{
    "uniprot_canonical_ac": "Q8K3U6-1",
    "uniprot_ac": "Q8K3U6",
    "uniprot_id": "FA7_RAT",
    "mass": {
        "chemical_mass": 50399.0,
        "monoisotopic_mass": 50399.0
    },
    "refseq": {
        "ac": "NP_690059",
        "name": "coagulation factor VII precursor",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_690059"
    },
    "gene_names": [
        {
            "name": "F7",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/Q8K3U6",
            "id": "Q8K3U6"
        },
        {
            "name": "F7",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_690059",
            "id": "NP_690059"
        }
    ],
    "protein_names": [
        {
            "name": "Coagulation factor VII",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "Q8K3U6"
        },
        {
            "name": "3.4.21.21",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q8K3U6"
        },
        {
            "name": "Serum prothrombin conversion accelerator",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q8K3U6"
        },
        {
            "name": "coagulation factor VII precursor",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_690059",
            "id": "NP_690059"
        },
        {
            "name": "serum prothrombin conversion accelerator",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_690059",
            "id": "NP_690059"
        }
    ],
    "function": [
        {
            "annotation": "Initiates the extrinsic pathway of blood coagulation. Serine protease that circulates in the blood in a zymogen form. Factor VII is converted to factor VIIa by factor Xa, factor XIIa, factor IXa, or thrombin by minor proteolysis. In the presence of tissue factor and calcium ions, factor VIIa then converts factor X to factor Xa by limited proteolysis. Factor VIIa will also convert factor IX to factor IXa in the presence of tissue factor and calcium (By similarity).",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q8K3U6",
                    "url": "https://www.uniprot.org/uniprot/Q8K3U6#function"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0080941",
            "recommended_name": {
                "id": "DOID:0080941",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0080941",
                "name": "acquired angioedema",
                "description": "An angioedema that is characterized by an acquired deficiency of (C1-INH) caused by either consumption or inactivation."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "0080941",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0080941"
                }
            ]
        },
        {
            "disease_id": "DOID:10763",
            "recommended_name": {
                "id": "DOID:10763",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries."
            },
            "synonyms": [
                {
                    "id": "DOID:10763",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10763",
                    "name": "HTN",
                    "description": ""
                },
                {
                    "id": "DOID:10763",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10763",
                    "name": "hyperpiesia",
                    "description": ""
                },
                {
                    "id": "DOID:10763",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10763",
                    "name": "vascular hypertensive disorder",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "10763",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:10763"
                }
            ]
        },
        {
            "disease_id": "DOID:1168",
            "recommended_name": {
                "id": "DOID:1168",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1168",
                "name": "familial hyperlipidemia",
                "description": ""
            },
            "synonyms": [
                {
                    "id": "DOID:1168",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1168",
                    "name": "familial hyperlipoproteinemia",
                    "description": ""
                },
                {
                    "id": "DOID:1168",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1168",
                    "name": "hyperlipemia",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1168",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1168"
                }
            ]
        },
        {
            "disease_id": "DOID:1459",
            "recommended_name": {
                "id": "DOID:1459",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1459",
                "name": "hypothyroidism",
                "description": "A thyroid gland disease which involves an underproduction of thyroid hormone."
            },
            "synonyms": [
                {
                    "id": "DOID:1459",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1459",
                    "name": "Thyroid deficiency",
                    "description": ""
                },
                {
                    "id": "DOID:1459",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1459",
                    "name": "Thyroid insufficiency",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1459",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1459"
                }
            ]
        },
        {
            "disease_id": "DOID:14735",
            "recommended_name": {
                "id": "DOID:14735",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:14735",
                "name": "hereditary angioedema",
                "description": "An angioedema that is characterized by recurrent episodes of severe swelling of the skin and mucous membranes."
            },
            "synonyms": [
                {
                    "id": "DOID:14735",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:14735",
                    "name": "HANE",
                    "description": ""
                },
                {
                    "id": "DOID:14735",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:14735",
                    "name": "Hereditary angioneurotic edema",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "14735",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:14735"
                }
            ]
        },
        {
            "disease_id": "DOID:1588",
            "recommended_name": {
                "id": "DOID:1588",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1588",
                "name": "thrombocytopenia",
                "description": "A blood platelet disease that is characterized by low a platelet count in the blood."
            },
            "synonyms": [
                {
                    "id": "MONDO:0012775",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012775",
                    "name": "thrombocytopenia 4",
                    "description": "Any thrombocytopenia in which the cause of the disease is a mutation in the CYCS gene."
                },
                {
                    "id": "MONDO:0012775",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012775",
                    "name": "CYCS thrombocytopenia",
                    "description": ""
                },
                {
                    "id": "MONDO:0012775",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012775",
                    "name": "thrombocytopenia 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012775",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012775",
                    "name": "thrombocytopenia caused by mutation in CYCS",
                    "description": ""
                },
                {
                    "id": "MONDO:0012775",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012775",
                    "name": "thrombocytopenia type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012775",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012775",
                    "name": "THC4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012775",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012775",
                    "name": "thrombocytopenia, autosomal dominant, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0010308",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010308",
                    "name": "thrombocytopenia, X-linked, with or without dyserythropoietic anemia",
                    "description": "An X-linked condition caused by mutation(s) in the GATA1 gene, encoding erythroid transcription factor. It is characterized by thrombocytopenia, as well as abnormal platelet function and morphology. Dyserythropoietic anemia of variable severity may also be present."
                },
                {
                    "id": "MONDO:0010308",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010308",
                    "name": "X-linked thrombocytopenia, with or without dyserythropoietic Anaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0010308",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010308",
                    "name": "X-linked thrombocytopenia, with or without dyserythropoietic Anemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0010308",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010308",
                    "name": "thrombocytopenia, X-linked, with or without dyserythropoietic anemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0010308",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010308",
                    "name": "thrombocytopenia, X-linked, with or without dyserythropoietic anemia, X-linked recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0010308",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010308",
                    "name": "XLTDA",
                    "description": ""
                },
                {
                    "id": "MONDO:0008555",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008555",
                    "name": "thrombocytopenia 2",
                    "description": "An autosomal dominant disorder caused by mutation(s) in the ANKRD26 gene, encoding ANKRD26 protein. Additionally, in one family, a mutation(s) has been identified in the MASTL gene, encoding serine/threonine-protein kinase greatwall. The condition is characterized by mild to moderate bruisability."
                },
                {
                    "id": "MONDO:0008555",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008555",
                    "name": "thrombocytopenia 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0008555",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008555",
                    "name": "thrombocytopenia type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0008555",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008555",
                    "name": "THC2",
                    "description": ""
                },
                {
                    "id": "MONDO:0008555",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008555",
                    "name": "thrombocytopenia autosomal dominant 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0008555",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008555",
                    "name": "thrombocytopenia, autosomal dominant, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0010120",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010120",
                    "name": "thrombocytopenia 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010120",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010120",
                    "name": "THC3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010120",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010120",
                    "name": "thrombocytopenia 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010120",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010120",
                    "name": "thrombocytopenia, autosomal recessive, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "thrombocytopenia 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "X-linked thrombocytopenia with normal platelets",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "thrombocytopenia 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "thrombocytopenia type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "thrombocytopenia, X-linked, X-linked recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "thrombocytopenia, X-linked, intermittent, X-linked recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "THC",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "THC1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "X-linked thrombocytopenia",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "XLT",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "thrombocytopenia, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "thrombocytopenia, X-linked, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010743",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010743",
                    "name": "thrombocytopenia, X-linked, intermittent",
                    "description": ""
                },
                {
                    "id": "MIM:612004",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/612004",
                    "name": "Thrombocytopenia 4",
                    "description": "Thrombocytopenia 4"
                },
                {
                    "id": "MIM:300367",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/300367",
                    "name": "X-linked dyserythropoietic anemia and thrombocytopenia",
                    "description": "X-linked dyserythropoietic anemia and thrombocytopenia"
                },
                {
                    "id": "MIM:188000",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/188000",
                    "name": "Thrombocytopenia 2",
                    "description": "Thrombocytopenia 2"
                },
                {
                    "id": "MIM:273900",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/273900",
                    "name": "Thrombocytopenia 3",
                    "description": "Thrombocytopenia 3"
                },
                {
                    "id": "MIM:313900",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/313900",
                    "name": "Thrombocytopenia 1",
                    "description": "Thrombocytopenia 1"
                }
            ],
            "evidence": [
                {
                    "id": "1588",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1588"
                }
            ]
        },
        {
            "disease_id": "DOID:1612",
            "recommended_name": {
                "id": "DOID:1612",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1612",
                "name": "breast cancer",
                "description": "A thoracic cancer that originates in the mammary gland."
            },
            "synonyms": [
                {
                    "id": "DOID:1612",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1612",
                    "name": "breast tumor",
                    "description": ""
                },
                {
                    "id": "DOID:1612",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1612",
                    "name": "malignant neoplasm of breast",
                    "description": ""
                },
                {
                    "id": "DOID:1612",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1612",
                    "name": "malignant tumor of the breast",
                    "description": ""
                },
                {
                    "id": "DOID:1612",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1612",
                    "name": "mammary cancer",
                    "description": ""
                },
                {
                    "id": "DOID:1612",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1612",
                    "name": "mammary tumor",
                    "description": ""
                },
                {
                    "id": "DOID:1612",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1612",
                    "name": "primary breast cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "hereditary breast carcinoma",
                    "description": "Breast carcinoma that has developed in relatives of patients with history of breast carcinoma."
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "breast cancer susceptibility, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "breast cancer, early-onset, susceptibility to, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "breast cancer, invasive ductal, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "breast cancer, lobular, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "breast cancer, male, susceptibility to, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "breast cancer, protection against, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "breast cancer, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "breast cancer, susceptibility to, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "familial breast cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "familial breast carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "familial cancer of breast",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "familial cancer of the breast",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "hereditary breast cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "hereditary breast carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "breast cancer, familial",
                    "description": ""
                },
                {
                    "id": "MONDO:0016419",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                    "name": "breast cancer, familial Male",
                    "description": ""
                },
                {
                    "id": "MIM:114480",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/114480",
                    "name": "Breast cancer",
                    "description": "Breast cancer"
                }
            ],
            "evidence": [
                {
                    "id": "1612",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1612"
                }
            ]
        },
        {
            "disease_id": "DOID:2215",
            "recommended_name": {
                "id": "DOID:2215",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2215",
                "name": "factor VII deficiency",
                "description": "A blood coagulation disease that is characterized by easy bleeding, has_symptom epistaxis, bleeding of the gums, menorrhagia, and occasionally hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation in the F7 gene, which encodes coagulation factor VII, an important factor in the clotting cascade."
            },
            "synonyms": [
                {
                    "id": "DOID:2215",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2215",
                    "name": "deficiency, stable",
                    "description": ""
                },
                {
                    "id": "MONDO:0009211",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009211",
                    "name": "congenital factor VII deficiency",
                    "description": "Factor VII (FVII) deficiency is a rare hereditary hemorrhagic disease caused by the diminution or absence of this coagulation factor."
                },
                {
                    "id": "MONDO:0009211",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009211",
                    "name": "congenital factor VII deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009211",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009211",
                    "name": "congenital proconvertin deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009211",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009211",
                    "name": "hypoproconvertinemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0009211",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009211",
                    "name": "F7 deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009211",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009211",
                    "name": "factor 7 deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009211",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009211",
                    "name": "factor VII deficiency",
                    "description": ""
                },
                {
                    "id": "MIM:227500",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/227500",
                    "name": "Factor VII deficiency",
                    "description": "Factor VII deficiency"
                }
            ],
            "evidence": [
                {
                    "id": "2215",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2215"
                }
            ]
        },
        {
            "disease_id": "DOID:2235",
            "recommended_name": {
                "id": "DOID:2235",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2235",
                "name": "prothrombin deficiency",
                "description": "A thrombophilia that is characterized by bleeding symptoms due to low levels of circulating prothrombin, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the gene encoding coagulation factor II, also known as prothrombin, on chromosome 11p11."
            },
            "synonyms": [
                {
                    "id": "DOID:2235",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2235",
                    "name": "Congenital factor II deficiency",
                    "description": ""
                },
                {
                    "id": "DOID:2235",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2235",
                    "name": "hypoprothrombinemia",
                    "description": ""
                },
                {
                    "id": "DOID:2235",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2235",
                    "name": "Hereditary factor II deficiency disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0013361",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013361",
                    "name": "congenital prothrombin deficiency",
                    "description": "Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms."
                },
                {
                    "id": "MONDO:0013361",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013361",
                    "name": "factor 2 deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0013361",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013361",
                    "name": "factor II deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0013361",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013361",
                    "name": "hypoprothrombinemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0013361",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013361",
                    "name": "prothrombin deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0013361",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013361",
                    "name": "Dysprothrombinemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0013361",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013361",
                    "name": "congenital prothrombin deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0013361",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013361",
                    "name": "hereditary prothrombin deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0013361",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013361",
                    "name": "congenital factor II deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0013361",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013361",
                    "name": "prothrombin deficiency, congenital",
                    "description": ""
                },
                {
                    "id": "MIM:613679",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/613679",
                    "name": "Factor II deficiency",
                    "description": "Factor II deficiency"
                }
            ],
            "evidence": [
                {
                    "id": "2235",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2235"
                }
            ]
        },
        {
            "disease_id": "DOID:2349",
            "recommended_name": {
                "id": "DOID:2349",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2349",
                "name": "arteriosclerosis",
                "description": "An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries."
            },
            "synonyms": [
                {
                    "id": "DOID:2349",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2349",
                    "name": "Arteriosclerotic vascular disease",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "2349",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2349"
                }
            ]
        },
        {
            "disease_id": "DOID:2394",
            "recommended_name": {
                "id": "DOID:2394",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary."
            },
            "synonyms": [
                {
                    "id": "DOID:2394",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2394",
                    "name": "malignant Ovarian tumor",
                    "description": ""
                },
                {
                    "id": "DOID:2394",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2394",
                    "name": "malignant tumour of ovary",
                    "description": ""
                },
                {
                    "id": "DOID:2394",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2394",
                    "name": "ovarian neoplasm",
                    "description": ""
                },
                {
                    "id": "DOID:2394",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2394",
                    "name": "ovary neoplasm",
                    "description": ""
                },
                {
                    "id": "DOID:2394",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2394",
                    "name": "primary ovarian cancer",
                    "description": ""
                },
                {
                    "id": "DOID:2394",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2394",
                    "name": "tumor of the Ovary",
                    "description": ""
                },
                {
                    "id": "MONDO:0011931",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011931",
                    "name": "ovarian cancer, susceptibility to, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011931",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011931",
                    "name": "OVCAS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011931",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011931",
                    "name": "ovarian cancer, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0011931",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011931",
                    "name": "ovarian cancer, susceptibility to, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "ovarian cancer",
                    "description": "A primary or metastatic malignant neoplasm involving the ovary. Most primary malignant ovarian neoplasms are either carcinomas (serous, mucinous, or endometrioid adenocarcinomas) or malignant germ cell tumors. Metastatic malignant neoplasms to the ovary include carcinomas, lymphomas, and melanomas."
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "ovarian neoplasm",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "ovary neoplasm",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "tumor of the ovary",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "tumour of the ovary",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "cancer of ovary",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "cancer of the ovary",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "malignant neoplasm of ovary",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "malignant neoplasm of the ovary",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "malignant ovarian neoplasm",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "malignant ovarian tumor",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "malignant ovarian tumour",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "malignant ovary neoplasm",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "malignant tumor of ovary",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "malignant tumor of the ovary",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "malignant tumour of ovary",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "malignant tumour of the ovary",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "ovarian cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "ovarian cancer, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "ovarian malignant tumor",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "ovarian malignant tumour",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "ovary cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "ovarian cancer, epithelial",
                    "description": ""
                },
                {
                    "id": "MONDO:0008170",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008170",
                    "name": "primary ovarian cancer",
                    "description": ""
                },
                {
                    "id": "MIM:167000",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/167000",
                    "name": "Ovarian cancer",
                    "description": "Ovarian cancer"
                }
            ],
            "evidence": [
                {
                    "id": "2394",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2394"
                }
            ]
        },
        {
            "disease_id": "DOID:2741",
            "recommended_name": {
                "id": "DOID:2741",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2741",
                "name": "bilirubin metabolic disorder",
                "description": "An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism."
            },
            "synonyms": [
                {
                    "id": "DOID:2741",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2741",
                    "name": "hereditary hyperbilirubinemia",
                    "description": ""
                },
                {
                    "id": "DOID:2741",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2741",
                    "name": "hyperbilirubinemia",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "2741",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2741"
                }
            ]
        },
        {
            "disease_id": "DOID:2841",
            "recommended_name": {
                "id": "DOID:2841",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing."
            },
            "synonyms": [
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "Exercise induced asthma",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "bronchial hyperreactivity",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "chronic obstructive asthma",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "chronic obstructive asthma with acute exacerbation",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "chronic obstructive asthma with status asthmaticus",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "exercise-induced asthma",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "inherited susceptibility to asthma",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, nocturnal, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, bronchial",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, diminished response to Antileukotriene treatment 1N",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, protection against",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma-related traits, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MIM:600807",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/600807",
                    "name": "Asthma",
                    "description": "Asthma"
                }
            ],
            "evidence": [
                {
                    "id": "2841",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2841"
                }
            ]
        },
        {
            "disease_id": "DOID:2913",
            "recommended_name": {
                "id": "DOID:2913",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2913",
                "name": "acute pancreatitis",
                "description": "A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "2913",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2913"
                }
            ]
        },
        {
            "disease_id": "DOID:3393",
            "recommended_name": {
                "id": "DOID:3393",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3393",
                "name": "coronary artery disease",
                "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles."
            },
            "synonyms": [
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "CHD",
                    "description": ""
                },
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "Coronary disease",
                    "description": ""
                },
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "coronary arteriosclerosis",
                    "description": ""
                },
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "coronary heart disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "coronary heart disease, susceptibility to, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "coronary heart disease, susceptibility to, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "coronary heart disease, susceptibility to, type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "Chds4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "coronary heart disease, susceptibility to, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "coronary heart disease, susceptibility to, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "coronary heart disease, susceptibility to, type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "Chds2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform mole, recurrent, 2",
                    "description": "Any complete hydatidiform mole in which the cause of the disease is a mutation in the KHDC3L gene."
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "KHDC3L complete hydatidiform mole",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "complete hydatidiform mole caused by mutation in KHDC3L",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform Mole, recurrent, type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform mole, recurrent, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "HYDM2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform MOLE, recurrent, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform Mole, complete",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to, 1",
                    "description": "Any coronary artery disease in which the cause of the disease is a mutation in the CX3CR1 gene."
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "CX3CR1 coronary artery disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary artery disease caused by mutation in CX3CR1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary artery disease, resistance to",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "Chds1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease, autosomal dominant, 1",
                    "description": "Any coronary artery disease in which the cause of the disease is a mutation in the MEF2A gene."
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "MEF2A coronary artery disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease caused by mutation in MEF2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease, autosomal dominant, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease, autosomal dominant, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "ADCAD1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease with myocardial infarction",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant 2",
                    "description": "Any coronary artery disease in which the cause of the disease is a mutation in the LRP6 gene."
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "LRP6 coronary artery disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease caused by mutation in LRP6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "ADCAD2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012788",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012788",
                    "name": "coronary heart disease, susceptibility to, 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012788",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012788",
                    "name": "CHDS9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012788",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012788",
                    "name": "coronary heart disease, susceptibility to, 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "coronary heart disease, susceptibility to, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "coronary heart disease, susceptibility to, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "coronary heart disease, susceptibility to, type 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "Chds3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012628",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012628",
                    "name": "coronary heart disease, susceptibility to, 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0012628",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012628",
                    "name": "CHDS8",
                    "description": ""
                },
                {
                    "id": "MONDO:0012628",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012628",
                    "name": "coronary heart disease, susceptibility to, 8",
                    "description": ""
                },
                {
                    "id": "MIM:614293",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/614293",
                    "name": "Hydatidiform mole, recurrent, 2",
                    "description": "Hydatidiform mole, recurrent, 2"
                },
                {
                    "id": "MIM:608320",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/608320",
                    "name": "Coronary artery disease, autosomal dominant, 1",
                    "description": "Coronary artery disease, autosomal dominant, 1"
                },
                {
                    "id": "MIM:610947",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/610947",
                    "name": "Coronary artery disease, autosomal dominant, 2",
                    "description": "Coronary artery disease, autosomal dominant, 2"
                }
            ],
            "evidence": [
                {
                    "id": "3393",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3393"
                }
            ]
        },
        {
            "disease_id": "DOID:3526",
            "recommended_name": {
                "id": "DOID:3526",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3526",
                "name": "cerebral infarction",
                "description": "A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain."
            },
            "synonyms": [
                {
                    "id": "DOID:3526",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3526",
                    "name": "CVA - Cerebral infarction",
                    "description": ""
                },
                {
                    "id": "DOID:3526",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3526",
                    "name": "Cerebral infarct",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "obsolete susceptibility to ischemic stroke",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "cerebral infarction, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "ischemic stroke, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "stroke, ischemic, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "stroke, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "cerebral infarction",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "cerebrovascular accident",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "stroke, ischemic",
                    "description": ""
                },
                {
                    "id": "MIM:601367",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/601367",
                    "name": "Ischemic stroke",
                    "description": "Ischemic stroke"
                }
            ],
            "evidence": [
                {
                    "id": "3526",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3526"
                }
            ]
        },
        {
            "disease_id": "DOID:4195",
            "recommended_name": {
                "id": "DOID:4195",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:4195",
                "name": "hyperglycemia",
                "description": ""
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "4195",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:4195"
                }
            ]
        },
        {
            "disease_id": "DOID:557",
            "recommended_name": {
                "id": "DOID:557",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:557",
                "name": "kidney disease",
                "description": "A urinary system disease that is located_in the kidney."
            },
            "synonyms": [
                {
                    "id": "DOID:557",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:557",
                    "name": "impaired renal function disease",
                    "description": ""
                },
                {
                    "id": "DOID:557",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:557",
                    "name": "nephropathy",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "557",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:557"
                }
            ]
        },
        {
            "disease_id": "DOID:576",
            "recommended_name": {
                "id": "DOID:576",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:576",
                "name": "proteinuria",
                "description": "A kidney disease that is characterized by the presence of excess proteins in the urine."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "576",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:576"
                }
            ]
        },
        {
            "disease_id": "DOID:5844",
            "recommended_name": {
                "id": "DOID:5844",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia."
            },
            "synonyms": [
                {
                    "id": "DOID:5844",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5844",
                    "name": "Myocardial infarct",
                    "description": ""
                },
                {
                    "id": "DOID:5844",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5844",
                    "name": "heart attack",
                    "description": ""
                },
                {
                    "id": "MONDO:0012058",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012058",
                    "name": "myocardial infarction, susceptibility to, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012058",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012058",
                    "name": "myocardial infarction, susceptibility to, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012058",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012058",
                    "name": "myocardial infarction, susceptibility to, type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012058",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012058",
                    "name": "Mci2",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "5844",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:5844"
                }
            ]
        },
        {
            "disease_id": "DOID:8805",
            "recommended_name": {
                "id": "DOID:8805",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:8805",
                "name": "intermediate coronary syndrome",
                "description": ""
            },
            "synonyms": [
                {
                    "id": "DOID:8805",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:8805",
                    "name": "Angina at rest",
                    "description": ""
                },
                {
                    "id": "DOID:8805",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:8805",
                    "name": "Anginal chest pain at rest",
                    "description": ""
                },
                {
                    "id": "DOID:8805",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:8805",
                    "name": "Impending infarction",
                    "description": ""
                },
                {
                    "id": "DOID:8805",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:8805",
                    "name": "Preinfarction angina",
                    "description": ""
                },
                {
                    "id": "DOID:8805",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:8805",
                    "name": "Unstable angina",
                    "description": ""
                },
                {
                    "id": "DOID:8805",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:8805",
                    "name": "Worsening angina",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "8805",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:8805"
                }
            ]
        },
        {
            "disease_id": "DOID:8947",
            "recommended_name": {
                "id": "DOID:8947",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:8947",
                "name": "diabetic retinopathy",
                "description": ""
            },
            "synonyms": [
                {
                    "id": "DOID:8947",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:8947",
                    "name": "Retinal abnormality - diabetes-related",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "8947",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:8947"
                }
            ]
        },
        {
            "disease_id": "DOID:9256",
            "recommended_name": {
                "id": "DOID:9256",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
            },
            "synonyms": [
                {
                    "id": "MONDO:0005575",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                    "name": "colorectal cancer",
                    "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                },
                {
                    "id": "MONDO:0005575",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                    "name": "cancer of colorectum",
                    "description": ""
                },
                {
                    "id": "MONDO:0005575",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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            "start_aa": "Thr",
            "end_pos": 101,
            "end_aa": "Thr",
            "residue": "Thr",
            "site_lbl": "Thr101",
            "evidence": [
                {
                    "id": "Q8K3U6",
                    "database": "UniProtKB",
                    "url": "https://www.uniprot.org/uniprot/Q8K3U6#ptm_processing"
                }
            ]
        },
        {
            "glytoucan_ac": "",
            "type": "N-linked",
            "subtype": "",
            "site_category": "predicted",
            "site_seq": "N",
            "relation": "attached",
            "comment": "N-linked (GlcNAc...) asparagine",
            "start_pos": 186,
            "start_aa": "Asn",
            "end_pos": 186,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn186",
            "evidence": [
                {
                    "id": "Q8K3U6",
                    "database": "UniProtKB",
                    "url": "https://www.uniprot.org/uniprot/Q8K3U6#ptm_processing"
                }
            ]
        },
        {
            "glytoucan_ac": "",
            "type": "N-linked",
            "subtype": "",
            "site_category": "predicted",
            "site_seq": "N",
            "relation": "attached",
            "comment": "N-linked (GlcNAc...) asparagine",
            "start_pos": 244,
            "start_aa": "Asn",
            "end_pos": 244,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn244",
            "evidence": [
                {
                    "id": "Q8K3U6",
                    "database": "UniProtKB",
                    "url": "https://www.uniprot.org/uniprot/Q8K3U6#ptm_processing"
                }
            ]
        },
        {
            "glytoucan_ac": "",
            "type": "O-linked",
            "subtype": "",
            "site_category": "predicted",
            "site_seq": "S",
            "relation": "attached",
            "comment": "O-linked (Xyl...) serine; alternate",
            "start_pos": 93,
            "start_aa": "Ser",
            "end_pos": 93,
            "end_aa": "Ser",
            "residue": "Ser",
            "site_lbl": "Ser93",
            "evidence": [
                {
                    "id": "Q8K3U6",
                    "database": "UniProtKB",
                    "url": "https://www.uniprot.org/uniprot/Q8K3U6#ptm_processing"
                }
            ]
        }
    ],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [
        "enzyme",
        "glycoprotein",
        "glycoprotein_predicted"
    ],
    "publication": [],
    "pathway": [
        {
            "id": "rno:260320",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:260320",
            "resource": "KEGG Pathway"
        },
        {
            "id": "R-RNO-140834",
            "name": "Extrinsic Pathway of Fibrin Clot Formation",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-140834",
            "resource": "Reactome",
            "description": "Extrinsic Pathway of Fibrin Clot Formation"
        },
        {
            "id": "R-RNO-159740",
            "name": "Gamma-carboxylation of protein precursors",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-159740",
            "resource": "Reactome",
            "description": "Gamma-carboxylation of protein precursors"
        },
        {
            "id": "R-RNO-159763",
            "name": "Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-159763",
            "resource": "Reactome",
            "description": "Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus"
        },
        {
            "id": "R-RNO-159782",
            "name": "Removal of aminoterminal propeptides from gamma-carboxylated proteins",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-159782",
            "resource": "Reactome",
            "description": "Removal of aminoterminal propeptides from gamma-carboxylated proteins"
        }
    ],
    "orthologs": [
        {
            "uniprot_canonical_ac": "P08709-1",
            "protein_name": "Coagulation factor VII",
            "gene_name": "F7",
            "tax_id": 9606,
            "organism": "Homo sapiens",
            "sequence": {
                "sequence": "MVSQALRLLCLLLGLQGCLAAGGVAKASGGETRDMPWKPGPHRVFVTQEEAHGVLHRRRRANAFLEELRPGSLERECKEEQCSFEEAREIFKDAERTKLFWISYSDGDQCASSPCQNGGSCKDQLQSYICFCLPAFEGRNCETHKDDQLICVNENGGCEQYCSDHTGTKRSCRCHEGYSLLADGVSCTPTVEYPCGKIPILEKRNASKPQGRIVGGKVCPKGECPWQVLLLVNGAQLCGGTLINTIWVVSAAHCFDKIKNWRNLIAVLGEHDLSEHDGDEQSRRVAQVIIPSTYVPGTTNHDIALLRLHQPVVLTDHVVPLCLPERTFSERTLAFVRFSLVSGWGQLLDRGATALELMVLNVPRLMTQDCLQQSRKVGDSPNITEYMFCAGYSDGSKDSCKGDSGGPHATHYRGTWYLTGIVSWGQGCATVGHFGVYTRVSQYIEWLQKLMRSEPRPGVLLRAPFP",
                "length": 466
            },
            "evidence": [
                {
                    "id": "45224272",
                    "url": "http://www.informatics.jax.org/homology/45224272",
                    "database": "MGI"
                },
                {
                    "id": "Q8K3U6",
                    "url": "https://omabrowser.org/oma/group/Q8K3U6/",
                    "database": "OMA"
                }
            ],
            "common_name": "Human"
        },
        {
            "uniprot_canonical_ac": "P70375-1",
            "protein_name": "Coagulation factor VII",
            "gene_name": "F7",
            "tax_id": 10090,
            "organism": "Mus musculus",
            "sequence": {
                "sequence": "MVPQAHGLLLLCFLLQLQGPLGTAVFITQEEAHGVLHRQRRANSLLEELWPGSLERECNEEQCSFEEAREIFKSPERTKQFWIVYSDGDQCASNPCQNGGTCQDHLKSYVCFCLLDFEGRNCEKSKNEQLICANENGDCDQYCRDHVGTKRTCSCHEDYTLQPDEVSCKPKVEYPCGRIPVVEKRNSSSRQGRIVGGNVCPKGECPWQAVLKINGLLLCGAVLLDARWIVTAAHCFDNIRYWGNITVVMGEHDFSEKDGDEQVRRVTQVIMPDKYIRGKINHDIALLRLHRPVTFTDYVVPLCLPEKSFSENTLARIRFSRVSGWGQLLDRGATALELMSIEVPRLMTQDCLEHAKHSSNTPKITENMFCAGYMDGTKDACKGDSGGPHATHYHGTWYLTGVVSWGEGCAAIGHIGVYTRVSQYIDWLVRHMDSKLQVGVFRLPLL",
                "length": 446
            },
            "evidence": [
                {
                    "id": "45224272",
                    "url": "http://www.informatics.jax.org/homology/45224272",
                    "database": "MGI"
                },
                {
                    "id": "Q8K3U6",
                    "url": "https://omabrowser.org/oma/group/Q8K3U6/",
                    "database": "OMA"
                }
            ],
            "common_name": "Mouse"
        }
    ],
    "go_annotation": {
        "categories": [
            {
                "name": "Biological Process",
                "total": 27,
                "go_terms": [
                    {
                        "name": "response to thyroxine",
                        "id": "GO:0097068",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097068",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "proteolysis",
                        "id": "GO:0006508",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "protein processing",
                        "id": "GO:0016485",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016485",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of protein kinase B signaling",
                        "id": "GO:0051897",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051897",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to hypoxia",
                        "id": "GO:0001666",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001666",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "blood coagulation",
                        "id": "GO:0007596",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007596",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to organic cyclic compound",
                        "id": "GO:0014070",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0014070",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to nutrient levels",
                        "id": "GO:0031667",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031667",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "circadian rhythm",
                        "id": "GO:0007623",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007623",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to estradiol",
                        "id": "GO:0032355",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032355",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to hormone",
                        "id": "GO:0009725",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009725",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "animal organ regeneration",
                        "id": "GO:0031100",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031100",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to estrogen",
                        "id": "GO:0043627",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043627",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to thyroid hormone",
                        "id": "GO:0097066",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097066",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of blood coagulation",
                        "id": "GO:0030194",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030194",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of leukocyte chemotaxis",
                        "id": "GO:0002690",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002690",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to growth hormone",
                        "id": "GO:0060416",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060416",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to vitamin K",
                        "id": "GO:0032571",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032571",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of positive chemotaxis",
                        "id": "GO:0050927",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050927",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to cholesterol",
                        "id": "GO:0070723",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070723",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to carbon dioxide",
                        "id": "GO:0010037",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010037",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of platelet-derived growth factor receptor signaling pathway",
                        "id": "GO:0010641",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010641",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to genistein",
                        "id": "GO:0033595",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033595",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to Thyroid stimulating hormone",
                        "id": "GO:1904400",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1904400",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to 2,3,7,8-tetrachlorodibenzodioxine",
                        "id": "GO:1904612",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1904612",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to astaxanthin",
                        "id": "GO:1905217",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905217",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to thyrotropin-releasing hormone",
                        "id": "GO:1905225",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905225",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 4,
                "go_terms": [
                    {
                        "name": "endopeptidase activity",
                        "id": "GO:0004175",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004175",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "serine-type endopeptidase activity",
                        "id": "GO:0004252",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004252",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "signaling receptor binding",
                        "id": "GO:0005102",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005102",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "calcium ion binding",
                        "id": "GO:0005509",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005509",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 6,
                "go_terms": [
                    {
                        "name": "extracellular space",
                        "id": "GO:0005615",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "vesicle",
                        "id": "GO:0031982",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031982",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "protein-containing complex",
                        "id": "GO:0032991",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032991",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "serine-type peptidase complex",
                        "id": "GO:1905286",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905286",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "serine-type endopeptidase complex",
                        "id": "GO:1905370",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905370",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "extracellular region",
                        "id": "GO:0005576",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8K3U6",
                                "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 186,
            "end_pos": 188,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 244,
            "end_pos": 246,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [
        {
            "id": "R-RNO-140736",
            "name": "factor X -> factor Xa + factor X activation peptide (TF:F7a catalyst)",
            "equation": "",
            "summary": "This event has been computationally inferred from an event that has been demonstrated in another species.<p>The inference is based on the homology mapping from PANTHER. Briefly, reactions for which all involved PhysicalEntities (in input, output and catalyst) have a mapped orthologue/paralogue (for complexes at least 75% of components must have a mapping) are inferred to the other species. High level events are also inferred for these events to allow for easier navigation.<p><a href='/electronic_inference_compara.html' target = 'NEW'>More details and caveats of the event inference in Reactome.</a> For details on PANTHER see also: <a href='http://www.pantherdb.org/about.jsp' target='NEW'>http://www.pantherdb.org/about.jsp</a>",
            "cellular_location": "extracellular region, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [
                "R-RNO-140785"
            ],
            "enzyme_list": [
                "Q63207-1",
                "Q8K3U6-1"
            ],
            "evidence": [
                {
                    "id": "R-RNO-140736",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-140736"
                }
            ]
        },
        {
            "id": "R-RNO-140748",
            "name": "tissue factor (TF) + activated factor VII (F7a) -> TF:F7a complex",
            "equation": "",
            "summary": "This event has been computationally inferred from an event that has been demonstrated in another species.<p>The inference is based on the homology mapping from PANTHER. Briefly, reactions for which all involved PhysicalEntities (in input, output and catalyst) have a mapped orthologue/paralogue (for complexes at least 75% of components must have a mapping) are inferred to the other species. High level events are also inferred for these events to allow for easier navigation.<p><a href='/electronic_inference_compara.html' target = 'NEW'>More details and caveats of the event inference in Reactome.</a> For details on PANTHER see also: <a href='http://www.pantherdb.org/about.jsp' target='NEW'>http://www.pantherdb.org/about.jsp</a>",
            "cellular_location": "extracellular region, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q8K3U6-1"
            ],
            "evidence": [
                {
                    "id": "R-RNO-140748",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-140748"
                }
            ]
        },
        {
            "id": "R-RNO-140769",
            "name": "factor VII -> factor VIIa",
            "equation": "",
            "summary": "This event has been computationally inferred from an event that has been demonstrated in another species.<p>The inference is based on the homology mapping from PANTHER. Briefly, reactions for which all involved PhysicalEntities (in input, output and catalyst) have a mapped orthologue/paralogue (for complexes at least 75% of components must have a mapping) are inferred to the other species. High level events are also inferred for these events to allow for easier navigation.<p><a href='/electronic_inference_compara.html' target = 'NEW'>More details and caveats of the event inference in Reactome.</a> For details on PANTHER see also: <a href='http://www.pantherdb.org/about.jsp' target='NEW'>http://www.pantherdb.org/about.jsp</a>",
            "cellular_location": "extracellular region",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q63207-1",
                "Q8K3U6-1"
            ],
            "evidence": [
                {
                    "id": "R-RNO-140769",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-140769"
                }
            ]
        },
        {
            "id": "R-RNO-140777",
            "name": "factor X -> factor Xa + factor X activation peptide (TF:F7 catalyst)",
            "equation": "",
            "summary": "This event has been computationally inferred from an event that has been demonstrated in another species.<p>The inference is based on the homology mapping from PANTHER. Briefly, reactions for which all involved PhysicalEntities (in input, output and catalyst) have a mapped orthologue/paralogue (for complexes at least 75% of components must have a mapping) are inferred to the other species. High level events are also inferred for these events to allow for easier navigation.<p><a href='/electronic_inference_compara.html' target = 'NEW'>More details and caveats of the event inference in Reactome.</a> For details on PANTHER see also: <a href='http://www.pantherdb.org/about.jsp' target='NEW'>http://www.pantherdb.org/about.jsp</a>",
            "cellular_location": "extracellular region, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q63207-1",
                "Q8K3U6-1"
            ],
            "evidence": [
                {
                    "id": "R-RNO-140777",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-140777"
                }
            ]
        },
        {
            "id": "R-RNO-140783",
            "name": "tissue factor (TF) + factor VII (F7) -> TF:F7 complex",
            "equation": "",
            "summary": "This event has been computationally inferred from an event that has been demonstrated in another species.<p>The inference is based on the homology mapping from PANTHER. Briefly, reactions for which all involved PhysicalEntities (in input, output and catalyst) have a mapped orthologue/paralogue (for complexes at least 75% of components must have a mapping) are inferred to the other species. High level events are also inferred for these events to allow for easier navigation.<p><a href='/electronic_inference_compara.html' target = 'NEW'>More details and caveats of the event inference in Reactome.</a> For details on PANTHER see also: <a href='http://www.pantherdb.org/about.jsp' target='NEW'>http://www.pantherdb.org/about.jsp</a>",
            "cellular_location": "extracellular region, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q8K3U6-1"
            ],
            "evidence": [
                {
                    "id": "R-RNO-140783",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-140783"
                }
            ]
        },
        {
            "id": "R-RNO-140823",
            "name": "factor IX -> factor IXa + factor IX activation peptide (TF:F7a catalyst)",
            "equation": "",
            "summary": "This event has been computationally inferred from an event that has been demonstrated in another species.<p>The inference is based on the homology mapping from PANTHER. Briefly, reactions for which all involved PhysicalEntities (in input, output and catalyst) have a mapped orthologue/paralogue (for complexes at least 75% of components must have a mapping) are inferred to the other species. High level events are also inferred for these events to allow for easier navigation.<p><a href='/electronic_inference_compara.html' target = 'NEW'>More details and caveats of the event inference in Reactome.</a> For details on PANTHER see also: <a href='http://www.pantherdb.org/about.jsp' target='NEW'>http://www.pantherdb.org/about.jsp</a>",
            "cellular_location": "extracellular region, plasma membrane",
            "input_participant_list": [
                "R-RNO-140886"
            ],
            "output_participant_list": [
                "R-RNO-140897"
            ],
            "enzyme_list": [
                "P16296-1",
                "Q8K3U6-1"
            ],
            "evidence": [
                {
                    "id": "R-RNO-140823",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-140823"
                }
            ]
        },
        {
            "id": "R-RNO-140825",
            "name": "TFPI + TF:F7a + factor Xa -> TFPI:TF:F7a:factor Xa",
            "equation": "",
            "summary": "This event has been computationally inferred from an event that has been demonstrated in another species.<p>The inference is based on the homology mapping from PANTHER. Briefly, reactions for which all involved PhysicalEntities (in input, output and catalyst) have a mapped orthologue/paralogue (for complexes at least 75% of components must have a mapping) are inferred to the other species. High level events are also inferred for these events to allow for easier navigation.<p><a href='/electronic_inference_compara.html' target = 'NEW'>More details and caveats of the event inference in Reactome.</a> For details on PANTHER see also: <a href='http://www.pantherdb.org/about.jsp' target='NEW'>http://www.pantherdb.org/about.jsp</a>",
            "cellular_location": "extracellular region, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q63207-1",
                "Q8K3U6-1"
            ],
            "evidence": [
                {
                    "id": "R-RNO-140825",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-140825"
                }
            ]
        },
        {
            "id": "R-RNO-159761",
            "name": "GGCX gamma-carboxylates F7(21-466) (pro-factor VII)",
            "equation": "",
            "summary": "This event has been computationally inferred from an event that has been demonstrated in another species.<p>The inference is based on the homology mapping from PANTHER. Briefly, reactions for which all involved PhysicalEntities (in input, output and catalyst) have a mapped orthologue/paralogue (for complexes at least 75% of components must have a mapping) are inferred to the other species. High level events are also inferred for these events to allow for easier navigation.<p><a href='/electronic_inference_compara.html' target = 'NEW'>More details and caveats of the event inference in Reactome.</a> For details on PANTHER see also: <a href='http://www.pantherdb.org/about.jsp' target='NEW'>http://www.pantherdb.org/about.jsp</a>",
            "cellular_location": "endoplasmic reticulum lumen, endoplasmic reticulum membrane",
            "input_participant_list": [
                "R-RNO-159848"
            ],
            "output_participant_list": [
                "R-RNO-159722"
            ],
            "enzyme_list": [
                "Q8K3U6-1",
                "O88496-1"
            ],
            "evidence": [
                {
                    "id": "R-RNO-159761",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-159761"
                }
            ]
        },
        {
            "id": "R-RNO-159783",
            "name": "Gamma-carboxy pro-factor VII transport from the endoplasmic reticulum to the Golgi apparatus",
            "equation": "",
            "summary": "This event has been computationally inferred from an event that has been demonstrated in another species.<p>The inference is based on the homology mapping from PANTHER. Briefly, reactions for which all involved PhysicalEntities (in input, output and catalyst) have a mapped orthologue/paralogue (for complexes at least 75% of components must have a mapping) are inferred to the other species. High level events are also inferred for these events to allow for easier navigation.<p><a href='/electronic_inference_compara.html' target = 'NEW'>More details and caveats of the event inference in Reactome.</a> For details on PANTHER see also: <a href='http://www.pantherdb.org/about.jsp' target='NEW'>http://www.pantherdb.org/about.jsp</a>",
            "cellular_location": "COPII-coated ER to Golgi transport vesicle, Golgi lumen, endoplasmic reticulum lumen",
            "input_participant_list": [],
            "output_participant_list": [
                "R-RNO-159767"
            ],
            "enzyme_list": [
                "Q8K3U6-1"
            ],
            "evidence": [
                {
                    "id": "R-RNO-159783",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-159783"
                }
            ]
        },
        {
            "id": "R-RNO-159868",
            "name": "Furin cleaves pro-factor VII to factor VII",
            "equation": "",
            "summary": "This event has been computationally inferred from an event that has been demonstrated in another species.<p>The inference is based on the homology mapping from PANTHER. Briefly, reactions for which all involved PhysicalEntities (in input, output and catalyst) have a mapped orthologue/paralogue (for complexes at least 75% of components must have a mapping) are inferred to the other species. High level events are also inferred for these events to allow for easier navigation.<p><a href='/electronic_inference_compara.html' target = 'NEW'>More details and caveats of the event inference in Reactome.</a> For details on PANTHER see also: <a href='http://www.pantherdb.org/about.jsp' target='NEW'>http://www.pantherdb.org/about.jsp</a>",
            "cellular_location": "Golgi lumen, Golgi membrane",
            "input_participant_list": [],
            "output_participant_list": [
                "R-RNO-159808",
                "R-RNO-159847"
            ],
            "enzyme_list": [
                "P23377-1",
                "Q8K3U6-1"
            ],
            "evidence": [
                {
                    "id": "R-RNO-159868",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-159868"
                }
            ]
        }
    ],
    "reaction_participants": [
        {
            "participant_id": "R-RNO-140785",
            "participant_name": "F10 [extracellular region]",
            "crossref": [
                {
                    "id": "Q63207",
                    "database": "UniProt",
                    "url": ""
                },
                {
                    "id": "Q63207",
                    "database": "ZINC target",
                    "url": ""
                },
                {
                    "id": "Q63207",
                    "database": "PRO",
                    "url": ""
                },
                {
                    "id": "NP_058839.1",
                    "database": "RefSeq",
                    "url": ""
                },
                {
                    "id": "FA10_RAT",
                    "database": "ZINC - Substances",
                    "url": ""
                },
                {
                    "id": "ENSG00000126218",
                    "database": "OpenTargets",
                    "url": ""
                },
                {
                    "id": "61850",
                    "database": "RGD",
                    "url": ""
                },
                {
                    "id": "FA10_RAT",
                    "database": "ZINC - Predictions - Purchasable",
                    "url": ""
                }
            ]
        },
        {
            "participant_id": "R-RNO-140886",
            "participant_name": "12xCbxE-3D-F9(47-461) [extracellular region]",
            "crossref": [
                {
                    "id": "NP_113728.1",
                    "database": "RefSeq",
                    "url": ""
                },
                {
                    "id": "P16296",
                    "database": "UniProt",
                    "url": ""
                },
                {
                    "id": "2589",
                    "database": "RGD",
                    "url": ""
                },
                {
                    "id": "P16296",
                    "database": "PRO",
                    "url": ""
                }
            ]
        },
        {
            "participant_id": "R-RNO-140897",
            "participant_name": "factor IX activation peptide [extracellular region]",
            "crossref": [
                {
                    "id": "P16296",
                    "database": "UniProt",
                    "url": ""
                },
                {
                    "id": "2589",
                    "database": "RGD",
                    "url": ""
                },
                {
                    "id": "NP_113728.1",
                    "database": "RefSeq",
                    "url": ""
                },
                {
                    "id": "P16296",
                    "database": "PRO",
                    "url": ""
                }
            ]
        },
        {
            "participant_id": "R-RNO-159722",
            "participant_name": "10xCbxE-F7(21-466) [endoplasmic reticulum lumen]",
            "crossref": [
                {
                    "id": "Q8K3U6",
                    "database": "UniProt",
                    "url": ""
                },
                {
                    "id": "3.4.21.21",
                    "database": "IntEnz",
                    "url": ""
                },
                {
                    "id": "ENSRNOT00000037806",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "628678",
                    "database": "RGD",
                    "url": ""
                },
                {
                    "id": "ENSRNOP00000038466",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "ENSRNOG00000032737",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "NP_690059.1",
                    "database": "RefSeq",
                    "url": ""
                },
                {
                    "id": "Q8K3U6",
                    "database": "PRO",
                    "url": ""
                }
            ]
        },
        {
            "participant_id": "R-RNO-159767",
            "participant_name": "pro-factor VII [Golgi lumen]",
            "crossref": [
                {
                    "id": "Q8K3U6",
                    "database": "UniProt",
                    "url": ""
                },
                {
                    "id": "3.4.21.21",
                    "database": "IntEnz",
                    "url": ""
                },
                {
                    "id": "ENSRNOT00000037806",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "628678",
                    "database": "RGD",
                    "url": ""
                },
                {
                    "id": "ENSRNOP00000038466",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "ENSRNOG00000032737",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "NP_690059.1",
                    "database": "RefSeq",
                    "url": ""
                },
                {
                    "id": "Q8K3U6",
                    "database": "PRO",
                    "url": ""
                }
            ]
        },
        {
            "participant_id": "R-RNO-159808",
            "participant_name": "factor VII [Golgi lumen]",
            "crossref": [
                {
                    "id": "Q8K3U6",
                    "database": "UniProt",
                    "url": ""
                },
                {
                    "id": "3.4.21.21",
                    "database": "IntEnz",
                    "url": ""
                },
                {
                    "id": "ENSRNOT00000037806",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "628678",
                    "database": "RGD",
                    "url": ""
                },
                {
                    "id": "ENSRNOP00000038466",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "ENSRNOG00000032737",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "NP_690059.1",
                    "database": "RefSeq",
                    "url": ""
                },
                {
                    "id": "Q8K3U6",
                    "database": "PRO",
                    "url": ""
                }
            ]
        },
        {
            "participant_id": "R-RNO-159847",
            "participant_name": "factor VII propeptide [Golgi lumen]",
            "crossref": [
                {
                    "id": "Q8K3U6",
                    "database": "UniProt",
                    "url": ""
                },
                {
                    "id": "3.4.21.21",
                    "database": "IntEnz",
                    "url": ""
                },
                {
                    "id": "ENSRNOT00000037806",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "628678",
                    "database": "RGD",
                    "url": ""
                },
                {
                    "id": "ENSRNOP00000038466",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "ENSRNOG00000032737",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "NP_690059.1",
                    "database": "RefSeq",
                    "url": ""
                },
                {
                    "id": "Q8K3U6",
                    "database": "PRO",
                    "url": ""
                }
            ]
        },
        {
            "participant_id": "R-RNO-159848",
            "participant_name": "F7(21-466) [endoplasmic reticulum lumen]",
            "crossref": [
                {
                    "id": "NP_690059.1",
                    "database": "RefSeq",
                    "url": ""
                },
                {
                    "id": "ENSRNOT00000037806",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "ENSRNOP00000038466",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "Q8K3U6",
                    "database": "UniProt",
                    "url": ""
                },
                {
                    "id": "628678",
                    "database": "RGD",
                    "url": ""
                },
                {
                    "id": "Q8K3U6",
                    "database": "PRO",
                    "url": ""
                },
                {
                    "id": "ENSRNOG00000032737",
                    "database": "Ensembl",
                    "url": ""
                },
                {
                    "id": "3.4.21.21",
                    "database": "IntEnz",
                    "url": ""
                }
            ]
        }
    ],
    "reaction_enzymes": [
        {
            "uniprot_ac": "O88496",
            "gene_name": "Ggcx",
            "activity": [
                {
                    "ec_number": "4.1.1.90",
                    "activity": "2,3-epoxyphylloquinone + 4-carboxy-L-glutamyl-[protein] + H(+) + H2O = CO2 + L-glutamyl-[protein] + O2 + phylloquinol.",
                    "evidence": [
                        {
                            "id": "O88496",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/O88496"
                        }
                    ]
                },
                {
                    "ec_number": "4.1.1.90",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "O88496",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/O88496"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P16296",
            "gene_name": "F9",
            "activity": [
                {
                    "ec_number": "3.4.21.22",
                    "activity": "Selective cleavage of Arg-|-Ile bond in factor X to form factor Xa.",
                    "evidence": [
                        {
                            "id": "P16296",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P16296"
                        }
                    ]
                },
                {
                    "ec_number": "3.4.21.22",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P16296",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P16296"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P23377",
            "gene_name": "Furin",
            "activity": [
                {
                    "ec_number": "3.4.21.75",
                    "activity": "Release of mature proteins from their proproteins by cleavage of -Arg-Xaa-Yaa-Arg-|-Zaa- bonds, where Xaa can be any amino acid and Yaa is Arg or Lys. Releases albumin, complement component C3 and von Willebrand factor from their respective precursors.",
                    "evidence": [
                        {
                            "id": "P23377",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P23377"
                        }
                    ]
                },
                {
                    "ec_number": "3.4.21.75",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P23377",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P23377"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "Q63207",
            "gene_name": "F10",
            "activity": [
                {
                    "ec_number": "3.4.21.6",
                    "activity": "Selective cleavage of Arg-|-Thr and then Arg-|-Ile bonds in prothrombin to form thrombin.",
                    "evidence": [
                        {
                            "id": "Q63207",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q63207"
                        }
                    ]
                },
                {
                    "ec_number": "3.4.21.6",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "Q63207",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q63207"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "Q8K3U6",
            "gene_name": "F7",
            "activity": [
                {
                    "ec_number": "3.4.21.21",
                    "activity": "Selective cleavage of Arg-|-Ile bond in factor X to form factor Xa.",
                    "evidence": [
                        {
                            "id": "Q8K3U6",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                        }
                    ]
                },
                {
                    "ec_number": "3.4.21.21",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "Q8K3U6",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q8K3U6"
                        }
                    ]
                }
            ]
        }
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