{
    "uniprot_canonical_ac": "A0A0B4KG59-1",
    "uniprot_ac": "A0A0B4KG59",
    "uniprot_id": "A0A0B4KG59_DROME",
    "mass": {
        "chemical_mass": 59207.0,
        "monoisotopic_mass": 59207.0
    },
    "refseq": {
        "ac": "NP_001262574",
        "name": "punt, isoform C",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262574"
    },
    "gene_names": [
        {
            "name": "put",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "Act-r; Atr; Atr-II; Atr88CD; atrII; AtrII; CG7904; dlhC; Dmel\\CG7904; l(3)10460; l(3)j5A5; pun; Punt; PUNT; Put; STK-C; TGF-B; TGF-beta; Tgf-r",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262574",
            "id": "NP_001262574"
        },
        {
            "name": "Act-r",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "Atr-II",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "Atr88CD",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "AtrII",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "Atr",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "CG7904",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "Dmel\\CG7904",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "Dmel_CG7904",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "PUNT",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "Punt",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "Put",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "STK-C",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "TGF-B",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "TGF-beta",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "Tgf-r",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "atrII",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "dlhC",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "l(3)10460",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "l(3)j5A5",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "pun",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KG59",
            "id": "A0A0B4KG59"
        },
        {
            "name": "put",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262574",
            "id": "NP_001262574"
        }
    ],
    "protein_names": [
        {
            "name": "Serine/threonine-protein kinase receptor",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "A0A0B4KG59"
        },
        {
            "name": "2.7.11.30",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A0B4KG59"
        },
        {
            "name": "CG7904-PB; put-PB; punt; DPP receptor; activin receptor; activin receptor type II; TGF-beta-type-receptor-like; dorsal holes C; Activin-A-receptor-88CD",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262575",
            "id": "NP_001262575"
        },
        {
            "name": "CG7904-PC; put-PC; punt; DPP receptor; activin receptor; activin receptor type II; TGF-beta-type-receptor-like; dorsal holes C; Activin-A-receptor-88CD",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262574",
            "id": "NP_001262574"
        },
        {
            "name": "punt, isoform B",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262575",
            "id": "NP_001262575"
        },
        {
            "name": "punt, isoform C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262574",
            "id": "NP_001262574"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0050545",
            "recommended_name": {
                "id": "DOID:0050545",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050545",
                "name": "visceral heterotaxy",
                "description": "A physical disorder characterized by the abnormal distribution of the major visceral organs within the chest and abdomen."
            },
            "synonyms": [
                {
                    "id": "DOID:0050545",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050545",
                    "name": "heterotaxia",
                    "description": ""
                },
                {
                    "id": "DOID:0050545",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050545",
                    "name": "situs ambiguus",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "heterotaxy, visceral, 2, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "DTGA2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "heterotaxy, visceral, 2, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "transposition of the great arteries, dextro-looped 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "HTX2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "Htx",
                    "description": ""
                },
                {
                    "id": "MONDO:0011659",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011659",
                    "name": "heterotaxy, visceral, 3, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0011659",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011659",
                    "name": "HTX3",
                    "description": ""
                },
                {
                    "id": "MONDO:0011659",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011659",
                    "name": "heterotaxy, visceral, 3, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, 1, X-linked",
                    "description": "X-linked visceral heterotaxy type 1 is a very rare form of heterotaxy that has only been reported in a few families. Heterotaxy is the right/left transposition of thoracic and/or abdominal organs. This condition is caused by mutations in the ZIC3 gene, is inherited in an X-linked recessive fashion, and is usually seen in males. Physical features include heart abnormalities such as dextrocardia, transposition of great vessels, ventricular septal defect, patent ductus arteriosus, pulmonic stenosis ; situs inversus, and missing (asplenia) and/or extra spleens (polysplenia).Affected individualscan also experience abnormalities in the development of the midline of the body, which can cause holoprosencephaly, myelomeningocele, urological anomalies, widely spaced eyes (hypertelorism), cleft palate, and abnormalities of the sacral spine and anus. Heterotaxia with recurrent respiratory infections are called primary ciliary dyskinesia."
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "ZIC3 visceral heterotaxy",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "congenital heart defects, nonsyndromic, 1, X-linked, X-linked recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, 1, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, 1, X-linked, X-linked recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "visceral heterotaxy caused by mutation in ZIC3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "HTX1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "X-linked visceral heterotaxy 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "congenital heart defects, multiple types, 1, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "dextrocardia with Other Cardiac malformations",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "laterality, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "situs inversus, Complex Cardiac defects, and splenic defects, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "heterotaxy, visceral, 6, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "heterotaxy, visceral, 6, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "heterotaxy, visceral, 6, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "HTX6",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "heterotaxy, visceral, 4, autosomal",
                    "description": "Any visceral heterotaxy in which the cause of the disease is a mutation in the ACVR2B gene."
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "ACVR2B visceral heterotaxy",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "heterotaxy, visceral, 4, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "visceral heterotaxy caused by mutation in ACVR2B",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "HTX4",
                    "description": ""
                },
                {
                    "id": "MIM:605376",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/605376",
                    "name": "Heterotaxy, visceral, 2, autosomal",
                    "description": "Heterotaxy, visceral, 2, autosomal"
                },
                {
                    "id": "MIM:306955",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/306955",
                    "name": "Heterotaxy, visceral, 1, X-linked",
                    "description": "Heterotaxy, visceral, 1, X-linked"
                },
                {
                    "id": "MIM:614779",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/614779",
                    "name": "Heterotaxy, visceral, 6, autosomal",
                    "description": "Heterotaxy, visceral, 6, autosomal"
                },
                {
                    "id": "MIM:613751",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/613751",
                    "name": "Heterotaxy, visceral, 4, autosomal",
                    "description": "Heterotaxy, visceral, 4, autosomal"
                }
            ],
            "evidence": [
                {
                    "id": "0050545",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050545"
                }
            ]
        },
        {
            "disease_id": "DOID:0050787",
            "recommended_name": {
                "id": "DOID:0050787",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050787",
                "name": "juvenile polyposis syndrome",
                "description": "A gastrointestinal system disease that is characterized by predisposition to hamartomatous benign polyps in the gastrointestinal tract, specifically in the stomach, small intestine, colon, and rectum."
            },
            "synonyms": [
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "juvenile polyposis syndrome",
                    "description": "Juvenile gastrointestinal polyposis (JIP) is a rare condition characterized by the presence of juvenile hamartomatous polyps in the gastrointestinal (GI) tract."
                },
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "JIP",
                    "description": ""
                },
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "jPS",
                    "description": ""
                },
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "juvenile gastrointestinal polyposis",
                    "description": ""
                },
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "juvenile intestinal polyposis",
                    "description": ""
                },
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "juvenile multiple polyps syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "juvenile polyposis",
                    "description": ""
                },
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "juvenile polyposis syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "polyposis, juvenile intestinal",
                    "description": ""
                },
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "PJI",
                    "description": ""
                },
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "polyposis familial of entire gastrointestinal tract",
                    "description": ""
                },
                {
                    "id": "MONDO:0017380",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0017380",
                    "name": "polyposis juvenile intestinal",
                    "description": ""
                },
                {
                    "id": "MIM:174900",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/174900",
                    "name": "Juvenile polyposis syndrome",
                    "description": "Juvenile polyposis syndrome"
                }
            ],
            "evidence": [
                {
                    "id": "0050787",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050787"
                }
            ]
        },
        {
            "disease_id": "DOID:0060856",
            "recommended_name": {
                "id": "DOID:0060856",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0060856",
                "name": "right atrial isomerism",
                "description": "A visceral heterotaxy that is characterized by complete atrioventricular septal defect with a common atrium and univentricular AV connection, total anomalous pulmonary drainage, and transposition or malposition of the great arteries and that has_material_basis_in homozygous mutation in the GDF1 gene on chromosome 19p12."
            },
            "synonyms": [
                {
                    "id": "DOID:0060856",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060856",
                    "name": "Ivemark syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:0060856",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060856",
                    "name": "asplenia with cardiovascular anomalies",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "right atrial isomerism",
                    "description": "A visceral heterotaxy characterized by complete atrioventricular septal defect with a common atrium and univentricular AV connection, total anomalous pulmonary drainage, and transposition or malposition of the great arteries and may be associated with bilateral trilobed lungs, midline liver, asplenia and situs inversus affecting other organs that has material basis in homozygous mutation in the GDF1 gene on chromosome 19p12."
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "Ivemark syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "asplenia with cardiovascular anomalies",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "right atrial isomerism",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "right atrial isomerism (disease)",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "right atrial isomerism (ivemark)",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "Polyasplenia",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "RAI",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "Vah, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "asplenia syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "bilateral right-sidedness sequence",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "heterotaxy, Visceroatrial, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "polysplenia syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "right isomerism",
                    "description": ""
                },
                {
                    "id": "MONDO:0008832",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008832",
                    "name": "splenic agenesis syndrome",
                    "description": ""
                },
                {
                    "id": "MIM:208530",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/208530",
                    "name": "Right atrial isomerism",
                    "description": "Right atrial isomerism"
                }
            ],
            "evidence": [
                {
                    "id": "0060856",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0060856"
                }
            ]
        },
        {
            "disease_id": "DOID:10591",
            "recommended_name": {
                "id": "DOID:10591",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10591",
                "name": "pre-eclampsia",
                "description": "A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy."
            },
            "synonyms": [
                {
                    "id": "DOID:10591",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10591",
                    "name": "gestational hypertension",
                    "description": ""
                },
                {
                    "id": "DOID:10591",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10591",
                    "name": "hypertension induced by pregnancy",
                    "description": ""
                },
                {
                    "id": "DOID:10591",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10591",
                    "name": "pre-eclamptic toxaemia",
                    "description": ""
                },
                {
                    "id": "DOID:10591",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10591",
                    "name": "preeclampsia",
                    "description": ""
                },
                {
                    "id": "DOID:10591",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10591",
                    "name": "preeclampsia/eclampsia",
                    "description": ""
                },
                {
                    "id": "DOID:10591",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10591",
                    "name": "pregnancy associated hypertension",
                    "description": ""
                },
                {
                    "id": "DOID:10591",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10591",
                    "name": "pregnancy toxemia",
                    "description": ""
                },
                {
                    "id": "DOID:10591",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10591",
                    "name": "proteinuric hypertension of pregnancy",
                    "description": ""
                },
                {
                    "id": "DOID:10591",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10591",
                    "name": "toxaemia of pregnancy",
                    "description": ""
                },
                {
                    "id": "MONDO:0012266",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012266",
                    "name": "preeclampsia/eclampsia 4",
                    "description": "Any preeclampsia in which the cause of the disease is a mutation in the STOX1 gene."
                },
                {
                    "id": "MONDO:0012266",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012266",
                    "name": "Preeclampsia/eclampsia type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012266",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012266",
                    "name": "STOX1 preeclampsia",
                    "description": ""
                },
                {
                    "id": "MONDO:0012266",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012266",
                    "name": "preeclampsia caused by mutation in STOX1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012266",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012266",
                    "name": "preeclampsia/eclampsia 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012266",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012266",
                    "name": "PEE4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012266",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012266",
                    "name": "PREECLAMPSIA/eclampsia 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012265",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012265",
                    "name": "preeclampsia/eclampsia 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012265",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012265",
                    "name": "PEE3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012265",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012265",
                    "name": "PREECLAMPSIA/eclampsia 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012264",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012264",
                    "name": "preeclampsia/eclampsia 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012264",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012264",
                    "name": "PEE2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012264",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012264",
                    "name": "PREECLAMPSIA/eclampsia 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0100467",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100467",
                    "name": "preeclampsia/eclampsia 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0100467",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100467",
                    "name": "toxaemia of pregnancy",
                    "description": ""
                },
                {
                    "id": "MONDO:0100467",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100467",
                    "name": "toxemia of pregnancy",
                    "description": ""
                },
                {
                    "id": "MONDO:0100467",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100467",
                    "name": "PEE1",
                    "description": ""
                },
                {
                    "id": "MONDO:0100467",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100467",
                    "name": "PREECLAMPSIA/eclampsia 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0100467",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100467",
                    "name": "PREG1",
                    "description": ""
                },
                {
                    "id": "MONDO:0100467",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100467",
                    "name": "hemolysis, elevated liver enzymes, and low platelet count",
                    "description": ""
                },
                {
                    "id": "MONDO:0100467",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100467",
                    "name": "hypertension, pregnancy-induced",
                    "description": ""
                },
                {
                    "id": "MONDO:0013815",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013815",
                    "name": "bent bone dysplasia syndrome 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0013815",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013815",
                    "name": "FGFR2-related bent bone dysplasia",
                    "description": ""
                },
                {
                    "id": "MONDO:0013815",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013815",
                    "name": "perinatal lethal bent bone dysplasia",
                    "description": ""
                },
                {
                    "id": "MONDO:0013815",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013815",
                    "name": "BBDS",
                    "description": ""
                },
                {
                    "id": "MONDO:0013815",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013815",
                    "name": "bent bone dysplasia (BBD)-FGFR2 type",
                    "description": ""
                },
                {
                    "id": "MONDO:0013815",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013815",
                    "name": "bent bone dysplasia syndrome",
                    "description": ""
                },
                {
                    "id": "MIM:609404",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/609404",
                    "name": "Pre-eclampsia/eclampsia 4",
                    "description": "Pre-eclampsia/eclampsia 4"
                },
                {
                    "id": "MIM:614592",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/614592",
                    "name": "Bent bone dysplasia syndrome 1",
                    "description": "Bent bone dysplasia syndrome 1"
                }
            ],
            "evidence": [
                {
                    "id": "10591",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:10591"
                }
            ]
        },
        {
            "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: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"
                }
            ]
        },
        {
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            "recommended_name": {
                "id": "DOID:4258",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:4258",
                "name": "Weissenbacher-Zweymuller syndrome",
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                {
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                    "url": "http://disease-ontology.org/term/DOID:4258",
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                    "description": ""
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                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
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                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
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                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
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                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
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                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
                    "name": "Piere-Robin syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
                    "name": "Pierre Robin malformation",
                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
                    "name": "Pierre Robin sequence-fetal chondrodysplasia syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
                    "name": "Pierre Robin syndrome with fetal chondrodysplasia",
                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
                    "name": "Pierre Robin syndrome with fetal chondrodysplasia Stickler syndrome, Nonocular type",
                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
                    "name": "Pierre Robin syndrome with fetal chondrodysplasia Stickler syndrome, Nonocular type, formerly",
                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
                    "name": "Pierre Robin syndrome with foetal chondrodysplasia",
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                },
                {
                    "id": "MONDO:0008490",
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                    "name": "Pierre Robin syndrome with foetal chondrodysplasia Stickler syndrome, Nonocular type",
                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
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                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
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                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
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                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
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                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
                    "name": "Stickler syndrome caused by mutation in COL11A2",
                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
                    "name": "Stickler syndrome, non-ocular type",
                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
                    "name": "Stickler syndrome, type 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
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                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
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                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
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                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
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                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
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                {
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                {
                    "id": "MONDO:0008490",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008490",
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                    "description": ""
                },
                {
                    "id": "MONDO:0008490",
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                {
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                {
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                {
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                {
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                {
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                {
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        "sequence": "MSKYDLLYLTAQLTLVCCLIGIHGSILPGSHGIIECEHFDEKMCNTTQQCETRIEHCKMEADKFPSCYVLWSVNETTGILRIKMKGCFTDMHECNQTECVTSAEPRQGNIHFCCCKGSRCNSNQKYIKSTTEATTQVPKEKTQDGSNLIYIYIGTSVFSVLMVIVGMGLLLYRRRKQAHFNEIPTHEAEITNSSPLLSNRPIQLLEQKASGRFGDVWQAKLNNQDVAVKIFRMQEKESWTTEHDIYKLPRMRHPNILEFLGVEKHMDKPEYWLISTYQHNGSLCDYLKSHTISWPELCRIAESMANGLAHLHEEIPASKTDGLKPSIAHRDFKSKNVLLKSDLTACIADFGLAMIFQPGKPCGDTHGQVGTRRYMAPEVLEGAINFNRDAFLRIDVYACGLVLWEMVSRCDFAGPVGEFQLPFEAELGLRPSLDEVQESVVMKKLRPRLLNSWRAHPGLNVFCDTMEECWDHDAEARLSSSCVMERFAQLNKYPSTQLLIKNHTNIDDAKESTNCLXKRY",
        "length": 520,
        "header": "tr|A0A0B4KG59-1|A0A0B4KG59_DROME Isoform 1 of Serine/threonine-protein kinase receptor  OS=Drosophila melanogaster OX=7227 GN=put PE=1 SV=1 CANONICAL=A0A0B4KG59-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A0B4KG59-1",
            "url": "",
            "sequence": {
                "sequence": "MSKYDLLYLTAQLTLVCCLIGIHGSILPGSHGIIECEHFDEKMCNTTQQCETRIEHCKMEADKFPSCYVLWSVNETTGILRIKMKGCFTDMHECNQTECVTSAEPRQGNIHFCCCKGSRCNSNQKYIKSTTEATTQVPKEKTQDGSNLIYIYIGTSVFSVLMVIVGMGLLLYRRRKQAHFNEIPTHEAEITNSSPLLSNRPIQLLEQKASGRFGDVWQAKLNNQDVAVKIFRMQEKESWTTEHDIYKLPRMRHPNILEFLGVEKHMDKPEYWLISTYQHNGSLCDYLKSHTISWPELCRIAESMANGLAHLHEEIPASKTDGLKPSIAHRDFKSKNVLLKSDLTACIADFGLAMIFQPGKPCGDTHGQVGTRRYMAPEVLEGAINFNRDAFLRIDVYACGLVLWEMVSRCDFAGPVGEFQLPFEAELGLRPSLDEVQESVVMKKLRPRLLNSWRAHPGLNVFCDTMEECWDHDAEARLSSSCVMERFAQLNKYPSTQLLIKNHTNIDDAKESTNCLXKRY",
                "length": 520,
                "header": "tr|A0A0B4KG59-1|A0A0B4KG59_DROME Isoform 1 of Serine/threonine-protein kinase receptor  OS=Drosophila melanogaster OX=7227 GN=put PE=1 SV=1 CANONICAL=A0A0B4KG59-1"
            },
            "locus": {
                "chromosome": "3R",
                "start_pos": 14625245,
                "end_pos": 14621025,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0330227",
                        "url": "https://www.ensembl.org/id/FBtr0330227"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0303260",
                        "url": "https://www.ensembl.org/id/FBpp0303260"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q24468-1",
            "url": "",
            "sequence": {
                "sequence": "MSKYDLLYLTAQLTLVCCLIGIHGSILPGSHGIIECEHFDEKMCNTTQQCETRIEHCKMEADKFPSCYVLWSVNETTGILRIKMKGCFTDMHECNQTECVTSAEPRQGNIHFCCCKGSRCNSNQKYIKSTTEATTQVPKEKTQDGSNLIYIYIGTSVFSVLMVIVGMGLLLYRRRKQAHFNEIPTHEAEITNSSPLLSNRPIQLLEQKASGRFGDVWQAKLNNQDVAVKIFRMQEKESWTTEHDIYKLPRMRHPNILEFLGVEKHMDKPEYWLISTYQHNGSLCDYLKSHTISWPELCRIAESMANGLAHLHEEIPASKTDGLKPSIAHRDFKSKNVLLKSDLTACIADFGLAMIFQPGKPCGDTHGQVGTRRYMAPEVLEGAINFNRDAFLRIDVYACGLVLWEMVSRCDFAGPVGEFQLPFEAELGLRPSLDEVQESVVMKKLRPRLLNSWRAHPGLNVFCDTMEECWDHDAEARLSSSCVMERFAQLNKYPSTQLLIKNHTNIDDAKESTNCL",
                "length": 516,
                "header": "tr|Q24468-1|A0A0B4KG59_DROME Computationally mapped isoform of Serine/threonine-protein kinase receptor  OS=Drosophila melanogaster OX=7227 GN=put PE=1 SV=1 CANONICAL=A0A0B4KG59-1"
            },
            "locus": {
                "chromosome": "3R",
                "start_pos": 14625245,
                "end_pos": 14621037,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0334030",
                        "url": "https://www.ensembl.org/id/FBtr0334030"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0306147",
                        "url": "https://www.ensembl.org/id/FBpp0306147"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [
        "enzyme"
    ],
    "publication": [
        {
            "title": "An absolute requirement for both the type II and type I receptors, punt and thick veins, for dpp signaling in vivo.",
            "journal": "Cell",
            "date": "1995",
            "authors": "Ruberte E, Marty T, Nellen D, Affolter M, Basler K",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q24468",
                    "url": "https://www.uniprot.org/uniprot/Q24468"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "7697719",
                    "url": "https://glygen.org/publication/PubMed/7697719"
                }
            ]
        }
    ],
    "pathway": [
        {
            "id": "dme:Dmel_CG7904",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG7904",
            "resource": "KEGG Pathway"
        },
        {
            "id": "R-DME-1502540",
            "name": "Signaling by Activin",
            "url": "https://www.reactome.org/PathwayBrowser/#R-DME-1502540",
            "resource": "Reactome",
            "description": "Signaling by Activin"
        },
        {
            "id": "R-DME-201451",
            "name": "Signaling by BMP",
            "url": "https://www.reactome.org/PathwayBrowser/#R-DME-201451",
            "resource": "Reactome",
            "description": "Signaling by BMP"
        },
        {
            "id": "R-DME-2173788",
            "name": "Downregulation of TGF-beta receptor signaling",
            "url": "https://www.reactome.org/PathwayBrowser/#R-DME-2173788",
            "resource": "Reactome",
            "description": "Downregulation of TGF-beta receptor signaling"
        },
        {
            "id": "R-DME-2173789",
            "name": "TGF-beta receptor signaling activates SMADs",
            "url": "https://www.reactome.org/PathwayBrowser/#R-DME-2173789",
            "resource": "Reactome",
            "description": "TGF-beta receptor signaling activates SMADs"
        },
        {
            "id": "R-DME-2173791",
            "name": "TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition)",
            "url": "https://www.reactome.org/PathwayBrowser/#R-DME-2173791",
            "resource": "Reactome",
            "description": "TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition)"
        }
    ],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Molecular Function",
                "total": 7,
                "go_terms": [
                    {
                        "name": "ATP binding",
                        "id": "GO:0005524",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "metal ion binding",
                        "id": "GO:0046872",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "activin binding",
                        "id": "GO:0048185",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048185",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "activin receptor activity",
                        "id": "GO:0017002",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0017002",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "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": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "BMP receptor activity",
                        "id": "GO:0098821",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098821",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "activin receptor activity, type II",
                        "id": "GO:0016362",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016362",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 4,
                "go_terms": [
                    {
                        "name": "plasma membrane",
                        "id": "GO:0005886",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "activin receptor complex",
                        "id": "GO:0048179",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048179",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "basolateral plasma membrane",
                        "id": "GO:0016323",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016323",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "BMP receptor complex",
                        "id": "GO:0070724",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070724",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Biological Process",
                "total": 23,
                "go_terms": [
                    {
                        "name": "cellular response to growth factor stimulus",
                        "id": "GO:0071363",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071363",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "phosphorylation",
                        "id": "GO:0016310",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016310",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "activin receptor signaling pathway",
                        "id": "GO:0032924",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032924",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "neuron development",
                        "id": "GO:0048666",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048666",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "axon guidance",
                        "id": "GO:0007411",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007411",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "germ-line stem cell population maintenance",
                        "id": "GO:0030718",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030718",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "primary branching, open tracheal system",
                        "id": "GO:0007428",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007428",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "dorsal closure",
                        "id": "GO:0007391",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007391",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "open tracheal system development",
                        "id": "GO:0007424",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007424",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "Malpighian tubule morphogenesis",
                        "id": "GO:0007443",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007443",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "head involution",
                        "id": "GO:0008258",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008258",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "germ-line stem cell division",
                        "id": "GO:0042078",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042078",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "negative regulation of salivary gland boundary specification",
                        "id": "GO:0045705",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045705",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of glycogen catabolic process",
                        "id": "GO:0045819",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045819",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cellular response to glucose stimulus",
                        "id": "GO:0071333",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071333",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "glucose homeostasis",
                        "id": "GO:0042593",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042593",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "BMP signaling pathway",
                        "id": "GO:0030509",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030509",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "dorsal/ventral pattern formation",
                        "id": "GO:0009953",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009953",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of SMAD protein signal transduction",
                        "id": "GO:0060391",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060391",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of neuromuscular junction development",
                        "id": "GO:1904398",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1904398",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "imaginal disc-derived wing morphogenesis",
                        "id": "GO:0007476",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007476",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "wing disc pattern formation",
                        "id": "GO:0035222",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035222",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "R8 cell fate specification",
                        "id": "GO:0045464",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045464",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4KG59",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4KG59"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 192,
            "end_pos": 194,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 280,
            "end_pos": 282,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 45,
            "end_pos": 47,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 502,
            "end_pos": 504,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 74,
            "end_pos": 76,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 95,
            "end_pos": 97,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [
        {
            "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-DME-1181149",
            "name": "ACVR2A,B (ActRIIA,B) phosphorylates ACVR1B (ActRIB, ALK4) in response to Activin",
            "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": [
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-1181149",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-1181149"
                }
            ]
        },
        {
            "id": "R-DME-1181153",
            "name": "Activin A,AB,B binds Activin Receptor ACVR2A,B:ACVR1B",
            "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": [
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-1181153",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-1181153"
                }
            ]
        },
        {
            "id": "R-DME-1549526",
            "name": "Phosphorylation of SMAD2,3 by Activin:Activin 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": "cytosol, plasma membrane",
            "input_participant_list": [
                "R-DME-3006353"
            ],
            "output_participant_list": [
                "R-DME-3009186"
            ],
            "enzyme_list": [
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-1549526",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-1549526"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-170835",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-170835"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-170843",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-170843"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A0A0B4KG59-1",
                "A1Z7L8-1",
                "P48375-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-170846",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-170846"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-170850",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-170850"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A0A0B4KG59-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-170861",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-170861"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-170868",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-170868"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-173512",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-173512"
                }
            ]
        },
        {
            "id": "R-DME-201443",
            "name": "Type II receptor phosphorylates type I 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": "cytosol, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "A0A0B4KG59-1",
                "M9PE88-1",
                "Q9VMT1-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-201443",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-201443"
                }
            ]
        },
        {
            "id": "R-DME-201453",
            "name": "Phospho-R-Smad1/5/8 dissociates from the 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": "early endosome",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "A0A0B4KG59-1",
                "M9PE88-1",
                "Q9VMT1-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-201453",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-201453"
                }
            ]
        },
        {
            "id": "R-DME-201457",
            "name": "BMP2 binds to the 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": "extracellular region, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "A0A0B4KG59-1",
                "M9PE88-1",
                "Q9VMT1-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-201457",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-201457"
                }
            ]
        },
        {
            "id": "R-DME-201475",
            "name": "I-Smad competes with R-Smad1/5/8 for type I 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": "cytosol, extracellular region, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "A0A0B4KG59-1",
                "M9PE88-1",
                "Q9VMT1-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-201475",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-201475"
                }
            ]
        },
        {
            "id": "R-DME-201476",
            "name": "Activated type I receptor phosphorylates R-Smad1/5/8 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": "plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "A0A0B4KG59-1",
                "M9PE88-1",
                "Q9VMT1-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-201476",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-201476"
                }
            ]
        },
        {
            "id": "R-DME-201648",
            "name": "An anchoring protein, Endofin, recruits R-Smad1/5/8",
            "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, early endosome membrane, plasma membrane",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [
                "A0A0B4KG59-1",
                "M9PE88-1",
                "Q9VMT1-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-201648",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-201648"
                }
            ]
        },
        {
            "id": "R-DME-201821",
            "name": "I-Smad binds to type I receptor, preventing Smad1/5/8 from being activated",
            "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": [
                "Q9V853-1",
                "A0A0B4KG59-1",
                "M9PE88-1",
                "Q9VMT1-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-201821",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-201821"
                }
            ]
        },
        {
            "id": "R-DME-202604",
            "name": "Formation of a heteromeric BMP 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": [
                "A0A0B4KG59-1",
                "M9PE88-1",
                "Q9VMT1-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-202604",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-202604"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-2128994",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-2128994"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A1Z9X0-1",
                "Q9V853-1",
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-2160931",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-2160931"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A1Z9X0-1",
                "Q9V853-1",
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-2160932",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-2160932"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A1Z9X0-1",
                "Q9V853-1",
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-2160935",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-2160935"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A0A0B4KG59-1",
                "A1Z7L8-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-2169046",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-2169046"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "A0A0B4KG59-1",
                "Q9VSK2-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-4332235",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-4332235"
                }
            ]
        },
        {
            "id": "R-DME-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": [
                "Q9VSF3-1",
                "A0A0B4KG59-1",
                "Q9VSK2-1"
            ],
            "evidence": [
                {
                    "id": "R-DME-4332236",
                    "database": "Reactome",
                    "url": "https://www.reactome.org/PathwayBrowser/#R-DME-4332236"
                }
            ]
        }
    ],
    "reaction_participants": [
        {
            "participant_id": "R-DME-3006353",
            "participant_name": "Smox [cytosol]",
            "crossref": [
                {
                    "id": "O96660",
                    "database": "UniProt",
                    "url": ""
                },
                {
                    "id": "NP_001285006.1",
                    "database": "RefSeq",
                    "url": ""
                },
                {
                    "id": "FBgn0025800",
                    "database": "Flybase",
                    "url": ""
                },
                {
                    "id": "NP_511079.1",
                    "database": "RefSeq",
                    "url": ""
                }
            ]
        },
        {
            "participant_id": "R-DME-3009186",
            "participant_name": "phospho-Smox [cytosol]",
            "crossref": [
                {
                    "id": "NP_001285006.1",
                    "database": "RefSeq",
                    "url": ""
                },
                {
                    "id": "NP_511079.1",
                    "database": "RefSeq",
                    "url": ""
                },
                {
                    "id": "O96660",
                    "database": "UniProt",
                    "url": ""
                },
                {
                    "id": "FBgn0025800",
                    "database": "Flybase",
                    "url": ""
                }
            ]
        }
    ],
    "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": "A1Z7L8",
            "gene_name": "babo",
            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "A1Z7L8",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/A1Z7L8"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "A1Z7L8",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/A1Z7L8"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "A1Z9X0",
            "gene_name": "aPKC",
            "activity": [
                {
                    "ec_number": "2.7.11.13",
                    "activity": "ATP + L-seryl-[protein] = ADP + H(+) + O-phospho-L-seryl-[protein].",
                    "evidence": [
                        {
                            "id": "A1Z9X0",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/A1Z9X0"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.13",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "A1Z9X0",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/A1Z9X0"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.-",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "A1Z9X0",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/A1Z9X0"
                        }
                    ]
                }
            ]
        },
        {
            "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": "M9PE88",
            "gene_name": "wit",
            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "M9PE88",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/M9PE88"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "M9PE88",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/M9PE88"
                        }
                    ]
                }
            ]
        },
        {
            "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": "P27037",
            "gene_name": "ACVR2A",
            "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": "",
                    "evidence": [
                        {
                            "id": "P27037",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P27037"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P27038",
            "gene_name": "Acvr2a",
            "activity": [
                {
                    "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"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P27040",
            "gene_name": "Acvr2b",
            "activity": [
                {
                    "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"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P36894",
            "gene_name": "BMPR1A",
            "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"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P36895",
            "gene_name": "Bmpr1a",
            "activity": [
                {
                    "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",
            "gene_name": "ACVR1B",
            "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",
            "activity": [
                {
                    "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",
            "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": "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",
            "gene_name": "ACVRL1",
            "activity": [
                {
                    "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"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P37172",
            "gene_name": "Acvr1",
            "activity": [
                {
                    "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": "",
                    "evidence": [
                        {
                            "id": "P37172",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P37172"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P37173",
            "gene_name": "TGFBR2",
            "activity": [
                {
                    "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"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P38438",
            "gene_name": "Tgfbr2",
            "activity": [
                {
                    "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",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P38438",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P38438"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P38444",
            "gene_name": "Acvr2a",
            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P38444",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P38444"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P38444",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P38444"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P38445",
            "gene_name": "Acvr2b",
            "activity": [
                {
                    "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"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P48375",
            "gene_name": "Fkbp12",
            "activity": [
                {
                    "ec_number": "5.2.1.8",
                    "activity": "[protein]-peptidylproline (omega=180) = [protein]-peptidylproline (omega=0).",
                    "evidence": [
                        {
                            "id": "P48375",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P48375"
                        }
                    ]
                },
                {
                    "ec_number": "5.2.1.8",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P48375",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P48375"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P70539",
            "gene_name": "Acvr1c",
            "activity": [
                {
                    "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"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P80201",
            "gene_name": "Acvr1",
            "activity": [
                {
                    "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",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P80201",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80201"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P80202",
            "gene_name": "Acvr1b",
            "activity": [
                {
                    "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"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P80202",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80202"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "P80203",
            "gene_name": "Acvrl1",
            "activity": [
                {
                    "ec_number": "2.7.11.30",
                    "activity": "ATP + L-threonyl-[receptor-protein] = ADP + H(+) + O-phospho-L-threonyl-[receptor-protein].",
                    "evidence": [
                        {
                            "id": "P80203",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80203"
                        }
                    ]
                },
                {
                    "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",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "P80204",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/P80204"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "Q04771",
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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": "Q04771",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q04771"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "Q04771",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q04771"
                        }
                    ]
                }
            ]
        },
        {
            "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"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "Q13705",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q13705"
                        }
                    ]
                }
            ]
        },
        {
            "uniprot_ac": "Q13873",
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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": "Q13873",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q13873"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                        {
                            "id": "Q13873",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q13873"
                        }
                    ]
                }
            ]
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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": "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"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
                    "evidence": [
                        {
                            "id": "Q61271",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q61271"
                        }
                    ]
                }
            ]
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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": "Q61288",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q61288"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                            "id": "Q61288",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q61288"
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                    ]
                }
            ]
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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": "Q62312",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q62312"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                        {
                            "id": "Q62312",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q62312"
                        }
                    ]
                }
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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": "Q62893",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q62893"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                            "id": "Q62893",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q62893"
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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": "Q64729",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q64729"
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                    ]
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                {
                    "ec_number": "2.7.11.30",
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                            "id": "Q64729",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q64729"
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                }
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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": "Q78EA7",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q78EA7"
                        }
                    ]
                },
                {
                    "ec_number": "2.7.11.30",
                    "activity": "",
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                            "id": "Q78EA7",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q78EA7"
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                    ]
                }
            ]
        },
        {
            "uniprot_ac": "Q8K348",
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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": "Q8K348",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q8K348"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                            "id": "Q8K348",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q8K348"
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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": "Q8K592",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q8K592"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                            "id": "Q8K592",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q8K592"
                        }
                    ]
                }
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        },
        {
            "uniprot_ac": "Q8NER5",
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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": "Q8NER5",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q8NER5"
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                    ]
                },
                {
                    "ec_number": "2.7.11.30",
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                            "id": "Q8NER5",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q8NER5"
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                }
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        {
            "uniprot_ac": "Q9V853",
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                {
                    "ec_number": "2.3.2.26",
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                    "evidence": [
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                            "id": "Q9V853",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q9V853"
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                },
                {
                    "ec_number": "2.3.2.26",
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                            "id": "Q9V853",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q9V853"
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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": "Q9VMT1",
                            "database": "UniProtKB",
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                },
                {
                    "ec_number": "2.7.11.30",
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                }
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                {
                    "ec_number": "2.3.2.34",
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                    "evidence": [
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                            "id": "Q9VSF3",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q9VSF3"
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                    ]
                },
                {
                    "ec_number": "2.3.2.34",
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                            "id": "Q9VSF3",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q9VSF3"
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                    ]
                }
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                {
                    "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.",
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                            "id": "Q9VSK2",
                            "database": "UniProtKB",
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                    ]
                },
                {
                    "ec_number": "2.3.2.27",
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                            "id": "Q9VSK2",
                            "database": "UniProtKB",
                            "url": "https://www.uniprot.org/uniprot/Q9VSK2"
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                    ]
                }
            ]
        }
    ],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
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    ],
    "section_stats": [
        {
            "table_id": "glycosylation",
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                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
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                {
                    "field": "n_linked_glycans",
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                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
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                {
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