{
    "uniprot_canonical_ac": "F7ESI5-1",
    "uniprot_ac": "F7ESI5",
    "uniprot_id": "F7ESI5_RAT",
    "mass": {
        "chemical_mass": 32704.0,
        "monoisotopic_mass": 32704.0
    },
    "refseq": {},
    "gene_names": [
        {
            "name": "Cfhr1",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/F7ESI5",
            "id": "F7ESI5"
        },
        {
            "name": "Cfhl1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/F7ESI5",
            "id": "F7ESI5"
        }
    ],
    "protein_names": [
        {
            "name": "Complement factor H-related 1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "F7ESI5"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0080301",
            "recommended_name": {
                "id": "DOID:0080301",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0080301",
                "name": "atypical hemolytic-uremic syndrome",
                "description": "A complement deficiency that is characterized by mechanical hemolytic anemia, thrombocytopenia, and renal dysfunction."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "0080301",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0080301"
                }
            ]
        },
        {
            "disease_id": "DOID:0110014",
            "recommended_name": {
                "id": "DOID:0110014",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110014",
                "name": "age related macular degeneration 1",
                "description": "An age related macular degeneration associated with polymorphism in the hemicentin gene (HMCN1) on chromosome 1q25.3-q31.1."
            },
            "synonyms": [
                {
                    "id": "DOID:0110014",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110014",
                    "name": "ARMD1",
                    "description": ""
                },
                {
                    "id": "DOID:0110014",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110014",
                    "name": "age related maculopathy 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011285",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011285",
                    "name": "age related macular degeneration 1",
                    "description": "An age related macular degeneration associated with polymorphism in the hemicentin gene (HMCN1) on chromosome 1q25.3-q31.1."
                },
                {
                    "id": "MONDO:0011285",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011285",
                    "name": "macular degeneration, age-related",
                    "description": ""
                },
                {
                    "id": "MONDO:0011285",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011285",
                    "name": "ARMD1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011285",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011285",
                    "name": "age related macular degeneration type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011285",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011285",
                    "name": "age related maculopathy 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011285",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011285",
                    "name": "macular Degeneration, age-related, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011285",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011285",
                    "name": "macular degeneration, age-related, reduced risk of",
                    "description": ""
                },
                {
                    "id": "MONDO:0011285",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011285",
                    "name": "macular degeneration, age-related, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011285",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011285",
                    "name": "maculopathy, age-related, 1",
                    "description": ""
                },
                {
                    "id": "MIM:603075",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/603075",
                    "name": "Macular degeneration, age-related, 1",
                    "description": "Macular degeneration, age-related, 1"
                }
            ],
            "evidence": [
                {
                    "id": "0110014",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110014"
                }
            ]
        },
        {
            "disease_id": "DOID:9119",
            "recommended_name": {
                "id": "DOID:9119",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:9119",
                "name": "acute myeloid leukemia",
                "description": "A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells."
            },
            "synonyms": [
                {
                    "id": "DOID:9119",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9119",
                    "name": "AML - acute Myeloid Leukemia",
                    "description": ""
                },
                {
                    "id": "DOID:9119",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9119",
                    "name": "Leukemia, Myelocytic, acute",
                    "description": ""
                },
                {
                    "id": "DOID:9119",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9119",
                    "name": "acute myeloblastic leukaemia",
                    "description": ""
                },
                {
                    "id": "DOID:9119",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9119",
                    "name": "acute myeloblastic leukemia",
                    "description": ""
                },
                {
                    "id": "DOID:9119",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9119",
                    "name": "acute myelogenous leukaemia",
                    "description": ""
                },
                {
                    "id": "DOID:9119",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9119",
                    "name": "acute myelogenous leukemia",
                    "description": ""
                },
                {
                    "id": "DOID:9119",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9119",
                    "name": "acute myeloid leukaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myeloid leukemia",
                    "description": "Acute myeloid leukemia (AML) is a group of neoplasms arising from precursor cells committed to the myeloid cell-line differentiation. All of them are characterized by clonal expansion of myeloid blasts. AML manifests by fever, pallor, anemia, hemorrhages and recurrent infections."
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "AML",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "AML - acute myeloid leukaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "AML - acute myeloid leukemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "ANLL",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute Nonlymphocytic leukaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute Nonlymphocytic leukemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute granulocytic leukaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute granulocytic leukemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myeloblastic leukaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myeloblastic leukemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myelocytic leukaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myelocytic leukemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myelogenous leukaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myelogenous leukemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myelogenous leukemias",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myeloid leukaemia (AML)",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myeloid leukemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myeloid leukemia (AML)",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute myeloid leukemia, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute nonlymphocytic leukaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute nonlymphocytic leukemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "hematopoeitic - acute Myleogenous leukaemia (AML)",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "hematopoeitic - acute Myleogenous leukemia (AML)",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "leukemia, acute myeloid, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "leukemia, acute myeloid, reduced survival in, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "leukemia, acute myeloid, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "leukemia, acute myeloid, susceptibility to, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "leukemia, myelocytic, acute",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "myeloid leukemia, acute",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "myeloid leukemia, acute, M4/M4Eo subtype, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute non lymphoblastic leukaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "acute non lymphoblastic leukemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "leukemia, acute myelogenous",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "leukemia, acute myeloid",
                    "description": ""
                },
                {
                    "id": "MONDO:0018874",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0018874",
                    "name": "leukemia, acute myeloid, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MIM:601626",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/601626",
                    "name": "Leukemia, acute myelogenous",
                    "description": "Leukemia, acute myelogenous"
                }
            ],
            "evidence": [
                {
                    "id": "9119",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:9119"
                }
            ]
        },
        {
            "disease_id": "DOID:9538",
            "recommended_name": {
                "id": "DOID:9538",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:9538",
                "name": "multiple myeloma",
                "description": "A myeloid neoplasm that is located_in the plasma cells in bone marrow."
            },
            "synonyms": [
                {
                    "id": "DOID:9538",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9538",
                    "name": "myeloma",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "plasma cell myeloma",
                    "description": "A bone marrow-based plasma cell neoplasm characterized by a serum monoclonal protein and skeletal destruction with osteolytic lesions, pathological fractures, bone pain, hypercalcemia, and anemia. Clinical variants include non-secretory myeloma, smoldering myeloma, indolent myeloma, and plasma cell leukemia. (WHO, 2001)"
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "Kahler disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "Kahler's disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "medullary plasmacytoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "multiple myeloma",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "multiple myeloma, resistance to, Somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "multiple myeloma, susceptibility to, Somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "multiple myeloma/plasma cell myeloma",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "myeloid neoplasm of plasma cell",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "myeloma",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "myeloma, multiple",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "myeloma, plasma cell, malignant",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "myelomatosis",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "plasma cell myeloid neoplasm",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "plasma cell myeloma",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "Al amyloidosis",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "amyloidosis, systemic",
                    "description": ""
                },
                {
                    "id": "MONDO:0009693",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693",
                    "name": "myeloma - multiple",
                    "description": ""
                },
                {
                    "id": "MIM:254500",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/254500",
                    "name": "Multiple myeloma",
                    "description": "Multiple myeloma"
                }
            ],
            "evidence": [
                {
                    "id": "9538",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:9538"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "F7ESI5",
                    "url": "https://www.uniprot.org/uniprot/F7ESI5"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "gene": [
        {
            "name": "Cfhr1",
            "url": "https://www.uniprot.org/uniprot/F7ESI5",
            "locus": {
                "chromosome": "13",
                "start_pos": 51369211,
                "end_pos": 51410592,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSRNOG00000042901",
                        "url": "https://www.ensembl.org/id/ENSRNOG00000042901"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "ENSRNOG00000042901",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000042901",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "cd00033",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd00033",
            "database": "CDD",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR000436",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR000436",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR035892",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR035892",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR035976",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR035976",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "GKYFYYT",
            "url": "https://omabrowser.org/oma/group/GKYFYYT/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR45785",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR45785",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR45785:SF7",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR45785:SF7",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF00084",
            "url": "http://pfam.xfam.org/family/PF00084",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "1310510",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1310510",
            "database": "RGD",
            "categories": [
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            "id": "A0A8I5XVW2",
            "url": "https://www.uniprot.org/uniprot/A0A8I5XVW2",
            "database": "UniProtKB",
            "categories": [
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            "id": "A0A8I5XVW2-1",
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            "database": "UniProtKB",
            "categories": [
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            "id": "F7ESI5",
            "url": "https://www.uniprot.org/uniprot/F7ESI5",
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            "categories": [
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            "id": "F7ESI5-1",
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    },
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                "header": "tr|A0A8I5XVW2-1|F7ESI5_RAT Computationally mapped isoform of Complement factor H-related 1  OS=Rattus norvegicus OX=10116 GN=Cfhr1 PE=1 SV=1 CANONICAL=F7ESI5-1"
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                        "id": "ENSRNOP00000017195.6",
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                    }
                ]
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        },
        {
            "isoform_ac": "Q7TP43-1",
            "url": "",
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                "length": 253,
                "header": "tr|Q7TP43-1|F7ESI5_RAT Computationally mapped isoform of Complement factor H-related 1  OS=Rattus norvegicus OX=10116 GN=Cfhr1 PE=1 SV=1 CANONICAL=F7ESI5-1"
            },
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                "chromosome": "13",
                "start_pos": 51410532,
                "end_pos": 51369214,
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                "evidence": [
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                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000079040.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000079040.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000071663.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000071663.1"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
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    "pathway": [],
    "orthologs": [],
    "go_annotation": {
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            {
                "name": "Cellular Component",
                "total": 2,
                "go_terms": [
                    {
                        "name": "extracellular space",
                        "id": "GO:0005615",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
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                        ],
                        "pmid": ""
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                    {
                        "name": "protein-containing complex",
                        "id": "GO:0032991",
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                ]
            },
            {
                "name": "Molecular Function",
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                        "name": "identical protein binding",
                        "id": "GO:0042802",
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                    },
                    {
                        "name": "complement component C3b binding",
                        "id": "GO:0001851",
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                                "id": "F7ESI5",
                                "url": "https://www.uniprot.org/uniprot/F7ESI5"
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                        "pmid": ""
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                ]
            },
            {
                "name": "Biological Process",
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                    {
                        "name": "negative regulation of protein binding",
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                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032091",
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                                "id": "F7ESI5",
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                    {
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                                "database": "UniProtKB",
                                "id": "F7ESI5",
                                "url": "https://www.uniprot.org/uniprot/F7ESI5"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "complement activation",
                        "id": "GO:0006956",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006956",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "F7ESI5",
                                "url": "https://www.uniprot.org/uniprot/F7ESI5"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
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        {
            "start_pos": 146,
            "end_pos": 148,
            "annotation": "n_glycosylation_sequon"
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    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
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