{
    "uniprot_canonical_ac": "Q62312-2",
    "uniprot_ac": "Q62312",
    "uniprot_id": "TGFR2_MOUSE",
    "mass": {
        "chemical_mass": 64219.0,
        "monoisotopic_mass": 64219.0
    },
    "refseq": {
        "ac": "NP_033397",
        "name": "TGF-beta receptor type-2 isoform 1 precursor",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033397"
    },
    "gene_names": [
        {
            "name": "Tgfbr2",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/Q62312",
            "id": "Q62312"
        },
        {
            "name": "1110020H15Rik; DNIIR; RIIDN; TbetaR-II; TbetaRII; TBR-II",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033397",
            "id": "NP_033397"
        },
        {
            "name": "Tgfbr2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033397",
            "id": "NP_033397"
        }
    ],
    "protein_names": [
        {
            "name": "TGF-beta receptor type-2",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "Q62312"
        },
        {
            "name": "2.7.11.30",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q62312"
        },
        {
            "name": "TGF-beta receptor type II",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q62312"
        },
        {
            "name": "TGF-beta receptor type-2 isoform 1 precursor",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033397",
            "id": "NP_033397"
        },
        {
            "name": "TGF-beta receptor type-2; TGF-beta receptor II; TGFR-2; TGF-beta receptor type II; TGF-beta type II receptor; transforming growth factor-beta receptor type II",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033397",
            "id": "NP_033397"
        },
        {
            "name": "TGF-beta type II receptor",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q62312"
        },
        {
            "name": "TGFR-2",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q62312"
        },
        {
            "name": "TbetaR-II",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q62312"
        },
        {
            "name": "Transforming growth factor-beta receptor type II",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q62312"
        }
    ],
    "function": [
        {
            "annotation": "Has transforming growth factor beta-activated receptor activity.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q62312",
                    "url": "https://www.uniprot.org/uniprot/Q62312#function"
                },
                {
                    "database": "UniProtKB",
                    "id": "P37173",
                    "url": "https://www.uniprot.org/uniprot/P37173#function"
                }
            ]
        },
        {
            "annotation": "Neuropilin-1 interacts with VE-cadherin and TGFBR2 to stabilize adherens junctions and prevent activation of endothelium under flow.",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_033397",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033397"
                },
                {
                    "database": "PubMed",
                    "id": "37220183",
                    "url": "https://glygen.org/publication/PubMed/37220183"
                }
            ]
        },
        {
            "annotation": "Transforming growth factor beta receptor 2 (Tgfbr2) deficiency in keratocytes results in corneal ectasia.",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_033397",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033397"
                },
                {
                    "database": "PubMed",
                    "id": "37393064",
                    "url": "https://glygen.org/publication/PubMed/37393064"
                }
            ]
        },
        {
            "annotation": "Transmembrane serine/threonine kinase forming with the TGF-beta type I serine/threonine kinase receptor, TGFBR1, the non-promiscuous receptor for the TGF-beta cytokines TGFB1, TGFB2 and TGFB3. Transduces the TGFB1, TGFB2 and TGFB3 signal from the cell surface to the cytoplasm and is thus regulating a plethora of physiological and pathological processes including cell cycle arrest in epithelial and hematopoietic cells, control of mesenchymal cell proliferation and differentiation, wound healing, extracellular matrix production, immunosuppression and carcinogenesis. The formation of the receptor complex composed of 2 TGFBR1 and 2 TGFBR2 molecules symmetrically bound to the cytokine dimer results in the phosphorylation and the activation of TGFRB1 by the constitutively active TGFBR2. Activated TGFBR1 phosphorylates SMAD2 which dissociates from the receptor and interacts with SMAD4. The SMAD2-SMAD4 complex is subsequently translocated to the nucleus where it modulates the transcription of the TGF-beta-regulated genes. This constitutes the canonical SMAD-dependent TGF-beta signaling cascade. Also involved in non-canonical, SMAD-independent TGF-beta signaling pathways (By similarity).",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q62312",
                    "url": "https://www.uniprot.org/uniprot/Q62312#function"
                },
                {
                    "database": "UniProtKB",
                    "id": "P37173",
                    "url": "https://www.uniprot.org/uniprot/P37173#function"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0050466",
            "recommended_name": {
                "id": "DOID:0050466",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050466",
                "name": "Loeys-Dietz syndrome",
                "description": "A syndrome that is characterized by increased risk of aortic aneurysm and dissection, elongated limbs, hypertelorism, bifid uvula and easy skin bruising due to mutations in TGFB3 that results in connective tissue defects."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "0050466",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050466"
                }
            ]
        },
        {
            "disease_id": "DOID:0070234",
            "recommended_name": {
                "id": "DOID:0070234",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0070234",
                "name": "Loeys-Dietz syndrome 2",
                "description": "A Loeys-Dietz syndrome that has_material_basis_in heterozygous mutation in the TGFBR2 gene on chromosome 3p24."
            },
            "synonyms": [
                {
                    "id": "DOID:0070234",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0070234",
                    "name": "AAT3",
                    "description": ""
                },
                {
                    "id": "DOID:0070234",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0070234",
                    "name": "LDS2",
                    "description": ""
                },
                {
                    "id": "DOID:0070234",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0070234",
                    "name": "Marfan syndrome type II",
                    "description": ""
                },
                {
                    "id": "DOID:0070234",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0070234",
                    "name": "familial throacic aortic aneurysm 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012427",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012427",
                    "name": "Loeys-Dietz syndrome 2",
                    "description": "A rare autosomal dominant inherited disorder of connective tissue caused by mutations in either the TGFBR1 or TGFBR2 gene. Like Loeys-Dietz syndrome type I the disease is characterized by enlargement of the aorta and other arteries, and arterial tortuosity, but skeletal signs are typically less severe or absent in type 2. Skin abnormalities, such as velvety skin are often present in type 2."
                },
                {
                    "id": "MONDO:0012427",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012427",
                    "name": "Loeys-Dietz syndrome 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012427",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012427",
                    "name": "Loeys-Dietz syndrome caused by mutation in TGFBR2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012427",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012427",
                    "name": "Loeys-Dietz syndrome type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012427",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012427",
                    "name": "Loeys-Dietz syndrome type II",
                    "description": ""
                },
                {
                    "id": "MONDO:0012427",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012427",
                    "name": "TGFBR2 Loeys-Dietz syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0012427",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012427",
                    "name": "LDS2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012427",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012427",
                    "name": "Marfan syndrome, type II",
                    "description": ""
                },
                {
                    "id": "MONDO:0012427",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012427",
                    "name": "Marfan syndrome, type II, formerly",
                    "description": ""
                },
                {
                    "id": "MONDO:0012427",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012427",
                    "name": "aortic aneurysm, familial thoracic 3",
                    "description": ""
                },
                {
                    "id": "MIM:610168",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/610168",
                    "name": "Loeys-Dietz syndrome 2",
                    "description": "Loeys-Dietz syndrome 2"
                }
            ],
            "evidence": [
                {
                    "id": "0070234",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0070234"
                }
            ]
        },
        {
            "disease_id": "DOID:0070273",
            "recommended_name": {
                "id": "DOID:0070273",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0070273",
                "name": "hereditary nonpolyposis colorectal cancer type 6",
                "description": "A Lynch syndrome that has_material_basis_in heterozygous mutation in the TGFBR2 gene on chromosome 3p22."
            },
            "synonyms": [
                {
                    "id": "DOID:0070273",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0070273",
                    "name": "HNPCC6",
                    "description": ""
                },
                {
                    "id": "MONDO:0013695",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013695",
                    "name": "colorectal cancer, hereditary nonpolyposis, type 6",
                    "description": "Any hereditary nonpolyposis colon cancer in which the cause of the disease is a mutation in the TGFBR2 gene."
                },
                {
                    "id": "MONDO:0013695",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013695",
                    "name": "TGFBR2 hereditary nonpolyposis colon cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0013695",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013695",
                    "name": "colorectal cancer, hereditary nonpolyposis, type 6",
                    "description": ""
                },
                {
                    "id": "MONDO:0013695",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013695",
                    "name": "hereditary nonpolyposis colon cancer caused by mutation in TGFBR2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013695",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013695",
                    "name": "HNPCC6",
                    "description": ""
                },
                {
                    "id": "MONDO:0013695",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013695",
                    "name": "colon cancer, hereditary nonpolyposis, type 6",
                    "description": ""
                },
                {
                    "id": "MIM:614331",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/614331",
                    "name": "Hereditary non-polyposis colorectal cancer 6",
                    "description": "Hereditary non-polyposis colorectal cancer 6"
                }
            ],
            "evidence": [
                {
                    "id": "0070273",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0070273"
                }
            ]
        },
        {
            "disease_id": "DOID:0110214",
            "recommended_name": {
                "id": "DOID:0110214",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110214",
                "name": "cleft soft palate",
                "description": "A cleft palate that is characterized as a fissure type embryopathy that affects in varying degrees the soft palate."
            },
            "synonyms": [
                {
                    "id": "DOID:0110214",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110214",
                    "name": "cleft velum",
                    "description": ""
                },
                {
                    "id": "DOID:0110214",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110214",
                    "name": "cleft velum palatinum",
                    "description": ""
                },
                {
                    "id": "DOID:0110214",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110214",
                    "name": "soft cleft palate",
                    "description": ""
                },
                {
                    "id": "MONDO:0007338",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007338",
                    "name": "cleft soft palate",
                    "description": "Cleft velum is a fissure type embryopathy that affects in varying degrees the soft palate."
                },
                {
                    "id": "MONDO:0007338",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007338",
                    "name": "cleft soft palate",
                    "description": ""
                },
                {
                    "id": "MONDO:0007338",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007338",
                    "name": "cleft velum",
                    "description": ""
                },
                {
                    "id": "MONDO:0007338",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007338",
                    "name": "cleft velum palatinum",
                    "description": ""
                },
                {
                    "id": "MONDO:0007338",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007338",
                    "name": "soft cleft palate",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "0110214",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110214"
                }
            ]
        },
        {
            "disease_id": "DOID:0112182",
            "recommended_name": {
                "id": "DOID:0112182",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0112182",
                "name": "mismatch repair cancer syndrome",
                "description": "A syndrome characterized by predisposition for development of a broad spectrum of malignancies during childhood, including mainly brain, hematological and gastrointestinal cancers that has_material_basis_in homozygous or compound heterozygous mutation in the mismatch repair genes MLH1, MSH2, MSH6, or PMS2 on chromosomes 3p22.2, 2p21-p16, 2p16.3, and 7p22.1, respectively."
            },
            "synonyms": [
                {
                    "id": "DOID:0112182",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112182",
                    "name": "BTP1 syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:0112182",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112182",
                    "name": "BTPS1",
                    "description": ""
                },
                {
                    "id": "DOID:0112182",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112182",
                    "name": "CMMRDS",
                    "description": ""
                },
                {
                    "id": "DOID:0112182",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112182",
                    "name": "MMR deficiency",
                    "description": ""
                },
                {
                    "id": "DOID:0112182",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112182",
                    "name": "Turcot syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:0112182",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112182",
                    "name": "CMMR-D syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:0112182",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112182",
                    "name": "brain tumor-polyposis syndrome 1",
                    "description": ""
                },
                {
                    "id": "DOID:0112182",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112182",
                    "name": "childhood cancer syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:0112182",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112182",
                    "name": "constitutional mismatch repair deficiency syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "mismatch repair cancer syndrome 1",
                    "description": "A rare childhood cancer predisposition syndrome caused by biallelic inheritance of mutations in MLH1, MSH2, MSH6, or PMS2 genes. It is characterized by the development of childhood cancers, usually hematological malignancies and/or brain tumors, and colorectal cancers with multiple intestinal polyps. The majority of patients show signs of neurofibromatosis type 1."
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "BTP1 syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "CMMR-D",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "CMMR-D syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "MMRCS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "brain tumor-polyposis syndrome 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "constitutional MIS-match repair deficiency syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "constitutional mismatch repair deficiency syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "mismatch repair cancer syndrome 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "CNS tumors with familial polyposis of the colon",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "CNS tumours with familial polyposis of the colon",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "MMR deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "MMRCS",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "Turcot syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "brain tumor-polyposis syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "childhood cancer syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "glioma-polyposis syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "malignant tumors of the central nervous system associated with familial polyposis of the colon",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "malignant tumours of the central nervous system associated with familial polyposis of the colon",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "mismatch repair cancer syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0010159",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010159",
                    "name": "mismatch repair deficiency",
                    "description": ""
                },
                {
                    "id": "MIM:276300",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/276300",
                    "name": "Mismatch repair cancer syndrome 1",
                    "description": "Mismatch repair cancer syndrome 1"
                }
            ],
            "evidence": [
                {
                    "id": "0112182",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0112182"
                }
            ]
        },
        {
            "disease_id": "DOID:10283",
            "recommended_name": {
                "id": "DOID:10283",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate."
            },
            "synonyms": [
                {
                    "id": "DOID:10283",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10283",
                    "name": "NGP - new growth of prostate",
                    "description": ""
                },
                {
                    "id": "DOID:10283",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10283",
                    "name": "hereditary prostate cancer",
                    "description": ""
                },
                {
                    "id": "DOID:10283",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10283",
                    "name": "malignant tumor of the prostate",
                    "description": ""
                },
                {
                    "id": "DOID:10283",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10283",
                    "name": "prostate cancer, familial",
                    "description": ""
                },
                {
                    "id": "DOID:10283",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10283",
                    "name": "prostate neoplasm",
                    "description": ""
                },
                {
                    "id": "DOID:10283",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10283",
                    "name": "prostatic cancer",
                    "description": ""
                },
                {
                    "id": "DOID:10283",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10283",
                    "name": "prostatic neoplasm",
                    "description": ""
                },
                {
                    "id": "DOID:10283",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10283",
                    "name": "tumor of the prostate",
                    "description": ""
                },
                {
                    "id": "MONDO:0012597",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                    "name": "prostate cancer, hereditary, 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012597",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                    "name": "prostate cancer, hereditary, 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012597",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                    "name": "prostate cancer, hereditary, type 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012597",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                    "name": "HPC9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012741",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                    "name": "prostate cancer, hereditary, 12",
                    "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene."
                },
                {
                    "id": "MONDO:0012741",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                    "name": "EHBP1 familial prostate cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0012741",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                    "name": "familial prostate cancer caused by mutation in EHBP1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012741",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                    "name": "prostate cancer, hereditary, 12",
                    "description": ""
                },
                {
                    "id": "MONDO:0012741",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                    "name": "prostate cancer, hereditary, type 12",
                    "description": ""
                },
                {
                    "id": "MONDO:0012741",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                    "name": "HPC12",
                    "description": ""
                },
                {
                    "id": "MONDO:0012244",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                    "name": "prostate cancer, hereditary, 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0012244",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                    "name": "prostate cancer, hereditary, 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0012244",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                    "name": "prostate cancer, hereditary, type 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0012244",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                    "name": "HPC5",
                    "description": ""
                },
                {
                    "id": "MONDO:0012093",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                    "name": "prostate cancer, hereditary, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012093",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                    "name": "prostate cancer, hereditary, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012093",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                    "name": "prostate cancer, hereditary, type 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012093",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                    "name": "prostate cancer, susceptibility to, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012093",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                    "name": "HPC3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012094",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                    "name": "prostate cancer, hereditary, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012094",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                    "name": "prostate cancer, hereditary, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012094",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                    "name": "prostate cancer, hereditary, type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012094",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                    "name": "prostate cancer, susceptibility to, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012094",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                    "name": "HPC4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012094",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                    "name": "prostate cancer, hereditary, on chromosome 7",
                    "description": ""
                },
                {
                    "id": "MONDO:0012758",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                    "name": "prostate cancer, hereditary, 13",
                    "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene."
                },
                {
                    "id": "MONDO:0012758",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                    "name": "MSMB familial prostate cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0012758",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                    "name": "familial prostate cancer caused by mutation in MSMB",
                    "description": ""
                },
                {
                    "id": "MONDO:0012758",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                    "name": "prostate cancer, hereditary, 13",
                    "description": ""
                },
                {
                    "id": "MONDO:0012758",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                    "name": "prostate cancer, hereditary, type 13",
                    "description": ""
                },
                {
                    "id": "MONDO:0012758",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                    "name": "HPC13",
                    "description": ""
                },
                {
                    "id": "MONDO:0011270",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                    "name": "prostate cancer, hereditary, 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0011270",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                    "name": "prostate cancer, hereditary, 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0011270",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                    "name": "prostate cancer, hereditary, type 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0011270",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                    "name": "HPC8",
                    "description": ""
                },
                {
                    "id": "MONDO:0011270",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                    "name": "predisposing for prostate cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0011270",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                    "name": "prostate cancer, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0012300",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                    "name": "prostate cancer, hereditary, 6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012300",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                    "name": "prostate cancer, hereditary, 6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012300",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                    "name": "prostate cancer, hereditary, type 6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012300",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                    "name": "HPC6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012300",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                    "name": "prostate cancer, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0012620",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                    "name": "prostate cancer, hereditary, 10",
                    "description": ""
                },
                {
                    "id": "MONDO:0012620",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                    "name": "HPC10",
                    "description": ""
                },
                {
                    "id": "MONDO:0012620",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                    "name": "prostate cancer, hereditary, 10",
                    "description": ""
                },
                {
                    "id": "MONDO:0023122",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                    "name": "familial prostate carcinoma",
                    "description": "Prostate carcinoma that has developed in relatives of patients with a history of prostate carcinoma."
                },
                {
                    "id": "MONDO:0023122",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                    "name": "familial prostate cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0023122",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                    "name": "hereditary prostate cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0023122",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                    "name": "hereditary prostate carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0023122",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                    "name": "prostate cancer, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0023122",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                    "name": "prostate cancer, familial, susceptibility to, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0023122",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                    "name": "prostate cancer, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0023122",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                    "name": "prostate cancer, susceptibility to, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0023122",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                    "name": "prostate cancer, familial",
                    "description": ""
                },
                {
                    "id": "MONDO:0023122",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                    "name": "prostate cancer, hereditary",
                    "description": ""
                },
                {
                    "id": "MONDO:0012470",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                    "name": "prostate cancer, hereditary, 7",
                    "description": ""
                },
                {
                    "id": "MONDO:0012470",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                    "name": "HPC7",
                    "description": ""
                },
                {
                    "id": "MONDO:0012470",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                    "name": "prostate cancer, hereditary, 7",
                    "description": ""
                },
                {
                    "id": "MONDO:0012470",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                    "name": "prostate cancer aggressiveness",
                    "description": ""
                },
                {
                    "id": "MONDO:0011098",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                    "name": "prostate cancer, hereditary, 1",
                    "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene."
                },
                {
                    "id": "MONDO:0011098",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                    "name": "RNASEL familial prostate cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0011098",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                    "name": "familial prostate cancer caused by mutation in RNASEL",
                    "description": ""
                },
                {
                    "id": "MONDO:0011098",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                    "name": "prostate cancer 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011098",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                    "name": "prostate cancer, hereditary, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011098",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                    "name": "prostate cancer, hereditary, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011098",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                    "name": "HPC1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011098",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                    "name": "Prca1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012768",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                    "name": "prostate cancer, hereditary, 11",
                    "description": ""
                },
                {
                    "id": "MONDO:0012768",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                    "name": "HPC11",
                    "description": ""
                },
                {
                    "id": "MONDO:0012768",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                    "name": "prostate cancer, hereditary, 11",
                    "description": ""
                },
                {
                    "id": "MONDO:0012769",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                    "name": "prostate cancer, hereditary, 14",
                    "description": ""
                },
                {
                    "id": "MONDO:0012769",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                    "name": "HPC14",
                    "description": ""
                },
                {
                    "id": "MONDO:0012769",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                    "name": "prostate cancer, hereditary, 14",
                    "description": ""
                },
                {
                    "id": "MONDO:0012770",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                    "name": "prostate cancer, hereditary, 15",
                    "description": ""
                },
                {
                    "id": "MONDO:0012770",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                    "name": "HPC15",
                    "description": ""
                },
                {
                    "id": "MONDO:0012770",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                    "name": "prostate cancer, hereditary, 15",
                    "description": ""
                },
                {
                    "id": "MONDO:0010257",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                    "name": "prostate cancer, hereditary, X-linked 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010257",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                    "name": "HPCX1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010257",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                    "name": "prostate cancer, hereditary, X-linked 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010257",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                    "name": "prostate cancer susceptibility, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010405",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                    "name": "prostate cancer, hereditary, X-linked 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0010405",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                    "name": "HPCX2",
                    "description": ""
                },
                {
                    "id": "MONDO:0010405",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                    "name": "prostate cancer, hereditary, X-linked 2",
                    "description": ""
                },
                {
                    "id": "MIM:611868",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/611868",
                    "name": "Prostate cancer, hereditary, 12",
                    "description": "Prostate cancer, hereditary, 12"
                },
                {
                    "id": "MIM:611928",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/611928",
                    "name": "Prostate cancer, hereditary, 13",
                    "description": "Prostate cancer, hereditary, 13"
                },
                {
                    "id": "MIM:176807",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/176807",
                    "name": "Prostate cancer",
                    "description": "Prostate cancer"
                },
                {
                    "id": "MIM:601518",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/601518",
                    "name": "Prostate cancer, hereditary, 1",
                    "description": "Prostate cancer, hereditary, 1"
                },
                {
                    "id": "MIM:611955",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/611955",
                    "name": "Prostate cancer, hereditary, 11",
                    "description": "Prostate cancer, hereditary, 11"
                }
            ],
            "evidence": [
                {
                    "id": "10283",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:10283"
                }
            ]
        },
        {
            "disease_id": "DOID:11198",
            "recommended_name": {
                "id": "DOID:11198",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:11198",
                "name": "DiGeorge syndrome",
                "description": "A syndrome that has_material_basis_in a large deletion of the chromosome 22q11.2 region which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production."
            },
            "synonyms": [
                {
                    "id": "DOID:11198",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11198",
                    "name": "22q11.2 deletion syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:11198",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11198",
                    "name": "DiGeorge sequence",
                    "description": ""
                },
                {
                    "id": "DOID:11198",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11198",
                    "name": "DiGeorge's syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:11198",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11198",
                    "name": "Pharyngeal pouch syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "DiGeorge syndrome",
                    "description": "A congenital anomaly characterized by immunodeficiency, abnormal facies, congenital heart disease, hypocalcemia, and increased susceptibility to infections. Pathologic characteristics include conotruncal abnormalities and absence or hypoplasia of thymus and parathyroid glands. DiGeorge syndrome is associated with abnormalities of chromosome 22. Also known as DiGeorge anomaly."
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "22q deletion syndrome(s)",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "22q11.2 Deletion syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "DGS",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "DGS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "Di-George syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "DiGeorge anomaly",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "DiGeorge syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "DiGeorge syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "DiGeorge's syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "pharyngeal pouch syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "Shprintzen syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "Sphrintzen",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "Catch22",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "DiGeorge syndrome chromosome region",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "Takao VCF syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "VCF",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "chromosome 22Q11.2 deletion syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "hypoplasia of thymus and parathyroids",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "third and fourth pharyngeal pouch syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "velo-cardio-facial syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008564",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008564",
                    "name": "velocardiofacial syndrome",
                    "description": ""
                },
                {
                    "id": "MIM:188400",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/188400",
                    "name": "DiGeorge syndrome",
                    "description": "DiGeorge syndrome"
                }
            ],
            "evidence": [
                {
                    "id": "11198",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:11198"
                }
            ]
        },
        {
            "disease_id": "DOID:14323",
            "recommended_name": {
                "id": "DOID:14323",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:14323",
                "name": "Marfan syndrome",
                "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens."
            },
            "synonyms": [
                {
                    "id": "DOID:14323",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:14323",
                    "name": "Marfan's syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0007947",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                    "name": "Marfan syndrome",
                    "description": "A disorder of the connective tissue. Connective tissue provides strength and flexibility to structures throughout the body such as bones, ligaments, muscles, walls of blood vessels, and heart valves. Marfan syndrome affects most organs and tissues, especially the skeleton, lungs, eyes, heart, and the large blood vessel that distributes blood from the heart to the rest of the body (the aorta). It is caused by mutations in the FBN1 gene, which provides instructions for making a protein called fibrillin-1. Marfan syndrome is inherited in an autosomal dominant pattern. At least 25% of cases are due to a new (de novo) mutation. Treatment is based on the signs and symptoms in each person."
                },
                {
                    "id": "MONDO:0007947",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                    "name": "MFS",
                    "description": ""
                },
                {
                    "id": "MONDO:0007947",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                    "name": "MFS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007947",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                    "name": "Marfan syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0007947",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                    "name": "Marfan syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007947",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                    "name": "Marfan syndrome, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007947",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                    "name": "Marfan's syndrome",
                    "description": ""
                },
                {
                    "id": "MIM:154700",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/154700",
                    "name": "Marfan syndrome",
                    "description": "Marfan syndrome"
                }
            ],
            "evidence": [
                {
                    "id": "14323",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:14323"
                }
            ]
        },
        {
            "disease_id": "DOID:1793",
            "recommended_name": {
                "id": "DOID:1793",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas."
            },
            "synonyms": [
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "Ca body of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "Ca head of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "Ca tail of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "malignant neoplasm of body of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "malignant neoplasm of head of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "malignant neoplasm of tail of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "pancreas neoplasm",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "pancreatic neoplasm",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "pancreatic tumor",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1793",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1793"
                }
            ]
        },
        {
            "disease_id": "DOID:219",
            "recommended_name": {
                "id": "DOID:219",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:219",
                "name": "colon cancer",
                "description": "A colorectal cancer that is located_in the colon."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "219",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:219"
                }
            ]
        },
        {
            "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:2920",
            "recommended_name": {
                "id": "DOID:2920",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2920",
                "name": "membranoproliferative glomerulonephritis",
                "description": ""
            },
            "synonyms": [
                {
                    "id": "DOID:2920",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2920",
                    "name": "Lobular glomerulonephritis",
                    "description": ""
                },
                {
                    "id": "DOID:2920",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2920",
                    "name": "chronic glomerulonephritis, lobular",
                    "description": ""
                },
                {
                    "id": "MONDO:0010596",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010596",
                    "name": "membranoproliferative glomerulonephritis, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010596",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010596",
                    "name": "membranoproliferative glomerulonephritis, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010596",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010596",
                    "name": "Mesangiocapillary glomerulonephritis, X-linked",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "2920",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2920"
                }
            ]
        },
        {
            "disease_id": "DOID:3587",
            "recommended_name": {
                "id": "DOID:3587",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3587",
                "name": "pancreatic ductal carcinoma",
                "description": "A pancreatic carcinoma located_in the pancreatic duct."
            },
            "synonyms": [
                {
                    "id": "DOID:3587",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3587",
                    "name": "malignant neoplasm of duct of Wirsung",
                    "description": ""
                },
                {
                    "id": "DOID:3587",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3587",
                    "name": "pancreatic duct cancer",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "3587",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3587"
                }
            ]
        },
        {
            "disease_id": "DOID:3770",
            "recommended_name": {
                "id": "DOID:3770",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3770",
                "name": "pulmonary fibrosis",
                "description": "An interstitial lung disease that is characterized by destruction, scarring, and thickening of the interstitial lung tissues and progressive pulmonary function loss in a restrictive pattern, has_symptom progressive shortness of breath, fatigue, and chronic cough, possibly has_material_basis_in exposure to certain chemicals, autoimmune conditions, and radiation."
            },
            "synonyms": [
                {
                    "id": "DOID:3770",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3770",
                    "name": "Fibrosis of lung",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "3770",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3770"
                }
            ]
        },
        {
            "disease_id": "DOID:3883",
            "recommended_name": {
                "id": "DOID:3883",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3883",
                "name": "Lynch syndrome",
                "description": "A syndrome that is characterized by an increased risk for colon cancer and cancers of the endometrium, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and skin and has_material_basis_in mutation of mismatch repair genes that increases the risk of many types of cancers."
            },
            "synonyms": [
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "COCA 1",
                    "description": ""
                },
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "HNPCC - hereditary nonpolyposis colon cancer",
                    "description": ""
                },
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "Hereditary Defective Mismatch Repair syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "hereditary nonpolyposis colorectal cancer",
                    "description": ""
                },
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "hereditary nonpolyposis colorectal neoplasm",
                    "description": ""
                },
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "Hereditary non-polyposis colon cancer",
                    "description": ""
                },
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "Hereditary non-polyposis colon cancer syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "Hereditary non-polyposis colorectal cancer",
                    "description": ""
                },
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "Hereditary nonpolyposis colon cancer",
                    "description": ""
                },
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "Hereditary nonpolyposis colon cancer syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "Hereditary nonpolyposis colorectal cancer syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:3883",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3883",
                    "name": "Hereditary non-polyposis colorectal cancer syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "Lynch syndrome 1",
                    "description": "Any Lynch syndrome in which the cause of the disease is a mutation in the MSH2 gene."
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "HNPCC1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "Hereditary non-polyposis colon cancer type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "Lynch 1 syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "Lynch syndrome 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "Lynch syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "familial non-polyposis colon cancer type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "hereditary nonpolyposis colorectal cancer type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "COCA1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "LYNCH syndrome I",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "Lynch syndrome 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "colon cancer, familial nonpolyposis, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007356",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007356",
                    "name": "colorectal cancer, hereditary nonpolyposis, type 1",
                    "description": ""
                },
                {
                    "id": "MIM:120435",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/120435",
                    "name": "Lynch syndrome 1",
                    "description": "Lynch syndrome 1"
                }
            ],
            "evidence": [
                {
                    "id": "3883",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3883"
                }
            ]
        },
        {
            "disease_id": "DOID:4762",
            "recommended_name": {
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                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:4762",
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        },
        {
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            },
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                    "description": ""
                },
                {
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:4947",
                    "name": "adult primary cholangiocellular carcinoma",
                    "description": ""
                },
                {
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:4947",
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                    "description": ""
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            ],
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                "resource": "Disease Ontology",
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                {
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                {
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                    "description": ""
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                {
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                    "resource": "Disease Ontology",
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                    "description": ""
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                {
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                    "description": ""
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                {
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                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "esophageal cancer",
                    "description": "A primary or metastatic malignant neoplasm involving the esophagus."
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                {
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                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "cancer of esophagus",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "cancer of oesophagus",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "esophageal cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "esophageal cancer, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "esophageal carcinoma, somatic",
                    "description": ""
                },
                {
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                    "resource": "MONDO",
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                    "name": "esophageal squamous cell carcinoma, somatic",
                    "description": ""
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                {
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                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "esophagus cancer",
                    "description": ""
                },
                {
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                    "resource": "MONDO",
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                {
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                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
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                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
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                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
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                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
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                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
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                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
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                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "malignant neoplasm of the oesophagus",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "malignant oesophagus neoplasm",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "malignant oesophagus tumour",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "malignant tumor of esophagus",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
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                    "name": "malignant tumor of the esophagus",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
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                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
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                    "description": ""
                },
                {
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                    "resource": "MONDO",
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                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
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                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
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                    "name": "Ca lower third oesophagus",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "Ca middle third esophagus",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "Ca middle third oesophagus",
                    "description": ""
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                {
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                {
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                {
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                    "resource": "MONDO",
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                    "description": ""
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                {
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                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
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                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
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                    "resource": "MONDO",
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                {
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                    "resource": "MONDO",
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                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "malignant tumour of the middle third of the oesophagus",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                    "name": "Aerodigestive tract cancer, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
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                    "description": ""
                },
                {
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                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
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                    "description": ""
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                {
                    "id": "MONDO:0007576",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007576",
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                    "description": ""
                },
                {
                    "id": "MIM:133239",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/133239",
                    "name": "Esophageal cancer",
                    "description": "Esophageal cancer"
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            ],
            "evidence": [
                {
                    "id": "5041",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:5041"
                }
            ]
        },
        {
            "disease_id": "DOID:557",
            "recommended_name": {
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                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:557",
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                "description": "A urinary system disease that is located_in the kidney."
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            "synonyms": [
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:557",
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                    "description": ""
                },
                {
                    "id": "DOID:557",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:557",
                    "name": "nephropathy",
                    "description": ""
                }
            ],
            "evidence": [
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                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:557"
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            ]
        },
        {
            "disease_id": "DOID:5844",
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                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:5844",
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                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia."
            },
            "synonyms": [
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                    "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",
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                    "name": "myocardial infarction, susceptibility to, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012058",
                    "resource": "MONDO",
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                    "name": "myocardial infarction, susceptibility to, type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012058",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012058",
                    "name": "Mci2",
                    "description": ""
                }
            ],
            "evidence": [
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                    "id": "5844",
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                    "url": "https://www.alliancegenome.org/disease/DOID:5844"
                }
            ]
        },
        {
            "disease_id": "DOID:6432",
            "recommended_name": {
                "id": "DOID:6432",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:6432",
                "name": "pulmonary hypertension",
                "description": "A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "6432",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:6432"
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        {
            "disease_id": "DOID:684",
            "recommended_name": {
                "id": "DOID:684",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver."
            },
            "synonyms": [
                {
                    "id": "DOID:684",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:684",
                    "name": "Hepatoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
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                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "HCC",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "cancer, hepatocellular",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma of liver",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma of liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma of the liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma, hepatocellular, malignant",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoblastoma, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular adenocarcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular cancer, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma, childhood type, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver cell cancer (hepatocellular carcinoma)",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver cell carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "primary carcinoma of liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "primary carcinoma of the liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "adult hepatoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "adult primary hepatocellular carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoblastoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoblastoma caused by somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver and intrahepatic bile duct carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma",
                    "description": "A malignant tumor that arises from hepatocytes. Hepatocellular carcinoma is relatively rare in the United States but very common in all African countries south of the Sahara and in Southeast Asia. Most cases are seen in patients over the age of 50 years, but this tumor can also occur in younger individuals and even in children. Hepatocellular carcinoma is more common in males than females and is associated with hepatitis B, hepatitis C, chronic alcohol abuse and cirrhosis. Serum elevation of alpha-fetoprotein occurs in a large percentage of patients with hepatocellular carcinoma. Grossly, hepatocellular carcinoma may present as a single mass, as multiple nodules, or as diffuse liver involvement. Microscopically, there is a wide range of differentiation from tumor to tumor (well differentiated to poorly differentiated tumors). Hepatocellular carcinomas quickly metastasize to regional lymph nodes and lung. The overall median survival of untreated liver cell carcinoma is about 4 months. The most effective treatment of hepatocellular carcinoma is complete resection of the tumor. Lately, an increasing number of tumors have been treated with liver transplantation."
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "HCC",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "cancer, hepatocellular",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma of liver",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma of liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma of the liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma, hepatocellular, malignant",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoblastoma, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular adenocarcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular cancer, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma, childhood type, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver cell cancer (hepatocellular carcinoma)",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver cell carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "primary carcinoma of liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "primary carcinoma of the liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "adult hepatoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "adult primary hepatocellular carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoblastoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoblastoma caused by somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver and intrahepatic bile duct carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver cancer",
                    "description": ""
                },
                {
                    "id": "MIM:114550",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/114550",
                    "name": "Hepatocellular carcinoma",
                    "description": "Hepatocellular carcinoma"
                }
            ],
            "evidence": [
                {
                    "id": "684",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:684"
                }
            ]
        },
        {
            "disease_id": "DOID:9352",
            "recommended_name": {
                "id": "DOID:9352",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin."
            },
            "synonyms": [
                {
                    "id": "DOID:9352",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9352",
                    "name": "NIDDM",
                    "description": ""
                },
                {
                    "id": "DOID:9352",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9352",
                    "name": "non-insulin-dependent diabetes mellitus",
                    "description": ""
                },
                {
                    "id": "DOID:9352",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9352",
                    "name": "type 2 diabetes",
                    "description": ""
                },
                {
                    "id": "DOID:9352",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9352",
                    "name": "type II diabetes mellitus",
                    "description": ""
                },
                {
                    "id": "DOID:9352",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9352",
                    "name": "insulin resistance",
                    "description": ""
                },
                {
                    "id": "MONDO:0011955",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011955",
                    "name": "diabetes mellitus, noninsulin-dependent, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0011955",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011955",
                    "name": "diabetes mellitus, noninsulin-dependent, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0011955",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011955",
                    "name": "diabetes mellitus, noninsulin-dependent, type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0011955",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011955",
                    "name": "Niddm4",
                    "description": ""
                },
                {
                    "id": "MONDO:0011955",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011955",
                    "name": "noninsulin-dependent diabetes mellitus 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "type 2 diabetes mellitus",
                    "description": "A type of diabetes mellitus that is characterized by insulin resistance or desensitization and increased blood glucose levels. This is a chronic disease that can develop gradually over the life of a patient and can be linked to both environmental factors and heredity."
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "NIDDM",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "T2DM - type 2 diabetes mellitus",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "adult onset diabetes",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "adult-onset diabetes",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitis type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitis type II",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitus, noninsulin-dependent",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitus, noninsulin-dependent, association with",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitus, noninsulin-dependent, late onset",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitus, type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitus, type II",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes, type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "insulin resistance, severe, digenic",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "non-insulin dependent diabetes",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "non-insulin dependent diabetes mellitus",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "non-insulin-dependent diabetes mellitus",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "noninsulin dependent diabetes",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "noninsulin-dependent diabetes mellitus",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "type 2 diabetes",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "type 2 diabetes mellitus",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "type 2 diabetes mellitus non-insulin dependent",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "type II diabetes",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "type II diabetes mellitus",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitus, noninsulin-dependent, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitus, non-insulin-dependent, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitus, noninsulin-dependent, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitus, type 2, protection against",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitus, type 2, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "diabetes mellitus, type II, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "hypertension, insulin resistance-related, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "insulin resistance, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "maturity-onset diabetes",
                    "description": ""
                },
                {
                    "id": "MONDO:0005148",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                    "name": "type 2 diabetes mellitus, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0011027",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                    "name": "diabetes mellitus, noninsulin-dependent, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011027",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                    "name": "diabetes mellitus, noninsulin-dependent 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011027",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                    "name": "diabetes mellitus, noninsulin-dependent, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011027",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                    "name": "diabetes mellitus, noninsulin-dependent, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011027",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                    "name": "NIDDM1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011027",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                    "name": "noninsulin-dependent diabetes mellitus 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011072",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011072",
                    "name": "diabetes mellitus, noninsulin-dependent, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011072",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011072",
                    "name": "NIDDM2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011072",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011072",
                    "name": "diabetes mellitus, noninsulin-dependent, 2",
                    "description": ""
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                {
                    "id": "MONDO:0011072",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011072",
                    "name": "noninsulin-dependent diabetes mellitus 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011363",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011363",
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                {
                    "id": "MONDO:0011363",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                    "name": "diabetes mellitus, noninsulin-dependent, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0011363",
                    "resource": "MONDO",
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                    "name": "diabetes mellitus, noninsulin-dependent, type 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0011363",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                    "name": "type 2 diabetes mellitus 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0011363",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                    "name": "NIDDM3",
                    "description": ""
                },
                {
                    "id": "MONDO:0011363",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                    "name": "noninsulin-dependent diabetes mellitus 3",
                    "description": ""
                },
                {
                    "id": "MIM:125853",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/125853",
                    "name": "Type 2 diabetes mellitus",
                    "description": "Type 2 diabetes mellitus"
                },
                {
                    "id": "MIM:601283",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/601283",
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                    "description": "Type 2 diabetes mellitus 1"
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            ],
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                {
                    "id": "9352",
                    "database": "Alliance of Genome Resources",
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        }
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    "expression_tissue": [],
    "expression_disease": [],
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        {
            "name": "Mus musculus",
            "taxid": 10090,
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            "id": "GPDB0005592",
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            "id": "IPR000719",
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        {
            "id": "IPR011009",
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        {
            "id": "IPR015013",
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        },
        {
            "id": "IPR017194",
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        {
            "id": "IPR017441",
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            "database": "InterPro",
            "categories": [
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        {
            "id": "IPR045860",
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        {
            "id": "98729",
            "url": "http://www.informatics.jax.org/marker/MGI:98729",
            "database": "MGI",
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            ]
        },
        {
            "id": "QMPNLCK",
            "url": "https://omabrowser.org/oma/group/QMPNLCK/",
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        },
        {
            "id": "3900892at2759",
            "url": "http://www.orthodb.org/?query=3900892at2759",
            "database": "OrthoDB",
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            ]
        },
        {
            "id": "PTHR23255",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR23255",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR23255:SF55",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR23255:SF55",
            "database": "PANTHER",
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        },
        {
            "id": "PF07714",
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        },
        {
            "id": "PF08917",
            "url": "http://pfam.xfam.org/family/PF08917",
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            ]
        },
        {
            "id": "PR_Q62312",
            "url": "http://purl.obolibrary.org/obo/PR_Q62312",
            "database": "PRO",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "R-MMU-2173788",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-2173788",
            "database": "Reactome",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "R-MMU-2173789",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-2173789",
            "database": "Reactome",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "R-MMU-2173791",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-2173791",
            "database": "Reactome",
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                "Protein Classification"
            ]
        },
        {
            "id": "NP_033397",
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        },
        {
            "id": "18673",
            "url": "https://www.rhea-db.org/rhea/18673",
            "database": "Rhea",
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        },
        {
            "id": "44880",
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        },
        {
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            ]
        },
        {
            "id": "Q62312-1",
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            ]
        },
        {
            "id": "Q62312-2",
            "url": "https://www.uniprot.org/uniprot/Q62312-2",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
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        "length": 567,
        "header": "sp|Q62312-2|TGFR2_MOUSE Isoform 2 of TGF-beta receptor type-2  OS=Mus musculus OX=10090 GN=Tgfbr2 PE=1 SV=2 CANONICAL=Q62312-2"
    },
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        {
            "isoform_ac": "Q62312-1",
            "url": "",
            "sequence": {
                "sequence": "MGRGLLRGLWPLHIVLWTRIASTIPPHVPKSDVEMEAQKDASIHLSCNRTIHPLKHFNSDVMASDNGGAVKLPQLCKFCDVRLSTCDNQKSCMSNCSITAICEKPHEVCVAVWRKNDKNITLETVCHDPKLTYHGFTLEDAASPKCVMKEKKRAGETFFMCACNMEECNDYIIFSEEYTTSSPDLLLVIIQVTGVSLLPPLGIAIAVIIIFYCYRVHRQQKLSPSWESSKPRKLMDFSDNCAIILEDDRSDISSTCANNINHNTELLPIELDTLVGKGRFAEVYKAKLKQNTSEQFETVAVKIFPYEEYSSWKTEKDIFSDINLKHENILQFLTAEERKTELGKQYWLITAFHAKGNLQEYLTRHVISWEDLRKLGSSLARGIAHLHSDHTPCGRPKMPIVHRDLKSSNILVKNDLTCCLCDFGLSLRLDPTLSVDDLANSGQVGTARYMAPEVLESRMNLENVESFKQTDVYSMALVLWEMTSRCNAVGEVKDYEPPFGSKVREHPCVESMKDSVLRDRGRPEIPSFWLNHQGIQIVCETLTECWDHDPEARLTAQCVAERFSELEHPERLSGRSCSQEKIPEDGSLNTTK",
                "length": 592,
                "header": "sp|Q62312-1|TGFR2_MOUSE Isoform 1 of TGF-beta receptor type-2  OS=Mus musculus OX=10090 GN=Tgfbr2 PE=1 SV=2 CANONICAL=Q62312-2"
            },
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                "start_pos": 116004105,
                "end_pos": 115919449,
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                "evidence": [
                    {
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                        "id": "ENSMUST00000061101",
                        "url": "https://www.ensembl.org/id/ENSMUST00000061101"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSMUSP00000062333",
                        "url": "https://www.ensembl.org/id/ENSMUSP00000062333"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q62312-2",
            "url": "",
            "sequence": {
                "sequence": "MGRGLLRGLWPLHIVLWTRIASTIPPHVPKSVNSDVMASDNGGAVKLPQLCKFCDVRLSTCDNQKSCMSNCSITAICEKPHEVCVAVWRKNDKNITLETVCHDPKLTYHGFTLEDAASPKCVMKEKKRAGETFFMCACNMEECNDYIIFSEEYTTSSPDLLLVIIQVTGVSLLPPLGIAIAVIIIFYCYRVHRQQKLSPSWESSKPRKLMDFSDNCAIILEDDRSDISSTCANNINHNTELLPIELDTLVGKGRFAEVYKAKLKQNTSEQFETVAVKIFPYEEYSSWKTEKDIFSDINLKHENILQFLTAEERKTELGKQYWLITAFHAKGNLQEYLTRHVISWEDLRKLGSSLARGIAHLHSDHTPCGRPKMPIVHRDLKSSNILVKNDLTCCLCDFGLSLRLDPTLSVDDLANSGQVGTARYMAPEVLESRMNLENVESFKQTDVYSMALVLWEMTSRCNAVGEVKDYEPPFGSKVREHPCVESMKDSVLRDRGRPEIPSFWLNHQGIQIVCETLTECWDHDPEARLTAQCVAERFSELEHPERLSGRSCSQEKIPEDGSLNTTK",
                "length": 567,
                "header": "sp|Q62312-2|TGFR2_MOUSE Isoform 2 of TGF-beta receptor type-2  OS=Mus musculus OX=10090 GN=Tgfbr2 PE=1 SV=2 CANONICAL=Q62312-2"
            },
            "locus": {
                "chromosome": "9",
                "start_pos": 116004105,
                "end_pos": 115919449,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSMUST00000035014",
                        "url": "https://www.ensembl.org/id/ENSMUST00000035014"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSMUSP00000035014",
                        "url": "https://www.ensembl.org/id/ENSMUSP00000035014"
                    }
                ]
            }
        }
    ],
    "glycosylation": [
        {
            "glytoucan_ac": "",
            "type": "N-linked",
            "subtype": "",
            "site_category": "predicted",
            "site_seq": "N",
            "relation": "attached",
            "comment": "N-linked (GlcNAc...) asparagine",
            "start_pos": 70,
            "start_aa": "Asn",
            "end_pos": 70,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn70",
            "evidence": [
                {
                    "id": "Q62312",
                    "database": "UniProtKB",
                    "url": "https://www.uniprot.org/uniprot/Q62312#ptm_processing"
                }
            ]
        },
        {
            "glytoucan_ac": "",
            "type": "N-linked",
            "subtype": "",
            "site_category": "predicted",
            "site_seq": "N",
            "relation": "attached",
            "comment": "N-linked (GlcNAc...) asparagine",
            "start_pos": 94,
            "start_aa": "Asn",
            "end_pos": 94,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn94",
            "evidence": [
                {
                    "id": "Q62312",
                    "database": "UniProtKB",
                    "url": "https://www.uniprot.org/uniprot/Q62312#ptm_processing"
                }
            ]
        }
    ],
    "phosphorylation": [
        {
            "start_pos": 284,
            "end_pos": 284,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Tyr",
            "comment": "",
            "evidence": [
                {
                    "database": "iPTMnet",
                    "id": "Q62312",
                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/Q62312"
                },
                {
                    "database": "PubMed",
                    "id": "18174260",
                    "url": "https://glygen.org/publication/PubMed/18174260"
                }
            ],
            "site_lbl": "Tyr284"
        },
        {
            "start_pos": 409,
            "end_pos": 409,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q62312",
                    "url": "https://www.uniprot.org/uniprot/Q62312"
                },
                {
                    "database": "PubMed",
                    "id": "21183079",
                    "url": "https://glygen.org/publication/PubMed/21183079"
                }
            ],
            "site_lbl": "Ser409"
        },
        {
            "start_pos": 548,
            "end_pos": 548,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q62312",
                    "url": "https://www.uniprot.org/uniprot/Q62312"
                }
            ],
            "site_lbl": "Ser548"
        },
        {
            "start_pos": 553,
            "end_pos": 553,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q62312",
                    "url": "https://www.uniprot.org/uniprot/Q62312"
                },
                {
                    "database": "PubMed",
                    "id": "21183079",
                    "url": "https://glygen.org/publication/PubMed/21183079"
                },
                {
                    "database": "PubMed",
                    "id": "19144319",
                    "url": "https://glygen.org/publication/PubMed/19144319"
                }
            ],
            "site_lbl": "Ser553"
        }
    ],
    "glycation": [],
    "keywords": [
        "enzyme",
        "glycoprotein",
        "glycoprotein_predicted"
    ],
    "publication": [
        {
            "title": "Grb2 binding to Tyr284 in TbetaR-II is essential for mammary tumor growth and metastasis stimulated by TGF-beta.",
            "journal": "Carcinogenesis",
            "date": "2008",
            "authors": "Galliher-Beckley AJ, Schiemann WP",
            "evidence": [
                {
                    "database": "iPTMnet",
                    "id": "Q62312",
                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/Q62312"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "18174260",
                    "url": "https://glygen.org/publication/PubMed/18174260"
                }
            ]
        },
        {
            "title": "The phagosomal proteome in interferon-gamma-activated macrophages.",
            "journal": "Immunity",
            "date": "2009",
            "authors": "Trost M, English L, Lemieux S, Courcelles M, Desjardins M, Thibault P",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q62312",
                    "url": "https://www.uniprot.org/uniprot/Q62312"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "19144319",
                    "url": "https://glygen.org/publication/PubMed/19144319"
                }
            ]
        },
        {
            "title": "A tissue-specific atlas of mouse protein phosphorylation and expression.",
            "journal": "Cell",
            "date": "2010",
            "authors": "Huttlin EL, Jedrychowski MP, Elias JE, Goswami T, Rad R, Beausoleil SA, Villen J, Haas W, Sowa ME, Gygi SP",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q62312",
                    "url": "https://www.uniprot.org/uniprot/Q62312"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "21183079",
                    "url": "https://glygen.org/publication/PubMed/21183079"
                }
            ]
        },
        {
            "title": "Neuropilin-1 interacts with VE-cadherin and TGFBR2 to stabilize adherens junctions and prevent activation of endothelium under flow.",
            "journal": "Science signaling",
            "date": "2023-05-23",
            "authors": "Bosseboeuf Emy, Chikh Anissa, Chaker Ahmed Bey, Mitchell Tom P, Vignaraja Dhilakshani, Rajendrakumar Ridhi, Khambata Rayomand S, Nightingale Thomas D, Mason Justin C, Randi Anna M, Ahluwalia Amrita, Raimondi Claudio",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_033397",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033397"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "37220183",
                    "url": "https://glygen.org/publication/PubMed/37220183"
                }
            ]
        },
        {
            "title": "Transforming growth factor beta receptor 2 (Tgfbr2) deficiency in keratocytes results in corneal ectasia.",
            "journal": "The ocular surface",
            "date": "2023-07",
            "authors": "Wang Yen-Chiao, Zolnik Olivia Betty, Yasoda Shingo, Yeh Lung-Kun, Yuan Yong, Kao Winston, Saika Shizuya, Liu Chia-Yang",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_033397",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033397"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "37393064",
                    "url": "https://glygen.org/publication/PubMed/37393064"
                }
            ]
        },
        {
            "title": "Cloning of an isoform of mouse TGF-beta type II receptor gene.",
            "journal": "FEBS Lett.",
            "date": "1994",
            "authors": "Maeda T., Suzuki A., Tada M., Ueno N., Shioda N.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q62312",
                    "url": "https://www.uniprot.org/uniprot/Q62312"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "7957954",
                    "url": "https://glygen.org/publication/PubMed/7957954"
                }
            ]
        },
        {
            "title": "The murine type II TGF-beta receptor has a coincident embryonic expression and binding preference for TGF-beta 1.",
            "journal": "Development",
            "date": "1994",
            "authors": "Derynck R., Ebner R., Moses H.L., Shum L., Wright C.V., Lawler S., Lopez A.R., Candia A.F.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q62312",
                    "url": "https://www.uniprot.org/uniprot/Q62312"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "8119124",
                    "url": "https://glygen.org/publication/PubMed/8119124"
                }
            ]
        }
    ],
    "pathway": [
        {
            "id": "mmu:21813",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+mmu:21813",
            "resource": "KEGG Pathway"
        },
        {
            "id": "R-MMU-2173788",
            "name": "Downregulation of TGF-beta receptor signaling",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-2173788",
            "resource": "Reactome",
            "description": "Downregulation of TGF-beta receptor signaling"
        },
        {
            "id": "R-MMU-2173789",
            "name": "TGF-beta receptor signaling activates SMADs",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-2173789",
            "resource": "Reactome",
            "description": "TGF-beta receptor signaling activates SMADs"
        },
        {
            "id": "R-MMU-2173791",
            "name": "TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition)",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-2173791",
            "resource": "Reactome",
            "description": "TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition)"
        }
    ],
    "orthologs": [
        {
            "uniprot_canonical_ac": "P37173-1",
            "protein_name": "TGF-beta receptor type-2",
            "gene_name": "TGFBR2",
            "tax_id": 9606,
            "organism": "Homo sapiens",
            "sequence": {
                "sequence": "MGRGLLRGLWPLHIVLWTRIASTIPPHVQKSVNNDMIVTDNNGAVKFPQLCKFCDVRFSTCDNQKSCMSNCSITSICEKPQEVCVAVWRKNDENITLETVCHDPKLPYHDFILEDAASPKCIMKEKKKPGETFFMCSCSSDECNDNIIFSEEYNTSNPDLLLVIFQVTGISLLPPLGVAISVIIIFYCYRVNRQQKLSSTWETGKTRKLMEFSEHCAIILEDDRSDISSTCANNINHNTELLPIELDTLVGKGRFAEVYKAKLKQNTSEQFETVAVKIFPYEEYASWKTEKDIFSDINLKHENILQFLTAEERKTELGKQYWLITAFHAKGNLQEYLTRHVISWEDLRKLGSSLARGIAHLHSDHTPCGRPKMPIVHRDLKSSNILVKNDLTCCLCDFGLSLRLDPTLSVDDLANSGQVGTARYMAPEVLESRMNLENVESFKQTDVYSMALVLWEMTSRCNAVGEVKDYEPPFGSKVREHPCVESMKDNVLRDRGRPEIPSFWLNHQGIQMVCETLTECWDHDPEARLTAQCVAERFSELEHLDRLSGRSCSEEKIPEDGSLNTTK",
                "length": 567
            },
            "evidence": [
                {
                    "id": "45225323",
                    "url": "http://www.informatics.jax.org/homology/45225323",
                    "database": "MGI"
                },
                {
                    "id": "Q62312",
                    "url": "https://omabrowser.org/oma/group/Q62312/",
                    "database": "OMA"
                }
            ],
            "common_name": "Human"
        },
        {
            "uniprot_canonical_ac": "P38438-1",
            "protein_name": "TGF-beta receptor type-2",
            "gene_name": "Tgfbr2",
            "tax_id": 10116,
            "organism": "Rattus norvegicus",
            "sequence": {
                "sequence": "MGRGLLRGLWPLHIVLWTRIASTIPPHVPKSVNSDLMAGDNSGAVKLPQLCKFCDVTLSTCDNQKSCMSNCSVTSICEKPQEVCVAVWRKNDKNITLETVCHDPKFTYHGFTLEDATSPTCVMKEKKRAGETFFMCSCNTEECNDYIIFNEEYTTSSPDLLLVIIQVTGVSLLPPLGIAIAVIAIFYCYRVHRQQKLSPSWESSKPRKLMDFSDNCAIILEDDRSDISSTCANNINHNTELLPIELDTLVGKGRFAEVYKAKLKQNTSEQFETVAVKIFPYEEYSSWKTEKDIFSDINLKHENILQFLTAEERKTEMGKQYWLITAFHAKGNLQEYLTRHVISWEDLRKLGSSLARGIAHLHSDHTPCGRPKMPIVHRDLKSSNILVKNDLTCCLCDFGLSLRLDPTLSVDDLANSGQVGTARYMAPEVLESRMNLENMESFKQTDVYSMALVLWEMTSRCNAVGEVKDYEPPFGSKVREHPCVESMKDNVLRDRGRPEIPSFWLNHQGIQIVCETLTECWDHDPEARLTAQCVAERFSELEHPDRLSGRSCSQEKIPEDGSLNTTK",
                "length": 567
            },
            "evidence": [
                {
                    "id": "45225323",
                    "url": "http://www.informatics.jax.org/homology/45225323",
                    "database": "MGI"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "go_annotation": {
        "categories": [
            {
                "name": "Biological Process",
                "total": 70,
                "go_terms": [
                    {
                        "name": "positive regulation of T cell tolerance induction",
                        "id": "GO:0002666",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002666",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "lens fiber cell apoptotic process",
                        "id": "GO:1990086",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990086",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "trachea morphogenesis",
                        "id": "GO:0060439",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060439",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "embryonic hemopoiesis",
                        "id": "GO:0035162",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035162",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "mammary gland morphogenesis",
                        "id": "GO:0060443",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060443",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "vasculogenesis",
                        "id": "GO:0001570",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001570",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "in utero embryonic development",
                        "id": "GO:0001701",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001701",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "protein phosphorylation",
                        "id": "GO:0006468",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006468",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "Notch signaling pathway",
                        "id": "GO:0007219",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007219",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "heart development",
                        "id": "GO:0007507",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007507",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "negative regulation of cell population proliferation",
                        "id": "GO:0008285",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008285",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "regulation of cell population proliferation",
                        "id": "GO:0042127",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042127",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "apoptotic process",
                        "id": "GO:0006915",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006915",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "lung development",
                        "id": "GO:0030324",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030324",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of angiogenesis",
                        "id": "GO:0045766",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045766",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "transforming growth factor beta receptor signaling pathway",
                        "id": "GO:0007179",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007179",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "brain development",
                        "id": "GO:0007420",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007420",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of smooth muscle cell proliferation",
                        "id": "GO:0048661",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048661",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cellular response to growth factor stimulus",
                        "id": "GO:0071363",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071363",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "animal organ morphogenesis",
                        "id": "GO:0009887",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009887",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of reactive oxygen species metabolic process",
                        "id": "GO:2000379",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:2000379",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "receptor-mediated endocytosis",
                        "id": "GO:0006898",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006898",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of pathway-restricted SMAD protein phosphorylation",
                        "id": "GO:0010862",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010862",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "peptidyl-threonine phosphorylation",
                        "id": "GO:0018107",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0018107",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "embryonic cranial skeleton morphogenesis",
                        "id": "GO:0048701",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048701",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of NK T cell differentiation",
                        "id": "GO:0051138",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051138",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "roof of mouth development",
                        "id": "GO:0060021",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060021",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "branching involved in blood vessel morphogenesis",
                        "id": "GO:0001569",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001569",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "atrioventricular valve morphogenesis",
                        "id": "GO:0003181",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003181",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "endocardial cushion fusion",
                        "id": "GO:0003274",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003274",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "pathway-restricted SMAD protein phosphorylation",
                        "id": "GO:0060389",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060389",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "ventricular septum morphogenesis",
                        "id": "GO:0060412",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060412",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of epithelial to mesenchymal transition involved in endocardial cushion formation",
                        "id": "GO:1905007",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905007",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "heart looping",
                        "id": "GO:0001947",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001947",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "peptidyl-serine phosphorylation",
                        "id": "GO:0018105",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0018105",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "regulation of stem cell proliferation",
                        "id": "GO:0072091",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072091",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "regulation of gene expression",
                        "id": "GO:0010468",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010468",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of epithelial to mesenchymal transition",
                        "id": "GO:0010718",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010718",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to xenobiotic stimulus",
                        "id": "GO:0009410",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009410",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "smoothened signaling pathway",
                        "id": "GO:0007224",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007224",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "aorta morphogenesis",
                        "id": "GO:0035909",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035909",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "gastrulation",
                        "id": "GO:0007369",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007369",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "artery morphogenesis",
                        "id": "GO:0048844",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048844",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of epithelial cell migration",
                        "id": "GO:0010634",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010634",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cartilage development",
                        "id": "GO:0051216",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051216",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "outflow tract morphogenesis",
                        "id": "GO:0003151",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003151",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "negative regulation of cardiac muscle cell proliferation",
                        "id": "GO:0060044",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060044",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "growth plate cartilage chondrocyte growth",
                        "id": "GO:0003430",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003430",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "miRNA transport",
                        "id": "GO:1990428",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990428",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of mesenchymal cell proliferation",
                        "id": "GO:0002053",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002053",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "outflow tract septum morphogenesis",
                        "id": "GO:0003148",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003148",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "membranous septum morphogenesis",
                        "id": "GO:0003149",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003149",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "aortic valve morphogenesis",
                        "id": "GO:0003180",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003180",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "tricuspid valve morphogenesis",
                        "id": "GO:0003186",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003186",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "common-partner SMAD protein phosphorylation",
                        "id": "GO:0007182",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007182",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "lung morphogenesis",
                        "id": "GO:0060425",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060425",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "bronchus development",
                        "id": "GO:0060433",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060433",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "trachea formation",
                        "id": "GO:0060440",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060440",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "lens development in camera-type eye",
                        "id": "GO:0002088",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002088",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cardiac left ventricle morphogenesis",
                        "id": "GO:0003214",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003214",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to cholesterol",
                        "id": "GO:0070723",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070723",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of CD4-positive, alpha-beta T cell proliferation",
                        "id": "GO:2000563",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:2000563",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of tolerance induction to self antigen",
                        "id": "GO:0002651",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002651",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of B cell tolerance induction",
                        "id": "GO:0002663",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002663",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "bronchus morphogenesis",
                        "id": "GO:0060434",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060434",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "inferior endocardial cushion morphogenesis",
                        "id": "GO:1905317",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905317",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "growth plate cartilage development",
                        "id": "GO:0003417",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003417",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "lung lobe morphogenesis",
                        "id": "GO:0060463",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060463",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "secondary palate development",
                        "id": "GO:0062009",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0062009",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "Langerhans cell differentiation",
                        "id": "GO:0061520",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061520",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 15,
                "go_terms": [
                    {
                        "name": "kinase activator activity",
                        "id": "GO:0019209",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019209",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "type III transforming growth factor beta receptor binding",
                        "id": "GO:0034714",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034714",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "molecular adaptor activity",
                        "id": "GO:0060090",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060090",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "ATP binding",
                        "id": "GO:0005524",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "metal ion binding",
                        "id": "GO:0046872",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "transmembrane receptor protein serine/threonine kinase activity",
                        "id": "GO:0004675",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004675",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "transforming growth factor beta receptor activity",
                        "id": "GO:0005024",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005024",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "SMAD binding",
                        "id": "GO:0046332",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046332",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "activin binding",
                        "id": "GO:0048185",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048185",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "transforming growth factor beta binding",
                        "id": "GO:0050431",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050431",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "transforming growth factor beta receptor activity, type II",
                        "id": "GO:0005026",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005026",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "glycosaminoglycan binding",
                        "id": "GO:0005539",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005539",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "type I transforming growth factor beta receptor binding",
                        "id": "GO:0034713",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034713",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "mitogen-activated protein kinase kinase kinase binding",
                        "id": "GO:0031435",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031435",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "activin receptor activity",
                        "id": "GO:0017002",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0017002",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 9,
                "go_terms": [
                    {
                        "name": "extracellular space",
                        "id": "GO:0005615",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "plasma membrane",
                        "id": "GO:0005886",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cell surface",
                        "id": "GO:0009986",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009986",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "membrane",
                        "id": "GO:0016020",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "receptor complex",
                        "id": "GO:0043235",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043235",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "membrane raft",
                        "id": "GO:0045121",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045121",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "external side of plasma membrane",
                        "id": "GO:0009897",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009897",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "caveola",
                        "id": "GO:0005901",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005901",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "transforming growth factor beta ligand-receptor complex",
                        "id": "GO:0070021",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070021",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q62312",
                                "url": "https://www.uniprot.org/uniprot/Q62312"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 266,
            "end_pos": 268,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 564,
            "end_pos": 566,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 70,
            "end_pos": 72,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 94,
            "end_pos": 96,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [
        {
            "id": "18673",
            "name": "",
            "equation": "ATP + L-seryl-[receptor-protein] = ADP + H(+) + O-phospho-L-seryl-[receptor-protein]",
            "summary": "",
            "cellular_location": "",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "P38445-1",
                "P80202-1",
                "Q78EA7-1",
                "P80201-1",
                "P70539-1",
                "P80203-1",
                "Q62893-1",
                "P38444-1",
                "P38438-1",
                "P80204-1",
                "F1LQC5-1",
                "A0A8I5ZJI2-1",
                "P36894-1",
                "Q13873-1",
                "Q13705-1",
                "P37023-1",
                "Q8NER5-1",
                "P36896-1",
                "Q16671-1",
                "Q04771-1",
                "O00238-1",
                "P27037-1",
                "P36897-1",
                "P37173-1",
                "Q8K348-1",
                "Q61288-1",
                "Q8K592-1",
                "Q61271-1",
                "P37172-1",
                "P27040-1",
                "P36895-1",
                "O35607-1",
                "P36898-1",
                "P27038-1",
                "Q62312-2",
                "Q64729-1"
            ],
            "evidence": [
                {
                    "id": "18673",
                    "database": "Rhea",
                    "url": "https://www.rhea-db.org/rhea/18673"
                }
            ]
        },
        {
            "id": "44880",
            "name": "",
            "equation": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein]",
            "summary": "",
            "cellular_location": "",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "P38445-1",
                "P80201-1",
                "P80202-1",
                "Q78EA7-1",
                "P70539-1",
                "P80203-1",
                "Q62893-1",
                "P38444-1",
                "P38438-1",
                "P80204-1",
                "F1LQC5-1",
                "A0A8I5ZJI2-1",
                "P36894-1",
                "Q13873-1",
                "Q13705-1",
                "P37023-1",
                "Q8NER5-1",
                "P36896-1",
                "Q16671-1",
                "Q04771-1",
                "O00238-1",
                "P27037-1",
                "P36897-1",
                "P37173-1",
                "Q8K348-1",
                "Q61288-1",
                "Q8K592-1",
                "P37172-1",
                "Q61271-1",
                "P27040-1",
                "P36895-1",
                "O35607-1",
                "P36898-1",
                "P27038-1",
                "Q62312-2",
                "Q64729-1",
                "A0A0B4KG59-1"
            ],
            "evidence": [
                {
                    "id": "44880",
                    "database": "Rhea",
                    "url": "https://www.rhea-db.org/rhea/44880"
                }
            ]
        },
        {
            "id": "R-MMU-170835",
            "name": "An anchoring protein, ZFYVE9 (SARA), recruits SMAD2/3",
            "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": "cytoplasmic side of plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q64729-1",
                "Q62312-2"
            ],
            "evidence": [
                {
                    "id": "R-MMU-170835",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-170835"
                }
            ]
        },
        {
            "id": "R-MMU-170843",
            "name": "TGFBR2 phosphorylates TGFBR1",
            "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": "cytosol, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q64729-1",
                "Q62312-2"
            ],
            "evidence": [
                {
                    "id": "R-MMU-170843",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-170843"
                }
            ]
        },
        {
            "id": "R-MMU-170846",
            "name": "TGFBR2 recruits TGFBR1",
            "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": "cytosol, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q64729-1",
                "P26883-1",
                "Q62312-2"
            ],
            "evidence": [
                {
                    "id": "R-MMU-170846",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-170846"
                }
            ]
        },
        {
            "id": "R-MMU-170850",
            "name": "Phosphorylated SMAD2/3 dissociates from TGFBR",
            "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": "early endosome",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q64729-1",
                "Q62312-2"
            ],
            "evidence": [
                {
                    "id": "R-MMU-170850",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-170850"
                }
            ]
        },
        {
            "id": "R-MMU-170861",
            "name": "Dimeric TGF-beta-1 binds to the receptor",
            "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": [
                "Q62312-2"
            ],
            "evidence": [
                {
                    "id": "R-MMU-170861",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-170861"
                }
            ]
        },
        {
            "id": "R-MMU-170868",
            "name": "Activated type I receptor phosphorylates SMAD2/3 directly",
            "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": "early endosome membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q64729-1",
                "Q62312-2"
            ],
            "evidence": [
                {
                    "id": "R-MMU-170868",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-170868"
                }
            ]
        },
        {
            "id": "R-MMU-173483",
            "name": "BAMBI interferes with the interaction of type I receptor with type II receptor",
            "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": "plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q64729-1",
                "Q62312-2"
            ],
            "evidence": [
                {
                    "id": "R-MMU-173483",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-173483"
                }
            ]
        },
        {
            "id": "R-MMU-173512",
            "name": "I-SMAD competes with SMAD2/3 for type I receptor (TGFBR1)",
            "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": "cytoplasmic side of plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q64729-1",
                "Q62312-2"
            ],
            "evidence": [
                {
                    "id": "R-MMU-173512",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-173512"
                }
            ]
        },
        {
            "id": "R-MMU-2128994",
            "name": "STRAP stabilizes interaction of activated TGF-beta receptor complex with SMAD7",
            "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": "cytosol, extracellular region, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q64729-1",
                "Q62312-2"
            ],
            "evidence": [
                {
                    "id": "R-MMU-2128994",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-2128994"
                }
            ]
        },
        {
            "id": "R-MMU-2160931",
            "name": "Disassembly of tight junctions",
            "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": "cell junction",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q9QUI0-1",
                "Q64729-1",
                "Q62312-2",
                "Q02956-1",
                "Q9CUN6-1"
            ],
            "evidence": [
                {
                    "id": "R-MMU-2160931",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-2160931"
                }
            ]
        },
        {
            "id": "R-MMU-2160932",
            "name": "SMURF1 binds phosphorylated PARD6A",
            "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": "cell junction, cytosol, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q9QUI0-1",
                "Q64729-1",
                "Q62312-2",
                "Q02956-1",
                "Q9CUN6-1"
            ],
            "evidence": [
                {
                    "id": "R-MMU-2160932",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-2160932"
                }
            ]
        },
        {
            "id": "R-MMU-2160935",
            "name": "SMURF1 ubiquitinates RHOA",
            "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": "cell junction, cytosol, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q9QUI0-1",
                "Q64729-1",
                "Q62312-2",
                "Q02956-1",
                "Q9CUN6-1"
            ],
            "evidence": [
                {
                    "id": "R-MMU-2160935",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-2160935"
                }
            ]
        },
        {
            "id": "R-MMU-2169046",
            "name": "Degradation of TGF-beta receptor 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": "plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q64729-1",
                "Q62312-2"
            ],
            "evidence": [
                {
                    "id": "R-MMU-2169046",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-2169046"
                }
            ]
        },
        {
            "id": "R-MMU-4332235",
            "name": "CBL binds TGFBR2",
            "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": "cytosol, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q62312-2",
                "P22682-1"
            ],
            "evidence": [
                {
                    "id": "R-MMU-4332235",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-4332235"
                }
            ]
        },
        {
            "id": "R-MMU-4332236",
            "name": "CBL neddylates TGFBR2",
            "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": "cytosol, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "Q62312-2",
                "P22682-1",
                "P61082-1"
            ],
            "evidence": [
                {
                    "id": "R-MMU-4332236",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-4332236"
                }
            ]
        }
    ],
    "reaction_participants": [],
    "reaction_enzymes": [
        {
            "uniprot_ac": "A0A0B4KG59",
            "gene_name": "put",
            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "A0A0B4KG59",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "A0A0B4KG59",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "A0A8I5ZJI2",
            "gene_name": "Bmpr1b",
            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "A0A8I5ZJI2",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/A0A8I5ZJI2"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "A0A8I5ZJI2",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/A0A8I5ZJI2"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "F1LQC5",
            "gene_name": "Bmpr2",
            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "F1LQC5",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/F1LQC5"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "F1LQC5",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/F1LQC5"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "O00238",
            "gene_name": "BMPR1B",
            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "O00238",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/O00238"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "O00238",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/O00238"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "O35607",
            "gene_name": "Bmpr2",
            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "O35607",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/O35607"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "O35607",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/O35607"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P22682",
            "gene_name": "Cbl",
            "activity": [
                {
                    "ec_number": "2.3.2.27",
                    "activity": "S-ubiquitinyl-[E2 ubiquitin-conjugating enzyme]-L-cysteine + [acceptor protein]-L-lysine = [E2 ubiquitin-conjugating enzyme]-L-cysteine + N(6)-ubiquitinyl-[acceptor protein]-L-lysine.",
                    "evidence": [
                        {
                            "id": "P22682",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P22682"
                        }
                    ]
                },
                {
                    "ec_number": "2.3.2.27",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P22682",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P22682"
                        }
                    ]
                }
            ]
        },
        {
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            "activity": [
                {
                    "ec_number": "5.2.1.8",
                    "activity": "[protein]-peptidylproline (omega=180) = [protein]-peptidylproline (omega=0).",
                    "evidence": [
                        {
                            "id": "P26883",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P26883"
                        }
                    ]
                },
                {
                    "ec_number": "5.2.1.8",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P26883",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P26883"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P27037",
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            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P27037",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P27037"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
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                        {
                            "id": "P27037",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P27037"
                        }
                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P27038",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P27038"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P27038",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P27038"
                        }
                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P27040",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P27040"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P27040",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P27040"
                        }
                    ]
                }
            ]
        },
        {
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            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P36894",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P36894"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P36894",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P36894"
                        }
                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P36895",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P36895"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P36895",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P36895"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P36896",
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            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P36896",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P36896"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P36896",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P36896"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P36897",
            "gene_name": "TGFBR1",
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P36897",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P36897"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P36897",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P36897"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P36898",
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P36898",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P36898"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P36898",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P36898"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P37023",
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P37023",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P37023"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P37023",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P37023"
                        }
                    ]
                }
            ]
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        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P37172",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P37172"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
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                        {
                            "id": "P37172",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P37172"
                        }
                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P37173",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P37173"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P37173",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P37173"
                        }
                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P38438",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P38438"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                    "evidence": [
                        {
                            "id": "P38438",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P38438"
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                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
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                        {
                            "id": "P38444",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P38444"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                    "evidence": [
                        {
                            "id": "P38444",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P38444"
                        }
                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P38445",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P38445"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P38445",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P38445"
                        }
                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.3.2.34",
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                    "evidence": [
                        {
                            "id": "P61082",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P61082"
                        }
                    ]
                },
                {
                    "ec_number": "2.3.2.34",
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                        {
                            "id": "P61082",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P61082"
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                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P70539",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P70539"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P70539",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P70539"
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                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P80201",
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P80201",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80201"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                        {
                            "id": "P80201",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80201"
                        }
                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P80202",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80202"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                        {
                            "id": "P80202",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80202"
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                    ]
                }
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        {
            "uniprot_ac": "P80203",
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
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                            "id": "P80203",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80203"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P80203",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80203"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P80204",
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P80204",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80204"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                    "evidence": [
                        {
                            "id": "P80204",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80204"
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                    ]
                }
            ]
        },
        {
            "uniprot_ac": "Q02956",
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                {
                    "ec_number": "2.7.11.13",
                    "activity": "ATP + L-seryl-[protein] = ADP + H(+) + O-phospho-L-seryl-[protein].",
                    "evidence": [
                        {
                            "id": "Q02956",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q02956"
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                    ]
                },
                {
                    "ec_number": "2.7.11.13",
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                    "evidence": [
                        {
                            "id": "Q02956",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q02956"
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                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
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                        {
                            "id": "Q04771",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q04771"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
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                            "id": "Q04771",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q04771"
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                    ]
                }
            ]
        },
        {
            "uniprot_ac": "Q13705",
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "Q13705",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q13705"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                    "evidence": [
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                            "id": "Q13705",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q13705"
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                    ]
                }
            ]
        },
        {
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "Q13873",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q13873"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "Q13873",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q13873"
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                    ]
                }
            ]
        },
        {
            "uniprot_ac": "Q16671",
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "Q16671",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q16671"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "Q16671",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q16671"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "Q61271",
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "Q61271",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q61271"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                    "evidence": [
                        {
                            "id": "Q61271",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q61271"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "Q61288",
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                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "Q61288",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q61288"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                    "evidence": [
                        {
                            "id": "Q61288",
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