012154",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012154",
                    "name": "SCO2 myopia (disease)",
                    "description": ""
                },
                {
                    "id": "MONDO:0012154",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012154",
                    "name": "myopia (disease) caused by mutation in SCO2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012154",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012154",
                    "name": "myopia 6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012154",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012154",
                    "name": "myopia type 6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012154",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012154",
                    "name": "MYP6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012154",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012154",
                    "name": "myopia, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0012389",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012389",
                    "name": "myopia 12, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0012389",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012389",
                    "name": "MYP12",
                    "description": ""
                },
                {
                    "id": "MONDO:0012389",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012389",
                    "name": "myopia 12",
                    "description": ""
                },
                {
                    "id": "MONDO:0012389",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012389",
                    "name": "myopia 12, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0012388",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012388",
                    "name": "myopia 11, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0012388",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012388",
                    "name": "MYP11",
                    "description": ""
                },
                {
                    "id": "MONDO:0012388",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012388",
                    "name": "myopia 11",
                    "description": ""
                },
                {
                    "id": "MONDO:0012388",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012388",
                    "name": "myopia 11, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0010377",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010377",
                    "name": "myopia 13, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010377",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010377",
                    "name": "MYP13",
                    "description": ""
                },
                {
                    "id": "MONDO:0010377",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010377",
                    "name": "myopia 13",
                    "description": ""
                },
                {
                    "id": "MONDO:0010377",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010377",
                    "name": "myopia 13, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0012021",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012021",
                    "name": "myopia 17, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0012021",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012021",
                    "name": "MYP17",
                    "description": ""
                },
                {
                    "id": "MONDO:0012021",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012021",
                    "name": "myopia 17, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0012021",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012021",
                    "name": "myopia 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012021",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012021",
                    "name": "myopia 4, formerly",
                    "description": ""
                },
                {
                    "id": "MONDO:0012469",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012469",
                    "name": "myopia 14",
                    "description": ""
                },
                {
                    "id": "MONDO:0012469",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012469",
                    "name": "MYP14",
                    "description": ""
                },
                {
                    "id": "MONDO:0012469",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012469",
                    "name": "myopia 14",
                    "description": ""
                },
                {
                    "id": "MONDO:0012045",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012045",
                    "name": "myopia 5, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0012045",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012045",
                    "name": "MYP5",
                    "description": ""
                },
                {
                    "id": "MONDO:0012045",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012045",
                    "name": "myopia 5, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0008053",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008053",
                    "name": "myopia 2, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0008053",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008053",
                    "name": "MYP2",
                    "description": ""
                },
                {
                    "id": "MONDO:0008053",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008053",
                    "name": "myopia 2, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0013603",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013603",
                    "name": "myopia 20, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0013603",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013603",
                    "name": "MYP20",
                    "description": ""
                },
                {
                    "id": "MONDO:0013603",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013603",
                    "name": "myopia 20, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0013508",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013508",
                    "name": "myopia 19, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0013508",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013508",
                    "name": "MYP19",
                    "description": ""
                },
                {
                    "id": "MONDO:0013508",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013508",
                    "name": "myopia 19, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0012932",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012932",
                    "name": "myopia 16, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0012932",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012932",
                    "name": "MYP16",
                    "description": ""
                },
                {
                    "id": "MONDO:0012932",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012932",
                    "name": "myopia 16",
                    "description": ""
                },
                {
                    "id": "MONDO:0012932",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012932",
                    "name": "myopia 16, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MIM:614167",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/614167",
                    "name": "Myopia 21, autosomal dominant",
                    "description": "Myopia 21, autosomal dominant"
                },
                {
                    "id": "MIM:615420",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/615420",
                    "name": "Myopia 22, autosomal dominant",
                    "description": "Myopia 22, autosomal dominant"
                },
                {
                    "id": "MIM:615946",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/615946",
                    "name": "Myopia 24, autosomal dominant",
                    "description": "Myopia 24, autosomal dominant"
                },
                {
                    "id": "MIM:615431",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/615431",
                    "name": "Myopia 23, autosomal recessive",
                    "description": "Myopia 23, autosomal recessive"
                },
                {
                    "id": "MIM:608908",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/608908",
                    "name": "Myopia 6",
                    "description": "Myopia 6"
                }
            ],
            "evidence": [
                {
                    "id": "11830",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:11830"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0G2JYV2",
                    "url": "https://www.uniprot.org/uniprot/A0A0G2JYV2"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "gene": [
        {
            "name": "Cpsf1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JYV2",
            "locus": {
                "chromosome": "7",
                "start_pos": 108319434,
                "end_pos": 108329934,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSRNOG00000030705",
                        "url": "https://www.ensembl.org/id/ENSRNOG00000030705"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "IPR004871",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR004871",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR015943",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR015943",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR018846",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR018846",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PMTKFKL",
            "url": "https://omabrowser.org/oma/group/PMTKFKL/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10644",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10644",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10644:SF2",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10644:SF2",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF03178",
            "url": "http://pfam.xfam.org/family/PF03178",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF10433",
            "url": "http://pfam.xfam.org/family/PF10433",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "1306406",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1306406",
            "database": "RGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "A0A0G2JYV2",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JYV2",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0G2JYV2-1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JYV2-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MYAVYKQAHPPTGLEFAMYCNFFNNSERNLVVAGTSQLYVYRLNRDAEALTKNDGSTEGKAHREKLELVASFSFFGNVMSMASVQLAGAKRDALLLSFKDAKVSSVGPAGGPGHSGVTEQRRLGCISVIKVGIERAMLLTSYLQLSVVEYDPGTHDLKTLSLHYFEEPELRDGFVQNVHTPRVRVDPDGRCAAMLIYGTRLVVLPFRRESLAEEHEGLMGEGQRSSFLPSYIIDVRALDEKLLNIIDLQFLHGYYEPTLLILFEPNQTWPGRVAVRQDTCSIVAISLNITQKVHPVIWSLTSLPFDCTQALAVPKPIGGVVIFAVNSLLYLNQSVPPYGVALNSLTTGTTAFPLRTQEGVRITLDCAQAAFISYDKMVISLKGGEIYVLTLITDGMRSVRAFHFDKAAASVLTTSMVTMEPGYLFLGSRLGNSLLLKYTEKLQEPPASSVREAADKEEPPSKKKRVDPTVGWTGGKTQDEVDEIEVYGSEAQSGTQLATYSFEVCDSMLNIGPCANAAVGEPAFLSEEFQNSPEPDLEIVVCSGYGKNGALSVLQKSIRPQVVTTFELPGCYDMWTVIAPVRKEEEETPKAESTEQEPSAPKAEEDGRRHGFLILSREDSTMILQTGQEIMELDTSGFATQGPTVFAGNIGDNRYIVQVSPLGIRLLEGVNQLHFIPVDLGAPIVQCAVADPYVVIMSAEGHVTMFLLKSDSYGGRHHRLALHKPPLHHQSKVIALCLYRDVSGMFTTESRLGGARDELGGRSGSEAEGLGSETSPTVDDEEEMLYGDSSSLFSPSKEEARRSNQPPADRDPAPFRADPTHWCLLVRENGTMEIYQLPDWRLVFLVKNFPVGQRVLVDSSFGQPTTQGEVRKEEATRQGELPLVKEVLLVALGSRQSRPYLLVHVDQELLIYEAFPHDSQLGQGNLKVRFKKVPHNINFREKKPKPSKKKAEGCSTEEGSGVRGRVARFRYFEDIYGYSGVFICGPSPHWLLVTGRGALRLHPMGIDGPIDSFAPFHNVNCPRGFLYFNRQGELRISVLPAYLSYDAPWPVRKIPLRCTAHYVAYHVESKVYAVATSTNTPCTRIPRMTGEEKEFEAIERDDRYIHPQQEAFSIQLISPVSWEAIPNARIELEEWEHVTCMKTVSLRSEETVSGLKGYVAAGTCLMQGEEVTCRGRILIMDVIEVVPEPGQPLTKNKFKVLYEKEQKGPVTALCHCNGHLVSAIGQKIFLWSLRASELTGMAFIDTQLYIHQMISVKNFILAADVMKSISLLRYQEESKTLSLVSRDAKPLEVYSVDFMVDNAQLGFLVSDRDRNLMVYMYLPEAKESFGGMRLLRRADFHVGAHVNTFWRTPCRGAAEGPSKKSVMWENKHITWFATLDGGIGLLLPMQEKTYRRLLMLQNALTTMLPHHAGLNPRAFRMLHVDRRILQNAVRNVLDGELLNRYLYLSTMERSELAKKIGTTPDIILDDLLETDRVTAHF",
        "length": 1481,
        "header": "tr|A0A0G2JYV2-1|A0A0G2JYV2_RAT Isoform 1 of Cleavage and polyadenylation specific factor 1  OS=Rattus norvegicus OX=10116 GN=Cpsf1 PE=1 SV=1 CANONICAL=A0A0G2JYV2-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A0G2JYV2-1",
            "url": "",
            "sequence": {
                "sequence": "MYAVYKQAHPPTGLEFAMYCNFFNNSERNLVVAGTSQLYVYRLNRDAEALTKNDGSTEGKAHREKLELVASFSFFGNVMSMASVQLAGAKRDALLLSFKDAKVSSVGPAGGPGHSGVTEQRRLGCISVIKVGIERAMLLTSYLQLSVVEYDPGTHDLKTLSLHYFEEPELRDGFVQNVHTPRVRVDPDGRCAAMLIYGTRLVVLPFRRESLAEEHEGLMGEGQRSSFLPSYIIDVRALDEKLLNIIDLQFLHGYYEPTLLILFEPNQTWPGRVAVRQDTCSIVAISLNITQKVHPVIWSLTSLPFDCTQALAVPKPIGGVVIFAVNSLLYLNQSVPPYGVALNSLTTGTTAFPLRTQEGVRITLDCAQAAFISYDKMVISLKGGEIYVLTLITDGMRSVRAFHFDKAAASVLTTSMVTMEPGYLFLGSRLGNSLLLKYTEKLQEPPASSVREAADKEEPPSKKKRVDPTVGWTGGKTQDEVDEIEVYGSEAQSGTQLATYSFEVCDSMLNIGPCANAAVGEPAFLSEEFQNSPEPDLEIVVCSGYGKNGALSVLQKSIRPQVVTTFELPGCYDMWTVIAPVRKEEEETPKAESTEQEPSAPKAEEDGRRHGFLILSREDSTMILQTGQEIMELDTSGFATQGPTVFAGNIGDNRYIVQVSPLGIRLLEGVNQLHFIPVDLGAPIVQCAVADPYVVIMSAEGHVTMFLLKSDSYGGRHHRLALHKPPLHHQSKVIALCLYRDVSGMFTTESRLGGARDELGGRSGSEAEGLGSETSPTVDDEEEMLYGDSSSLFSPSKEEARRSNQPPADRDPAPFRADPTHWCLLVRENGTMEIYQLPDWRLVFLVKNFPVGQRVLVDSSFGQPTTQGEVRKEEATRQGELPLVKEVLLVALGSRQSRPYLLVHVDQELLIYEAFPHDSQLGQGNLKVRFKKVPHNINFREKKPKPSKKKAEGCSTEEGSGVRGRVARFRYFEDIYGYSGVFICGPSPHWLLVTGRGALRLHPMGIDGPIDSFAPFHNVNCPRGFLYFNRQGELRISVLPAYLSYDAPWPVRKIPLRCTAHYVAYHVESKVYAVATSTNTPCTRIPRMTGEEKEFEAIERDDRYIHPQQEAFSIQLISPVSWEAIPNARIELEEWEHVTCMKTVSLRSEETVSGLKGYVAAGTCLMQGEEVTCRGRILIMDVIEVVPEPGQPLTKNKFKVLYEKEQKGPVTALCHCNGHLVSAIGQKIFLWSLRASELTGMAFIDTQLYIHQMISVKNFILAADVMKSISLLRYQEESKTLSLVSRDAKPLEVYSVDFMVDNAQLGFLVSDRDRNLMVYMYLPEAKESFGGMRLLRRADFHVGAHVNTFWRTPCRGAAEGPSKKSVMWENKHITWFATLDGGIGLLLPMQEKTYRRLLMLQNALTTMLPHHAGLNPRAFRMLHVDRRILQNAVRNVLDGELLNRYLYLSTMERSELAKKIGTTPDIILDDLLETDRVTAHF",
                "length": 1481,
                "header": "tr|A0A0G2JYV2-1|A0A0G2JYV2_RAT Isoform 1 of Cleavage and polyadenylation specific factor 1  OS=Rattus norvegicus OX=10116 GN=Cpsf1 PE=1 SV=1 CANONICAL=A0A0G2JYV2-1"
            },
            "locus": {
                "chromosome": "7",
                "start_pos": 108329890,
                "end_pos": 108319513,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000086796.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000086796.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000070801.2",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000070801.2"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Cellular Component",
                "total": 3,
                "go_terms": [
                    {
                        "name": "nucleus",
                        "id": "GO:0005634",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JYV2",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JYV2"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "nucleoplasm",
                        "id": "GO:0005654",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JYV2",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JYV2"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "mRNA cleavage and polyadenylation specificity factor complex",
                        "id": "GO:0005847",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005847",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JYV2",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JYV2"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Biological Process",
                "total": 1,
                "go_terms": [
                    {
                        "name": "mRNA polyadenylation",
                        "id": "GO:0006378",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006378",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JYV2",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JYV2"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 2,
                "go_terms": [
                    {
                        "name": "enzyme binding",
                        "id": "GO:0019899",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019899",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JYV2",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JYV2"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "mRNA 3'-UTR AU-rich region binding",
                        "id": "GO:0035925",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035925",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JYV2",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JYV2"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 24,
            "end_pos": 26,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 266,
            "end_pos": 268,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 288,
            "end_pos": 290,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 332,
            "end_pos": 334,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 829,
            "end_pos": 831,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [],
    "section_stats": [
        {
            "table_id": "glycosylation",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported_with_glycan",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_predicted",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_automatic_literature_mining",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "phosphorylation",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "snv",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "snv_disease",
            "table_stats": [
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                    "field": "total",
                    "count": 0
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                {
                    "field": "total_sites",
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            ],
            "sort_fields": []
        },
        {
            "table_id": "snv_non_disease",
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                    "field": "total",
                    "count": 0
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                {
                    "field": "total_sites",
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            ],
            "sort_fields": []
        },
        {
            "table_id": "publication",
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                    "field": "total",
                    "count": 0
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            ],
            "sort_fields": []
        }
    ]
}