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                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "CD27 receptor binding",
                "id": "GO:0005175",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005175",
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                    {
                        "database": "UniProtKB",
                        "id": "A8JUS8",
                        "url": "https://www.uniprot.org/uniprotkb/A8JUS8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
        "uniprot_canonical_ac": "B7YZH0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                        "id": "B7YZH0",
                        "url": "https://www.uniprot.org/uniprotkb/B7YZH0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 145,
        "chemical_mass": 16296.0,
        "gene_names": "CG13353;CG13353;CG42287;Dmel\\CG42287;Dmel_CG42287",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "B7YZH0-1"
    },
    {
        "uniprot_canonical_ac": "B7YZL9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7YZL9",
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                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1500,
        "chemical_mass": 166756.0,
        "gene_names": "Fak;CG10023;CT28129;DFAK;DFak56;DFak;Dfak56;Dfak;DmFAK;Dmel\\CG10023;Dmel_CG10023;FAK65D;FAK;Fak56D;Fak56;Fak;dFak;fak56D;fak56;fak;pFAK;ptk2",
        "protein_name": "",
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                    {
                        "id": "0060074",
                        "database": "AGR",
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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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                ],
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            },
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                ],
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                ],
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                ],
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            },
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                        "url": "https://www.alliancegenome.org/disease/DOID:2316"
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                ],
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                    {
                        "id": "289",
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                ],
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                    {
                        "id": "2893",
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                ],
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                    {
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                        "url": "https://www.alliancegenome.org/disease/DOID:2921"
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                ],
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                ],
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                        "url": "https://www.alliancegenome.org/disease/DOID:4001"
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                        "url": "https://www.alliancegenome.org/disease/DOID:4362"
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                ],
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            },
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                ],
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4780"
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                ],
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                        "id": "5409",
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                ],
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                        "database": "AGR",
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                ],
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            },
            {
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                    {
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                ],
                "pmid": ""
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        ],
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                "name": "positive regulation of cell population proliferation",
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                ],
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            },
            {
                "name": "animal organ morphogenesis",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009887",
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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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            },
            {
                "name": "negative regulation of synaptic assembly at neuromuscular junction",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045886",
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                    {
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                ],
                "pmid": ""
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        ],
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        ],
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        "gene_names": "BBS9;BBS9;BcDNA:RH67628;CG15666;Dmel\\CG15666;Dmel_CG15666",
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                ],
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            },
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                "name": "Bardet-Biedl syndrome",
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                "url": "https://disease-ontology.org/term/DOID:1935",
                "evidence": [
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                        "id": "1935",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1935"
                    }
                ],
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            },
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                "name": "craniosynostosis",
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                "url": "https://disease-ontology.org/term/DOID:2340",
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                        "url": "https://www.alliancegenome.org/disease/DOID:2340"
                    }
                ],
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            },
            {
                "disease_id": "DOID:5426",
                "name": "primary ovarian insufficiency",
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                "url": "https://disease-ontology.org/term/DOID:5426",
                "evidence": [
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5426"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "cilium",
                "id": "GO:0005929",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005929",
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                    {
                        "database": "UniProtKB",
                        "id": "B7YZM8",
                        "url": "https://www.uniprot.org/uniprotkb/B7YZM8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
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                    {
                        "database": "UniProtKB",
                        "id": "B7YZM8",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "BBSome",
                "id": "GO:0034464",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034464",
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                    {
                        "database": "UniProtKB",
                        "id": "B7YZM8",
                        "url": "https://www.uniprot.org/uniprotkb/B7YZM8"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cilium assembly",
                "id": "GO:0060271",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060271",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7YZM8",
                        "url": "https://www.uniprot.org/uniprotkb/B7YZM8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "B7YZM8-1"
    },
    {
        "uniprot_canonical_ac": "B7YZN3-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7YZN3",
                        "url": "https://www.uniprot.org/uniprotkb/B7YZN3"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 202,
        "chemical_mass": 23493.0,
        "gene_names": "Dmel\\CG42364;CG15675;CG42364;Dmel\\CG42364;Dmel_CG42364",
        "protein_name": "",
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        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "B7YZN3-1"
    },
    {
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                        "id": "B7YZQ6",
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                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
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        ],
        "length": 574,
        "chemical_mass": 66287.0,
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            {
                "name": "detection of chemical stimulus",
                "id": "GO:0009593",
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                "evidence": [
                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "ligand-gated monoatomic ion channel activity",
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                    {
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                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
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                    {
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                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
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                ],
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        ],
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            {
                "name": "nucleus",
                "id": "GO:0005634",
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                    {
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                        "id": "B7YZU6",
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                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
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                    {
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                        "id": "B7YZU6",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "lipid droplet",
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                    {
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                        "id": "B7YZU6",
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                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "lipid transport",
                "id": "GO:0006869",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006869",
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                    {
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                        "id": "B7YZU6",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule-based movement",
                "id": "GO:0007018",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007018",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7YZU6",
                        "url": "https://www.uniprot.org/uniprotkb/B7YZU6"
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                ],
                "pmid": ""
            },
            {
                "name": "lipid droplet transport along microtubule",
                "id": "GO:0031887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7YZU6",
                        "url": "https://www.uniprot.org/uniprotkb/B7YZU6"
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "kinesin binding",
                "id": "GO:0019894",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019894",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7YZU6",
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                ],
                "pmid": ""
            }
        ],
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    {
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                "name": "Drosophila melanogaster",
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                        "id": "B7Z0E0",
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
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        ],
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        "chemical_mass": 53643.0,
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        "protein_name": "Isocitrate dehydrogenase [NADP]",
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                "disease_id": "DOID:0050575",
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                        "id": "0050575",
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                        "id": "0050908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050908"
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                ],
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                "name": "cancer",
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                "url": "https://disease-ontology.org/term/DOID:162",
                "evidence": [
                    {
                        "id": "162",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:162"
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                ],
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            },
            {
                "disease_id": "DOID:3068",
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                "description": "A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes.",
                "url": "https://disease-ontology.org/term/DOID:3068",
                "evidence": [
                    {
                        "id": "3068",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3068"
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                ],
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            },
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                "disease_id": "DOID:3070",
                "name": "high grade glioma",
                "description": "A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine.",
                "url": "https://disease-ontology.org/term/DOID:3070",
                "evidence": [
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                        "id": "3070",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3070"
                    }
                ],
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            },
            {
                "disease_id": "DOID:3907",
                "name": "lung squamous cell carcinoma",
                "description": "A non-small cell lung carcinoma that has_material_basis_in the squamous cell.",
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                "evidence": [
                    {
                        "id": "3907",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3907"
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                ],
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            {
                "disease_id": "DOID:3910",
                "name": "lung adenocarcinoma",
                "description": "A lung non-small cell carcinoma that derives_from epithelial cells of glandular origin.",
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                "evidence": [
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                        "id": "3910",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3910"
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                ],
                "weight": 0.0
            },
            {
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                "name": "autoimmune disease",
                "description": "An immune system disease that is an overactive immune response of the body against substances and tissues normally present in the body resulting from an abnormal functioning of the immune system that results in the production of antibodies or T cell directed against the host tissues.",
                "url": "https://disease-ontology.org/term/DOID:417",
                "evidence": [
                    {
                        "id": "417",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:417"
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                ],
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            },
            {
                "disease_id": "DOID:5016",
                "name": "hepatocellular clear cell carcinoma",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:5016",
                "evidence": [
                    {
                        "id": "5016",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5016"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9119",
                "name": "acute myeloid leukemia",
                "description": "A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells.",
                "url": "https://disease-ontology.org/term/DOID:9119",
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                    {
                        "id": "9119",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9119"
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                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "NADP+ metabolic process",
                "id": "GO:0006739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tricarboxylic acid cycle",
                "id": "GO:0006099",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006099",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "isocitrate metabolic process",
                "id": "GO:0006102",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006102",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellular response to oxidative stress",
                "id": "GO:0034599",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034599",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glyoxylate cycle",
                "id": "GO:0006097",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006097",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "magnesium ion binding",
                "id": "GO:0000287",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000287",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "NAD binding",
                "id": "GO:0051287",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051287",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "isocitrate dehydrogenase (NADP+) activity",
                "id": "GO:0004450",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004450",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial matrix",
                "id": "GO:0005759",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005759",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "peroxisome",
                "id": "GO:0005777",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005777",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "B7Z0E0-1"
    },
    {
        "uniprot_canonical_ac": "B7Z0E3-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0E3",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0E3"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 323,
        "chemical_mass": 37840.0,
        "gene_names": "CT32600;Dmel\\CG13305;BcDNA:RE33542;CG13305;CT32600;Dmel\\CG13305;Dmel_CG13305",
        "protein_name": "",
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        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "B7Z0E3-1"
    },
    {
        "uniprot_canonical_ac": "B7Z0K3-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0K3",
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                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 455,
        "chemical_mass": 51193.0,
        "gene_names": "Dmel\\CG14866;CG14866;Dmel\\CG14866;Dmel_CG14866",
        "protein_name": "C-type lectin domain-containing protein",
        "disease": [
            {
                "disease_id": "DOID:0050598",
                "name": "extrapulmonary tuberculosis",
                "description": "A tuberculosis that occurs at body sites other than the lung.",
                "url": "https://disease-ontology.org/term/DOID:0050598",
                "evidence": [
                    {
                        "id": "0050598",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050598"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050827",
                "name": "rheumatic heart disease",
                "description": "A heart valve disease that is characterized by repeated inflammation with fibrinous repair caused by an autoimmune reaction to Group A beta-hemolytic streptococci (GAS) that results in valvular damage. The cardinal anatomic changes of the valve include leaflet thickening, commissural fusion, and shortening and thickening of the tendinous cords.",
                "url": "https://disease-ontology.org/term/DOID:0050827",
                "evidence": [
                    {
                        "id": "0050827",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050827"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080599",
                "name": "Coronavirus infectious disease",
                "description": "A viral infectious disease that has_material_basis_in Coronavirus.",
                "url": "https://disease-ontology.org/term/DOID:0080599",
                "evidence": [
                    {
                        "id": "0080599",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080599"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11650",
                "name": "bronchopulmonary dysplasia",
                "description": "A lung disease that is characterized by underdeveloped lungs in newborns that can be easily irritated or inflamed after birth resulting in damage to the alveoli of the lungs and bronchi. Most newborns who develop BPD are born more than 10 weeks before their due dates, weigh less than 2 pounds at birth, and have breathing problems.",
                "url": "https://disease-ontology.org/term/DOID:11650",
                "evidence": [
                    {
                        "id": "11650",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11650"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12205",
                "name": "dengue disease",
                "description": "A viral infectious disease that results in infection, has_material_basis_in Dengue virus (Orthoflavivirus denguei), which are transmitted by Aedes mosquito bite. The infection has symptom fever, has symptom severe headache, has symptom severe pain behind the eyes, has symptom joint pain, has symptom muscle and bone pain, has symptom rash, and has symptom mild bleeding.",
                "url": "https://disease-ontology.org/term/DOID:12205",
                "evidence": [
                    {
                        "id": "12205",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12205"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12206",
                "name": "dengue hemorrhagic fever",
                "description": "A dengue disease that occurs when a person experiences a second infection with a heterologous Dengue virus (Orthoflavivirus denguei) serotype, which is transmitted_by Aedes mosquito bite. The infection has_symptom hemorrhagic lesions of the skin, has_symptom thrombocytopenia, has_symptom reduction in the fluid part of the blood, and has_symptom high fever. Four distinct Dengue virus serotypes have been identified.",
                "url": "https://disease-ontology.org/term/DOID:12206",
                "evidence": [
                    {
                        "id": "12206",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12206"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13564",
                "name": "aspergillosis",
                "description": "An opportunistic mycosis that involves a spectrum of diseases of humans and animals caused by members of the genus Aspergillus infecting lungs, brain, kidney, heart, bone, eyes, sinuses, skin and gastrointestinal tract. It is a serious illnesses in people with a weakened immune system.",
                "url": "https://disease-ontology.org/term/DOID:13564",
                "evidence": [
                    {
                        "id": "13564",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13564"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing.",
                "url": "https://disease-ontology.org/term/DOID:2841",
                "evidence": [
                    {
                        "id": "2841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2957",
                "name": "pulmonary tuberculosis",
                "description": "A tuberculosis that is a contagious disease located_in lungs. The infection has_symptom fever, has_symptom cough, has_symptom difficulty in breathing, has_symptom inflammatory infiltrations, has_symptom formation of tubercles, has_symptom caseation, has_symptom pleural effusion, and has_symptom fibrosis.",
                "url": "https://disease-ontology.org/term/DOID:2957",
                "evidence": [
                    {
                        "id": "2957",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2957"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:399",
                "name": "tuberculosis",
                "description": "A primary bacterial infectious disease that is located_in lungs, located_in lymph nodes, located_in pericardium, located_in brain, located_in pleura or located_in gastrointestinal tract, has_material_basis_in Mycobacterium tuberculosis, which is transmitted_by droplets released into the air when an infected person coughs or sneezes.",
                "url": "https://disease-ontology.org/term/DOID:399",
                "evidence": [
                    {
                        "id": "399",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:399"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:526",
                "name": "human immunodeficiency virus infectious disease",
                "description": "A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 (Lentivirus humimdef1) or Human immunodeficiency virus 2 (Lentivirus humimdef2), which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands.",
                "url": "https://disease-ontology.org/term/DOID:526",
                "evidence": [
                    {
                        "id": "526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:526"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:635",
                "name": "acquired immunodeficiency syndrome",
                "description": "A Human immunodeficiency virus infectious disease that results_in reduction in the numbers of CD4-bearing helper T cells below 200 per microliter of blood or 14% of all lymphocytes thereby rendering the subject highly vulnerable to life-threatening infections and cancers, has_material_basis_in Human immunodeficiency virus 1 (Lentivirus humimdef1) or Human immunodeficiency virus 2 (Lentivirus humimdef2), which are transmitted_by sexual contact, transmitted_by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted_by congenital method, and transmitted_by contaminated needles. Opportunistic infections are common in people with AIDS.",
                "url": "https://disease-ontology.org/term/DOID:635",
                "evidence": [
                    {
                        "id": "635",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:635"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6432",
                "name": "pulmonary hypertension",
                "description": "A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries.",
                "url": "https://disease-ontology.org/term/DOID:6432",
                "evidence": [
                    {
                        "id": "6432",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6432"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "immune response",
                "id": "GO:0006955",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006955",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0K3",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0K3"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "external side of plasma membrane",
                "id": "GO:0009897",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009897",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0K3",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0K3"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "carbohydrate binding",
                "id": "GO:0030246",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030246",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0K3",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0K3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "pattern recognition receptor activity",
                "id": "GO:0038187",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0038187",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0K3",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0K3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "B7Z0K3-1"
    },
    {
        "uniprot_canonical_ac": "B7Z0L3-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0L3",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0L3"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 282,
        "chemical_mass": 31019.0,
        "gene_names": "CG5240;CG31266;CG5240;Dmel\\CG31266;Dmel_CG31266;SPH146a;SPH146",
        "protein_name": "Peptidase S1 domain-containing protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "endopeptidase activity",
                "id": "GO:0004175",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004175",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0L3",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0L3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "serine-type peptidase activity",
                "id": "GO:0008236",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008236",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0L3",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0L3"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0L3",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0L3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0L3",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0L3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein processing",
                "id": "GO:0016485",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016485",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0L3",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0L3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "B7Z0L3-1"
    },
    {
        "uniprot_canonical_ac": "B7Z0S9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0S9",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0S9"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 243,
        "chemical_mass": 27841.0,
        "gene_names": "GstD11;BcDNA:RE72392;CG17639;DmGSTD11;Dmel\\CG17639;Dmel_CG17639;GSTD11;GstD11;cg17639;gstd11",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "glutathione transferase activity",
                "id": "GO:0004364",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004364",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0S9",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0S9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glutathione peroxidase activity",
                "id": "GO:0004602",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004602",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0S9",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0S9"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0S9",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0S9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "glutathione metabolic process",
                "id": "GO:0006749",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006749",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0S9",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0S9"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "B7Z0S9-1"
    },
    {
        "uniprot_canonical_ac": "B7Z0X5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0X5",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0X5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 608,
        "chemical_mass": 71243.0,
        "gene_names": "Ir7e;7e;CG15327;CG42293;DmelIR7e;Dmel\\CG42293;Dmel_CG42293;IR7e;Ir7e",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "detection of chemical stimulus",
                "id": "GO:0009593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009593",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0X5",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0X5"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0X5",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0X5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0X5",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0X5"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "ligand-gated monoatomic ion channel activity",
                "id": "GO:0015276",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015276",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0X5",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0X5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "B7Z0X5-1"
    },
    {
        "uniprot_canonical_ac": "E1JH12-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JH12",
                        "url": "https://www.uniprot.org/uniprotkb/E1JH12"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 67,
        "chemical_mass": 7996.0,
        "gene_names": "Dmel\\CG42615;CG42615;Dmel\\CG42615;Dmel_CG42615;gft",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "E1JH12-1"
    },
    {
        "uniprot_canonical_ac": "E1JHF6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JHF6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JHF6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 91,
        "chemical_mass": 10709.0,
        "gene_names": "Dmel\\CG42470;CG42470;Dmel\\CG42470;Dmel_CG42470",
        "protein_name": "Seminal fluid protein",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "E1JHF6-1"
    },
    {
        "uniprot_canonical_ac": "E1JHF9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JHF9",
                        "url": "https://www.uniprot.org/uniprotkb/E1JHF9"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 215,
        "chemical_mass": 24011.0,
        "gene_names": "Dmel\\CG14932;CG14932;Dmel\\CG14932;Dmel_CG14932",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "E1JHF9-1",
                "start_pos": "149",
                "end_pos": "149",
                "site_lbl": "Thr149",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 149,
                        "start_aa": "Thr",
                        "end_pos": 149,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr149",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "E1JHF9-1"
    },
    {
        "uniprot_canonical_ac": "E1JHS7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JHS7",
                        "url": "https://www.uniprot.org/uniprotkb/E1JHS7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 82,
        "chemical_mass": 9623.0,
        "gene_names": "Dmel\\CG42467;CG42467;Dmel\\CG42467;Dmel_CG42467",
        "protein_name": "Seminal fluid protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "serine-type endopeptidase inhibitor activity",
                "id": "GO:0004867",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004867",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JHS7",
                        "url": "https://www.uniprot.org/uniprotkb/E1JHS7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "E1JHS7-1"
    },
    {
        "uniprot_canonical_ac": "E1JHT4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JHT4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JHT4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 496,
        "chemical_mass": 54978.0,
        "gene_names": "Dmel\\CG12194;anon-EST:Posey105;CG12194;Dmel\\CG12194;Dmel_CG12194;anon-EST:Posey105",
        "protein_name": "Lysosomal dipeptide transporter MFSD1",
        "disease": [],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JHT4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JHT4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "lysosome",
                "id": "GO:0005764",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005764",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JHT4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JHT4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "lysosomal membrane",
                "id": "GO:0005765",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005765",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JHT4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JHT4"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane transporter activity",
                "id": "GO:0022857",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022857",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JHT4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JHT4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "transmembrane transport",
                "id": "GO:0055085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055085",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JHT4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JHT4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "E1JHT4-1"
    },
    {
        "uniprot_canonical_ac": "E1JJ15-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JJ15",
                        "url": "https://www.uniprot.org/uniprotkb/E1JJ15"
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                ]
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                ],
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                ],
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        ],
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    {
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                ],
                "common_name": "Fruit fly",
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        ],
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                ],
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        ],
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    {
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                "name": "Drosophila melanogaster",
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                ],
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        ],
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                "name": "mitochondrial inner membrane",
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        ],
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                "name": "mitochondrial electron transport, ubiquinol to cytochrome c",
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        ],
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        ],
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            {
                "disease_id": "DOID:0060037",
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                "url": "https://disease-ontology.org/term/DOID:0060037",
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                    {
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                ],
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        ],
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            {
                "name": "establishment of apical/basal cell polarity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035089",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                ],
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            },
            {
                "name": "synapse assembly",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007416",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                ],
                "pmid": ""
            },
            {
                "name": "adherens junction organization",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034332",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of filopodium assembly",
                "id": "GO:0051490",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051490",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "branching involved in open tracheal system development",
                "id": "GO:0060446",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060446",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "asymmetric neuroblast division",
                "id": "GO:0055059",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055059",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "zonula adherens assembly",
                "id": "GO:0045186",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045186",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "photoreceptor cell morphogenesis",
                "id": "GO:0008594",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008594",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "establishment or maintenance of epithelial cell apical/basal polarity",
                "id": "GO:0045197",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045197",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "asymmetric protein localization involved in cell fate determination",
                "id": "GO:0045167",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045167",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "follicle cell of egg chamber-cell adhesion",
                "id": "GO:0007299",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007299",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Malpighian tubule development",
                "id": "GO:0072002",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072002",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "germarium-derived oocyte fate determination",
                "id": "GO:0007294",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007294",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "border follicle cell migration",
                "id": "GO:0007298",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007298",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "oocyte anterior/posterior axis specification",
                "id": "GO:0007314",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007314",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                ],
                "pmid": ""
            },
            {
                "name": "germ-band extension",
                "id": "GO:0007377",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007377",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                ],
                "pmid": ""
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            {
                "name": "oocyte microtubule cytoskeleton organization",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016325",
                "evidence": [
                    {
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                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                ],
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            {
                "name": "border follicle cell delamination",
                "id": "GO:0030709",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030709",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                ],
                "pmid": ""
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            {
                "name": "cell adhesion",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007155",
                "evidence": [
                    {
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                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                ],
                "pmid": ""
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            {
                "name": "positive regulation of Notch signaling pathway",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045747",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
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            {
                "name": "intracellular protein localization",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008104",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                ],
                "pmid": ""
            },
            {
                "name": "microtubule cytoskeleton organization",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000226",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                "pmid": ""
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            {
                "name": "establishment of cell polarity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030010",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                ],
                "pmid": ""
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            {
                "name": "establishment or maintenance of cell polarity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007163",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
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            {
                "name": "axis elongation",
                "id": "GO:0003401",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003401",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
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                ],
                "pmid": ""
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            {
                "name": "regulation of establishment of planar polarity",
                "id": "GO:0090175",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090175",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "apical protein localization",
                "id": "GO:0045176",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045176",
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                        "id": "Q0KHR3",
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                ],
                "pmid": ""
            }
        ],
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                "name": "adherens junction",
                "id": "GO:0005912",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005912",
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                ],
                "pmid": ""
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                "name": "apical plasma membrane",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "apical junction complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043296",
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                        "id": "Q0KHR3",
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                ],
                "pmid": ""
            },
            {
                "name": "zonula adherens",
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                "pmid": ""
            },
            {
                "name": "spot adherens junction",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005914",
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                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasmic side of apical plasma membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098592",
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                    {
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                        "id": "Q0KHR3",
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                ],
                "pmid": ""
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            {
                "name": "cell cortex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005938",
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                        "id": "Q0KHR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHR3"
                    }
                ],
                "pmid": ""
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                "name": "PAR polarity complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0120157",
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                        "id": "Q0KHR3",
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                        "id": "Q0KHR3",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "phosphatidic acid binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070300",
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                "name": "Drosophila melanogaster",
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                ],
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                ],
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                "name": "Down syndrome",
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                "url": "https://disease-ontology.org/term/DOID:14250",
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                ],
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        ],
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                "name": "regulation of axonogenesis",
                "id": "GO:0050770",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050770",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/Q0E9H9"
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                ],
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                "name": "central nervous system morphogenesis",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0021551",
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                        "id": "Q0E9H9",
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            },
            {
                "name": "detection of mechanical stimulus involved in sensory perception of touch",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050976",
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                    {
                        "database": "UniProtKB",
                        "id": "Q0E9H9",
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                    }
                ],
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            },
            {
                "name": "cell adhesion",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007155",
                "evidence": [
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                        "id": "Q0E9H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E9H9"
                    }
                ],
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            },
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048814",
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                ],
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                "name": "phagocytosis",
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                        "id": "Q0E9H9",
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                        "url": "https://www.uniprot.org/uniprotkb/Q0E9H9"
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                ],
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                "name": "axonal fasciculation",
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                        "id": "Q0E9H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E9H9"
                    }
                ],
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            },
            {
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                        "id": "Q0E9H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E9H9"
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                "pmid": ""
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007411",
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                ],
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                "name": "dendrite self-avoidance",
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                        "id": "Q0E9H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E9H9"
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                ],
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            },
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032490",
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                        "database": "UniProtKB",
                        "id": "Q0E9H9",
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                ],
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                        "id": "Q0E9H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E9H9"
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                ],
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007419",
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                ],
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                "name": "mushroom body development",
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                        "url": "https://www.uniprot.org/uniprotkb/Q0E9H9"
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                "pmid": ""
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                "pmid": ""
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                "name": "neuronal cell body",
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                "name": "perikaryon",
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                ],
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                "name": "neuron projection",
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        ],
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                        "database": "UniProtKB",
                        "id": "Q0E9H9",
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                        "database": "UniProtKB",
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                            }
                        ]
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                ]
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                "uniprot_canonical_ac": "Q0E9H9-1",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
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                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 755,
                        "start_aa": "Thr",
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                        "end_aa": "Thr",
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                        "site_lbl": "Thr755",
                        "evidence": [
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                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
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            {
                "uniprot_canonical_ac": "Q0E9H9-1",
                "start_pos": "820",
                "end_pos": "820",
                "site_lbl": "Asn820",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
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                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
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                        "comment": "N-linked (GlcNAc...) asparagine",
                        "icn3d_view": {},
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                        "start_aa": "Asn",
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                        "residue": "Asn",
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                                "id": "Q0E9H9",
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                            },
                            {
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                ]
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            {
                "uniprot_canonical_ac": "Q0E9H9-1",
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                "site_lbl": "Arg530",
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                "mutagenesis": [
                    {
                        "sequence_org": "R",
                        "sequence_mut": "W",
                        "comment": "In DscamR496W; loss of function probably due to disruption of the intramolecular binding interface between Ig-like domains 5 and 6; dorsal lobe nerve tract does not form and the medial lobe fails to extend to the midline.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
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                            },
                            {
                                "database": "PubMed",
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                    }
                ]
            }
        ],
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    {
        "uniprot_canonical_ac": "Q9VB15-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "chemical_mass": 77997.0,
        "gene_names": "tau;BcDNA:RE16764;CG12881;CG31057;CG31058;CG34294;CG45110;CG5606;Dmel\\CG45110;Dmel_CG45110;Tau;d-tau;dTAU;dTau;dtau;tao;tau",
        "protein_name": "Microtubule-associated protein",
        "disease": [
            {
                "disease_id": "DOID:0050741",
                "name": "alcohol dependence",
                "description": "A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol.",
                "url": "https://disease-ontology.org/term/DOID:0050741",
                "evidence": [
                    {
                        "id": "0050741",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050741"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0051060",
                "name": "frontotemporal dementia 1",
                "description": "A frontotemporal dementia that has_material_basis_in heterozygous mutation in the MAPT gene, which encodes microtubule-associated protein tau, on chromosome 17q21.",
                "url": "https://disease-ontology.org/term/DOID:0051060",
                "evidence": [
                    {
                        "id": "0051060",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0051060"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0060892",
                "name": "late onset Parkinson's disease",
                "description": "A Parkinson's disease characterized by onset of motor symptoms typically after 60 years of age.",
                "url": "https://disease-ontology.org/term/DOID:0060892",
                "evidence": [
                    {
                        "id": "0060892",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060892"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080855",
                "name": "Parkinsonism",
                "description": "A movement disorder that is characterized by disturbances of balance, gait and posture.",
                "url": "https://disease-ontology.org/term/DOID:0080855",
                "evidence": [
                    {
                        "id": "0080855",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080855"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081292",
                "name": "traumatic brain injury",
                "description": "A brain disease that is characterized by brain dysfunction caused by an outside force, usually a violent blow to the head.",
                "url": "https://disease-ontology.org/term/DOID:0081292",
                "evidence": [
                    {
                        "id": "0081292",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081292"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10914",
                "name": "amnestic disorder",
                "description": "A cognitive disorder where the memory is disturbed or lost and involves the loss of memories previously established, loss of the ability to create new memories, or loss of the ability to learn new information.",
                "url": "https://disease-ontology.org/term/DOID:10914",
                "evidence": [
                    {
                        "id": "10914",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10914"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11870",
                "name": "Pick's disease",
                "description": "A frontotemporal dementia that is characterized by a spectrum of neuropsychiatric symptoms ranging from those that affect the patient's personality to those that cause a decline in cognitive function.",
                "url": "https://disease-ontology.org/term/DOID:11870",
                "evidence": [
                    {
                        "id": "11870",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11870"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11949",
                "name": "Creutzfeldt-Jakob disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11949",
                "evidence": [
                    {
                        "id": "11949",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11949"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1289",
                "name": "neurodegenerative disease",
                "description": "A central nervous system disease that results in the progressive deterioration of function or structure of neurons.",
                "url": "https://disease-ontology.org/term/DOID:1289",
                "evidence": [
                    {
                        "id": "1289",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1289"
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1307",
                "name": "dementia",
                "description": "A cognitive disorder resulting from a loss of brain function affecting memory, thinking, language, judgement and behavior.",
                "url": "https://disease-ontology.org/term/DOID:1307",
                "evidence": [
                    {
                        "id": "1307",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1307"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14330",
                "name": "Parkinson's disease",
                "description": "A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions.",
                "url": "https://disease-ontology.org/term/DOID:14330",
                "evidence": [
                    {
                        "id": "14330",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14330"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1561",
                "name": "cognitive disorder",
                "description": "A disease of mental health that affects cognitive functions including memory processing, perception and problem solving.",
                "url": "https://disease-ontology.org/term/DOID:1561",
                "evidence": [
                    {
                        "id": "1561",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1561"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1826",
                "name": "epilepsy",
                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.",
                "url": "https://disease-ontology.org/term/DOID:1826",
                "evidence": [
                    {
                        "id": "1826",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1826"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2316",
                "name": "brain ischemia",
                "description": "An ischemia that is characterized by insufficient blood flow to the brain to meet metabolic demand.",
                "url": "https://disease-ontology.org/term/DOID:2316",
                "evidence": [
                    {
                        "id": "2316",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2316"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:332",
                "name": "amyotrophic lateral sclerosis",
                "description": "A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.",
                "url": "https://disease-ontology.org/term/DOID:332",
                "evidence": [
                    {
                        "id": "332",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:332"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3328",
                "name": "temporal lobe epilepsy",
                "description": "A focal epilepsy that is characterized by recurrent, unprovoked focal seizures that originate in the temporal lobe of the brain and last about one or two minutes.",
                "url": "https://disease-ontology.org/term/DOID:3328",
                "evidence": [
                    {
                        "id": "3328",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3328"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3525",
                "name": "middle cerebral artery infarction",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3525",
                "evidence": [
                    {
                        "id": "3525",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3525"
                    }
                ],
                "weight": 0.0
            },
            {
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                "name": "progressive supranuclear palsy",
                "description": "A movement disease that is characterized by serious and progressive problems with control of gait and balance, along with complex eye movement and thinking problems. It involves gradual deterioration and death of specific volumes of the brain.",
                "url": "https://disease-ontology.org/term/DOID:678",
                "evidence": [
                    {
                        "id": "678",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:678"
                    }
                ],
                "weight": 0.0
            },
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                "name": "tauopathy",
                "description": "A neurodegenerative disease that has_material_basis_in the pathological aggregation of tau protein in so-called neurofibrillary tangles (NFT) in the human brain.",
                "url": "https://disease-ontology.org/term/DOID:680",
                "evidence": [
                    {
                        "id": "680",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:680"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8725",
                "name": "vascular dementia",
                "description": "A dementia that involves impairments in cognitive function caused by problems in blood vessels that feed the brain.",
                "url": "https://disease-ontology.org/term/DOID:8725",
                "evidence": [
                    {
                        "id": "8725",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8725"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9255",
                "name": "frontotemporal dementia",
                "description": "A dementia characterized by progressive neuronal loss predominantly involving the frontal and/or temporal lobes of the brain resulting in a gradual and progressive decline in behavior or language.",
                "url": "https://disease-ontology.org/term/DOID:9255",
                "evidence": [
                    {
                        "id": "9255",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9255"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9970",
                "name": "obesity",
                "description": "An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness.",
                "url": "https://disease-ontology.org/term/DOID:9970",
                "evidence": [
                    {
                        "id": "9970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9970"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "microtubule",
                "id": "GO:0005874",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005874",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB15",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB15"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axon",
                "id": "GO:0030424",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030424",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB15",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB15"
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                ],
                "pmid": ""
            },
            {
                "name": "dendrite",
                "id": "GO:0030425",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030425",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "Q9VB15",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB15"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoskeleton",
                "id": "GO:0005856",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005856",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB15",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB15"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron projection",
                "id": "GO:0043005",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043005",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB15",
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                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "microtubule binding",
                "id": "GO:0008017",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008017",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB15",
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                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "microtubule cytoskeleton organization",
                "id": "GO:0000226",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000226",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB15",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB15"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "rhabdomere morphogenesis",
                "id": "GO:0061541",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061541",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB15",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB15"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron projection development",
                "id": "GO:0031175",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031175",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB15",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB15"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "branching involved in open tracheal system development",
                "id": "GO:0060446",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060446",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "Q9VB15",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "lumen formation, open tracheal system",
                "id": "GO:0035149",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035149",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB15",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB15"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9VB15-1",
                "start_pos": "486",
                "end_pos": "486",
                "site_lbl": "Thr486",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 486,
                        "start_aa": "Thr",
                        "end_pos": 486,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr486",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "Q9VB15-1"
    },
    {
        "uniprot_canonical_ac": "Q9V435-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 890,
        "chemical_mass": 101860.0,
        "gene_names": "yuri;BG:DS05639.1;BG:DS07851.11;CG11860;CG12635;CG31732;Dmel\\CG31732;Dmel_CG31732;Yuri;yuri",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "nuclear envelope",
                "id": "GO:0005635",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005635",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear lamina",
                "id": "GO:0005652",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005652",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "investment cone",
                "id": "GO:0070865",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070865",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "gravitaxis",
                "id": "GO:0042332",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042332",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein localization to nuclear envelope",
                "id": "GO:0090435",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090435",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear envelope organization",
                "id": "GO:0006998",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006998",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sperm individualization",
                "id": "GO:0007291",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007291",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "heterochromatin formation",
                "id": "GO:0031507",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031507",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear migration",
                "id": "GO:0007097",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007097",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ciliary basal body organization",
                "id": "GO:0032053",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032053",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear pore localization",
                "id": "GO:0051664",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051664",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "structural constituent of cytoskeleton",
                "id": "GO:0005200",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005200",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V435",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V435"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9V435-1"
    },
    {
        "uniprot_canonical_ac": "Q9VHR2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHR2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHR2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1876,
        "chemical_mass": 206681.0,
        "gene_names": "CG11729;CG42286;CT32186;GS3056;MRE1;anon-EST:Posey178;43462;BcDNA:AT05815;BcDNA:GH22170;CG11718;CG11729;CG11730;CG11731;CG11733;CG31264;CG31369;CG31462;CG42285;CG42286;CG43462;CG45263;CT32186;Dmel\\CG45263;Dmel_CG45263;GH22170;GS3056;MRE1;anon-EST:Posey178",
        "protein_name": "Ig-like domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHR2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHR2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHR2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHR2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell-cell junction",
                "id": "GO:0005911",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005911",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHR2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHR2"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "cell adhesion molecule binding",
                "id": "GO:0050839",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050839",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHR2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHR2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cell-cell adhesion",
                "id": "GO:0098609",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098609",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHR2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHR2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9VHR2-1",
                "start_pos": "1617",
                "end_pos": "1617",
                "site_lbl": "Thr1617",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1617,
                        "start_aa": "Thr",
                        "end_pos": 1617,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1617",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q9VHR2-1",
                "start_pos": "1652",
                "end_pos": "1652",
                "site_lbl": "Thr1652",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1652,
                        "start_aa": "Thr",
                        "end_pos": 1652,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1652",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q9VHR2-1",
                "start_pos": "1838",
                "end_pos": "1838",
                "site_lbl": "Thr1838",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1838,
                        "start_aa": "Thr",
                        "end_pos": 1838,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1838",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q9VHR2-1",
                "start_pos": "326",
                "end_pos": "326",
                "site_lbl": "Ser326",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "G49108TO",
                        "type": "O-linked",
                        "subtype": "O-GlcNAcylation",
                        "prediction_tool_list": [],
                        "site_category": "reported_with_glycan",
                        "site_category_dict": {
                            "reported_with_glycan": true
                        },
                        "site_seq": "S",
                        "relation": "attached",
                        "comment": "O-GlcNAcylation",
                        "icn3d_view": {},
                        "start_pos": 326,
                        "start_aa": "Ser",
                        "end_pos": 326,
                        "end_aa": "Ser",
                        "residue": "Ser",
                        "site_lbl": "Ser326",
                        "evidence": [
                            {
                                "id": "40245499",
                                "database": "PubMed",
                                "url": "https://glygen.org/publication/PubMed/40245499"
                            },
                            {
                                "id": "Q9VHR2",
                                "database": "O-GlcNAc Database",
                                "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q9VHR2"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q9VHR2-1",
                "start_pos": "334",
                "end_pos": "334",
                "site_lbl": "Thr334",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "G49108TO",
                        "type": "O-linked",
                        "subtype": "O-GlcNAcylation",
                        "prediction_tool_list": [],
                        "site_category": "reported_with_glycan",
                        "site_category_dict": {
                            "reported_with_glycan": true
                        },
                        "site_seq": "T",
                        "relation": "attached",
                        "comment": "O-GlcNAcylation",
                        "icn3d_view": {},
                        "start_pos": 334,
                        "start_aa": "Thr",
                        "end_pos": 334,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr334",
                        "evidence": [
                            {
                                "id": "40245499",
                                "database": "PubMed",
                                "url": "https://glygen.org/publication/PubMed/40245499"
                            },
                            {
                                "id": "Q9VHR2",
                                "database": "O-GlcNAc Database",
                                "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q9VHR2"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "Q9VHR2-1"
    },
    {
        "uniprot_canonical_ac": "M9NFQ7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NFQ7",
                        "url": "https://www.uniprot.org/uniprotkb/M9NFQ7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 962,
        "chemical_mass": 96880.0,
        "gene_names": "Rbfox1;A2BP1;A2bp1;BcDNA:GM06073;CG14155;CG18441;CG32062;Dmel\\CG32062;Dmel_CG32062;Rbfox1;Rbox1;cg18441;dA2BP1;rbfox1",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:1059",
                "name": "intellectual disability",
                "description": "A specific developmental disorder that involves significant limitations both in mental functioning and in adaptive behavior such as communicating, taking care of him or herself, and social skills.",
                "url": "https://disease-ontology.org/term/DOID:1059",
                "evidence": [
                    {
                        "id": "1059",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1059"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11722",
                "name": "myotonic dystrophy type 1",
                "description": "A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region.",
                "url": "https://disease-ontology.org/term/DOID:11722",
                "evidence": [
                    {
                        "id": "11722",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11722"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12930",
                "name": "dilated cardiomyopathy",
                "description": "An intrinsic cardiomyopathy that is characterized by an an enlarged heart and damage to the myocardium causing the heart to pump blood inefficiently.",
                "url": "https://disease-ontology.org/term/DOID:12930",
                "evidence": [
                    {
                        "id": "12930",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12930"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1574",
                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:1574",
                "evidence": [
                    {
                        "id": "1574",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1574"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1682",
                "name": "congenital heart disease",
                "description": "A physical disorder that is characterized by problems with the heart's structure that are present at birth.",
                "url": "https://disease-ontology.org/term/DOID:1682",
                "evidence": [
                    {
                        "id": "1682",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1682"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3454",
                "name": "brain infarction",
                "description": "A cerebrovascular disease that is characterized by tissue necrosis located_in the brain, resulting from inadequate blood flow through the brain.",
                "url": "https://disease-ontology.org/term/DOID:3454",
                "evidence": [
                    {
                        "id": "3454",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3454"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3525",
                "name": "middle cerebral artery infarction",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3525",
                "evidence": [
                    {
                        "id": "3525",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3525"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9955",
                "name": "hypoplastic left heart syndrome",
                "description": "A congenital heart disease characterized by abnormal development of the left-sided structures of the heart.",
                "url": "https://disease-ontology.org/term/DOID:9955",
                "evidence": [
                    {
                        "id": "9955",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9955"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NFQ7",
                        "url": "https://www.uniprot.org/uniprotkb/M9NFQ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleoplasm",
                "id": "GO:0005654",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NFQ7",
                        "url": "https://www.uniprot.org/uniprotkb/M9NFQ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NFQ7",
                        "url": "https://www.uniprot.org/uniprotkb/M9NFQ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear stress granule",
                "id": "GO:0097165",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097165",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NFQ7",
                        "url": "https://www.uniprot.org/uniprotkb/M9NFQ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleolus",
                "id": "GO:0005730",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005730",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NFQ7",
                        "url": "https://www.uniprot.org/uniprotkb/M9NFQ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "P-body",
                "id": "GO:0000932",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000932",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NFQ7",
                        "url": "https://www.uniprot.org/uniprotkb/M9NFQ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Cajal body",
                "id": "GO:0015030",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015030",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NFQ7",
                        "url": "https://www.uniprot.org/uniprotkb/M9NFQ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasmic stress granule",
                "id": "GO:0010494",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010494",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NFQ7",
                        "url": "https://www.uniprot.org/uniprotkb/M9NFQ7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "mRNA processing",
                "id": "GO:0006397",
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                "name": "molecular condensate scaffold activity",
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                "name": "calcium-dependent phospholipid binding",
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                "name": "plasma membrane",
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                "name": "positive regulation of stress fiber assembly",
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    },
    {
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            {
                "name": "Drosophila melanogaster",
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                    {
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        ],
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            {
                "name": "visceral mesoderm-endoderm interaction involved in midgut development",
                "id": "GO:0007495",
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                    {
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                ],
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            {
                "name": "DNA-templated transcription",
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                "name": "regulation of transcription by RNA polymerase II",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of DNA-templated transcription",
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                ],
                "pmid": ""
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            {
                "name": "midgut development",
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                ],
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                    {
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                ],
                "pmid": ""
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                "name": "defense response to virus",
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                "name": "cellular response to virus",
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                ],
                "pmid": ""
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        ],
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                "pmid": ""
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            {
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                ],
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                ],
                "pmid": ""
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            {
                "name": "DNA-binding transcription factor activity, RNA polymerase II-specific",
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                    }
                ],
                "pmid": ""
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        ],
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                ],
                "pmid": ""
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            {
                "name": "anterograde synaptic vesicle transport",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048490",
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                ],
                "pmid": ""
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            {
                "name": "axon guidance",
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                    {
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                ],
                "pmid": ""
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            {
                "name": "axon extension",
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                ],
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            {
                "name": "regulation of axon extension involved in axon guidance",
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            {
                "name": "retinal ganglion cell axon guidance",
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                "pmid": ""
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            {
                "name": "photoreceptor cell morphogenesis",
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                ],
                "pmid": ""
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                "name": "presynaptic active zone organization",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990709",
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                ],
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        ],
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                "name": "focal adhesion",
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                ],
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            {
                "name": "synapse",
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                ],
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                ],
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                "name": "protein-containing complex",
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                ],
                "pmid": ""
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            {
                "name": "presynaptic cytosol",
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                    }
                ],
                "pmid": ""
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                ],
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        ],
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        "protein_name": "",
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                "disease_id": "DOID:0070283",
                "name": "primary autosomal recessive microcephaly 13",
                "description": "A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CENPE gene on chromosome 4q24.",
                "url": "https://disease-ontology.org/term/DOID:0070283",
                "evidence": [
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                "name": "plus-end-directed microtubule motor activity",
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                    }
                ],
                "pmid": ""
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            {
                "name": "microtubule motor activity",
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                    }
                ],
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        ],
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                ],
                "pmid": ""
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            {
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                ],
                "pmid": ""
            },
            {
                "name": "kinetochore",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000776",
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                        "id": "Q9VKI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKI0"
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                "pmid": ""
            }
        ],
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                "name": "microtubule-based movement",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VKI0"
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                "pmid": ""
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                "name": "mitotic cell cycle",
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                    }
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            {
                "name": "mitotic metaphase chromosome alignment",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of cell cycle",
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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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        "protein_name": "Protein SCAI",
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            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
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                        "id": "M9PER3",
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                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transcription corepressor activity",
                "id": "GO:0003714",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003714",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER3",
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                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PER3",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER3"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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                    }
                ],
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        ],
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        "protein_name": "Zasp-like motif domain-containing protein",
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            {
                "name": "mesoderm development",
                "id": "GO:0007498",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007498",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PF57",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin cytoskeleton organization",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030036",
                "evidence": [
                    {
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                        "id": "M9PF57",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cytoplasm",
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                    {
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                        "id": "M9PF57",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "microtubule binding",
                "id": "GO:0008017",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PF57",
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                    }
                ],
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            }
        ],
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            {
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                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
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                        "residue": "Thr",
                        "site_lbl": "Thr353",
                        "evidence": [
                            {
                                "id": "GLY_001163",
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                            }
                        ]
                    }
                ]
            },
            {
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                "start_pos": "471",
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                "site_lbl": "Thr471",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
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                        "subtype": "",
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                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 471,
                        "start_aa": "Thr",
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                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr471",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "M9PF57-1",
                "start_pos": "938",
                "end_pos": "938",
                "site_lbl": "Thr938",
                "weight": 0.0,
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                    {
                        "glytoucan_ac": "",
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                        "subtype": "",
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                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 938,
                        "start_aa": "Thr",
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                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr938",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "M9PER1-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
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                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 47924.0,
        "gene_names": "Atg18a;ATG18.1;ATG18a;ATG18;Atg18A;Atg18a;Atg18;CG7986;Dmel\\CG7986;Dmel_CG7986;atg18.1;atg18a;atg18",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:12858",
                "name": "Huntington's disease",
                "description": "A neurodegenerative disease that has_material_basis_in autosomal dominant inheritance and is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities.",
                "url": "https://disease-ontology.org/term/DOID:12858",
                "evidence": [
                    {
                        "id": "12858",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12858"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "autophagosome assembly",
                "id": "GO:0000045",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000045",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "defense response to virus",
                "id": "GO:0051607",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051607",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "macroautophagy",
                "id": "GO:0016236",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016236",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellular response to starvation",
                "id": "GO:0009267",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009267",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of defense response to virus",
                "id": "GO:0050688",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050688",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glycophagy",
                "id": "GO:0061723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "larval midgut histolysis",
                "id": "GO:0035069",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035069",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "larval midgut cell programmed cell death",
                "id": "GO:0035096",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035096",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein localization to phagophore assembly site",
                "id": "GO:0034497",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034497",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "T-tubule organization",
                "id": "GO:0033292",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033292",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "autophagy of mitochondrion",
                "id": "GO:0000422",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000422",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitophagy",
                "id": "GO:0000423",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000423",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleophagy",
                "id": "GO:0044804",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0044804",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "pexophagy",
                "id": "GO:0000425",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000425",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "autophagosome",
                "id": "GO:0005776",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005776",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phagophore assembly site membrane",
                "id": "GO:0034045",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034045",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "protein-macromolecule adaptor activity",
                "id": "GO:0030674",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030674",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phosphatidylinositol-3,5-bisphosphate binding",
                "id": "GO:0080025",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0080025",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phosphatidylinositol-3-phosphate binding",
                "id": "GO:0032266",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032266",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PER1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PER1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "record_id": "M9PER1-1"
    },
    {
        "uniprot_canonical_ac": "M9PGC0-1",
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                "name": "Drosophila melanogaster",
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                        "id": "M9PGC0",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGC0"
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                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "M6;CG7540;Dmel\\CG7540;Dmel_CG7540;M6;dM6a;m6",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0110773",
                "name": "hereditary spastic paraplegia 2",
                "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2.",
                "url": "https://disease-ontology.org/term/DOID:0110773",
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                    {
                        "id": "0110773",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110773"
                    }
                ],
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            },
            {
                "disease_id": "DOID:1059",
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                "url": "https://disease-ontology.org/term/DOID:1059",
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                ],
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            },
            {
                "disease_id": "DOID:1596",
                "name": "depressive disorder",
                "description": "A mood disorder characterized by persistent sadness, emptiness, or irritability and decreased ability to function.",
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                "evidence": [
                    {
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                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1826",
                "name": "epilepsy",
                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.",
                "url": "https://disease-ontology.org/term/DOID:1826",
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                ],
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            },
            {
                "disease_id": "DOID:3210",
                "name": "Pelizaeus-Merzbacher disease",
                "description": "A hypomyelinating leukodystrophy characterized by impaired myelin formation, nystagmus, spastic quadriplegia, ataxia, and developmental delay that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.",
                "url": "https://disease-ontology.org/term/DOID:3210",
                "evidence": [
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                        "id": "3210",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3210"
                    }
                ],
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            }
        ],
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            {
                "name": "plasma membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "lateral plasma membrane",
                "id": "GO:0016328",
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                ],
                "pmid": ""
            },
            {
                "name": "tricellular tight junction",
                "id": "GO:0061689",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061689",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        ],
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            {
                "name": "oogenesis",
                "id": "GO:0048477",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048477",
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                    }
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                "name": "chitin deacetylase activity",
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                "name": "hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds",
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                "name": "calcium ion transport from cytosol to endoplasmic reticulum",
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            {
                "name": "protein tyrosine phosphatase activity",
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        "chemical_mass": 135807.0,
        "gene_names": "stumps;0837/10;10;CG18485;CG31317;CG3375;C;DOF;Dmel\\CG31317;Dmel_CG31317;Dof/stumps/heartbroken;Dof;Hbr/Dof;Hbr;P1740;Stumps;anon-EST:CL47;anon-estC;dof/hbr/sms;dof/hbr;dof1;dof;gene C;hbr;heartbroken/dof;heartbroken;i21;i28;l(3)09904;l(3)S083710;sms;stumps/dof;stumps",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:1580",
                "name": "diffuse scleroderma",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1580",
                "evidence": [
                    {
                        "id": "1580",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1580"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:418",
                "name": "systemic scleroderma",
                "description": "A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies.",
                "url": "https://disease-ontology.org/term/DOID:418",
                "evidence": [
                    {
                        "id": "418",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:418"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7188",
                "name": "autoimmune thyroiditis",
                "description": "An autoimmune disease of endocrine system that involves inflammation located_in thyroid gland caused by the immune system reacting against its own tissues.",
                "url": "https://disease-ontology.org/term/DOID:7188",
                "evidence": [
                    {
                        "id": "7188",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7188"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8893",
                "name": "psoriasis",
                "description": "A skin disease that is characterized by patches of thick red skin and silvery scales.",
                "url": "https://disease-ontology.org/term/DOID:8893",
                "evidence": [
                    {
                        "id": "8893",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8893"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9074",
                "name": "systemic lupus erythematosus",
                "description": "A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart.",
                "url": "https://disease-ontology.org/term/DOID:9074",
                "evidence": [
                    {
                        "id": "9074",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9074"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9744",
                "name": "type 1 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by destruction of pancreatic beta cells resulting in absent or extremely low insulin production.",
                "url": "https://disease-ontology.org/term/DOID:9744",
                "evidence": [
                    {
                        "id": "9744",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9744"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "glial cell development",
                "id": "GO:0021782",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0021782",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mesodermal cell migration",
                "id": "GO:0008078",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008078",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mesoderm development",
                "id": "GO:0007498",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007498",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "open tracheal system development",
                "id": "GO:0007424",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007424",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mesodermal cell fate commitment",
                "id": "GO:0001710",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001710",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "fibroblast growth factor receptor signaling pathway",
                "id": "GO:0008543",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008543",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tracheal outgrowth, open tracheal system",
                "id": "GO:0007426",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007426",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "epithelial cell migration, open tracheal system",
                "id": "GO:0007427",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007427",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "epithelial cell fate determination, open tracheal system",
                "id": "GO:0007425",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007425",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane receptor protein tyrosine kinase adaptor activity",
                "id": "GO:0005068",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005068",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "fibroblast growth factor receptor binding",
                "id": "GO:0005104",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005104",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VFI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VFI0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9VFI0-1",
                "start_pos": "1057",
                "end_pos": "1057",
                "site_lbl": "Thr1057",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1057,
                        "start_aa": "Thr",
                        "end_pos": 1057,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1057",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q9VFI0-1",
                "start_pos": "1067",
                "end_pos": "1067",
                "site_lbl": "Thr1067",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1067,
                        "start_aa": "Thr",
                        "end_pos": 1067,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1067",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "Q9VFI0-1"
    },
    {
        "uniprot_canonical_ac": "Q8MLX0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8MLX0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8MLX0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1161,
        "chemical_mass": 130934.0,
        "gene_names": "Dmel\\CG3216;CG3216;Dmel\\CG3216;Dmel_CG3216;GYC",
        "protein_name": "Guanylate cyclase",
        "disease": [
            {
                "disease_id": "DOID:0070316",
                "name": "Miura type epiphyseal chondrodysplasia",
                "description": "A bone developmental disease characterized by tall stature, scoliosis and macrodactyly of the great toes that has_material_basis_in heterozygous mutation in the NPR2 gene on chromosome 9p13.",
                "url": "https://disease-ontology.org/term/DOID:0070316",
                "evidence": [
                    {
                        "id": "0070316",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070316"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080006",
                "name": "bone development disease",
                "description": "A bone disease that results_in abnormal growth and development located_in bone or located_in cartilage.",
                "url": "https://disease-ontology.org/term/DOID:0080006",
                "evidence": [
                    {
                        "id": "0080006",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080006"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080050",
                "name": "acromesomelic dysplasia, Maroteaux type",
                "description": "An acromesomelic dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in the NPR2 gene, which encodes natriuretic peptide receptor B, on chromosome 9p13.",
                "url": "https://disease-ontology.org/term/DOID:0080050",
                "evidence": [
                    {
                        "id": "0080050",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080050"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10825",
                "name": "essential hypertension",
                "description": "A hypertension with no known cause. It is the most common type of hypertension.",
                "url": "https://disease-ontology.org/term/DOID:10825",
                "evidence": [
                    {
                        "id": "10825",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10825"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4480",
                "name": "achondroplasia",
                "description": "An osteochondrodysplasia that is characterized by short stature caused by rhizomelic shortening of the limbs, characteristic facies with frontal bossing and midface hypoplasia, exaggerated lumbar lordosis, limitation of elbow extension, genu varum, and trident hand and that has_material_basis_in heterozygous mutation in the fibroblast growth factor receptor-3 gene (FGFR3) on chromosome 4p16.3. Achondroplasia results in dwarfism due to the abnormal ossification of cartilage in the long bone.",
                "url": "https://disease-ontology.org/term/DOID:4480",
                "evidence": [
                    {
                        "id": "4480",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4480"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "guanylate cyclase activity",
                "id": "GO:0004383",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004383",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8MLX0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8MLX0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8MLX0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8MLX0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "GTP binding",
                "id": "GO:0005525",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005525",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8MLX0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8MLX0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "signaling receptor activity",
                "id": "GO:0038023",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0038023",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8MLX0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8MLX0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "peptide receptor activity",
                "id": "GO:0001653",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001653",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8MLX0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8MLX0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8MLX0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8MLX0"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "intracellular signal transduction",
                "id": "GO:0035556",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035556",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8MLX0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8MLX0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cGMP biosynthetic process",
                "id": "GO:0006182",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006182",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8MLX0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8MLX0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "receptor guanylyl cyclase signaling pathway",
                "id": "GO:0007168",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007168",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8MLX0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8MLX0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q8MLX0-1"
    },
    {
        "uniprot_canonical_ac": "Q9VK51-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK51",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK51"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1112,
        "chemical_mass": 127938.0,
        "gene_names": "ACXA;AC62D;ACXA;AC;Ac62D;CG17176;DACXA;Dmel\\CG17176;Dmel_CG17176",
        "protein_name": "adenylate cyclase",
        "disease": [
            {
                "disease_id": "DOID:1682",
                "name": "congenital heart disease",
                "description": "A physical disorder that is characterized by problems with the heart's structure that are present at birth.",
                "url": "https://disease-ontology.org/term/DOID:1682",
                "evidence": [
                    {
                        "id": "1682",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1682"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3312",
                "name": "bipolar disorder",
                "description": "A mood disorder that involves alternating periods of mania and depression.",
                "url": "https://disease-ontology.org/term/DOID:3312",
                "evidence": [
                    {
                        "id": "3312",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3312"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "adenylate cyclase activity",
                "id": "GO:0004016",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004016",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK51",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK51",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK51",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK51"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "spermatogenesis",
                "id": "GO:0007283",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007283",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK51",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular signal transduction",
                "id": "GO:0035556",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035556",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK51",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cyclic nucleotide biosynthetic process",
                "id": "GO:0009190",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009190",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK51",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cAMP biosynthetic process",
                "id": "GO:0006171",
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                "name": "zinc ion binding",
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                "name": "metallocarboxypeptidase activity",
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                "name": "detection of chemical stimulus involved in sensory perception",
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                "url": "https://disease-ontology.org/term/DOID:0111779",
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                    {
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                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
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                        ],
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                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
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                        "comment": "",
                        "icn3d_view": {},
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                        "start_aa": "Thr",
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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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            }
        ],
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        "gene_names": "Dmel\\CG44195;CG44195;Dmel\\CG44195;Dmel_CG44195",
        "protein_name": "",
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            {
                "uniprot_canonical_ac": "M9PEG1-1",
                "start_pos": "297",
                "end_pos": "297",
                "site_lbl": "Thr297",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
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                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
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                            }
                        ],
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                        "site_category_dict": {
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                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
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                        "start_pos": 297,
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                        ]
                    }
                ]
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        ],
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    },
    {
        "uniprot_canonical_ac": "M9PEG2-1",
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            {
                "name": "Drosophila melanogaster",
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                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
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            }
        ],
        "length": 273,
        "chemical_mass": 30852.0,
        "gene_names": "Dmel\\CG13288;dmCG13288;CG13288;Dmel\\CG13288;Dmel_CG13288;dmCG13288",
        "protein_name": "",
        "disease": [],
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            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "Drosophila melanogaster",
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                    {
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                        "id": "M9PEJ6",
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                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 105,
        "chemical_mass": 11243.0,
        "gene_names": "Dmel\\CG43915;CG43915;Dmel\\CG43915;Dmel_CG43915",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PEJ6",
                        "url": "https://www.uniprot.org/uniprotkb/M9PEJ6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "M9PEJ6-1"
    },
    {
        "uniprot_canonical_ac": "M9PEP2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
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                    {
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                        "id": "M9PEP2",
                        "url": "https://www.uniprot.org/uniprotkb/M9PEP2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 188332.0,
        "gene_names": "Ac13E;AC 13E;AC13E;Ac13E;Ac35C;CG9210;DAC9;Dmel\\CG9210;Dmel_CG9210;ac13e;dADCY9",
        "protein_name": "Adenylate cyclase type 9",
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            {
                "disease_id": "DOID:12716",
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                "description": "A respiratory failure that is characterized by deficiency of the surfactant coating the inner surface of the lungs, by failure of the lungs to expand and contract properly during breathing with resulting collapse, and by the accumulation of a protein-containing film lining the alveoli and their ducts.",
                "url": "https://disease-ontology.org/term/DOID:12716",
                "evidence": [
                    {
                        "id": "12716",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12716"
                    }
                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:2841",
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                    {
                        "id": "2841",
                        "database": "AGR",
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                    }
                ],
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                "url": "https://disease-ontology.org/term/DOID:9415",
                "evidence": [
                    {
                        "id": "9415",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9415"
                    }
                ],
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            }
        ],
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            {
                "name": "adenylate cyclase activity",
                "id": "GO:0004016",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004016",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PEP2",
                        "url": "https://www.uniprot.org/uniprotkb/M9PEP2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
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                    {
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                        "id": "M9PEP2",
                        "url": "https://www.uniprot.org/uniprotkb/M9PEP2"
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                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PEP2",
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                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PEP2",
                        "url": "https://www.uniprot.org/uniprotkb/M9PEP2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cAMP biosynthetic process",
                "id": "GO:0006171",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006171",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            },
            {
                "name": "adenylate cyclase-activating G protein-coupled receptor signaling pathway",
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                    {
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                ],
                "pmid": ""
            },
            {
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035556",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PEP2",
                        "url": "https://www.uniprot.org/uniprotkb/M9PEP2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "adenylate cyclase-modulating G protein-coupled receptor signaling pathway",
                "id": "GO:0007188",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007188",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PEP2",
                        "url": "https://www.uniprot.org/uniprotkb/M9PEP2"
                    }
                ],
                "pmid": ""
            }
        ],
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        "record_id": "M9PEP2-1"
    },
    {
        "uniprot_canonical_ac": "M9PEY3-1",
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                "name": "Drosophila melanogaster",
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                        "url": "https://www.uniprot.org/uniprotkb/M9PEY3"
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 9573.0,
        "gene_names": "Dmel\\CG43993;CG43993;Dmel\\CG43993;Dmel_CG43993",
        "protein_name": "Seminal fluid protein",
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        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "M9PEY3-1"
    },
    {
        "uniprot_canonical_ac": "M9PF61-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                        "id": "M9PF61",
                        "url": "https://www.uniprot.org/uniprotkb/M9PF61"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 40137.0,
        "gene_names": "Ar1;34F4T;AR;Akr1B;CG6084;Dmel\\CG6084;ESTS:34F4T;dAR1",
        "protein_name": "Aldo-keto reductase 1B",
        "disease": [
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
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                ],
                "weight": 0.0
            },
            {
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                "name": "allergic disease",
                "description": "An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods.",
                "url": "https://disease-ontology.org/term/DOID:1205",
                "evidence": [
                    {
                        "id": "1205",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1205"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2349",
                "name": "arteriosclerosis",
                "description": "An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:2349",
                "evidence": [
                    {
                        "id": "2349",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2349"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4195",
                "name": "hyperglycemia",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:4195",
                "evidence": [
                    {
                        "id": "4195",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4195"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4500",
                "name": "hypokalemia",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:4500",
                "evidence": [
                    {
                        "id": "4500",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4500"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:83",
                "name": "cataract",
                "description": "A lens disease characterized by clouding of the lens inside the eye which leads to a decrease in vision.",
                "url": "https://disease-ontology.org/term/DOID:83",
                "evidence": [
                    {
                        "id": "83",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:83"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8947",
                "name": "diabetic retinopathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8947",
                "evidence": [
                    {
                        "id": "8947",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8947"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9743",
                "name": "diabetic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:9743",
                "evidence": [
                    {
                        "id": "9743",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9743"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9870",
                "name": "galactosemia",
                "description": "A carbohydrate metabolic disorder that involves a defect in galactose metabolism resulting in toxic levels of galactose 1-phosphate in various tissues.",
                "url": "https://disease-ontology.org/term/DOID:9870",
                "evidence": [
                    {
                        "id": "9870",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9870"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PF61",
                        "url": "https://www.uniprot.org/uniprotkb/M9PF61"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleoplasm",
                "id": "GO:0005654",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PF61",
                        "url": "https://www.uniprot.org/uniprotkb/M9PF61"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PF61",
                        "url": "https://www.uniprot.org/uniprotkb/M9PF61"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PF61",
                        "url": "https://www.uniprot.org/uniprotkb/M9PF61"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "aldose reductase (NADPH) activity",
                "id": "GO:0004032",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004032",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PF61",
                        "url": "https://www.uniprot.org/uniprotkb/M9PF61"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "L-glucuronate reductase activity",
                "id": "GO:0047939",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0047939",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PF61",
                        "url": "https://www.uniprot.org/uniprotkb/M9PF61"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "prostaglandin H2 endoperoxidase reductase activity",
                "id": "GO:0036130",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036130",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PF61",
                        "url": "https://www.uniprot.org/uniprotkb/M9PF61"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "all-trans-retinol dehydrogenase (NADP+) activity",
                "id": "GO:0052650",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0052650",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PF61",
                        "url": "https://www.uniprot.org/uniprotkb/M9PF61"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glycerol dehydrogenase (NADP+) activity",
                "id": "GO:0047956",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0047956",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PF61",
                        "url": "https://www.uniprot.org/uniprotkb/M9PF61"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "allyl-alcohol dehydrogenase activity",
                "id": "GO:0047655",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0047655",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PF61",
                        "url": "https://www.uniprot.org/uniprotkb/M9PF61"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "sorbitol biosynthetic process",
                "id": "GO:0006061",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006061",
                "evidence": [
                    {
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                ],
                "pmid": ""
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            {
                "name": "open tracheal system development",
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            {
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                "name": "regulation of cell shape",
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                "name": "melanotic encapsulation of foreign target",
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                    }
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                ],
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                "name": "GTP binding",
                "id": "GO:0005525",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005525",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PG08",
                        "url": "https://www.uniprot.org/uniprotkb/M9PG08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein kinase binding",
                "id": "GO:0019901",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019901",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PG08",
                        "url": "https://www.uniprot.org/uniprotkb/M9PG08"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoskeleton",
                "id": "GO:0005856",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005856",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PG08",
                        "url": "https://www.uniprot.org/uniprotkb/M9PG08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PG08",
                        "url": "https://www.uniprot.org/uniprotkb/M9PG08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasmic vesicle",
                "id": "GO:0031410",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031410",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PG08",
                        "url": "https://www.uniprot.org/uniprotkb/M9PG08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endosome membrane",
                "id": "GO:0010008",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010008",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PG08",
                        "url": "https://www.uniprot.org/uniprotkb/M9PG08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell projection",
                "id": "GO:0042995",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042995",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PG08",
                        "url": "https://www.uniprot.org/uniprotkb/M9PG08"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "M9PG08-1",
                "start_pos": "27",
                "end_pos": "27",
                "site_lbl": "Thr27",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "G49108TO",
                        "type": "O-linked",
                        "subtype": "O-GlcNAcylation",
                        "prediction_tool_list": [],
                        "site_category": "reported_with_glycan",
                        "site_category_dict": {
                            "reported_with_glycan": true
                        },
                        "site_seq": "T",
                        "relation": "attached",
                        "comment": "O-GlcNAcylation",
                        "icn3d_view": {},
                        "start_pos": 27,
                        "start_aa": "Thr",
                        "end_pos": 27,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr27",
                        "evidence": [
                            {
                                "id": "40245499",
                                "database": "PubMed",
                                "url": "https://glygen.org/publication/PubMed/40245499"
                            },
                            {
                                "id": "M9PG08",
                                "database": "O-GlcNAc Database",
                                "url": "https://www.oglcnac.mcw.edu/search/?query_protein=M9PG08"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "M9PG08-1"
    },
    {
        "uniprot_canonical_ac": "M9PGH7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1657,
        "chemical_mass": 183541.0,
        "gene_names": "G9a;CG2995;Dmel\\CG2995;Dmel_CG2995;EG:BACR37P7.2;EHMT;G9ae;G9a;cab65850 G9a Dm;dG9a",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050156",
                "name": "idiopathic pulmonary fibrosis",
                "description": "A pulmonary fibrosis that is characterized by scarring of the lung characterized by stiffness in the lungs and makes it difficult to breathe.",
                "url": "https://disease-ontology.org/term/DOID:0050156",
                "evidence": [
                    {
                        "id": "0050156",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050156"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050696",
                "name": "fetal alcohol spectrum disorder",
                "description": "A specific developmental disorder and physical disorder that is characterized by physical, behavioral and learning birth defects resulting from maternal ingestion of alcohol during pregnancy.",
                "url": "https://disease-ontology.org/term/DOID:0050696",
                "evidence": [
                    {
                        "id": "0050696",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050696"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060352",
                "name": "Kleefstra syndrome 1",
                "description": "A Kleefstra syndrome that is characterized by severe mental retardation, hypotonia, microcephaly, epileptic seizures, flat face with hypertelorism, synophrys, anteverted nares, everted lower lip, carp mouth with macroglossia, and heart defects and that has_material_basis_in a microdeletion in the chromosome region 9q34.3 or by a point mutation in the EHMT1 gene located in that region.",
                "url": "https://disease-ontology.org/term/DOID:0060352",
                "evidence": [
                    {
                        "id": "0060352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080597",
                "name": "Kleefstra syndrome",
                "description": "A syndrome that is characterized by developmental delay and intellectual disability, severely limited or absent speech, and weak muscle tone.",
                "url": "https://disease-ontology.org/term/DOID:0080597",
                "evidence": [
                    {
                        "id": "0080597",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080597"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1909",
                "name": "melanoma",
                "description": "A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye.",
                "url": "https://disease-ontology.org/term/DOID:1909",
                "evidence": [
                    {
                        "id": "1909",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1909"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3748",
                "name": "esophagus squamous cell carcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus.",
                "url": "https://disease-ontology.org/term/DOID:3748",
                "evidence": [
                    {
                        "id": "3748",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3748"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3910",
                "name": "lung adenocarcinoma",
                "description": "A lung non-small cell carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3910",
                "evidence": [
                    {
                        "id": "3910",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3910"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:934",
                "name": "viral infectious disease",
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                "url": "https://disease-ontology.org/term/DOID:934",
                "evidence": [
                    {
                        "id": "934",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:934"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:986",
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                "description": "An autoimmune disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots.",
                "url": "https://disease-ontology.org/term/DOID:986",
                "evidence": [
                    {
                        "id": "986",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:986"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "habituation",
                "id": "GO:0046959",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046959",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of transcription by RNA polymerase II",
                "id": "GO:0000122",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000122",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chromatin remodeling",
                "id": "GO:0006338",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006338",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
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                "name": "short-term memory",
                "id": "GO:0007614",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007614",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to virus",
                "id": "GO:0009615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of dendrite morphogenesis",
                "id": "GO:0050775",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050775",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "long-term memory",
                "id": "GO:0007616",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007616",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of gene expression",
                "id": "GO:0010468",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010468",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "methylation",
                "id": "GO:0032259",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032259",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "epigenetic regulation of gene expression",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040029",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "larval locomotory behavior",
                "id": "GO:0008345",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008345",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "facultative heterochromatin formation",
                "id": "GO:0140718",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140718",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chromatin",
                "id": "GO:0000785",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000785",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "euchromatin",
                "id": "GO:0000791",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000791",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "polytene chromosome interband",
                "id": "GO:0005705",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005705",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription corepressor activity",
                "id": "GO:0003714",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003714",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "p53 binding",
                "id": "GO:0002039",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002039",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H3K9 methyltransferase activity",
                "id": "GO:0046974",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046974",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H3K9 monomethyltransferase activity",
                "id": "GO:0140948",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140948",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H3K9 dimethyltransferase activity",
                "id": "GO:0140942",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140942",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H3K27 monomethyltransferase activity",
                "id": "GO:0140953",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140953",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H3K9 trimethyltransferase activity",
                "id": "GO:0140949",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140949",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H4 methyltransferase activity",
                "id": "GO:0140939",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140939",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H3K27 trimethyltransferase activity",
                "id": "GO:0140951",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140951",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H3K27 dimethyltransferase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140952",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGH7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGH7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "M9PGH7-1"
    },
    {
        "uniprot_canonical_ac": "M9PGR0-1",
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            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
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                        "id": "M9PGR0",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGR0"
                    }
                ],
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 176,
        "chemical_mass": 19794.0,
        "gene_names": "Dlip1;CG15367;DIP1;Dip1;Dlip1;Dmel\\CG15367;Dmel_CG15367;dip1;dlip",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PGR0",
                        "url": "https://www.uniprot.org/uniprotkb/M9PGR0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
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                        "url": "https://www.uniprot.org/uniprotkb/M9PGR0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "M9PHC0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHC0",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHC0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 261,
        "chemical_mass": 30604.0,
        "gene_names": "Dmel\\CG32718;CG32718;Dmel\\CG32718;Dmel_CG32718",
        "protein_name": "",
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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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            {
                "name": "regulation of transcription by RNA polymerase II",
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                ],
                "pmid": ""
            },
            {
                "name": "nervous system development",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "cell differentiation",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of transcription by RNA polymerase II",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045944",
                "evidence": [
                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "protein dimerization activity",
                "id": "GO:0046983",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046983",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
                "id": "GO:0000978",
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                "evidence": [
                    {
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                ],
                "pmid": ""
            },
            {
                "name": "DNA-binding transcription factor activity, RNA polymerase II-specific",
                "id": "GO:0000981",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000981",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PH26",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "sequence-specific double-stranded DNA binding",
                "id": "GO:1990837",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990837",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PH26",
                        "url": "https://www.uniprot.org/uniprotkb/M9PH26"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "uniprot_canonical_ac": "M9PH26-1",
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                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
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                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 73,
                        "start_aa": "Thr",
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                        "end_aa": "Thr",
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                        "site_lbl": "Thr73",
                        "evidence": [
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                                "id": "GLY_001163",
                                "database": "GlyGen",
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                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "M9PHF7-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                        "id": "M9PHF7",
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                    }
                ],
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        ],
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        "gene_names": "Dmel\\CG12992;CG12992;Dmel\\CG12992;Dmel_CG12992",
        "protein_name": "",
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        "record_id": "M9PHF7-1"
    },
    {
        "uniprot_canonical_ac": "M9PHI7-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                        "id": "M9PHI7",
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                    }
                ],
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        ],
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        "gene_names": "kri;CG5537;Dmel\\CG5537;Dmel_CG5537;anon-EST:Posey275;kri;uprt",
        "protein_name": "Uracil phosphoribosyltransferase homolog",
        "disease": [],
        "molecular_function": [
            {
                "name": "GTP binding",
                "id": "GO:0005525",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005525",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHI7",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "uracil phosphoribosyltransferase activity",
                "id": "GO:0004845",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004845",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHI7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHI7"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHI7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHI7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHI7",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHI7"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "M9PHK6-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHK6",
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "gene_names": "Dmel\\CG14221;CG14221;Dmel\\CG14221;Dmel_CG14221",
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        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "M9PHS8-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHS8",
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                    }
                ],
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        ],
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        "gene_names": "Dmel\\CG9784;CG9784;Dmel\\CG9784;Dmel_CG9784;IPP;lincRNA.S9473",
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            {
                "disease_id": "DOID:0050588",
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                    {
                        "id": "0050588",
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                    }
                ],
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            },
            {
                "disease_id": "DOID:0080197",
                "name": "congenital muscular dystrophy with cataracts and intellectual disability",
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                "url": "https://disease-ontology.org/term/DOID:0080197",
                "evidence": [
                    {
                        "id": "0080197",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080197"
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                ],
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            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PHS8",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHS8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron projection",
                "id": "GO:0043005",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043005",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHS8",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHS8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ruffle",
                "id": "GO:0001726",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001726",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHS8",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHS8"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "phosphatidylinositol dephosphorylation",
                "id": "GO:0046856",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046856",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHS8",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHS8"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity",
                "id": "GO:0004439",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004439",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHS8",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHS8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase activity",
                "id": "GO:0034485",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034485",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHS8",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHS8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "inositol trisphosphate phosphatase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046030",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHS8",
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                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
        "uniprot_canonical_ac": "M9PHT8-1",
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            {
                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PHT8",
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                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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            {
                "disease_id": "DOID:0112265",
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                "description": "A renal tubular transport disease characterized by impaired renal tube reabsorption of proline, hydroxyproline and glycine and elevated urine levels of the imino acids and glycine that has_material_basis_in homozygous mutation in SLC36A2 on chromosome 5q33.1 combined with either heterozygous mutation in SLC6A20 gene on chromosome 3p21.31 or homozygous mutation in SLC6A19 on chromosome 5p15.33.",
                "url": "https://disease-ontology.org/term/DOID:0112265",
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                    {
                        "id": "0112265",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0112265"
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                ],
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        ],
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            {
                "name": "L-amino acid transmembrane transporter activity",
                "id": "GO:0015179",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015179",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHT8",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHT8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "amino acid transmembrane transporter activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015171",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "vacuolar membrane",
                "id": "GO:0005774",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005774",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/M9PHT8"
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                ],
                "pmid": ""
            },
            {
                "name": "membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "amino acid transmembrane transport",
                "id": "GO:0003333",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003333",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PHT8",
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                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "M9PHX0-1",
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            {
                "name": "Drosophila melanogaster",
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                        "id": "M9PHX0",
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "gene_names": "Dmel\\CG43843;CG15049;CG43843;Dmel\\CG43843;Dmel_CG43843",
        "protein_name": "",
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        "biomarkers": [],
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        "record_id": "M9PHX0-1"
    },
    {
        "uniprot_canonical_ac": "M9PI41-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI41",
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                    }
                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "gene_names": "sti;CG10522;CIT-K;CIT;Citron K;Citron;DCK;Dmel\\CG10522;Dmel_CG10522;STI;anon-WO0118547.388;cit;ck;dck;l(3)7m-62;l(3)7m62;l(3)SG21;sti/Citron;sti",
        "protein_name": "non-specific serine/threonine protein kinase",
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            {
                "disease_id": "DOID:0070288",
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                "url": "https://disease-ontology.org/term/DOID:0070288",
                "evidence": [
                    {
                        "id": "0070288",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070288"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0070297",
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                "url": "https://disease-ontology.org/term/DOID:0070297",
                "evidence": [
                    {
                        "id": "0070297",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070297"
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081292",
                "name": "traumatic brain injury",
                "description": "A brain disease that is characterized by brain dysfunction caused by an outside force, usually a violent blow to the head.",
                "url": "https://disease-ontology.org/term/DOID:0081292",
                "evidence": [
                    {
                        "id": "0081292",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081292"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10907",
                "name": "microcephaly",
                "description": "A congenital nervous system abnormality that is characterized by a significantly smaller than normal head in infants.",
                "url": "https://disease-ontology.org/term/DOID:10907",
                "evidence": [
                    {
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10907"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1826",
                "name": "epilepsy",
                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.",
                "url": "https://disease-ontology.org/term/DOID:1826",
                "evidence": [
                    {
                        "id": "1826",
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                "name": "mitotic DNA replication checkpoint signaling",
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        ],
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                "disease_id": "DOID:0060269",
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                "url": "https://disease-ontology.org/term/DOID:0060269",
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                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 622,
        "chemical_mass": 70558.0,
        "gene_names": "Hexo1;CG1318;DmHex1;Dmel\\CG1318;Dmel_CG1318;HEX 1;HEX1;HEXO1;Hexo1",
        "protein_name": "beta-N-acetylhexosaminidase",
        "disease": [
            {
                "disease_id": "DOID:12377",
                "name": "spinal muscular atrophy",
                "description": "A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy.",
                "url": "https://disease-ontology.org/term/DOID:12377",
                "evidence": [
                    {
                        "id": "12377",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12377"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3211",
                "name": "lysosomal storage disease",
                "description": "An inherited metabolic disorder that involve an abnormal accumulation of substances inside the lysosome resulting from defects in lysosomal function.",
                "url": "https://disease-ontology.org/term/DOID:3211",
                "evidence": [
                    {
                        "id": "3211",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3211"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3320",
                "name": "Tay-Sachs disease",
                "description": "A GM2 gangliosidosis that is characterized onset in infancy of developmental retardation, followed by paralysis, dementia and blindness, with death in the second or third year of life and has_material_basis_in homozygous or compound heterozygous mutation in the alpha subunit of the hexosaminidase A gene (HEXA) on chromosome 15q23.",
                "url": "https://disease-ontology.org/term/DOID:3320",
                "evidence": [
                    {
                        "id": "3320",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3320"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3323",
                "name": "Sandhoff disease",
                "description": "A GM2 gangliosidosis that is characterized by an accumulation of GM2 gangliosides, particularly in neurons, and that has_material_basis_in mutation in the beta subunit of hexosaminidase (HEXB) on chromosome 5q13.",
                "url": "https://disease-ontology.org/term/DOID:3323",
                "evidence": [
                    {
                        "id": "3323",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3323"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8H9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "lysosome",
                "id": "GO:0005764",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005764",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8H9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "carbohydrate metabolic process",
                "id": "GO:0005975",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005975",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8H9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glycosaminoglycan metabolic process",
                "id": "GO:0030203",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030203",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8H9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chondroitin sulfate proteoglycan catabolic process",
                "id": "GO:0030207",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030207",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8H9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chitin catabolic process",
                "id": "GO:0006032",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006032",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8H9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "N-glycan processing",
                "id": "GO:0006491",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006491",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8H9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "rhodopsin biosynthetic process",
                "id": "GO:0016063",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016063",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8H9"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "beta-N-acetylglucosaminidase activity",
                "id": "GO:0016231",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016231",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8H9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "beta-N-acetylhexosaminidase activity",
                "id": "GO:0004563",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004563",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8H9",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8H9"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q0E8H9-1",
                "start_pos": "144",
                "end_pos": "144",
                "site_lbl": "Thr144",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 144,
                        "start_aa": "Thr",
                        "end_pos": 144,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr144",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "Q0E8H9-1"
    },
    {
        "uniprot_canonical_ac": "Q0E8V6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8V6",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8V6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 384,
        "chemical_mass": 43396.0,
        "gene_names": "Spn28Da;CG12318;CG31902;Dmel\\CG31902;Dmel_CG31902;Spn28Da",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050589",
                "name": "inflammatory bowel disease",
                "description": "An intestinal disease characterized by inflammation located in all parts of digestive tract.",
                "url": "https://disease-ontology.org/term/DOID:0050589",
                "evidence": [
                    {
                        "id": "0050589",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050589"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050831",
                "name": "familial encephalopathy with neuroserpin inclusion bodies",
                "description": "A neurodegenerative disease that is characterized by intraneuronal inclusions of mutant neuroserpin resulting in progressive encephalopathy, dementia and seizures and has_material_basis_in a mutation in the SERPINI1 gene inherited in an in autosomal dominant pattern.",
                "url": "https://disease-ontology.org/term/DOID:0050831",
                "evidence": [
                    {
                        "id": "0050831",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050831"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0051054",
                "name": "coarctation of the aorta",
                "description": "A congenital heart disease that is characterized by the luminal narrowing of the thoracic aortic arch, typically located just beyond the left subclavian artery. This narrowing creates an obstruction that can lead to significant cardiovascular complications, including systemic hypertension, left ventricular hypertrophy, and eventually heart failure.",
                "url": "https://disease-ontology.org/term/DOID:0051054",
                "evidence": [
                    {
                        "id": "0051054",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0051054"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0051061",
                "name": "stroke",
                "description": "A cerebrovascular disease that is characterized by disruption of blood flow to the brain resulting in damage to brain cells due to a lack of oxygen.",
                "url": "https://disease-ontology.org/term/DOID:0051061",
                "evidence": [
                    {
                        "id": "0051061",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0051061"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060186",
                "name": "chemical colitis",
                "description": "A colitis caused_by introduction of various chemicals.",
                "url": "https://disease-ontology.org/term/DOID:0060186",
                "evidence": [
                    {
                        "id": "0060186",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060186"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060189",
                "name": "ileitis",
                "description": "An inflammatory bowel disease characterized by inflammation located_in ileum, has_symptom diarrhea, has_symptom abdominal pain, often in the right lower quadrant, has_symptom weight loss.",
                "url": "https://disease-ontology.org/term/DOID:0060189",
                "evidence": [
                    {
                        "id": "0060189",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060189"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060224",
                "name": "atrial fibrillation",
                "description": "A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain.",
                "url": "https://disease-ontology.org/term/DOID:0060224",
                "evidence": [
                    {
                        "id": "0060224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060903",
                "name": "thrombosis",
                "description": "A vascular disease caused by the formation of a blood clot inside a blood vessel, obstructing the flow of blood through the circulatory system.",
                "url": "https://disease-ontology.org/term/DOID:0060903",
                "evidence": [
                    {
                        "id": "0060903",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060903"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070508",
                "name": "metabolic dysfunction and alcohol associated liver disease",
                "description": "A steatotic liver disease characterized by at least one of five specified cardiometabolic risk factors and elevated alcohol consumption. This disease is distinguished from MASLD by increased alcohol consumption and from ALD by the evidence of one or more of the specified cardiometabolic risk factors. The five cardiometabolic risk factors are: (1) higher than normal body mass index or waist circumference; (2) higher than normal serum glucose or glycated hemoglobin level, or type 2 diabetes; (3) higher than normal blood pressure or hypertensive treatment; (4) higher than normal plasma triglycerides or lipid lowering treatment; and (5) lower than normal plasma high-density lipoprotein cholesterol.",
                "url": "https://disease-ontology.org/term/DOID:0070508",
                "evidence": [
                    {
                        "id": "0070508",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070508"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070555",
                "name": "Nagashima-type palmoplantar keratosis",
                "description": "A nonepidermolytic palmoplantar keratoderma characterized by mild, well-demarcated, diffuse erythematous hyperkeratosis that is nonprogressive after the second decade of life which extends onto the dorsal surfaces of the palms and feet and the Achilles tendon area, with a high frequency of hyperhidrosis on the palms and soles and without flexion contractures or constricting bands that has_material_basis_in homozygous or compound heterozygous mutation in the SERPINB7 gene on chromosome 18q21.33.",
                "url": "https://disease-ontology.org/term/DOID:0070555",
                "evidence": [
                    {
                        "id": "0070555",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070555"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080322",
                "name": "polycystic kidney disease",
                "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure.",
                "url": "https://disease-ontology.org/term/DOID:0080322",
                "evidence": [
                    {
                        "id": "0080322",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0090030",
                "name": "corticosteroid-binding globulin deficiency",
                "description": "An adrenal gland disease characterized by decreased levels of serum corticosteroid-binding globulin and cortisol, and in some cases hypo- or hypertension, and muscle fatigue that has_material_basis_in heterozygous or homozygous mutation in the SERPINA6 gene on chromosome 14q32.",
                "url": "https://disease-ontology.org/term/DOID:0090030",
                "evidence": [
                    {
                        "id": "0090030",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0090030"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10159",
                "name": "osteonecrosis",
                "description": "An ischemic bone disease that results_in necrosis located_in bone.",
                "url": "https://disease-ontology.org/term/DOID:10159",
                "evidence": [
                    {
                        "id": "10159",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10159"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "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.",
                "url": "https://disease-ontology.org/term/DOID:10591",
                "evidence": [
                    {
                        "id": "10591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10591"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10762",
                "name": "portal hypertension",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:10762",
                "evidence": [
                    {
                        "id": "10762",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10762"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10808",
                "name": "gastric ulcer",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:10808",
                "evidence": [
                    {
                        "id": "10808",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10808"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10952",
                "name": "nephritis",
                "description": "A kidney disease that is characterized by an inflammation of the kidneys.",
                "url": "https://disease-ontology.org/term/DOID:10952",
                "evidence": [
                    {
                        "id": "10952",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10952"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11049",
                "name": "meconium aspiration syndrome",
                "description": "A lung disease that is characterized by a newborn breathing in a mixture of meconium and amniotic fluid into the lungs around the time of delivery.",
                "url": "https://disease-ontology.org/term/DOID:11049",
                "evidence": [
                    {
                        "id": "11049",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11049"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11111",
                "name": "hydronephrosis",
                "description": "An urinary system disease that is characterized by swelling of one or both kidneys due to incomplete voiding of urine.",
                "url": "https://disease-ontology.org/term/DOID:11111",
                "evidence": [
                    {
                        "id": "11111",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11111"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11123",
                "name": "IgA vasculitis",
                "description": "A hypersensitivity vasculitis that is characterized by purpura (purplish plaques), arthralgia, gastrointestinal upset, and/or glomerulonephritis, and may be related to increased immune response following an infection.",
                "url": "https://disease-ontology.org/term/DOID:11123",
                "evidence": [
                    {
                        "id": "11123",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11123"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11247",
                "name": "disseminated intravascular coagulation",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11247",
                "evidence": [
                    {
                        "id": "11247",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11247"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11394",
                "name": "adult respiratory distress syndrome",
                "description": "A respiratory failure that results from diffuse injury to the endothelium of the lung (as in sepsis, chest trauma, massive blood transfusion, aspiration of the gastric contents, or pneumonia) and is characterized by pulmonary edema with an abnormally high amount of protein in the edematous fluid and by difficult rapid breathing and hypoxemia.",
                "url": "https://disease-ontology.org/term/DOID:11394",
                "evidence": [
                    {
                        "id": "11394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11396",
                "name": "pulmonary edema",
                "description": "A respiratory failure that is characterized by the accumulation of fluid in the lung tissues causing disturbance of the gas exchange that may lead to respiratory failure.",
                "url": "https://disease-ontology.org/term/DOID:11396",
                "evidence": [
                    {
                        "id": "11396",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11396"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11446",
                "name": "sciatic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11446",
                "evidence": [
                    {
                        "id": "11446",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11446"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11716",
                "name": "prediabetes syndrome",
                "description": "A glucose metabolism disease that is characterized by blood glucose levels are high, but not high enough to be classified as type 2 diabetes.",
                "url": "https://disease-ontology.org/term/DOID:11716",
                "evidence": [
                    {
                        "id": "11716",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11716"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1184",
                "name": "nephrotic syndrome",
                "description": "A nephrosis characterized by marked increase in glomerular protein permeability resulting in marked elevation of urine protein levels, hypoalbuminemia, hyperlipidemia, and hypercoagulability.",
                "url": "https://disease-ontology.org/term/DOID:1184",
                "evidence": [
                    {
                        "id": "1184",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1184"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11949",
                "name": "Creutzfeldt-Jakob disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11949",
                "evidence": [
                    {
                        "id": "11949",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11949"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11984",
                "name": "hypertrophic cardiomyopathy",
                "description": "An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause.",
                "url": "https://disease-ontology.org/term/DOID:11984",
                "evidence": [
                    {
                        "id": "11984",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11984"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1205",
                "name": "allergic disease",
                "description": "An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods.",
                "url": "https://disease-ontology.org/term/DOID:1205",
                "evidence": [
                    {
                        "id": "1205",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1205"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12185",
                "name": "otosclerosis",
                "description": "An otitis interna characterized by isolated endochondral bone sclerosis of the labyrinthine capsule.",
                "url": "https://disease-ontology.org/term/DOID:12185",
                "evidence": [
                    {
                        "id": "12185",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12185"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12236",
                "name": "primary biliary cholangitis",
                "description": "A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts.",
                "url": "https://disease-ontology.org/term/DOID:12236",
                "evidence": [
                    {
                        "id": "12236",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12236"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12351",
                "name": "alcoholic hepatitis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:12351",
                "evidence": [
                    {
                        "id": "12351",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12351"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12930",
                "name": "dilated cardiomyopathy",
                "description": "An intrinsic cardiomyopathy that is characterized by an an enlarged heart and damage to the myocardium causing the heart to pump blood inefficiently.",
                "url": "https://disease-ontology.org/term/DOID:12930",
                "evidence": [
                    {
                        "id": "12930",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12930"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13025",
                "name": "retinopathy of prematurity",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:13025",
                "evidence": [
                    {
                        "id": "13025",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13025"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1312",
                "name": "focal segmental glomerulosclerosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1312",
                "evidence": [
                    {
                        "id": "1312",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1312"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13141",
                "name": "uveitis",
                "description": "An uveal disease is characterized by inflammation of any of the layers of the uvea of the eye, which includes the iris, ciliary body, and choroid.",
                "url": "https://disease-ontology.org/term/DOID:13141",
                "evidence": [
                    {
                        "id": "13141",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13141"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13372",
                "name": "alpha 1-antitrypsin deficiency",
                "description": "A plasma protein metabolism disease that has_material_basis_in defective production of the protease inhibitor alpha 1-antitrypsin (A1AT), leading to decreased A1AT activity in the blood and lungs, and deposition of excessive abnormal A1AT protein in liver cells.",
                "url": "https://disease-ontology.org/term/DOID:13372",
                "evidence": [
                    {
                        "id": "13372",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13372"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13884",
                "name": "sick sinus syndrome",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:13884",
                "evidence": [
                    {
                        "id": "13884",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13884"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14115",
                "name": "toxic shock syndrome",
                "description": "A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus, which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities.",
                "url": "https://disease-ontology.org/term/DOID:14115",
                "evidence": [
                    {
                        "id": "14115",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14115"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14499",
                "name": "Fabry disease",
                "description": "A sphingolipidosis that is characterized by the buildup of globotriaosylceramide in the body's cells and has_material_basis_in X-linked inherited mutations in the GLA gene, encoding alpha-galactosidase A, on chromosome Xq22.",
                "url": "https://disease-ontology.org/term/DOID:14499",
                "evidence": [
                    {
                        "id": "14499",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14499"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1485",
                "name": "cystic fibrosis",
                "description": "A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs.",
                "url": "https://disease-ontology.org/term/DOID:1485",
                "evidence": [
                    {
                        "id": "1485",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1485"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1580",
                "name": "diffuse scleroderma",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1580",
                "evidence": [
                    {
                        "id": "1580",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1580"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1875",
                "name": "impotence",
                "description": "A sexual dysfunction that is characterized by persistent or recurrent inability to achieve or to maintain an erection during sexual activity.",
                "url": "https://disease-ontology.org/term/DOID:1875",
                "evidence": [
                    {
                        "id": "1875",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1875"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1936",
                "name": "atherosclerosis",
                "description": "An arteriosclerotic cardiovascular disease that is characterized by the build-up of fatty material and calcium deposition in the arterial wall resulting in partial or complete occlusion of the arterial lumen. Disease is located within the tunica intima of large and small arteries.",
                "url": "https://disease-ontology.org/term/DOID:1936",
                "evidence": [
                    {
                        "id": "1936",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1936"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2018",
                "name": "hyperinsulinism",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:2018",
                "evidence": [
                    {
                        "id": "2018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2018"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
                "description": "A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.",
                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2349",
                "name": "arteriosclerosis",
                "description": "An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:2349",
                "evidence": [
                    {
                        "id": "2349",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2349"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2377",
                "name": "multiple sclerosis",
                "description": "A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring.",
                "url": "https://disease-ontology.org/term/DOID:2377",
                "evidence": [
                    {
                        "id": "2377",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2377"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2450",
                "name": "central retinal vein occlusion",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:2450",
                "evidence": [
                    {
                        "id": "2450",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2450"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:289",
                "name": "endometriosis",
                "description": "A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body.",
                "url": "https://disease-ontology.org/term/DOID:289",
                "evidence": [
                    {
                        "id": "289",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:289"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2913",
                "name": "acute pancreatitis",
                "description": "A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock.",
                "url": "https://disease-ontology.org/term/DOID:2913",
                "evidence": [
                    {
                        "id": "2913",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2913"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2921",
                "name": "glomerulonephritis",
                "description": "A nephritis that causes inflammation of the glomeruli located_in kidney.",
                "url": "https://disease-ontology.org/term/DOID:2921",
                "evidence": [
                    {
                        "id": "2921",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2921"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2945",
                "name": "severe acute respiratory syndrome",
                "description": "A Coronavirus infectious disease that results_in infection located_in respiratory tract, has_material_basis_in Severe acute respiratory syndrome coronavirus (SARS-CoV or SARS-CoV-1), a subtype of Betacoronavirus pandemicum, which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia.",
                "url": "https://disease-ontology.org/term/DOID:2945",
                "evidence": [
                    {
                        "id": "2945",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2945"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2986",
                "name": "IgA glomerulonephritis",
                "description": "A glomerulonephritis characterized by build up of IgA antibody in the glomerulus.",
                "url": "https://disease-ontology.org/term/DOID:2986",
                "evidence": [
                    {
                        "id": "2986",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2986"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3021",
                "name": "acute kidney failure",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3021",
                "evidence": [
                    {
                        "id": "3021",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3021"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3328",
                "name": "temporal lobe epilepsy",
                "description": "A focal epilepsy that is characterized by recurrent, unprovoked focal seizures that originate in the temporal lobe of the brain and last about one or two minutes.",
                "url": "https://disease-ontology.org/term/DOID:3328",
                "evidence": [
                    {
                        "id": "3328",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3328"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3393",
                "name": "coronary artery disease",
                "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles.",
                "url": "https://disease-ontology.org/term/DOID:3393",
                "evidence": [
                    {
                        "id": "3393",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3393"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3407",
                "name": "carotid artery disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3407",
                "evidence": [
                    {
                        "id": "3407",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3407"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3525",
                "name": "middle cerebral artery infarction",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3525",
                "evidence": [
                    {
                        "id": "3525",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3525"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3587",
                "name": "pancreatic ductal carcinoma",
                "description": "A pancreatic carcinoma located_in the pancreatic duct.",
                "url": "https://disease-ontology.org/term/DOID:3587",
                "evidence": [
                    {
                        "id": "3587",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3587"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3755",
                "name": "antithrombin III deficiency",
                "description": "A thrombophilia that is characterized by the tendency to form clots in the veins.",
                "url": "https://disease-ontology.org/term/DOID:3755",
                "evidence": [
                    {
                        "id": "3755",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3755"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3770",
                "name": "pulmonary fibrosis",
                "description": "An interstitial lung disease that is characterized by destruction, scarring, and thickening of the interstitial lung tissues and progressive pulmonary function loss in a restrictive pattern, has_symptom progressive shortness of breath, fatigue, and chronic cough, possibly has_material_basis_in exposure to certain chemicals, autoimmune conditions, and radiation. It can be caused by inhaling hazardous chemicals, certain diseases, medication and genetics or unknown causes.",
                "url": "https://disease-ontology.org/term/DOID:3770",
                "evidence": [
                    {
                        "id": "3770",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3770"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3910",
                "name": "lung adenocarcinoma",
                "description": "A lung non-small cell carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3910",
                "evidence": [
                    {
                        "id": "3910",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3910"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:409",
                "name": "liver disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:409",
                "evidence": [
                    {
                        "id": "409",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:409"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:418",
                "name": "systemic scleroderma",
                "description": "A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies.",
                "url": "https://disease-ontology.org/term/DOID:418",
                "evidence": [
                    {
                        "id": "418",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:418"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4448",
                "name": "macular degeneration",
                "description": "A retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye and has_symptom vision loss.",
                "url": "https://disease-ontology.org/term/DOID:4448",
                "evidence": [
                    {
                        "id": "4448",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4448"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4780",
                "name": "anti-basement membrane glomerulonephritis",
                "description": "A Goodpasture syndrome that is characterized by damage to only kidney capillaries.",
                "url": "https://disease-ontology.org/term/DOID:4780",
                "evidence": [
                    {
                        "id": "4780",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4780"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5082",
                "name": "liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:5082",
                "evidence": [
                    {
                        "id": "5082",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5082"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:526",
                "name": "human immunodeficiency virus infectious disease",
                "description": "A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 (Lentivirus humimdef1) or Human immunodeficiency virus 2 (Lentivirus humimdef2), which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands.",
                "url": "https://disease-ontology.org/term/DOID:526",
                "evidence": [
                    {
                        "id": "526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:526"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6000",
                "name": "congestive heart failure",
                "description": "A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body.",
                "url": "https://disease-ontology.org/term/DOID:6000",
                "evidence": [
                    {
                        "id": "6000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6000"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6432",
                "name": "pulmonary hypertension",
                "description": "A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries.",
                "url": "https://disease-ontology.org/term/DOID:6432",
                "evidence": [
                    {
                        "id": "6432",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6432"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6713",
                "name": "cerebrovascular disease",
                "description": "An vascular disease that is characterized by dysfunction of the blood vessels supplying the brain.",
                "url": "https://disease-ontology.org/term/DOID:6713",
                "evidence": [
                    {
                        "id": "6713",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6713"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8398",
                "name": "osteoarthritis",
                "description": "An arthritis that has_material_basis_in worn out cartilage located_in joint.",
                "url": "https://disease-ontology.org/term/DOID:8398",
                "evidence": [
                    {
                        "id": "8398",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8398"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8552",
                "name": "chronic myeloid leukemia",
                "description": "A myeloid leukemia that is characterized by over production of white blood cells.",
                "url": "https://disease-ontology.org/term/DOID:8552",
                "evidence": [
                    {
                        "id": "8552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8552"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:865",
                "name": "vasculitis",
                "description": "A vascular disease that is characterized by inflammation of the blood vessels.",
                "url": "https://disease-ontology.org/term/DOID:865",
                "evidence": [
                    {
                        "id": "865",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:865"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8805",
                "name": "intermediate coronary syndrome",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8805",
                "evidence": [
                    {
                        "id": "8805",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8805"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8923",
                "name": "skin melanoma",
                "description": "A skin cancer that has_material_basis_in melanocytes.",
                "url": "https://disease-ontology.org/term/DOID:8923",
                "evidence": [
                    {
                        "id": "8923",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8923"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8947",
                "name": "diabetic retinopathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8947",
                "evidence": [
                    {
                        "id": "8947",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8947"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9675",
                "name": "pulmonary emphysema",
                "description": "A chronic obstructive pulmonary disease that is characterized by permanent enlargement of air spaces distal to the terminal bronchioles and the destruction of the alveolar walls.",
                "url": "https://disease-ontology.org/term/DOID:9675",
                "evidence": [
                    {
                        "id": "9675",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9675"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:988",
                "name": "mitral valve prolapse",
                "description": "A mitral valve disease where one or both of the cusps of the mitral valve bulge or collapse backward in the left atrium during systole.",
                "url": "https://disease-ontology.org/term/DOID:988",
                "evidence": [
                    {
                        "id": "988",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:988"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9970",
                "name": "obesity",
                "description": "An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness.",
                "url": "https://disease-ontology.org/term/DOID:9970",
                "evidence": [
                    {
                        "id": "9970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9970"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "serine-type endopeptidase inhibitor activity",
                "id": "GO:0004867",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004867",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8V6",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8V6"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8V6",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8V6"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "negative regulation of proteolysis",
                "id": "GO:0045861",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045861",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8V6",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8V6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mating",
                "id": "GO:0007618",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007618",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8V6",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8V6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q0E8V6-1"
    },
    {
        "uniprot_canonical_ac": "Q0E9B1-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E9B1",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E9B1"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 180,
        "chemical_mass": 21484.0,
        "gene_names": "CR33632;CG33632;CR33632;Dmel\\CG33632;Dmel_CG33632",
        "protein_name": "MD-2-related lipid-recognition domain-containing protein",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q0E9B1-1"
    },
    {
        "uniprot_canonical_ac": "Q0KI05-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI05",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI05"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 4842,
        "chemical_mass": 553527.0,
        "gene_names": "Dmel\\CG3339;CG3339;DHC5;Dmel\\CG3339;Dmel_CG3339",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050144",
                "name": "Kartagener syndrome",
                "description": "A primary ciliary dyskinesia that is characterized by sinusitis, bronchiectasis and situs inversus with dextrocardia resulting from dysfunction of the cilia during embryologic development.",
                "url": "https://disease-ontology.org/term/DOID:0050144",
                "evidence": [
                    {
                        "id": "0050144",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050144"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110605",
                "name": "primary ciliary dyskinesia 7",
                "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with chronic respiratory infections, chronic sinusitis, recurrent bronchitis, and pneumonia beginning in infancy or early childhood and has_material_basis_in mutation in the DNAH11 gene on chromosome 7p21.",
                "url": "https://disease-ontology.org/term/DOID:0110605",
                "evidence": [
                    {
                        "id": "0110605",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110605"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111853",
                "name": "primary ciliary dyskinesia 40",
                "description": "A primary ciliary dyskinesia characterized by a subtle defect in the bend of the distal portion of the cilia, reduced ciliary clearance in-vitro, relatively mild respiratory phenotype and laterality defects in all reported patients that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH9 gene on chromosome 17p12.",
                "url": "https://disease-ontology.org/term/DOID:0111853",
                "evidence": [
                    {
                        "id": "0111853",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111853"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "cilium movement involved in cell motility",
                "id": "GO:0060294",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060294",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI05",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI05"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI05",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI05"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "minus-end-directed microtubule motor activity",
                "id": "GO:0008569",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008569",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI05",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI05"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dynein light intermediate chain binding",
                "id": "GO:0051959",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051959",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI05",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI05"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dynein intermediate chain binding",
                "id": "GO:0045505",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045505",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI05",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI05"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "microtubule",
                "id": "GO:0005874",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005874",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI05",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI05"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axoneme",
                "id": "GO:0005930",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005930",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI05",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI05"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dynein complex",
                "id": "GO:0030286",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030286",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI05",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI05"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "outer dynein arm",
                "id": "GO:0036157",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036157",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI05",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI05"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "9+2 motile cilium",
                "id": "GO:0097729",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097729",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI05",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI05"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q0KI05-1",
                "start_pos": "135",
                "end_pos": "135",
                "site_lbl": "Thr135",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 135,
                        "start_aa": "Thr",
                        "end_pos": 135,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr135",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "Q0KI05-1"
    },
    {
        "uniprot_canonical_ac": "Q0KI25-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI25",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI25"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1125,
        "chemical_mass": 126543.0,
        "gene_names": "CG13825;Dmel\\CG4467;CG13825;CG4467;Dmel\\CG4467;Dmel_CG4467",
        "protein_name": "Endoplasmic reticulum aminopeptidase 2",
        "disease": [
            {
                "disease_id": "DOID:127",
                "name": "leiomyoma",
                "description": "A cell type benign neoplasm that is a benign tumor of smooth muscle cells.",
                "url": "https://disease-ontology.org/term/DOID:127",
                "evidence": [
                    {
                        "id": "127",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:127"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13129",
                "name": "severe pre-eclampsia",
                "description": "A pre-eclampsia that has_symptom at least one of the following: SBP of 160mm HG or higher or DPB of 110mm HG or higher on 2 occasions at least 6 hours apart, proteinuria more than 5g in a 24-hour collection, pulmonary edema or cyanosis, oliguria, persistent headaches, epigastric pain and/or impaired liver function, thrombocytopenia, oligohydramnios, decreased fetal growth or placental abruption.",
                "url": "https://disease-ontology.org/term/DOID:13129",
                "evidence": [
                    {
                        "id": "13129",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13129"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2871",
                "name": "endometrial carcinoma",
                "description": "A endometrial cancer that is located_in the tissue lining the uterus.",
                "url": "https://disease-ontology.org/term/DOID:2871",
                "evidence": [
                    {
                        "id": "2871",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2871"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2893",
                "name": "cervix carcinoma",
                "description": "A cervical cancer that is located_in the cervix uteri or located_in the cervical area and that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:2893",
                "evidence": [
                    {
                        "id": "2893",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2893"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4450",
                "name": "renal cell carcinoma",
                "description": "A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney.",
                "url": "https://disease-ontology.org/term/DOID:4450",
                "evidence": [
                    {
                        "id": "4450",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4450"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8488",
                "name": "polyhydramnios",
                "description": "A placenta disease that is characterized by an excess of amniotic fluid in the amniotic sac.",
                "url": "https://disease-ontology.org/term/DOID:8488",
                "evidence": [
                    {
                        "id": "8488",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8488"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI25",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI25"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "hydrolase activity",
                "id": "GO:0016787",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016787",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI25",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI25"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI25",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI25"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KI25",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KI25"
                    }
                ],
                "pmid": ""
            }
        ],
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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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                "name": "myosin complex",
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                "name": "mushroom body development",
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                "name": "spermathecum morphogenesis",
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                "name": "genital disc development",
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                "name": "genital disc sexually dimorphic development",
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                "name": "brush border",
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                "name": "cerebrooculofacioskeletal syndrome 2",
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                "evidence": [
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                        "id": "0080912",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0080912"
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                "name": "xeroderma pigmentosum group D",
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                "evidence": [
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                        "id": "0110845",
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                "name": "photosensitive trichothiodystrophy 1",
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                    {
                        "id": "0111873",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111873"
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            },
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                "name": "Down syndrome",
                "description": "A chromosomal duplication syndrome that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability.",
                "url": "https://disease-ontology.org/term/DOID:14250",
                "evidence": [
                    {
                        "id": "14250",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14250"
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                ],
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            },
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                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
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                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
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                ],
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            },
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                        "id": "1793",
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                ],
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                    {
                        "id": "1909",
                        "database": "AGR",
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                ],
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            },
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                        "database": "AGR",
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                ],
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            },
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2960"
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                ],
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            },
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                "name": "Cockayne syndrome",
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                "url": "https://disease-ontology.org/term/DOID:2962",
                "evidence": [
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                        "id": "2962",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2962"
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                ],
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            },
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                "name": "high grade glioma",
                "description": "A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine.",
                "url": "https://disease-ontology.org/term/DOID:3070",
                "evidence": [
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                        "id": "3070",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3070"
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                ],
                "weight": 0.0
            },
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                "name": "coronary artery disease",
                "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles.",
                "url": "https://disease-ontology.org/term/DOID:3393",
                "evidence": [
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                        "id": "3393",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3393"
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                ],
                "weight": 0.0
            },
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                        "id": "37",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:37"
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                ],
                "weight": 0.0
            },
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                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
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                ],
                "weight": 0.0
            },
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                "description": "A retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye and has_symptom vision loss.",
                "url": "https://disease-ontology.org/term/DOID:4448",
                "evidence": [
                    {
                        "id": "4448",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4448"
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                ],
                "weight": 0.0
            },
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                "name": "acquired immunodeficiency syndrome",
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                "url": "https://disease-ontology.org/term/DOID:635",
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                    {
                        "id": "635",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:635"
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                ],
                "weight": 0.0
            },
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                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:8552",
                "name": "chronic myeloid leukemia",
                "description": "A myeloid leukemia that is characterized by over production of white blood cells.",
                "url": "https://disease-ontology.org/term/DOID:8552",
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                        "id": "8552",
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                        "url": "https://www.alliancegenome.org/disease/DOID:8552"
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                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:9119",
                "evidence": [
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                        "id": "9119",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9119"
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                ],
                "weight": 0.0
            },
            {
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                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
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                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
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                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:9538",
                "name": "multiple myeloma",
                "description": "A myeloid neoplasm that is located_in the plasma cells in bone marrow.",
                "url": "https://disease-ontology.org/term/DOID:9538",
                "evidence": [
                    {
                        "id": "9538",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9538"
                    }
                ],
                "weight": 0.0
            },
            {
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                "name": "oral mucosa leukoplakia",
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                "url": "https://disease-ontology.org/term/DOID:9655",
                "evidence": [
                    {
                        "id": "9655",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9655"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:9669",
                "name": "senile cataract",
                "description": "A cataract that is characterized by thickening and loss of transparency of the lens with age progression, caused by a multifactorial etiology related to aging.",
                "url": "https://disease-ontology.org/term/DOID:9669",
                "evidence": [
                    {
                        "id": "9669",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9669"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9952",
                "name": "acute lymphoblastic leukemia",
                "description": "A acute leukemia that is characterized by over production of lymphoblasts.",
                "url": "https://disease-ontology.org/term/DOID:9952",
                "evidence": [
                    {
                        "id": "9952",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9952"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "4 iron, 4 sulfur cluster binding",
                "id": "GO:0051539",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051539",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "damaged DNA binding",
                "id": "GO:0003684",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003684",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP hydrolysis activity",
                "id": "GO:0016887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA helicase activity",
                "id": "GO:0003678",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003678",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "5'-3' DNA helicase activity",
                "id": "GO:0043139",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043139",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription factor TFIIH holo complex",
                "id": "GO:0005675",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005675",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription factor TFIIH core complex",
                "id": "GO:0000439",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000439",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "polytene chromosome",
                "id": "GO:0005700",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005700",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "polytene chromosome puff",
                "id": "GO:0005703",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005703",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "polytene chromosome interband",
                "id": "GO:0005705",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005705",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "DNA damage response",
                "id": "GO:0006974",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006974",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to UV",
                "id": "GO:0009411",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009411",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription by RNA polymerase II",
                "id": "GO:0006366",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006366",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription initiation at RNA polymerase II promoter",
                "id": "GO:0006367",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006367",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of mitotic nuclear division",
                "id": "GO:0007088",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007088",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleotide-excision repair",
                "id": "GO:0006289",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006289",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of G2/M transition of mitotic cell cycle",
                "id": "GO:0010972",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010972",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA polymerase II promoter clearance",
                "id": "GO:0001111",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001111",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription open complex formation at RNA polymerase II promoter",
                "id": "GO:0001113",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001113",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of chromosome segregation",
                "id": "GO:0051983",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051983",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "hair cell differentiation",
                "id": "GO:0035315",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035315",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of mitotic recombination",
                "id": "GO:0045951",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045951",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of syncytial blastoderm mitotic cell cycle",
                "id": "GO:0007348",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007348",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVP9"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q7KVP9-1"
    },
    {
        "uniprot_canonical_ac": "Q7PLB8-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLB8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLB8"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 2394,
        "chemical_mass": 266851.0,
        "gene_names": "FASN3;80Ff;CG17374;DM_7289423;Dmel\\CG17374;Dmel_CG17374;FASN3;FASN[CG17374];FAS[CG17374];FAS;fasn3;l(3)80Ff;l(3)Lh4B;l4B",
        "protein_name": "Fatty acid synthase",
        "disease": [
            {
                "disease_id": "DOID:0080000",
                "name": "muscular disease",
                "description": "A musculoskeletal system disease that affects the muscles.",
                "url": "https://disease-ontology.org/term/DOID:0080000",
                "evidence": [
                    {
                        "id": "0080000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080000"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080208",
                "name": "metabolic dysfunction-associated steatotic liver disease",
                "description": "A steatotic liver disease characterized by at least one of five specified cardiometabolic risk factors and no other discernible cause with normal to no alcohol use. The five cardiometabolic risk factors are: (1) higher than normal body mass index or waist circumference; (2) higher than normal serum glucose or glycated hemoglobin level, or type 2 diabetes; (3) higher than normal blood pressure or hypertensive treatment; (4) higher than normal plasma triglycerides or lipid lowering treatment; and (5) lower than normal plasma high-density lipoprotein cholesterol.",
                "url": "https://disease-ontology.org/term/DOID:0080208",
                "evidence": [
                    {
                        "id": "0080208",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080208"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "fatty acid biosynthetic process",
                "id": "GO:0006633",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006633",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLB8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLB8"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "phosphopantetheine binding",
                "id": "GO:0031177",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031177",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLB8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLB8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "fatty acid synthase activity",
                "id": "GO:0004312",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004312",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLB8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLB8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "[acyl-carrier-protein] S-acetyltransferase activity",
                "id": "GO:0004313",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004313",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLB8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLB8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "3-oxoacyl-[acyl-carrier-protein] synthase activity",
                "id": "GO:0004315",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004315",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLB8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLB8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity",
                "id": "GO:0004316",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004316",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLB8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLB8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "fatty acyl-[ACP] hydrolase activity",
                "id": "GO:0016297",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016297",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLB8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLB8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "(3R)-hydroxyacyl-[acyl-carrier-protein] dehydratase activity",
                "id": "GO:0019171",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019171",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLB8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLB8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "enoyl-[acyl-carrier-protein] reductase (NADPH) activity",
                "id": "GO:0141148",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0141148",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLB8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLB8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q7PLB8-1"
    },
    {
        "uniprot_canonical_ac": "Q7PLI0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 781,
        "chemical_mass": 86823.0,
        "gene_names": "p120ctn;CG17484;Dmel\\CG17484;Dmel_CG17484;Dp120[ctn];Dp120ctn;P120-catenin;P120ctn;P120;dP120ctn;dp120ctn;p120[ctn];p120ctn;p120",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050431",
                "name": "arrhythmogenic right ventricular cardiomyopathy",
                "description": "An intrinsic cardiomyopathy that is characterized by hypokinetic areas involving the free wall of the right ventricle, with fibrofatty replacement of the right ventricular myocardium, with associated arrhythmias originating in the right ventricle and limited or no involvement of the left ventricle.",
                "url": "https://disease-ontology.org/term/DOID:0050431",
                "evidence": [
                    {
                        "id": "0050431",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050431"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050866",
                "name": "oral squamous cell carcinoma",
                "description": "An oral cavity cancer that has_material_basis_in squamous cells.",
                "url": "https://disease-ontology.org/term/DOID:0050866",
                "evidence": [
                    {
                        "id": "0050866",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050866"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060041",
                "name": "autism spectrum disorder",
                "description": "A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior.",
                "url": "https://disease-ontology.org/term/DOID:0060041",
                "evidence": [
                    {
                        "id": "0060041",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060041"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080346",
                "name": "blepharocheilodontic syndrome 2",
                "description": "A blepharocheilodontic syndrome that has_material_basis_in heterozygous mutation in the CTNND1 gene on chromosome 11q12.",
                "url": "https://disease-ontology.org/term/DOID:0080346",
                "evidence": [
                    {
                        "id": "0080346",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080346"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110077",
                "name": "arrhythmogenic right ventricular dysplasia 9",
                "description": "An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutations in the PKP2 gene on chromosome 12p11.",
                "url": "https://disease-ontology.org/term/DOID:0110077",
                "evidence": [
                    {
                        "id": "0110077",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110077"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11198",
                "name": "DiGeorge syndrome",
                "description": "A syndrome that has_material_basis_in a large deletion of the chromosome 22q11.2 region which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production.",
                "url": "https://disease-ontology.org/term/DOID:11198",
                "evidence": [
                    {
                        "id": "11198",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11198"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1470",
                "name": "major depressive disorder",
                "description": "A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality.",
                "url": "https://disease-ontology.org/term/DOID:1470",
                "evidence": [
                    {
                        "id": "1470",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1470"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2030",
                "name": "anxiety disorder",
                "description": "A cognitive disorder that involves an excessive, irrational dread of everyday situations.",
                "url": "https://disease-ontology.org/term/DOID:2030",
                "evidence": [
                    {
                        "id": "2030",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2030"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2121",
                "name": "ectodermal dysplasia",
                "description": "A syndrome characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings.",
                "url": "https://disease-ontology.org/term/DOID:2121",
                "evidence": [
                    {
                        "id": "2121",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2121"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.",
                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6432",
                "name": "pulmonary hypertension",
                "description": "A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries.",
                "url": "https://disease-ontology.org/term/DOID:6432",
                "evidence": [
                    {
                        "id": "6432",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6432"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "centrosome",
                "id": "GO:0005813",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005813",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "adherens junction",
                "id": "GO:0005912",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005912",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cell adhesion",
                "id": "GO:0007155",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007155",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell-cell adhesion",
                "id": "GO:0098609",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098609",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dendritic spine morphogenesis",
                "id": "GO:0060997",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060997",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "adherens junction maintenance",
                "id": "GO:0034334",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034334",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "compound eye morphogenesis",
                "id": "GO:0001745",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001745",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "cadherin binding",
                "id": "GO:0045296",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045296",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7PLI0",
                        "url": "https://www.uniprot.org/uniprotkb/Q7PLI0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q7PLI0-1"
    },
    {
        "uniprot_canonical_ac": "Q86BI5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q86BI5",
                        "url": "https://www.uniprot.org/uniprotkb/Q86BI5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 121,
        "chemical_mass": 13838.0,
        "gene_names": "CG13057;CG13057;CG33060;Dmel\\CG33060;Dmel_CG33060",
        "protein_name": "Protein dpy-30 homolog",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q86BI5-1"
    },
    {
        "uniprot_canonical_ac": "Q8IML0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IML0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IML0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 373,
        "chemical_mass": 42066.0,
        "gene_names": "Dmel\\CG14507;CG14507;Dmel\\CG14507;Dmel_CG14507",
        "protein_name": "Phospholipase A2",
        "disease": [
            {
                "disease_id": "DOID:0111677",
                "name": "familial benign fleck retina",
                "description": "A retinal disease characterized by a striking pattern of diffuse, yellow-white, fleck-like lesions extending to the far periphery of the retina but with no apparent visual or electrophysiologic deficits that has_material_basis_in homozygous or compound heterozygous mutation in the PLA2G5 gene on chromosome 1p36.13.",
                "url": "https://disease-ontology.org/term/DOID:0111677",
                "evidence": [
                    {
                        "id": "0111677",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111677"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11151",
                "name": "cholecystolithiasis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11151",
                "evidence": [
                    {
                        "id": "11151",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11151"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11204",
                "name": "allergic conjunctivitis",
                "description": "A chronic conjunctivitis that is an inflammation of the conjunctiva involing red, itchy, and watery eyes a resulting from an exposure to an allergen or an irritant.",
                "url": "https://disease-ontology.org/term/DOID:11204",
                "evidence": [
                    {
                        "id": "11204",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11204"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11394",
                "name": "adult respiratory distress syndrome",
                "description": "A respiratory failure that results from diffuse injury to the endothelium of the lung (as in sepsis, chest trauma, massive blood transfusion, aspiration of the gastric contents, or pneumonia) and is characterized by pulmonary edema with an abnormally high amount of protein in the edematous fluid and by difficult rapid breathing and hypoxemia.",
                "url": "https://disease-ontology.org/term/DOID:11394",
                "evidence": [
                    {
                        "id": "11394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1596",
                "name": "depressive disorder",
                "description": "A mood disorder characterized by persistent sadness, emptiness, or irritability and decreased ability to function.",
                "url": "https://disease-ontology.org/term/DOID:1596",
                "evidence": [
                    {
                        "id": "1596",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1596"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:526",
                "name": "human immunodeficiency virus infectious disease",
                "description": "A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 (Lentivirus humimdef1) or Human immunodeficiency virus 2 (Lentivirus humimdef2), which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands.",
                "url": "https://disease-ontology.org/term/DOID:526",
                "evidence": [
                    {
                        "id": "526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:526"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8534",
                "name": "gastroesophageal reflux disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8534",
                "evidence": [
                    {
                        "id": "8534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IML0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IML0"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "lipid catabolic process",
                "id": "GO:0016042",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016042",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IML0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IML0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "arachidonate secretion",
                "id": "GO:0050482",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050482",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IML0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IML0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phospholipid metabolic process",
                "id": "GO:0006644",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006644",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IML0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IML0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "calcium ion binding",
                "id": "GO:0005509",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005509",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IML0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IML0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phospholipase A2 activity",
                "id": "GO:0004623",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004623",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IML0",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IML0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q8IML0-1"
    },
    {
        "uniprot_canonical_ac": "Q8IMQ3-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMQ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMQ3"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 988,
        "chemical_mass": 110326.0,
        "gene_names": "Dmel\\CG31077;CG31077;Dmel\\CG31077;Dmel_CG31077",
        "protein_name": "Chitin-binding type-2 domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMQ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMQ3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "external encapsulating structure",
                "id": "GO:0030312",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030312",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMQ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMQ3"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "chitin binding",
                "id": "GO:0008061",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008061",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMQ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMQ3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q8IMQ3-1"
    },
    {
        "uniprot_canonical_ac": "Q8IMR4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMR4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMR4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 402,
        "chemical_mass": 44796.0,
        "gene_names": "Yif1;CG5484;COP;Dmel\\CG5484;Dmel_CG5484;Yif1;anon-WO0118547.366;doc",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:14330",
                "name": "Parkinson's disease",
                "description": "A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions.",
                "url": "https://disease-ontology.org/term/DOID:14330",
                "evidence": [
                    {
                        "id": "14330",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14330"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "Golgi membrane",
                "id": "GO:0000139",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000139",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMR4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMR4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endoplasmic reticulum membrane",
                "id": "GO:0005789",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005789",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMR4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMR4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endoplasmic reticulum-Golgi intermediate compartment",
                "id": "GO:0005793",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005793",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMR4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMR4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "COPII-coated ER to Golgi transport vesicle",
                "id": "GO:0030134",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030134",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMR4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMR4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endoplasmic reticulum exit site",
                "id": "GO:0070971",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070971",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMR4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMR4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cis-Golgi network",
                "id": "GO:0005801",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005801",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMR4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMR4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein transport",
                "id": "GO:0015031",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015031",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMR4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMR4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endoplasmic reticulum to Golgi vesicle-mediated transport",
                "id": "GO:0006888",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006888",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMR4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMR4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of synapse pruning",
                "id": "GO:1905808",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905808",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMR4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMR4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q8IMR4-1"
    },
    {
        "uniprot_canonical_ac": "Q8IMT4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMT4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMT4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 428,
        "chemical_mass": 49978.0,
        "gene_names": "CG13665;CG13665;CG31288;Dmel\\CG31288;Dmel_CG31288;Dro11-0",
        "protein_name": "CHK kinase-like domain-containing protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "ecdysteroid 22-kinase activity",
                "id": "GO:0106389",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0106389",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IMT4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IMT4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 548,
        "chemical_mass": 60406.0,
        "gene_names": "dock;2L19;CG3727;DOCK;Dm0447;Dmel\\CG3727;Dock;Nck;dck;dock;doc;l(2)04723",
        "protein_name": "SH2/SH3 adapter protein dreadlocks",
        "disease": [],
        "biological_process": [
            {
                "name": "negative regulation of insulin receptor signaling pathway",
                "id": "GO:0046627",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046627",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "myoblast fusion",
                "id": "GO:0007520",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007520",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axon guidance",
                "id": "GO:0007411",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007411",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "insulin receptor binding",
                "id": "GO:0005158",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005158",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein kinase binding",
                "id": "GO:0019901",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019901",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein-macromolecule adaptor activity",
                "id": "GO:0030674",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030674",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell adhesion molecule binding",
                "id": "GO:0050839",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050839",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "kinase binding",
                "id": "GO:0019900",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019900",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "growth cone",
                "id": "GO:0030426",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030426",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "perikaryon",
                "id": "GO:0043204",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043204",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear body",
                "id": "GO:0016604",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016604",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "clathrin-coated vesicle",
                "id": "GO:0030136",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030136",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell periphery",
                "id": "GO:0071944",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071944",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "male germline ring canal",
                "id": "GO:0035323",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035323",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q8IPW2-2",
                "start_pos": "186",
                "end_pos": "186",
                "site_lbl": "Trp186",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "W",
                        "sequence_mut": "K",
                        "comment": "Probably disrupts the binding pocket of SH3 domain 1. No effect on interaction with Pak. Unable to rescue R cell projection phenotype in loss of function mutants; when associated with Q-336.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8IPW2",
                                "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                            },
                            {
                                "database": "PubMed",
                                "id": "10399914",
                                "url": "https://glygen.org/publication/PubMed/10399914"
                            },
                            {
                                "database": "PubMed",
                                "id": "9482841",
                                "url": "https://glygen.org/publication/PubMed/9482841"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q8IPW2-2",
                "start_pos": "289",
                "end_pos": "289",
                "site_lbl": "Trp289",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "W",
                        "sequence_mut": "K",
                        "comment": "Probably disrupts the binding pocket of SH3 domain 2. Disrupts interaction with Pak. Unable to rescue R cell projection phenotype in loss of function mutants.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8IPW2",
                                "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                            },
                            {
                                "database": "PubMed",
                                "id": "10399914",
                                "url": "https://glygen.org/publication/PubMed/10399914"
                            },
                            {
                                "database": "PubMed",
                                "id": "9482841",
                                "url": "https://glygen.org/publication/PubMed/9482841"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q8IPW2-2",
                "start_pos": "363",
                "end_pos": "363",
                "site_lbl": "Trp363",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "W",
                        "sequence_mut": "K",
                        "comment": "Probably disrupts the binding pocket of SH3 domain 3. No effect on interaction with Pak. Unable to rescue R cell projection phenotype in loss of function mutants; when associated with Q-336.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8IPW2",
                                "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                            },
                            {
                                "database": "PubMed",
                                "id": "9482841",
                                "url": "https://glygen.org/publication/PubMed/9482841"
                            },
                            {
                                "database": "PubMed",
                                "id": "10399914",
                                "url": "https://glygen.org/publication/PubMed/10399914"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q8IPW2-2",
                "start_pos": "474",
                "end_pos": "474",
                "site_lbl": "Arg474",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "R",
                        "sequence_mut": "Q",
                        "comment": "Probably disrupts SH2 phosphotyrosine binding pocket. Unable to rescue R cell projection phenotype in loss of function mutants; when associated with K-48 or K-225.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q8IPW2",
                                "url": "https://www.uniprot.org/uniprotkb/Q8IPW2"
                            },
                            {
                                "database": "PubMed",
                                "id": "9482841",
                                "url": "https://glygen.org/publication/PubMed/9482841"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "Q8IPW2-2"
    },
    {
        "uniprot_canonical_ac": "Q8IPX4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPX4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPX4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 192,
        "chemical_mass": 21952.0,
        "gene_names": "CG16933;CG16933;CG31659;Dmel\\CG31659;Dmel_CG31659",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "insemination",
                "id": "GO:0007320",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007320",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPX4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPX4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "lipid metabolic process",
                "id": "GO:0006629",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006629",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPX4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPX4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to reactive oxygen species",
                "id": "GO:0000302",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000302",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPX4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPX4"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPX4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPX4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPX4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPX4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q8IPX4-1"
    },
    {
        "uniprot_canonical_ac": "Q8IQ06-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ06",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ06"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 109,
        "chemical_mass": 12293.0,
        "gene_names": "BEST:RH19272;BEST:RH19272;CG31777;Dmel\\CG31777;Dmel_CG31777",
        "protein_name": "BPTI/Kunitz inhibitor domain-containing protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "serine-type endopeptidase inhibitor activity",
                "id": "GO:0004867",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004867",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ06",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ06"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q8IQ06-1"
    },
    {
        "uniprot_canonical_ac": "Q8IQ79-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ79",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ79"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 253,
        "chemical_mass": 29067.0,
        "gene_names": "sphinx1;CG32383;CG8555;Dmel\\CG32383;Dmel_CG32383;SPH194a;SPH194;Sphinx-1;Sphinx1;Spx1;sphinx-1;sphinx1",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ79",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ79"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ79",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ79"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ79",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ79"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "innate immune response",
                "id": "GO:0045087",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045087",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ79",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ79"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "defense response to Gram-negative bacterium",
                "id": "GO:0050829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ79",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ79"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "defense response to Gram-positive bacterium",
                "id": "GO:0050830",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050830",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ79",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ79"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "defense response to fungus",
                "id": "GO:0050832",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050832",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ79",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ79"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mating",
                "id": "GO:0007618",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007618",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ79",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ79"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Toll receptor ligand protein activation cascade",
                "id": "GO:0160032",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0160032",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ79",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ79"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "hydrolase activity",
                "id": "GO:0016787",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016787",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ79",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ79"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q8IQ79-1"
    },
    {
        "uniprot_canonical_ac": "Q8IQ88-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ88",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ88"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 760,
        "chemical_mass": 83551.0,
        "gene_names": "Dmel\\CG14837;CG14837;Dmel\\CG14837;Dmel_CG14837",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q8IQ88-1"
    },
    {
        "uniprot_canonical_ac": "Q8IQ89-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ89",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ89"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 291,
        "chemical_mass": 33062.0,
        "gene_names": "Dmel\\CG32376;CG32376;CG8528;Dmel\\CG32376;Dmel_CG32376;SP148b;SP148",
        "protein_name": "Peptidase S1 domain-containing protein",
        "disease": [
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "serine-type endopeptidase activity",
                "id": "GO:0004252",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004252",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ89",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ89"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ89",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ89"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "digestion",
                "id": "GO:0007586",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007586",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQ89",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQ89"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "hemolymph coagulation",
                "id": "GO:0042381",
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                "name": "polyubiquitin modification-dependent protein binding",
                "id": "GO:0031593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031593",
                "evidence": [
                    {
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                        "url": "https://www.uniprot.org/uniprotkb/Q8IRD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP hydrolysis activity",
                "id": "GO:0016887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016887",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q8IRD1"
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                ],
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            {
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                    {
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                        "type": "O-linked",
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                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
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                        "site_category_dict": {
                            "predicted": true
                        },
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                        "relation": "attached",
                        "comment": "",
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        ],
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                "disease_id": "DOID:1682",
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                "url": "https://disease-ontology.org/term/DOID:3083",
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                    {
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                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:3312",
                "evidence": [
                    {
                        "id": "3312",
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            {
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                ],
                "pmid": ""
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            {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "plasma membrane",
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                "pmid": ""
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        ],
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            {
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            {
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        ],
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                ],
                "pmid": ""
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        ],
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    {
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                ],
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        ],
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            {
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                ],
                "pmid": ""
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        ],
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            {
                "name": "endosome",
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                ],
                "pmid": ""
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            {
                "name": "plasma membrane",
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                ],
                "pmid": ""
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                "name": "vesicle",
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                "pmid": ""
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                "name": "synaptic vesicle",
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                ],
                "pmid": ""
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            {
                "name": "trans-Golgi network transport vesicle",
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                ],
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                "name": "exocytosis",
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                "pmid": ""
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                "name": "endocytic recycling",
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                "name": "Rab protein signal transduction",
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        ],
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                ],
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        ],
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                "name": "nucleus",
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        ],
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                "name": "DNA-templated transcription",
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                "name": "nuclear-transcribed mRNA poly(A) tail shortening",
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                ],
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    {
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                ],
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        ],
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    },
    {
        "uniprot_canonical_ac": "Q8MMD6-1",
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                "name": "Drosophila melanogaster",
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                "evidence": [
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                        "id": "Q8MMD6",
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                    }
                ],
                "common_name": "Fruit fly",
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        ],
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        "gene_names": "MFS1;CG11682;CG30272;Dmel\\CG30272;Dmel_CG30272;MFS1",
        "protein_name": "Putative inorganic phosphate cotransporter",
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            {
                "name": "membrane",
                "id": "GO:0016020",
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            {
                "name": "symporter activity",
                "id": "GO:0015293",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015293",
                "evidence": [
                    {
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                        "url": "https://www.uniprot.org/uniprotkb/Q8MMD6"
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                ],
                "pmid": ""
            }
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                "name": "sodium ion transport",
                "id": "GO:0006814",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006814",
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            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                    {
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                ],
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            {
                "name": "negative regulation of ERK1 and ERK2 cascade",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070373",
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                    {
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                ],
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    {
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            {
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                        "id": "Q9I7M8",
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "gene_names": "Ku80;BG:DS09217.6;CG18801;DmKu80;Dmel\\CG18801;Dmel_CG18801;KU80;Ku80;Ku;ku80",
        "protein_name": "ATP-dependent DNA helicase II subunit 2",
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                "url": "https://disease-ontology.org/term/DOID:1574",
                "evidence": [
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                        "id": "1574",
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                ],
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                "disease_id": "DOID:1749",
                "name": "squamous cell carcinoma",
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                "url": "https://disease-ontology.org/term/DOID:1749",
                "evidence": [
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                        "id": "1749",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1749"
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                ],
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            },
            {
                "disease_id": "DOID:1993",
                "name": "rectum cancer",
                "description": "A colorectal cancer that is located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:1993",
                "evidence": [
                    {
                        "id": "1993",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1993"
                    }
                ],
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            },
            {
                "disease_id": "DOID:2513",
                "name": "basal cell carcinoma",
                "description": "A skin carcinoma affecting basal cells.",
                "url": "https://disease-ontology.org/term/DOID:2513",
                "evidence": [
                    {
                        "id": "2513",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2513"
                    }
                ],
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            },
            {
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                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9538",
                "name": "multiple myeloma",
                "description": "A myeloid neoplasm that is located_in the plasma cells in bone marrow.",
                "url": "https://disease-ontology.org/term/DOID:9538",
                "evidence": [
                    {
                        "id": "9538",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9538"
                    }
                ],
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            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
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                    {
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                        "id": "Q9I7M8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9I7M8"
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                ],
                "pmid": ""
            },
            {
                "name": "damaged DNA binding",
                "id": "GO:0003684",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003684",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9I7M8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9I7M8"
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                ],
                "pmid": ""
            },
            {
                "name": "ATP hydrolysis activity",
                "id": "GO:0016887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016887",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9I7M8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9I7M8"
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                ],
                "pmid": ""
            },
            {
                "name": "telomeric DNA binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042162",
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                    {
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                        "id": "Q9I7M8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9I7M8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA helicase activity",
                "id": "GO:0003678",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003678",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9I7M8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9I7M8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP-dependent activity, acting on DNA",
                "id": "GO:0008094",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008094",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9I7M8"
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "DNA recombination",
                "id": "GO:0006310",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006310",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9I7M8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9I7M8"
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                ],
                "pmid": ""
            },
            {
                "name": "response to ethanol",
                "id": "GO:0045471",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045471",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9I7M8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9I7M8"
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                ],
                "pmid": ""
            },
            {
                "name": "telomere maintenance",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9I7M8"
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                ],
                "pmid": ""
            },
            {
                "name": "double-strand break repair via nonhomologous end joining",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006303",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9I7M8"
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                ],
                "pmid": ""
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        ],
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            {
                "name": "Ku70:Ku80 complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043564",
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                ],
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        ],
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                "name": "extracellular space",
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                ],
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        ],
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            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
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                ],
                "pmid": ""
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        ],
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    },
    {
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                ],
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        ],
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        "protein_name": "Ankyrin repeat domain-containing protein 49",
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            {
                "name": "cytosol",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9V3Y0"
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                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9V3Y0"
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                ],
                "pmid": ""
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        ],
        "biological_process": [
            {
                "name": "regulation of establishment of planar polarity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090175",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V3Y0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V3Y0"
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                ],
                "pmid": ""
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        ],
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            {
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                        "sequence_org": "A",
                        "sequence_mut": "T",
                        "comment": "Lethal. Pupal wings containing clones display reduced levels of dsh, reduced asymmetric localization of stan, delayed trichome initiation, and formation of trichomes in the cell center rather than at the distal cell edge; when associated with A-87.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q9V3Y0",
                                "url": "https://www.uniprot.org/uniprotkb/Q9V3Y0"
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                                "id": "32750048",
                                "url": "https://glygen.org/publication/PubMed/32750048"
                            }
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                    {
                        "sequence_org": "H",
                        "sequence_mut": "Y",
                        "comment": "Lethal. Pupal wings containing clones display reduced levels of dsh, reduced asymmetric localization of stan, delayed trichome initiation, and formation of trichomes in the cell center rather than at the distal cell edge; when associated with T-156.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q9V3Y0",
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                            },
                            {
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        ],
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    {
        "uniprot_canonical_ac": "Q9V421-1",
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                "name": "Drosophila melanogaster",
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                        "id": "Q9V421",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V421"
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "gene_names": "BG:BACR44L22.3;BACR44L22.3;BG:BACR44L22.3;CG15253;Dmel\\CG15253;Dmel_CG15253",
        "protein_name": "Metalloendopeptidase",
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            {
                "name": "metalloendopeptidase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004222",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V421",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V421"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "zinc ion binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
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                        "id": "Q9V421",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V421"
                    }
                ],
                "pmid": ""
            }
        ],
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                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V421",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V421"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V421",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V421"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "Q9V9P0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9P0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9P0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 390,
        "chemical_mass": 44184.0,
        "gene_names": "Dmel\\CG6675;CG6675;Dmel\\CG6675;Dmel_CG6675",
        "protein_name": "Lipase domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9P0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9P0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9P0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9P0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "lipase activity",
                "id": "GO:0016298",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016298",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9P0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9P0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "triacylglycerol lipase activity",
                "id": "GO:0004806",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004806",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9P0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9P0"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "lipid catabolic process",
                "id": "GO:0016042",
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                    {
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                ],
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            {
                "name": "insemination",
                "id": "GO:0007320",
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                ],
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            }
        ],
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            {
                "name": "extracellular space",
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                ],
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                "name": "phosphatidylinositol bisphosphate binding",
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                    {
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                ],
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            }
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            {
                "name": "acetyl-CoA hydrolase activity",
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            },
            {
                "name": "fatty acyl-CoA hydrolase activity",
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                ],
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            }
        ],
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            {
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            },
            {
                "name": "mitochondrial matrix",
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            }
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                "name": "acyl-CoA metabolic process",
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                ],
                "pmid": ""
            }
        ],
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                ],
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            }
        ],
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            {
                "name": "kinetochore microtubule",
                "id": "GO:0005828",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9W7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9W7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RZZ complex",
                "id": "GO:1990423",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990423",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9W7",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                    {
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                        "id": "Q9V9W7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9W7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "spindle",
                "id": "GO:0005819",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005819",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9W7",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "spindle midzone",
                "id": "GO:0051233",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051233",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9W7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9W7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "kinetochore",
                "id": "GO:0000776",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000776",
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                    {
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                        "id": "Q9V9W7",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "Golgi stack",
                "id": "GO:0005795",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005795",
                "evidence": [
                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "acroblast",
                "id": "GO:0036063",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036063",
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                    {
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                        "id": "Q9V9W7",
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "regulation of chromosome separation",
                "id": "GO:1905818",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905818",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9W7",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein localization to kinetochore involved in kinetochore assembly",
                "id": "GO:1903394",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1903394",
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                    {
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                ],
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            },
            {
                "name": "mitotic spindle assembly checkpoint signaling",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007094",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of attachment of spindle microtubules to kinetochore",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051988",
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                    {
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                ],
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            },
            {
                "name": "regulation of mitotic metaphase/anaphase transition",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "Golgi organization",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007030",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
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            {
                "name": "mitotic sister chromatid segregation",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000070",
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                ],
                "pmid": ""
            },
            {
                "name": "protein localization to kinetochore",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034501",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9W7",
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "small GTPase binding",
                "id": "GO:0031267",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031267",
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                    {
                        "database": "UniProtKB",
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                ],
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        ],
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                ],
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        ],
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                "disease_id": "DOID:0050861",
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                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:0050997",
                "evidence": [
                    {
                        "id": "0050997",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0050997"
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                ],
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            },
            {
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                "evidence": [
                    {
                        "id": "0080199",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0080199"
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                ],
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            },
            {
                "disease_id": "DOID:0111371",
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                "description": "A skin disease characterized by excessive loss of salt in sweat resulting in low levels of salt in the blood in the absence of other symptoms that has_material_basis_in homozygous or compound heterozygous mutation in the CA12 gene on chromosome 15q22.2.",
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                "evidence": [
                    {
                        "id": "0111371",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0111371"
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                ],
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            },
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                "name": "lung cancer",
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                    {
                        "id": "1324",
                        "database": "AGR",
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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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                ],
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            },
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                ],
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                        "id": "5015",
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                ],
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            },
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                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
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                ],
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            }
        ],
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            {
                "name": "cytoplasm",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            },
            {
                "name": "carbonate dehydratase activity",
                "id": "GO:0004089",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004089",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                ],
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            }
        ],
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    {
        "uniprot_canonical_ac": "Q9VA61-1",
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            {
                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VA61",
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "gene_names": "PH4alphaNE2;CG9720;Dmel\\CG9720;Dmel_CG9720;PH4-alpha-NE2;PH4alphaNE2",
        "protein_name": "procollagen-proline 4-dioxygenase",
        "disease": [
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
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                    {
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                "name": "L-ascorbic acid binding",
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                "name": "endoplasmic reticulum",
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                "name": "endoplasmic reticulum lumen",
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                "name": "cell migration",
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                "pmid": ""
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                "name": "mating",
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                "pmid": ""
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                "pmid": ""
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                "name": "ceramide biosynthetic process",
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                "name": "hydrolase activity, acting on glycosyl bonds",
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                "name": "acid sphingomyelin phosphodiesterase activity",
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                ],
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            }
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        ],
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                "name": "hydrolase activity",
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                "name": "arylesterase activity",
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                ],
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            {
                "name": "lyase activity",
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                "pmid": ""
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                ],
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        ],
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        "protein_name": "Histone acetyltransferase",
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                "disease_id": "DOID:1612",
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                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
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                    }
                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:162",
                "evidence": [
                    {
                        "id": "162",
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                    }
                ],
                "weight": 0.0
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            {
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                "evidence": [
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                    }
                ],
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        ],
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                "name": "nucleus",
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                "pmid": ""
            },
            {
                "name": "NuA4 histone acetyltransferase complex",
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                "pmid": ""
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            {
                "name": "euchromatin",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VAV6"
                    }
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                "pmid": ""
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            {
                "name": "MSL complex",
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                ],
                "pmid": ""
            },
            {
                "name": "chromosome, telomeric region",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000781",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VAV6"
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                ],
                "pmid": ""
            },
            {
                "name": "NSL complex",
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                "pmid": ""
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        ],
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                "name": "regulation of DNA-templated transcription",
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                        "database": "UniProtKB",
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        ],
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                "name": "histone acetyltransferase activity",
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                    {
                        "database": "UniProtKB",
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            {
                "name": "histone H4K16 acetyltransferase activity",
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
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                ],
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        ],
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            {
                "name": "nucleus",
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                ],
                "pmid": ""
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                "name": "nucleoplasm",
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                "pmid": ""
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                "name": "cytoplasm",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VAW1"
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                "pmid": ""
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            {
                "name": "catalytic step 2 spliceosome",
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                ],
                "pmid": ""
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            {
                "name": "precatalytic spliceosome",
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                "pmid": ""
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        ],
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                "name": "protein folding",
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            {
                "name": "mRNA splicing, via spliceosome",
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                "name": "cyclosporin A binding",
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                ],
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            {
                "name": "peptidyl-prolyl cis-trans isomerase activity",
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                    }
                ],
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        ],
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                "name": "cytosol",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 91815.0,
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            {
                "disease_id": "DOID:0060259",
                "name": "renal-hepatic-pancreatic dysplasia",
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                "url": "https://disease-ontology.org/term/DOID:0060259",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0060259"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0060558",
                "name": "lethal congenital contracture syndrome",
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                    {
                        "id": "0060558",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0060558"
                    }
                ],
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                "disease_id": "DOID:0081378",
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                    }
                ],
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            },
            {
                "disease_id": "DOID:0110861",
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                    {
                        "id": "0110861",
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                    }
                ],
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            },
            {
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                    {
                        "id": "0111120",
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                    }
                ],
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        ],
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            {
                "name": "protein serine/threonine kinase activity",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
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                    {
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                    }
                ],
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            },
            {
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                "id": "GO:0046872",
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                    {
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                ],
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            }
        ],
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            {
                "name": "cytoplasm",
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                    {
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                    }
                ],
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            },
            {
                "name": "cilium",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
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            }
        ],
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    },
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                        "database": "UniProtKB",
                        "id": "Q9VC68",
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                    }
                ],
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        ],
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    },
    {
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            {
                "name": "Drosophila melanogaster",
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                    {
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                    }
                ],
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            }
        ],
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            {
                "name": "TSC1-TSC2 complex",
                "id": "GO:0033596",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033596",
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                    {
                        "database": "UniProtKB",
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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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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "GTPase activator activity",
                "id": "GO:0005096",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005096",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "TSC1-TSC2 complex binding",
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                    {
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                        "id": "Q9VCC4",
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                    }
                ],
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            }
        ],
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            {
                "name": "glucose homeostasis",
                "id": "GO:0042593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042593",
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                    {
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                    }
                ],
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            },
            {
                "name": "negative regulation of TOR signaling",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032007",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "Q9VCJ2-1",
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            {
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                    }
                ],
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        ],
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            {
                "name": "phosphatidylinositol bisphosphate binding",
                "id": "GO:1902936",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1902936",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "lipid transfer activity",
                "id": "GO:0120013",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0120013",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VCJ2",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "intermembrane lipid transfer",
                "id": "GO:0120009",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0120009",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VCJ2",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "Q9VCJ9-1",
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            {
                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VCJ9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCJ9"
                    }
                ],
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            }
        ],
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        "gene_names": "Dmel\\CG16710;CG16710;Dmel\\CG16710;Dmel_CG16710;SP16;cSP16",
        "protein_name": "CLIP domain-containing serine protease",
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        "molecular_function": [
            {
                "name": "serine-type endopeptidase activity",
                "id": "GO:0004252",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004252",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCJ9",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VCJ9",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VCJ9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCJ9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCJ9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCJ9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "innate immune response",
                "id": "GO:0045087",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045087",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCJ9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCJ9"
                    }
                ],
                "pmid": ""
            }
        ],
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        "record_id": "Q9VCJ9-1"
    },
    {
        "uniprot_canonical_ac": "Q9VCL3-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCL3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCL3"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 62243.0,
        "gene_names": "Ugt303B2;CG10168;Dmel\\CG10168;Dmel_CG10168;UGT303B2;Ugt303B2",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "UDP-glycosyltransferase activity",
                "id": "GO:0008194",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008194",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCL3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCL3"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "endoplasmic reticulum membrane",
                "id": "GO:0005789",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005789",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCL3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCL3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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            {
                "uniprot_canonical_ac": "Q9VCL3-1",
                "start_pos": "61",
                "end_pos": "61",
                "site_lbl": "Thr61",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 61,
                        "start_aa": "Thr",
                        "end_pos": 61,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr61",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "Q9VCM8-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCM8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCM8"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 479,
        "chemical_mass": 54385.0,
        "gene_names": "Dmel\\CG4408;BEST:GH09055;CG4408;Dmel\\CG4408;Dmel_CG4408",
        "protein_name": "Zinc carboxypeptidase A 1",
        "disease": [
            {
                "disease_id": "DOID:0060752",
                "name": "familial temporal lobe epilepsy 5",
                "description": "A temporal lobe epilepsy that has_material_basis_in heterozygous mutation in the CPA6 gene on chromosome 8q13.",
                "url": "https://disease-ontology.org/term/DOID:0060752",
                "evidence": [
                    {
                        "id": "0060752",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060752"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111308",
                "name": "familial febrile seizures 11",
                "description": "A familial febrile seizures that has_material_basis_in homozygous mutation in the CPA6 gene on chromosome 8p13.2.",
                "url": "https://disease-ontology.org/term/DOID:0111308",
                "evidence": [
                    {
                        "id": "0111308",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111308"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1184",
                "name": "nephrotic syndrome",
                "description": "A nephrosis characterized by marked increase in glomerular protein permeability resulting in marked elevation of urine protein levels, hypoalbuminemia, hyperlipidemia, and hypercoagulability.",
                "url": "https://disease-ontology.org/term/DOID:1184",
                "evidence": [
                    {
                        "id": "1184",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1184"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13241",
                "name": "Behcet's disease",
                "description": "An autoimmune disease that is characterized by mucocutaneous manifestations, including recurrent oral and genital ulcerations, ocular manifestations, especially chronic relapsing uveitis, and systemic vasculitis involving arteries and veins of all sizes.",
                "url": "https://disease-ontology.org/term/DOID:13241",
                "evidence": [
                    {
                        "id": "13241",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13241"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2228",
                "name": "thrombocytosis",
                "description": "A blood platelet disease that is characterized by the presence of high platelet counts in the blood.",
                "url": "https://disease-ontology.org/term/DOID:2228",
                "evidence": [
                    {
                        "id": "2228",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2228"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4989",
                "name": "pancreatitis",
                "description": "A pancreas disease that is characterized by inflammation of the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:4989",
                "evidence": [
                    {
                        "id": "4989",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4989"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:784",
                "name": "chronic kidney disease",
                "description": "A kidney failure that is characterized by the gradual loss of kidney function, present for a minimum of 3 months. CKD is classified based on cause, glomerular filtration rate (GFR) category (G2-G5), and albuminuria category (A1-A3).",
                "url": "https://disease-ontology.org/term/DOID:784",
                "evidence": [
                    {
                        "id": "784",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:784"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9351",
                "name": "diabetes mellitus",
                "description": "A glucose metabolism disease that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both.",
                "url": "https://disease-ontology.org/term/DOID:9351",
                "evidence": [
                    {
                        "id": "9351",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9351"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9970",
                "name": "obesity",
                "description": "An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness.",
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                "evidence": [
                    {
                        "id": "9970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9970"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCM8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCM8"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VCM8",
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                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "metallocarboxypeptidase activity",
                "id": "GO:0004181",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004181",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCM8",
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                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9VCM8-1",
                "start_pos": "457",
                "end_pos": "457",
                "site_lbl": "Thr457",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 457,
                        "start_aa": "Thr",
                        "end_pos": 457,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr457",
                        "evidence": [
                            {
                                "id": "GLY_001163",
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                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "Q9VCN6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
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                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
        "length": 718,
        "chemical_mass": 81738.0,
        "gene_names": "Cdc16;APC6;Apc6;CDC16;CG6759;Cdc16;Dmcdc16;Dmel\\CG6759;Dmel_CG6759;cdc16",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "mitotic cell cycle",
                "id": "GO:0000278",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000278",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell division",
                "id": "GO:0051301",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of canonical Wnt signaling pathway",
                "id": "GO:0090090",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090090",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCN6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of mitotic cell cycle",
                "id": "GO:0007346",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007346",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCN6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein ubiquitination",
                "id": "GO:0016567",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016567",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCN6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "anaphase-promoting complex-dependent catabolic process",
                "id": "GO:0031145",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031145",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCN6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of mitotic metaphase/anaphase transition",
                "id": "GO:0045842",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045842",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCN6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of mitotic metaphase/anaphase transition",
                "id": "GO:0030071",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030071",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCN6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein catabolic process",
                "id": "GO:0030163",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030163",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCN6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "compound eye photoreceptor cell differentiation",
                "id": "GO:0001751",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001751",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCN6"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCN6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "anaphase-promoting complex",
                "id": "GO:0005680",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005680",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCN6"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "enzyme-substrate adaptor activity",
                "id": "GO:0140767",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140767",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCN6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCN6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VCN6-1"
    },
    {
        "uniprot_canonical_ac": "Q9VCQ2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCQ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCQ2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 211,
        "chemical_mass": 23509.0,
        "gene_names": "Dmel\\CG13829;CG13829;Dmel\\CG13829;Dmel_CG13829",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "endoplasmic reticulum membrane",
                "id": "GO:0005789",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005789",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCQ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCQ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasmic vesicle",
                "id": "GO:0031410",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031410",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCQ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCQ2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "vacuolar proton-transporting V-type ATPase complex assembly",
                "id": "GO:0070072",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070072",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCQ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCQ2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VCQ2-1"
    },
    {
        "uniprot_canonical_ac": "Q9VCT6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCT6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCT6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 466,
        "chemical_mass": 53239.0,
        "gene_names": "Dmel\\CG13840;CG13840;Dmel\\CG13840;Dmel_CG13840",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VCT6-1"
    },
    {
        "uniprot_canonical_ac": "Q9VCV8-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCV8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCV8"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 772,
        "chemical_mass": 89202.0,
        "gene_names": "Dmel\\CG13842;CG13842;Dmel\\CG13842;Dmel_CG13842",
        "protein_name": "Coiled-coil protein 142 C-terminal domain-containing protein",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VCV8-1"
    },
    {
        "uniprot_canonical_ac": "Q9VCW2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCW2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 830,
        "chemical_mass": 92829.0,
        "gene_names": "cd;CG6969;Dmel\\CG6969;Dmel_CG6969;HPX6;PHS;cd",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050328",
                "name": "congenital hypothyroidism",
                "description": "A hypothyroidism that is present at birth.",
                "url": "https://disease-ontology.org/term/DOID:0050328",
                "evidence": [
                    {
                        "id": "0050328",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050328"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080162",
                "name": "lupus nephritis",
                "description": "A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus.",
                "url": "https://disease-ontology.org/term/DOID:0080162",
                "evidence": [
                    {
                        "id": "0080162",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080162"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080348",
                "name": "Alzheimer's disease 1",
                "description": "An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21.",
                "url": "https://disease-ontology.org/term/DOID:0080348",
                "evidence": [
                    {
                        "id": "0080348",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080348"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0112186",
                "name": "thyroid dyshormonogenesis 2A",
                "description": "A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TPO on chromosome 2p25.3.",
                "url": "https://disease-ontology.org/term/DOID:0112186",
                "evidence": [
                    {
                        "id": "0112186",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112186"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1287",
                "name": "cardiovascular system disease",
                "description": "A disease of anatomical entity which occurs in the blood, heart, blood vessels or the lymphatic system that passes nutrients (such as amino acids and electrolytes), gases, hormones, blood cells or lymph to and from cells in the body to help fight diseases and help stabilize body temperature and pH to maintain homeostasis.",
                "url": "https://disease-ontology.org/term/DOID:1287",
                "evidence": [
                    {
                        "id": "1287",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1287"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1485",
                "name": "cystic fibrosis",
                "description": "A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs.",
                "url": "https://disease-ontology.org/term/DOID:1485",
                "evidence": [
                    {
                        "id": "1485",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1485"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1591",
                "name": "renovascular hypertension",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1591",
                "evidence": [
                    {
                        "id": "1591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1591"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:161",
                "name": "keratosis",
                "description": "A skin disease characterized_by growth of keratin on the skin or mucous membranes.",
                "url": "https://disease-ontology.org/term/DOID:161",
                "evidence": [
                    {
                        "id": "161",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:161"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1679",
                "name": "cystitis",
                "description": "A bladder disease that is characterized by inflammation of the bladder.",
                "url": "https://disease-ontology.org/term/DOID:1679",
                "evidence": [
                    {
                        "id": "1679",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1679"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing.",
                "url": "https://disease-ontology.org/term/DOID:2841",
                "evidence": [
                    {
                        "id": "2841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2921",
                "name": "glomerulonephritis",
                "description": "A nephritis that causes inflammation of the glomeruli located_in kidney.",
                "url": "https://disease-ontology.org/term/DOID:2921",
                "evidence": [
                    {
                        "id": "2921",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2921"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3021",
                "name": "acute kidney failure",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3021",
                "evidence": [
                    {
                        "id": "3021",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3021"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3082",
                "name": "interstitial lung disease",
                "description": "A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough.",
                "url": "https://disease-ontology.org/term/DOID:3082",
                "evidence": [
                    {
                        "id": "3082",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3082"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5082",
                "name": "liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:5082",
                "evidence": [
                    {
                        "id": "5082",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5082"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:783",
                "name": "end stage renal disease",
                "description": "A chronic kidney disease is characterized by non-functioning kidneys, as the final stage in chronic kidney disease.",
                "url": "https://disease-ontology.org/term/DOID:783",
                "evidence": [
                    {
                        "id": "783",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:783"
                    }
                ],
                "weight": 0.0
            },
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                "name": "lung disease",
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                "url": "https://disease-ontology.org/term/DOID:850",
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                    {
                        "id": "850",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:850"
                    }
                ],
                "weight": 0.0
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            {
                "disease_id": "DOID:865",
                "name": "vasculitis",
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                        "id": "865",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:865"
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                ],
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            {
                "disease_id": "DOID:874",
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                "description": "A pneumonia involving inflammation of the lungs caused by bacteria.",
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                    {
                        "id": "874",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:874"
                    }
                ],
                "weight": 0.0
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            {
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                "url": "https://disease-ontology.org/term/DOID:9362",
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                    {
                        "id": "9362",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9362"
                    }
                ],
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            }
        ],
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            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCW2",
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                ],
                "pmid": ""
            },
            {
                "name": "lysosome",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005764",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCW2",
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                ],
                "pmid": ""
            },
            {
                "name": "pigment granule",
                "id": "GO:0048770",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048770",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCW2"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "response to oxidative stress",
                "id": "GO:0006979",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006979",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VCW2",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "kynurenine metabolic process",
                "id": "GO:0070189",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VCW2",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellular process involved in reproduction in multicellular organism",
                "id": "GO:0022412",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022412",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ommochrome biosynthetic process",
                "id": "GO:0006727",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006727",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCW2",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VCW2",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "heme binding",
                "id": "GO:0020037",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0020037",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCW2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "peroxidase activity",
                "id": "GO:0004601",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004601",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VCW2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCW2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VCW2-1"
    },
    {
        "uniprot_canonical_ac": "Q9VD47-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD47",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD47"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 444,
        "chemical_mass": 49232.0,
        "gene_names": "Dmel\\CG13407;CG13407;Dmel\\CG13407;Dmel_CG13407",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VD47-1"
    },
    {
        "uniprot_canonical_ac": "Q9VD62-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD62",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD62"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 562,
        "chemical_mass": 64813.0,
        "gene_names": "Qsox3;CG6690;Dmel\\CG6690;Dmel_CG6690;Qsox3",
        "protein_name": "Sulfhydryl oxidase",
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            {
                "disease_id": "DOID:14679",
                "name": "VACTERL association",
                "description": "A syndrome that is characterized by the presence of at least three of the following: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities.",
                "url": "https://disease-ontology.org/term/DOID:14679",
                "evidence": [
                    {
                        "id": "14679",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14679"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "insemination",
                "id": "GO:0007320",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007320",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD62",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD62"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein folding",
                "id": "GO:0006457",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006457",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD62",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD62"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mating",
                "id": "GO:0007618",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007618",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD62",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD62"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "Golgi membrane",
                "id": "GO:0000139",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000139",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD62",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD62"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD62",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD62"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD62",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD62"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "flavin-dependent sulfhydryl oxidase activity",
                "id": "GO:0016971",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016971",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD62",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD62"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein disulfide isomerase activity",
                "id": "GO:0003756",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003756",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD62",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD62"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VD62-1"
    },
    {
        "uniprot_canonical_ac": "Q9VD91-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD91",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD91"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 260,
        "chemical_mass": 29788.0,
        "gene_names": "Jhbp16;CG15497;Dmel\\CG15497;Dmel_CG15497;JHBP16;Jhbp16",
        "protein_name": "",
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        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD91",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD91"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "circadian rhythm",
                "id": "GO:0007623",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007623",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VD91",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VD91"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VD91-1"
    },
    {
        "uniprot_canonical_ac": "Q9VDA3-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDA3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDA3"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 200,
        "chemical_mass": 22517.0,
        "gene_names": "CheB93a;CG15503;CheB93a;Dmel\\CG15503;Dmel_CG15503",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDA3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDA3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDA3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDA3"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "lipid binding",
                "id": "GO:0008289",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008289",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDA3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDA3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "sensory perception of chemical stimulus",
                "id": "GO:0007606",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007606",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDA3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDA3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "detection of pheromone",
                "id": "GO:0043695",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043695",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDA3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDA3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VDA3-1"
    },
    {
        "uniprot_canonical_ac": "Q9VDA5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDA5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDA5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 526,
        "chemical_mass": 59654.0,
        "gene_names": "Ugt49B2;CG6475;Dmel\\CG6475;Dmel_CG6475;UGT49B2;Ugt49B2",
        "protein_name": "UDP-glucuronosyltransferase",
        "disease": [
            {
                "disease_id": "DOID:10211",
                "name": "cholelithiasis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:10211",
                "evidence": [
                    {
                        "id": "10211",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10211"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11151",
                "name": "cholecystolithiasis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11151",
                "evidence": [
                    {
                        "id": "11151",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11151"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1380",
                "name": "endometrial cancer",
                "description": "A uterine cancer that is located_in tissues lining the uterus.",
                "url": "https://disease-ontology.org/term/DOID:1380",
                "evidence": [
                    {
                        "id": "1380",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1380"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2043",
                "name": "hepatitis B",
                "description": "A viral hepatitis that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus (Orthohepadnavirus hominoidei), which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice.",
                "url": "https://disease-ontology.org/term/DOID:2043",
                "evidence": [
                    {
                        "id": "2043",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2043"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
                "url": "https://disease-ontology.org/term/DOID:2394",
                "evidence": [
                    {
                        "id": "2394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2739",
                "name": "Gilbert syndrome",
                "description": "A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin as bilirubin is not being conjugated as a result of reduced glucuronyltransferase activity.",
                "url": "https://disease-ontology.org/term/DOID:2739",
                "evidence": [
                    {
                        "id": "2739",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2739"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2741",
                "name": "bilirubin metabolic disorder",
                "description": "An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism.",
                "url": "https://disease-ontology.org/term/DOID:2741",
                "evidence": [
                    {
                        "id": "2741",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2741"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3803",
                "name": "Crigler-Najjar syndrome",
                "description": "A bilirubin metabolic disorder that involves a build up of bilirubin as bilirubin is not being broken down as a result of a lack or deficiency of the enzyme uridine diphosphate glycosyltransferase (UGT).",
                "url": "https://disease-ontology.org/term/DOID:3803",
                "evidence": [
                    {
                        "id": "3803",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3803"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
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                "name": "proteolysis",
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                "name": "insemination",
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                ],
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        ],
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            {
                "name": "extracellular space",
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                "disease_id": "DOID:0110734",
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                "description": "A neurodegenerative disease characterized by progressive iron accumulation in the basal ganglia and other regions of the brain, resulting in extrapyramidal movements, such as parkinsonism and dystonia.",
                "url": "https://disease-ontology.org/term/DOID:0110734",
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                "name": "mitochondrion",
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            {
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                "name": "fatty acid metabolic process",
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                "name": "fatty acid beta-oxidation using acyl-CoA oxidase",
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                "name": "carnitine metabolic process, CoA-linked",
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                "name": "DNA-templated transcription",
                "id": "GO:0006351",
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                    {
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                ],
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            },
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                "name": "positive regulation of transcription by RNA polymerase II",
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                    {
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            },
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            },
            {
                "name": "endoplasmic reticulum lumen",
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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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            },
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                    }
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                    }
                ],
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            {
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                    }
                ],
                "pmid": ""
            }
        ],
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                "name": "nucleus",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrion",
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                    }
                ],
                "pmid": ""
            }
        ],
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                "name": "nucleotide-excision repair",
                "id": "GO:0006289",
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                    }
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            },
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                "name": "base-excision repair, AP site formation",
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                    }
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                "name": "zinc ion binding",
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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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            }
        ],
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        "gene_names": "sac;CG14651;Dmel\\CG14651;Dmel_CG14651;sac",
        "protein_name": "",
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            {
                "name": "flagellated sperm motility",
                "id": "GO:0030317",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030317",
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                    {
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                        "id": "Q9VN30",
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                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "sperm flagellum",
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                "pmid": ""
            },
            {
                "name": "dynein complex",
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                "name": "dynein light intermediate chain binding",
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                    }
                ],
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            {
                "name": "dynein intermediate chain binding",
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                    {
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        ],
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                "name": "cytoplasm",
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                        "id": "A1ZAW0",
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                ],
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                "name": "detection of virus",
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            {
                "name": "heterochromatin formation",
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                    }
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            {
                "name": "RNAi-mediated antiviral immune response",
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                "evidence": [
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
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            {
                "name": "dosage compensation by hyperactivation of X chromosome",
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                "evidence": [
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                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
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            {
                "name": "positive regulation of Toll signaling pathway",
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            },
            {
                "name": "global gene silencing by mRNA cleavage",
                "id": "GO:0098795",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098795",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "lncRNA catabolic process",
                "id": "GO:0110064",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0110064",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "RNA binding",
                "id": "GO:0003723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP hydrolysis activity",
                "id": "GO:0016887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mRNA 3'-UTR binding",
                "id": "GO:0003730",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003730",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "siRNA binding",
                "id": "GO:0035197",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035197",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "helicase activity",
                "id": "GO:0004386",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004386",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ribonuclease III activity",
                "id": "GO:0004525",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004525",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "deoxyribonuclease I activity",
                "id": "GO:0004530",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004530",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP-dependent activity, acting on RNA",
                "id": "GO:0008186",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008186",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "perinuclear region of cytoplasm",
                "id": "GO:0048471",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048471",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasmic ribonucleoprotein granule",
                "id": "GO:0036464",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036464",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RISC complex",
                "id": "GO:0016442",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016442",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RISC-loading complex",
                "id": "GO:0070578",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070578",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "1566",
                "end_pos": "1566",
                "site_lbl": "Thr1566",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1566,
                        "start_aa": "Thr",
                        "end_pos": 1566,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1566",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "1210",
                "end_pos": "1210",
                "site_lbl": "Glu1210",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "E",
                        "sequence_mut": "V",
                        "comment": "No effect on RNAi silencing activity.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "15066283",
                                "url": "https://glygen.org/publication/PubMed/15066283"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "1217",
                "end_pos": "1217",
                "site_lbl": "Asp1217",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "D",
                        "sequence_mut": "A",
                        "comment": "Unable to unwind blunt termini (BLT) dsRNAs and fails to rescue loss of RNA silencing activity in mutants. No effect on binding to BLT or 3' overhanging (3'ovr) termini dsRNAs; when associated with A-1476. No effect on binding to 3' overhanging (3'ovr) termini but abolishes binding to BLT dsRNAs; when associated with A-34 and A-1476.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "25891075",
                                "url": "https://glygen.org/publication/PubMed/25891075"
                            },
                            {
                                "database": "PubMed",
                                "id": "29269422",
                                "url": "https://glygen.org/publication/PubMed/29269422"
                            },
                            {
                                "database": "PubMed",
                                "id": "27872309",
                                "url": "https://glygen.org/publication/PubMed/27872309"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "1237",
                "end_pos": "1237",
                "site_lbl": "Glu1237",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "E",
                        "sequence_mut": "A",
                        "comment": "No effect on RNAi silencing activity.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "15066283",
                                "url": "https://glygen.org/publication/PubMed/15066283"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "1330",
                "end_pos": "1330",
                "site_lbl": "Arg1330",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "R",
                        "sequence_mut": "A",
                        "comment": "Loss of dimerization, likely affecting formation of the initial binding complex with loqs and dsRNA.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "35768513",
                                "url": "https://glygen.org/publication/PubMed/35768513"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "1371",
                "end_pos": "1371",
                "site_lbl": "Glu1371",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "E",
                        "sequence_mut": "K",
                        "comment": "Loss of RNAi silencing activity. Decreased processing of dsRNAs into SiRNAs. No effect on mRNA cleavage.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "15066283",
                                "url": "https://glygen.org/publication/PubMed/15066283"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "1476",
                "end_pos": "1476",
                "site_lbl": "Asp1476",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "D",
                        "sequence_mut": "A",
                        "comment": "Unable to unwind blunt termini (BLT) dsRNAs and fails to rescue loss of RNA silencing activity in mutants. No effect on binding to BLT or 3' overhanging (3'ovr) termini dsRNAs; when associated with A-1217. No effect on binding to 3' overhanging (3'ovr) termini but abolishes binding to BLT dsRNAs; when associated with A-34 and A-1217.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "25891075",
                                "url": "https://glygen.org/publication/PubMed/25891075"
                            },
                            {
                                "database": "PubMed",
                                "id": "29269422",
                                "url": "https://glygen.org/publication/PubMed/29269422"
                            },
                            {
                                "database": "PubMed",
                                "id": "27872309",
                                "url": "https://glygen.org/publication/PubMed/27872309"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "1617",
                "end_pos": "1617",
                "site_lbl": "Glu1617",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "E",
                        "sequence_mut": "K",
                        "comment": "Loss of RNAi silencing activity. Decreased processing of dsRNAs into SiRNAs. No effect on mRNA cleavage.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "15066283",
                                "url": "https://glygen.org/publication/PubMed/15066283"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "173",
                "end_pos": "173",
                "site_lbl": "Gly173",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "G",
                        "sequence_mut": "E",
                        "comment": "Decreased production of siRNAs from dsRNA precursors.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "15066283",
                                "url": "https://glygen.org/publication/PubMed/15066283"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "225",
                "end_pos": "225",
                "site_lbl": "Phe225",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "F",
                        "sequence_mut": "G",
                        "comment": "Reduced RNAi activity due to decreased generation of siRNAs from endogenous and viral dsRNAs. In vitro, abolishes ATP-dependent cleavage of blunt termini (BLT) dsRNAs but has no effect on ATP-independent cleavage of 3' overhanging (3'ovr) termini dsRNAs. Decreased binding affinities for BLT and 3'ovr dsRNAs. Binding affinity for BLT dsRNAs is further decreased by addition of ATP. Also displays severely reduced binding to loqs (isoform PD). No effect on ATP hydrolysis. Abolishes binding to BLT and 3'ovr dsRNAs; when associated with A-493 and A-596.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "29269422",
                                "url": "https://glygen.org/publication/PubMed/29269422"
                            },
                            {
                                "database": "PubMed",
                                "id": "32843367",
                                "url": "https://glygen.org/publication/PubMed/32843367"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "31",
                "end_pos": "31",
                "site_lbl": "Gly31",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "G",
                        "sequence_mut": "R",
                        "comment": "Disrupts ATP binding and thus ATP hydrolysis. Also effects binding to dsRNA substrates and siRNA unwinding by the RISC-loading complex is decreased. Severely reduced RNAi activity due to decreased generation of siRNAs from endogenous and viral dsRNAs. Abolishes ATP-dependent cleavage of blunt termini (BLT) dsRNAs but has no effect on ATP-independent cleavage of 3' overhanging (3'ovr) termini dsRNAs. Decreased binding affinities for BLT and 3'ovr dsRNAs. Also reduces binding to loqs. Fails to rescue loss of RNA silencing activity in mutants.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "21419681",
                                "url": "https://glygen.org/publication/PubMed/21419681"
                            },
                            {
                                "database": "PubMed",
                                "id": "32843367",
                                "url": "https://glygen.org/publication/PubMed/32843367"
                            },
                            {
                                "database": "PubMed",
                                "id": "15550672",
                                "url": "https://glygen.org/publication/PubMed/15550672"
                            },
                            {
                                "database": "PubMed",
                                "id": "27872309",
                                "url": "https://glygen.org/publication/PubMed/27872309"
                            },
                            {
                                "database": "PubMed",
                                "id": "15066283",
                                "url": "https://glygen.org/publication/PubMed/15066283"
                            },
                            {
                                "database": "PubMed",
                                "id": "34590626",
                                "url": "https://glygen.org/publication/PubMed/34590626"
                            },
                            {
                                "database": "PubMed",
                                "id": "24488111",
                                "url": "https://glygen.org/publication/PubMed/24488111"
                            },
                            {
                                "database": "PubMed",
                                "id": "34257295",
                                "url": "https://glygen.org/publication/PubMed/34257295"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "324",
                "end_pos": "324",
                "site_lbl": "Arg324",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "R",
                        "sequence_mut": "E",
                        "comment": "Decreased binding to r2d2.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "35768503",
                                "url": "https://glygen.org/publication/PubMed/35768503"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "331",
                "end_pos": "331",
                "site_lbl": "Glu331",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "E",
                        "sequence_mut": "R",
                        "comment": "Decreased binding to r2d2.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "35768503",
                                "url": "https://glygen.org/publication/PubMed/35768503"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "34",
                "end_pos": "34",
                "site_lbl": "Lys34",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "K",
                        "sequence_mut": "A",
                        "comment": "ATPase-defective. Unable to unwind blunt termini (BLT) dsRNAs but is able to bind BLT dsRNAs. No effect on binding to 3' overhanging (3'ovr) termini but abolishes binding to BLT dsRNAs; when associated with A-1217 and A-1476.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "25891075",
                                "url": "https://glygen.org/publication/PubMed/25891075"
                            },
                            {
                                "database": "PubMed",
                                "id": "29269422",
                                "url": "https://glygen.org/publication/PubMed/29269422"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "500",
                "end_pos": "500",
                "site_lbl": "Ala500",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "A",
                        "sequence_mut": "V",
                        "comment": "Increased viral replication of the Sindbis virus (SINV).",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "24009507",
                                "url": "https://glygen.org/publication/PubMed/24009507"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "743",
                "end_pos": "743",
                "site_lbl": "His743",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "H",
                        "sequence_mut": "A",
                        "comment": "Partially rescues RNA silencing activity in mutants. Abolishes cleavage of 3' overhanging (3'ovr) termini dsRNAs but has no effect on cleavage of blunt termini (BLT) dsRNAs, when associated with A-752, A-759, A-943 and A-956.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "27872309",
                                "url": "https://glygen.org/publication/PubMed/27872309"
                            },
                            {
                                "database": "PubMed",
                                "id": "35768503",
                                "url": "https://glygen.org/publication/PubMed/35768503"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "752",
                "end_pos": "752",
                "site_lbl": "Arg752",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "R",
                        "sequence_mut": "A",
                        "comment": "Decreased siRNA length fidelity. Abundance of 21-nucleotide siRNAs produced by the enzyme is decreased whereas the abundance of both 20- and 22-nucleotide siRNAs is increased. Partially rescues RNA silencing activity in mutants. Abolishes cleavage of 3' overhanging (3'ovr) termini dsRNAs but has no effect on cleavage of blunt termini (BLT) dsRNAs, when associated with A-743, A-759, A-943 and A-956.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "27872309",
                                "url": "https://glygen.org/publication/PubMed/27872309"
                            },
                            {
                                "database": "PubMed",
                                "id": "35768503",
                                "url": "https://glygen.org/publication/PubMed/35768503"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "759",
                "end_pos": "759",
                "site_lbl": "Arg759",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "R",
                        "sequence_mut": "A",
                        "comment": "Decreased siRNA length fidelity. Abundance of 21-nucleotide siRNAs produced by the enzyme is decreased whereas the abundance of both 20- and 22-nucleotide siRNAs is increased. Partially rescues RNA silencing activity in mutants. Abolishes cleavage of 3' overhanging (3'ovr) termini dsRNAs but has no effect on cleavage of blunt termini (BLT) dsRNAs, when associated with A-743, A-752, A-943 and A-956.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "32843367",
                                "url": "https://glygen.org/publication/PubMed/32843367"
                            },
                            {
                                "database": "PubMed",
                                "id": "27872309",
                                "url": "https://glygen.org/publication/PubMed/27872309"
                            },
                            {
                                "database": "PubMed",
                                "id": "35768503",
                                "url": "https://glygen.org/publication/PubMed/35768503"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "943",
                "end_pos": "943",
                "site_lbl": "Arg943",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "R",
                        "sequence_mut": "A",
                        "comment": "Decreased siRNA length fidelity. Abundance of 21-nucleotide siRNAs produced by the enzyme is decreased whereas the abundance of both 20- and 22-nucleotide siRNAs is increased. However, has no effect on RNA cleavage rates, when associated with A-956. Decreased siRNA length fidelity, partially rescues RNA silencing activity in mutants and abolishes cleavage of 3' overhanging (3'ovr) termini dsRNAs but has no effect on cleavage of blunt termini (BLT) dsRNAs, when associated with A-743, A-752, A-759 and A-956. Abolishes binding to BLT and 3'ovr dsRNAs; when associated with G-225 and A-956.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "32843367",
                                "url": "https://glygen.org/publication/PubMed/32843367"
                            },
                            {
                                "database": "PubMed",
                                "id": "29269422",
                                "url": "https://glygen.org/publication/PubMed/29269422"
                            },
                            {
                                "database": "PubMed",
                                "id": "27872309",
                                "url": "https://glygen.org/publication/PubMed/27872309"
                            }
                        ]
                    },
                    {
                        "sequence_org": "R",
                        "sequence_mut": "E",
                        "comment": "Decreased siRNA length fidelity. Abundance of 21-nucleotide siRNAs produced by the enzyme is decreased whereas the abundance of both 20- and 22-nucleotide siRNAs is increased. However, has no effect on RNA cleavage rates, when associated with E-956.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "27872309",
                                "url": "https://glygen.org/publication/PubMed/27872309"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1ZAW0-1",
                "start_pos": "956",
                "end_pos": "956",
                "site_lbl": "Arg956",
                "weight": 0.0,
                "mutagenesis": [
                    {
                        "sequence_org": "R",
                        "sequence_mut": "A",
                        "comment": "Decreased siRNA length fidelity. Abundance of 21-nucleotide siRNAs produced by the enzyme is decreased whereas the abundance of both 20- and 22-nucleotide siRNAs is increased. However, has no effect on RNA cleavage rates when associated with A-943. Partially rescues RNA silencing activity in mutants. Abolishes cleavage of 3' overhanging (3'ovr) termini dsRNAs but has no effect on cleavage of blunt termini (BLT) dsRNAs, when associated with A-743, A-752, A-759 and A-943. Abolishes binding to BLT and 3'ovr dsRNAs; when associated with G-225 and A-493.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "29269422",
                                "url": "https://glygen.org/publication/PubMed/29269422"
                            },
                            {
                                "database": "PubMed",
                                "id": "32843367",
                                "url": "https://glygen.org/publication/PubMed/32843367"
                            },
                            {
                                "database": "PubMed",
                                "id": "27872309",
                                "url": "https://glygen.org/publication/PubMed/27872309"
                            }
                        ]
                    },
                    {
                        "sequence_org": "R",
                        "sequence_mut": "E",
                        "comment": "Decreased siRNA length fidelity. Abundance of 21-nucleotide siRNAs produced by the enzyme is decreased whereas the abundance of both 20- and 22-nucleotide siRNAs is increased. However, has no effect on RNA cleavage rates, when associated with E-943.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1ZAW0",
                                "url": "https://www.uniprot.org/uniprotkb/A1ZAW0"
                            },
                            {
                                "database": "PubMed",
                                "id": "27872309",
                                "url": "https://glygen.org/publication/PubMed/27872309"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "A1ZAW0-1"
    },
    {
        "uniprot_canonical_ac": "A0A126GUN8-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A126GUN8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A126GUN8"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 760,
        "chemical_mass": 83489.0,
        "gene_names": "Klp54D;CG15844;CG43323;DmKlp54D;Dmel\\CG43323;Dmel_CG43323;KIF 12;KIF12;KLP1;KLP54D;Klp1;Klp54D",
        "protein_name": "Kinesin-like protein",
        "disease": [
            {
                "disease_id": "DOID:0070221",
                "name": "progressive familial intrahepatic cholestasis",
                "description": "An intrahepatic cholestasis characterized by early onset of chronic unremitting cholestasis of hepatocellular origin that progresses to hepatic fibrosis, cirrhosis, and end-stage liver disease before adulthood.",
                "url": "https://disease-ontology.org/term/DOID:0070221",
                "evidence": [
                    {
                        "id": "0070221",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070221"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080547",
                "name": "metabolic dysfunction-associated steatohepatitis",
                "description": "A metabolic dysfunction-associated steatotic liver disease characterized by the presence of inflammation with hepatocyte injury such as ballooning, with or without fibrosis.",
                "url": "https://disease-ontology.org/term/DOID:0080547",
                "evidence": [
                    {
                        "id": "0080547",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080547"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A126GUN8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A126GUN8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule binding",
                "id": "GO:0008017",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008017",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A126GUN8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A126GUN8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule motor activity",
                "id": "GO:0003777",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003777",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A126GUN8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A126GUN8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP hydrolysis activity",
                "id": "GO:0016887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A126GUN8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A126GUN8"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "microtubule",
                "id": "GO:0005874",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005874",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A126GUN8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A126GUN8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A126GUN8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A126GUN8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "kinesin complex",
                "id": "GO:0005871",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005871",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A126GUN8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A126GUN8"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "microtubule-based movement",
                "id": "GO:0007018",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007018",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A126GUN8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A126GUN8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A126GUN8-1",
                "start_pos": "666",
                "end_pos": "666",
                "site_lbl": "Thr666",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 666,
                        "start_aa": "Thr",
                        "end_pos": 666,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr666",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "A0A126GUN8-1"
    },
    {
        "uniprot_canonical_ac": "A0A0B4K6N2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4K6N2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K6N2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 520,
        "chemical_mass": 59473.0,
        "gene_names": "FoxP;CG16899;CG32937;CG43067;DmFoxP;Dmcg16899;Dmel\\CG43067;Dmel_CG43067;FoxP;dFoxP;fd85E",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050200",
                "name": "Korean hemorrhagic fever",
                "description": "A hemorrhagic fever with renal syndrome that results_in infection located_in kidney, has_material_basis_in Hantaan virus, which is transmitted_by the eurasian field mouse, Apodemus agrarius, or has_material_basis_in Seoul virus, which is transmitted_by norwegian rat, Rattus norvegicus. The infection has_symptom headache, has_symptom back pain, has_symptom abdominal pain, has_symptom fever, has_symptom chills, has_symptom nausea, has_symptom blurred vision, has_symptom flushing of the face, has_symptom redness of the eyes, has_symptom rash, has_symptom low blood pressure, has_symptom acute shock, has_symptom vascular leakage, and has_symptom acute kidney failure, which can cause severe fluid overload.",
                "url": "https://disease-ontology.org/term/DOID:0050200",
                "evidence": [
                    {
                        "id": "0050200",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050200"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050523",
                "name": "adult T-cell leukemia/lymphoma",
                "description": "A T-cell acute leukemia that results_in abnormal increase of lymphocytes, derives_from T-cells, has_material_basis_in human T-cell leukemia virus type 1 (Deltaretrovirus priTlym1), which is transmitted_by sexual contact, transmitted_by contaminated needles used by intravenous-drug users, and transmitted_by breast feeding. The infection results_in_formation_of skin lesions.",
                "url": "https://disease-ontology.org/term/DOID:0050523",
                "evidence": [
                    {
                        "id": "0050523",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050523"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060038",
                "name": "specific developmental disorder",
                "description": "A developmental disorder of mental health that categorizes specific learning disabilities and developmental disorders affecting coordination.",
                "url": "https://disease-ontology.org/term/DOID:0060038",
                "evidence": [
                    {
                        "id": "0060038",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060038"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060041",
                "name": "autism spectrum disorder",
                "description": "A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior.",
                "url": "https://disease-ontology.org/term/DOID:0060041",
                "evidence": [
                    {
                        "id": "0060041",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060041"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081267",
                "name": "graft-versus-host disease",
                "description": "An immune system disease that is characterized by recognition by mature donor T cells, that contaminate the allogeneic bone marrow, of the recipient's tissue as foreign, causing a severe inflammatory disease characterized by rashes, diarrhea, and liver disease, and that has_material_basis_in an associated with variation in the interleukin-10 gene (IL10) on chromosome 1q32.",
                "url": "https://disease-ontology.org/term/DOID:0081267",
                "evidence": [
                    {
                        "id": "0081267",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081267"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0090110",
                "name": "immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome",
                "description": "An autoimmune disease that is characterized by onset in infancy of refractory diarrhea, endocrinopathies, type 1 diabetes mellitus, and dermatitis that has_material_basis_in X-linked recessive mutation in the forkhead box P3 (FOXP3) gene on chromosome Xp11.",
                "url": "https://disease-ontology.org/term/DOID:0090110",
                "evidence": [
                    {
                        "id": "0090110",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0090110"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0090131",
                "name": "complex cortical dysplasia with other brain malformations",
                "description": "A brain disease characterized by aberrant neuronal migration and disturbed axonal guidance resulting in variable brain malformations.",
                "url": "https://disease-ontology.org/term/DOID:0090131",
                "evidence": [
                    {
                        "id": "0090131",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0090131"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111275",
                "name": "speech-language disorder-1",
                "description": "A speech disorder characterized by severe orofacial dyspraxia resulting in largely incomprehensible speech that has_material_basis_in heterozygous mutation in FOXP2 on 7q31.1.",
                "url": "https://disease-ontology.org/term/DOID:0111275",
                "evidence": [
                    {
                        "id": "0111275",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111275"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111331",
                "name": "intellectual disability-severe speech delay-mild dysmorphism syndrome",
                "description": "A syndromic intellectual disability characterized by global developmental delay with moderate to severe speech delay, dysmorphic craniofacial features, and gross motor skill delays that particularly affects expressive speech that has_material_basis_in heterozygous mutation in the FOXP1 gene on chromosome 3p13.",
                "url": "https://disease-ontology.org/term/DOID:0111331",
                "evidence": [
                    {
                        "id": "0111331",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111331"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:106",
                "name": "pleural tuberculosis",
                "description": "An extrapulmonary tuberculosis that results_in lymphocyte-predominant exudative pleural effusion, located_in pleura. This results from an allergic response to tuberculoprotein causing the permeabiltity of the pleural vasculature to alter leading to a sub-pleural caseous focus rupture into the pleural sac.",
                "url": "https://disease-ontology.org/term/DOID:106",
                "evidence": [
                    {
                        "id": "106",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:106"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1094",
                "name": "attention deficit hyperactivity disorder",
                "description": "A specific developmental disorder that is characterized by co-existence of attentional problems and hyperactivity, with each behavior occurring infrequently alone and symptoms starting before seven years of age.",
                "url": "https://disease-ontology.org/term/DOID:1094",
                "evidence": [
                    {
                        "id": "1094",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1094"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11166",
                "name": "Human papillomavirus infectious disease",
                "description": "A viral infectious disease that has_material_basis_in human papillomaviruses, which establish productive infections only in the stratified epithelium of the skin or mucous membranes. These viruses cause warts and sometimes tumors. They are transmitted_by sexual contact.",
                "url": "https://disease-ontology.org/term/DOID:11166",
                "evidence": [
                    {
                        "id": "11166",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11166"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11168",
                "name": "anogenital venereal wart",
                "description": "A viral infectious disease that results_in infection located_in skin of vagina, cervix, uterus, anus, penis, scrotum, mouth, or throat, has_material_basis_in human papillomaviruses (types 6 and 11), which are transmitted_by direct contact with the skin during oral, genital, or anal sex with an infected partner. The infection has_symptom anogenital warts.",
                "url": "https://disease-ontology.org/term/DOID:11168",
                "evidence": [
                    {
                        "id": "11168",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11168"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11263",
                "name": "chlamydia",
                "description": "A commensal bacterial infectious disease that is caused by Chlamydia trachomatis.",
                "url": "https://disease-ontology.org/term/DOID:11263",
                "evidence": [
                    {
                        "id": "11263",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11263"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12236",
                "name": "primary biliary cholangitis",
                "description": "A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts.",
                "url": "https://disease-ontology.org/term/DOID:12236",
                "evidence": [
                    {
                        "id": "12236",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12236"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12365",
                "name": "malaria",
                "description": "A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle.",
                "url": "https://disease-ontology.org/term/DOID:12365",
                "evidence": [
                    {
                        "id": "12365",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12365"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1255",
                "name": "trichostrongyloidiasis",
                "description": "A parasitic helminthiasis infectious disease that involves parasitic infection of animals and humans by nematodes of the superfamily Trichostrongyloidea.",
                "url": "https://disease-ontology.org/term/DOID:1255",
                "evidence": [
                    {
                        "id": "1255",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1255"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12849",
                "name": "autistic disorder",
                "description": "An autism spectrum disorder that is characterized by symptoms across all three symptom domains (communication, social, restricted repetitive interests and behaviors), delayed language development, and symptom onset prior to age 3 years.",
                "url": "https://disease-ontology.org/term/DOID:12849",
                "evidence": [
                    {
                        "id": "12849",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12849"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12858",
                "name": "Huntington's disease",
                "description": "A neurodegenerative disease that has_material_basis_in autosomal dominant inheritance and is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities.",
                "url": "https://disease-ontology.org/term/DOID:12858",
                "evidence": [
                    {
                        "id": "12858",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12858"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1459",
                "name": "hypothyroidism",
                "description": "A thyroid gland disease which involves an underproduction of thyroid hormone.",
                "url": "https://disease-ontology.org/term/DOID:1459",
                "evidence": [
                    {
                        "id": "1459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1470",
                "name": "major depressive disorder",
                "description": "A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality.",
                "url": "https://disease-ontology.org/term/DOID:1470",
                "evidence": [
                    {
                        "id": "1470",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1470"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1682",
                "name": "congenital heart disease",
                "description": "A physical disorder that is characterized by problems with the heart's structure that are present at birth.",
                "url": "https://disease-ontology.org/term/DOID:1682",
                "evidence": [
                    {
                        "id": "1682",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1682"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1883",
                "name": "hepatitis C",
                "description": "A viral hepatitis that results_in inflammation located_in liver, has_material_basis_in hepatitis C virus (Hepacivirus hominis), which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice.",
                "url": "https://disease-ontology.org/term/DOID:1883",
                "evidence": [
                    {
                        "id": "1883",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1883"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2043",
                "name": "hepatitis B",
                "description": "A viral hepatitis that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus (Orthohepadnavirus hominoidei), which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice.",
                "url": "https://disease-ontology.org/term/DOID:2043",
                "evidence": [
                    {
                        "id": "2043",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2043"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2799",
                "name": "bronchiolitis obliterans",
                "description": "A obstructive lung disease involving obstruction of the bronchioles due to inflammation and fibrosis which occurs as a complication of various lung conditions or physiological insults.",
                "url": "https://disease-ontology.org/term/DOID:2799",
                "evidence": [
                    {
                        "id": "2799",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2799"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing.",
                "url": "https://disease-ontology.org/term/DOID:2841",
                "evidence": [
                    {
                        "id": "2841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:289",
                "name": "endometriosis",
                "description": "A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body.",
                "url": "https://disease-ontology.org/term/DOID:289",
                "evidence": [
                    {
                        "id": "289",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:289"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2938",
                "name": "Epstein-Barr virus infectious disease",
                "description": "A viral infectious disease that has_material_basis_in Human gammaherpesvirus 4 (Lymphocryptovirus humangamma4).",
                "url": "https://disease-ontology.org/term/DOID:2938",
                "evidence": [
                    {
                        "id": "2938",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2938"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2957",
                "name": "pulmonary tuberculosis",
                "description": "A tuberculosis that is a contagious disease located_in lungs. The infection has_symptom fever, has_symptom cough, has_symptom difficulty in breathing, has_symptom inflammatory infiltrations, has_symptom formation of tubercles, has_symptom caseation, has_symptom pleural effusion, and has_symptom fibrosis.",
                "url": "https://disease-ontology.org/term/DOID:2957",
                "evidence": [
                    {
                        "id": "2957",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2957"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:321",
                "name": "HTLV-1-associated myelopathy/tropical spastic paraparesis",
                "description": "A viral infectious disease that results in inflammation located in spinal cord, has_material_basis_in human T-cell leukemia virus type 1 (Deltaretrovirus priTlym1), which is transmitted by sexual contact, and transmitted by breast feeding. The infection has symptom spastic weakness of both legs, has symptom muscle stiffness, has symptom sensory disturbance, and has symptom spasms.",
                "url": "https://disease-ontology.org/term/DOID:321",
                "evidence": [
                    {
                        "id": "321",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:321"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3744",
                "name": "cervical squamous cell carcinoma",
                "description": "A cervix carcinoma that has_material_basis_in squamous cells of the cervix.",
                "url": "https://disease-ontology.org/term/DOID:3744",
                "evidence": [
                    {
                        "id": "3744",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3744"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3910",
                "name": "lung adenocarcinoma",
                "description": "A lung non-small cell carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3910",
                "evidence": [
                    {
                        "id": "3910",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3910"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:401",
                "name": "multidrug-resistant tuberculosis",
                "description": "A tuberculosis that is resistant to isoniazid and rifampicin, the two most powerful first-line anti-TB drugs.",
                "url": "https://disease-ontology.org/term/DOID:401",
                "evidence": [
                    {
                        "id": "401",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:401"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4166",
                "name": "syphilis",
                "description": "A primary bacterial infectious disease that is a sexually transmitted systemic disease, has_material_basis_in Treponema pallidum subsp pallidum, which is transmitted_by sexual contact, transmitted_by blood product transfusion, transmitted_by congenital method from mother to fetus or transmitted_by contact with infectious lesions. If left untreated, produces chancres, rashes, and systemic lesions in a clinical course with three stages continued over many years.",
                "url": "https://disease-ontology.org/term/DOID:4166",
                "evidence": [
                    {
                        "id": "4166",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4166"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4186",
                "name": "articulation disorder",
                "description": "A speech disorder that involves mispronouncing speech sounds by omitting, distorting, substituting, or adding sounds which can make speech difficult to understand.",
                "url": "https://disease-ontology.org/term/DOID:4186",
                "evidence": [
                    {
                        "id": "4186",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4186"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4428",
                "name": "dyslexia",
                "description": "A reading disorder resulting from a developmental reading disability involving the inability to process graphic symbols resulting in impairment of reading ability.",
                "url": "https://disease-ontology.org/term/DOID:4428",
                "evidence": [
                    {
                        "id": "4428",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4428"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4914",
                "name": "esophagus adenocarcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:4914",
                "evidence": [
                    {
                        "id": "4914",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4914"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4928",
                "name": "intrahepatic cholangiocarcinoma",
                "description": "A cholangiocarcinoma that arises from the intrahepatic bile duct epithelium in any site of the intrahepatic biliary tree.",
                "url": "https://disease-ontology.org/term/DOID:4928",
                "evidence": [
                    {
                        "id": "4928",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4928"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.",
                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6000",
                "name": "congestive heart failure",
                "description": "A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body.",
                "url": "https://disease-ontology.org/term/DOID:6000",
                "evidence": [
                    {
                        "id": "6000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6000"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8283",
                "name": "peritonitis",
                "description": "A gastrointestinal system disease that involves inflammation of the peritoneum resulting from perforation of the gastrointestinal tract, which produces immediate chemical inflammation followed shortly by infection from intestinal organisms. Peritonitis can also result from appendicitis, diverticulitis, strangulating intestinal obstruction, pancreatitis, pelvic inflammatory disease, mesenteric ischemia, intraperitoneal blood, barium, or peritoneo-systemic shunts, drains, and dialysis catheters in the peritoneal cavity. The symptoms include abdominal pain and tenderness, fever, fluid in the abdomen, nausea, vomiting and low urine output.",
                "url": "https://disease-ontology.org/term/DOID:8283",
                "evidence": [
                    {
                        "id": "8283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8568",
                "name": "infectious mononucleosis",
                "description": "A viral infectious disease that results in inflammation, located in pharynx, has_material_basis_in Human herpesvirus 4 (Lymphocryptovirus humangamma4) and has symptom fever, has symptom fatigue, has symptom lymphadenopathy, and has symptom splenomegaly.",
                "url": "https://disease-ontology.org/term/DOID:8568",
                "evidence": [
                    {
                        "id": "8568",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8568"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9111",
                "name": "cutaneous leishmaniasis",
                "description": "A leishmaniasis that involves skin infection caused by Leishmania species, resulting in one or more cutaneous lesions.",
                "url": "https://disease-ontology.org/term/DOID:9111",
                "evidence": [
                    {
                        "id": "9111",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9111"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9169",
                "name": "Wiskott-Aldrich syndrome",
                "description": "A syndrome that is characterized by abnormal immune system function and a reduced ability to form blood clots resulting from a decrease in the number and size of blood cell fragments involved in clotting (microthrombocytopenia).",
                "url": "https://disease-ontology.org/term/DOID:9169",
                "evidence": [
                    {
                        "id": "9169",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9169"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9206",
                "name": "Barrett's esophagus",
                "description": "An esophageal disease characterized by a change of normal esophageal squamous epithelium to a columnar and intestinal-type epithelium.",
                "url": "https://disease-ontology.org/term/DOID:9206",
                "evidence": [
                    {
                        "id": "9206",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9206"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:93",
                "name": "language disorder",
                "description": "A communication disorder that involves the processing of linguistic information.",
                "url": "https://disease-ontology.org/term/DOID:93",
                "evidence": [
                    {
                        "id": "93",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:93"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9744",
                "name": "type 1 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by destruction of pancreatic beta cells resulting in absent or extremely low insulin production.",
                "url": "https://disease-ontology.org/term/DOID:9744",
                "evidence": [
                    {
                        "id": "9744",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9744"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9955",
                "name": "hypoplastic left heart syndrome",
                "description": "A congenital heart disease characterized by abnormal development of the left-sided structures of the heart.",
                "url": "https://disease-ontology.org/term/DOID:9955",
                "evidence": [
                    {
                        "id": "9955",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9955"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "operant conditioning",
                "id": "GO:0035106",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035106",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4K6N2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K6N2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4K6N2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K6N2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "locomotion",
                "id": "GO:0040011",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040011",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4K6N2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K6N2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "male courtship behavior, veined wing generated song production",
                "id": "GO:0045433",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045433",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4K6N2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K6N2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4K6N2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K6N2"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "DNA-binding transcription factor activity",
                "id": "GO:0003700",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003700",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4K6N2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K6N2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sequence-specific DNA binding",
                "id": "GO:0043565",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043565",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4K6N2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K6N2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
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                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "phospholipid binding",
                "id": "GO:0005543",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005543",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "lipid binding",
                "id": "GO:0008289",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008289",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "GTPase activating protein binding",
                "id": "GO:0032794",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032794",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cleavage furrow",
                "id": "GO:0032154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "midbody",
                "id": "GO:0030496",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030496",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "vesicle membrane",
                "id": "GO:0012506",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0012506",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuromuscular junction",
                "id": "GO:0031594",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031594",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "endocytosis",
                "id": "GO:0006897",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006897",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane organization",
                "id": "GO:0007009",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007009",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "signal transduction",
                "id": "GO:0007165",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007165",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular protein localization",
                "id": "GO:0008104",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008104",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of actin nucleation",
                "id": "GO:0051126",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051126",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mesoderm development",
                "id": "GO:0007498",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007498",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of actin filament polymerization",
                "id": "GO:0030837",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030837",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane tubulation",
                "id": "GO:0097320",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097320",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of synaptic assembly at neuromuscular junction",
                "id": "GO:0008582",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008582",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "germarium-derived female germ-line cyst encapsulation",
                "id": "GO:0030708",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030708",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of adherens junction organization",
                "id": "GO:1903391",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1903391",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellularization",
                "id": "GO:0007349",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007349",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc-derived wing hair organization",
                "id": "GO:0035317",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035317",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of synaptic assembly at neuromuscular junction",
                "id": "GO:0045886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JNK4",
                        "url": "https://www.uniprot.org/uniprotkb/A8JNK4"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "X2JEY5-1",
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                "name": "Drosophila melanogaster",
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                "evidence": [
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                        "id": "X2JEY5",
                        "url": "https://www.uniprot.org/uniprotkb/X2JEY5"
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        ],
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        "protein_name": "AMP deaminase",
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                "disease_id": "DOID:0051064",
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                "url": "https://disease-ontology.org/term/DOID:0051064",
                "evidence": [
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                        "id": "0051064",
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                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:0060264",
                "evidence": [
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                        "id": "0060264",
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                ],
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            },
            {
                "disease_id": "DOID:0060278",
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                "url": "https://disease-ontology.org/term/DOID:0060278",
                "evidence": [
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                        "id": "0060278",
                        "database": "AGR",
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                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:0110814",
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                        "id": "0110814",
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                    }
                ],
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            {
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                "url": "https://disease-ontology.org/term/DOID:3393",
                "evidence": [
                    {
                        "id": "3393",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3393"
                    }
                ],
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                    }
                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:6000",
                "evidence": [
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                        "id": "6000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6000"
                    }
                ],
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        ],
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            {
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                    {
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                        "id": "X2JEY5",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
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                        "id": "X2JEY5",
                        "url": "https://www.uniprot.org/uniprotkb/X2JEY5"
                    }
                ],
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            },
            {
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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                "name": "IMP salvage",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032264",
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                    {
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                    }
                ],
                "pmid": ""
            },
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                    }
                ],
                "pmid": ""
            },
            {
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                    }
                ],
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            }
        ],
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                ],
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                "pmid": ""
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                ],
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            }
        ],
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                "pmid": ""
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        ],
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "N-methyltransferase activity",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VZ41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein methyltransferase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008276",
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                        "id": "Q9VZ41",
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                ],
                "pmid": ""
            },
            {
                "name": "S-adenosylmethionine-dependent methyltransferase activity",
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                "evidence": [
                    {
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                        "id": "Q9VZ41",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein-lysine N-methyltransferase activity",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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                        "database": "UniProtKB",
                        "id": "Q9W4S3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W4S3"
                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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        "protein_name": "BACK domain-containing protein",
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        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "Q9W4G6-1",
        "species": [
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                "name": "Drosophila melanogaster",
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                ],
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            }
        ],
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        "gene_names": "CG2861;Dmel\\CG2861;CG2861;Dmel\\CG2861;Dmel_CG2861",
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        "disease": [],
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        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9W4G6-1",
                "start_pos": "595",
                "end_pos": "595",
                "site_lbl": "Thr595",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
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                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "modulation of chemical synaptic transmission",
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                ],
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        ],
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        ],
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        "protein_name": "28S rRNA (uridine-N(3))-methyltransferase",
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            {
                "name": "nucleolus",
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                "pmid": ""
            },
            {
                "name": "S-adenosyl-L-methionine binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1904047",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z830",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "rRNA base methylation",
                "id": "GO:0070475",
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                    {
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                ],
                "pmid": ""
            }
        ],
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    {
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                ],
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            }
        ],
        "length": 2577,
        "chemical_mass": 276829.0,
        "gene_names": "shn;BEST:SD06302;CG7734;Dmel\\CG7734;EP(2)2359;EP2359;SD06302;SHN;Schnurri;Shn;l(2)04738;quo;shn",
        "protein_name": "Protein schnurri",
        "disease": [
            {
                "disease_id": "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.",
                "url": "https://disease-ontology.org/term/DOID:0050787",
                "evidence": [
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                ],
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            {
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                "url": "https://disease-ontology.org/term/DOID:1059",
                "evidence": [
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                    }
                ],
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                ],
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            {
                "disease_id": "DOID:5419",
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                        "id": "5419",
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                ],
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        ],
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            {
                "name": "nucleus",
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                "name": "DNA-templated transcription",
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                    {
                        "database": "UniProtKB",
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                "name": "ectoderm development",
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                "name": "negative regulation of salivary gland boundary specification",
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                    {
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                    {
                        "database": "UniProtKB",
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        ],
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                        "end_aa": "Thr",
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                            {
                                "id": "GLY_001163",
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                        "start_pos": 1514,
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                        "end_aa": "Thr",
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                                "id": "GLY_001163",
                                "database": "GlyGen",
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                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1Z8F4-1",
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                "site_lbl": "Thr823",
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                        "start_pos": 823,
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                ]
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            {
                "uniprot_canonical_ac": "A1Z8F4-1",
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                "site_lbl": "Cys517",
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                "mutagenesis": [
                    {
                        "sequence_org": "C",
                        "sequence_mut": "S",
                        "comment": "Results in ectopic venation of developing wings; when associated with 486-S--S-489. Phenotype is more severe when also associated with 1834-N--N-1838 and 1846-S--S-1849.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1Z8F4",
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                            },
                            {
                                "database": "PubMed",
                                "id": "38344065",
                                "url": "https://glygen.org/publication/PubMed/38344065"
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                        ]
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                ]
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        ],
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    },
    {
        "uniprot_canonical_ac": "Q9W2Z7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                ],
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        ],
        "length": 364,
        "chemical_mass": 38031.0,
        "gene_names": "CG12634;CG12649;CG18512;Dmel\\CG32694;BcDNA:RE02049;CG12634;CG12649;CG18512;CG32694;Dmel\\CG32694;Dmel_CG32694",
        "protein_name": "Cell wall protein DAN4",
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        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9W2Z7-1",
                "start_pos": "126",
                "end_pos": "126",
                "site_lbl": "Thr126",
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                    {
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        ],
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        "gene_names": "AMT;Dmel\\CG10226;AMT;CG10226;DmCG10226;Dmel\\CG10226;Dmel_CG10226",
        "protein_name": "Multidrug resistance protein homolog 65",
        "disease": [
            {
                "disease_id": "DOID:0050848",
                "name": "obstructive sleep apnea",
                "description": "A sleep apnea that is characterized by repeated collapse and obstruction of the upper airway during sleep, which results in reduced airflow (hypopnea) or complete airflow cessation (apnea), oxygen desaturation, and arousals from sleep.",
                "url": "https://disease-ontology.org/term/DOID:0050848",
                "evidence": [
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                ],
                "weight": 0.0
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            {
                "disease_id": "DOID:0050861",
                "name": "colorectal adenocarcinoma",
                "description": "A colorectal carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:0050861",
                "evidence": [
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                        "database": "AGR",
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060643",
                "name": "primary sclerosing cholangitis",
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                "url": "https://disease-ontology.org/term/DOID:0060643",
                "evidence": [
                    {
                        "id": "0060643",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060643"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060750",
                "name": "familial temporal lobe epilepsy 3",
                "description": "A temporal lobe epilepsy characterized by simple or complex partial seizures often accompanied by intense feelings of deja or altered awareness and that has_material_basis_in variation in the chromosome region 4q13.2-q21.3.",
                "url": "https://disease-ontology.org/term/DOID:0060750",
                "evidence": [
                    {
                        "id": "0060750",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060750"
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070223",
                "name": "progressive familial intrahepatic cholestasis 3",
                "description": "A progressive familial intrahepatic cholestasis characterized by autosomal recessive inheritance of intrahepatic cholestasis and elevated serum GGT1 activity that has_material_basis_in mutation in the ABCB4 gene on chromosome 7q21.12.",
                "url": "https://disease-ontology.org/term/DOID:0070223",
                "evidence": [
                    {
                        "id": "0070223",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070223"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070229",
                "name": "intrahepatic cholestasis of pregnancy 3",
                "description": "An intrahepatic cholestasis of pregnancy characterized by autosomal dominant inheritance that has_material_basis_in mutation in the ABCB4 gene on chromosome 7q21.",
                "url": "https://disease-ontology.org/term/DOID:0070229",
                "evidence": [
                    {
                        "id": "0070229",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070229"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080208",
                "name": "metabolic dysfunction-associated steatotic liver disease",
                "description": "A steatotic liver disease characterized by at least one of five specified cardiometabolic risk factors and no other discernible cause with normal to no alcohol use. The five cardiometabolic risk factors are: (1) higher than normal body mass index or waist circumference; (2) higher than normal serum glucose or glycated hemoglobin level, or type 2 diabetes; (3) higher than normal blood pressure or hypertensive treatment; (4) higher than normal plasma triglycerides or lipid lowering treatment; and (5) lower than normal plasma high-density lipoprotein cholesterol.",
                "url": "https://disease-ontology.org/term/DOID:0080208",
                "evidence": [
                    {
                        "id": "0080208",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080208"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080797",
                "name": "nasal type extranodal NK/T-cell lymphoma",
                "description": "A mature T-cell and NK-cell lymphoma that is characterized by an often angiocentric and angiodestructive cellular infiltrate composed of EBV positive NK/T cells.",
                "url": "https://disease-ontology.org/term/DOID:0080797",
                "evidence": [
                    {
                        "id": "0080797",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080797"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110893",
                "name": "inflammatory bowel disease 13",
                "description": "An inflammatory bowel disease that has_material_basis_in variation in the ABCB1 gene on chromosome 7q21.1.",
                "url": "https://disease-ontology.org/term/DOID:0110893",
                "evidence": [
                    {
                        "id": "0110893",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110893"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10159",
                "name": "osteonecrosis",
                "description": "An ischemic bone disease that results_in necrosis located_in bone.",
                "url": "https://disease-ontology.org/term/DOID:10159",
                "evidence": [
                    {
                        "id": "10159",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10159"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10939",
                "name": "antisocial personality disorder",
                "description": "A personality disorder that involves a pervasive pattern of disregard for, and violation of, the rights of others that begins in childhood or early adolescence and continues into adulthood.",
                "url": "https://disease-ontology.org/term/DOID:10939",
                "evidence": [
                    {
                        "id": "10939",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10939"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1168",
                "name": "familial hyperlipidemia",
                "description": "A lipid metabolism disease that is characterized by elevated levels of lipids in the blood.",
                "url": "https://disease-ontology.org/term/DOID:1168",
                "evidence": [
                    {
                        "id": "1168",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1168"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12236",
                "name": "primary biliary cholangitis",
                "description": "A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts.",
                "url": "https://disease-ontology.org/term/DOID:12236",
                "evidence": [
                    {
                        "id": "12236",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12236"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12365",
                "name": "malaria",
                "description": "A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle.",
                "url": "https://disease-ontology.org/term/DOID:12365",
                "evidence": [
                    {
                        "id": "12365",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12365"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13241",
                "name": "Behcet's disease",
                "description": "An autoimmune disease that is characterized by mucocutaneous manifestations, including recurrent oral and genital ulcerations, ocular manifestations, especially chronic relapsing uveitis, and systemic vasculitis involving arteries and veins of all sizes.",
                "url": "https://disease-ontology.org/term/DOID:13241",
                "evidence": [
                    {
                        "id": "13241",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13241"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13413",
                "name": "hepatic encephalopathy",
                "description": "A brain disease that is characterized by loss of brain function, the occurrence of confusion, altered level of consciousness, and coma that results when the liver is unable to remove toxins from the blood.",
                "url": "https://disease-ontology.org/term/DOID:13413",
                "evidence": [
                    {
                        "id": "13413",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13413"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13580",
                "name": "cholestasis",
                "description": "A bile duct disease that is characterized by where bile cannot flow from the liver to the duodenum.",
                "url": "https://disease-ontology.org/term/DOID:13580",
                "evidence": [
                    {
                        "id": "13580",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13580"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1485",
                "name": "cystic fibrosis",
                "description": "A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs.",
                "url": "https://disease-ontology.org/term/DOID:1485",
                "evidence": [
                    {
                        "id": "1485",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1485"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1824",
                "name": "status epilepticus",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1824",
                "evidence": [
                    {
                        "id": "1824",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1824"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1826",
                "name": "epilepsy",
                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.",
                "url": "https://disease-ontology.org/term/DOID:1826",
                "evidence": [
                    {
                        "id": "1826",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1826"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1849",
                "name": "cannabis dependence",
                "description": "A drug dependence that involves the continued use of cannabis despite problems related to use of the substance.",
                "url": "https://disease-ontology.org/term/DOID:1849",
                "evidence": [
                    {
                        "id": "1849",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1849"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1852",
                "name": "intrahepatic cholestasis",
                "description": "A cholestasis characterized by impairment of the bile flow caused by obstruction located_in liver.",
                "url": "https://disease-ontology.org/term/DOID:1852",
                "evidence": [
                    {
                        "id": "1852",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1852"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1949",
                "name": "cholecystitis",
                "description": "A cholangitis that is characterized by an inflammation that is located in the gallbladder.",
                "url": "https://disease-ontology.org/term/DOID:1949",
                "evidence": [
                    {
                        "id": "1949",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1949"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2154",
                "name": "nephroblastoma",
                "description": "A kidney cancer that affects the kidneys and typically occuring in children.",
                "url": "https://disease-ontology.org/term/DOID:2154",
                "evidence": [
                    {
                        "id": "2154",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2154"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2316",
                "name": "brain ischemia",
                "description": "An ischemia that is characterized by insufficient blood flow to the brain to meet metabolic demand.",
                "url": "https://disease-ontology.org/term/DOID:2316",
                "evidence": [
                    {
                        "id": "2316",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2316"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
                "url": "https://disease-ontology.org/term/DOID:2394",
                "evidence": [
                    {
                        "id": "2394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2559",
                "name": "opiate dependence",
                "description": "A drug dependence that involves the continued use of opiate drugs despite despite problems related to use of the substance.",
                "url": "https://disease-ontology.org/term/DOID:2559",
                "evidence": [
                    {
                        "id": "2559",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2559"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing.",
                "url": "https://disease-ontology.org/term/DOID:2841",
                "evidence": [
                    {
                        "id": "2841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2917",
                "name": "cryoglobulinemia",
                "description": "A hypersensitivity reaction type IV disease that involves large amounts of cryoglobulins in the blood which become thick or gel-like in cold temperatures.",
                "url": "https://disease-ontology.org/term/DOID:2917",
                "evidence": [
                    {
                        "id": "2917",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2917"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2957",
                "name": "pulmonary tuberculosis",
                "description": "A tuberculosis that is a contagious disease located_in lungs. The infection has_symptom fever, has_symptom cough, has_symptom difficulty in breathing, has_symptom inflammatory infiltrations, has_symptom formation of tubercles, has_symptom caseation, has_symptom pleural effusion, and has_symptom fibrosis.",
                "url": "https://disease-ontology.org/term/DOID:2957",
                "evidence": [
                    {
                        "id": "2957",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2957"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2987",
                "name": "familial Mediterranean fever",
                "description": "An autoinflammatory disease characterized by recurrent episodes of fever and acute inflammation of the membranes lining the abdomen, joints and lungs; that has_material_basis_in mutations in the MEFV gene, which encodes the protein pyrin.",
                "url": "https://disease-ontology.org/term/DOID:2987",
                "evidence": [
                    {
                        "id": "2987",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2987"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3008",
                "name": "invasive ductal carcinoma",
                "description": "A breast ductal carcinoma that is characterized by infiltration into the fibrous or fatty tissue of the breast outside of the duct where it originated.",
                "url": "https://disease-ontology.org/term/DOID:3008",
                "evidence": [
                    {
                        "id": "3008",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3008"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3070",
                "name": "high grade glioma",
                "description": "A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine.",
                "url": "https://disease-ontology.org/term/DOID:3070",
                "evidence": [
                    {
                        "id": "3070",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3070"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3328",
                "name": "temporal lobe epilepsy",
                "description": "A focal epilepsy that is characterized by recurrent, unprovoked focal seizures that originate in the temporal lobe of the brain and last about one or two minutes.",
                "url": "https://disease-ontology.org/term/DOID:3328",
                "evidence": [
                    {
                        "id": "3328",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3328"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3602",
                "name": "toxic encephalopathy",
                "description": "A nervous system disease that results from exposure to neurotoxicants and is characterized by an altered mental status, memory loss, and visual problems.",
                "url": "https://disease-ontology.org/term/DOID:3602",
                "evidence": [
                    {
                        "id": "3602",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3602"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4450",
                "name": "renal cell carcinoma",
                "description": "A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney.",
                "url": "https://disease-ontology.org/term/DOID:4450",
                "evidence": [
                    {
                        "id": "4450",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4450"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4481",
                "name": "allergic rhinitis",
                "description": "A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites.",
                "url": "https://disease-ontology.org/term/DOID:4481",
                "evidence": [
                    {
                        "id": "4481",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4481"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5082",
                "name": "liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:5082",
                "evidence": [
                    {
                        "id": "5082",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5082"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:526",
                "name": "human immunodeficiency virus infectious disease",
                "description": "A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 (Lentivirus humimdef1) or Human immunodeficiency virus 2 (Lentivirus humimdef2), which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands.",
                "url": "https://disease-ontology.org/term/DOID:526",
                "evidence": [
                    {
                        "id": "526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:526"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:635",
                "name": "acquired immunodeficiency syndrome",
                "description": "A Human immunodeficiency virus infectious disease that results_in reduction in the numbers of CD4-bearing helper T cells below 200 per microliter of blood or 14% of all lymphocytes thereby rendering the subject highly vulnerable to life-threatening infections and cancers, has_material_basis_in Human immunodeficiency virus 1 (Lentivirus humimdef1) or Human immunodeficiency virus 2 (Lentivirus humimdef2), which are transmitted_by sexual contact, transmitted_by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted_by congenital method, and transmitted_by contaminated needles. Opportunistic infections are common in people with AIDS.",
                "url": "https://disease-ontology.org/term/DOID:635",
                "evidence": [
                    {
                        "id": "635",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:635"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:783",
                "name": "end stage renal disease",
                "description": "A chronic kidney disease is characterized by non-functioning kidneys, as the final stage in chronic kidney disease.",
                "url": "https://disease-ontology.org/term/DOID:783",
                "evidence": [
                    {
                        "id": "783",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:783"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8552",
                "name": "chronic myeloid leukemia",
                "description": "A myeloid leukemia that is characterized by over production of white blood cells.",
                "url": "https://disease-ontology.org/term/DOID:8552",
                "evidence": [
                    {
                        "id": "8552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8552"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8577",
                "name": "ulcerative colitis",
                "description": "A colitis that is predominantly confined to the mucosa located_in colon and includes characteristic ulcers, or open sores.",
                "url": "https://disease-ontology.org/term/DOID:8577",
                "evidence": [
                    {
                        "id": "8577",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8577"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8778",
                "name": "Crohn's disease",
                "description": "An intestinal disease that involves inflammation located_in intestine.",
                "url": "https://disease-ontology.org/term/DOID:8778",
                "evidence": [
                    {
                        "id": "8778",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8778"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9952",
                "name": "acute lymphoblastic leukemia",
                "description": "A acute leukemia that is characterized by over production of lymphoblasts.",
                "url": "https://disease-ontology.org/term/DOID:9952",
                "evidence": [
                    {
                        "id": "9952",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9952"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9974",
                "name": "drug dependence",
                "description": "A substance dependence that involves the continued use of drugs despite problems related to use of the substance.",
                "url": "https://disease-ontology.org/term/DOID:9974",
                "evidence": [
                    {
                        "id": "9974",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9974"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9976",
                "name": "heroin dependence",
                "description": "An opiate dependence that involves the continued use of heroin despite problems related to use of the substance.",
                "url": "https://disease-ontology.org/term/DOID:9976",
                "evidence": [
                    {
                        "id": "9976",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9976"
                    }
                ],
                "weight": 0.0
            }
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                    {
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                "disease_id": "DOID:224",
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                ],
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                "name": "negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction",
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                "pmid": ""
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                "name": "determination of adult lifespan",
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            {
                "name": "meiotic spindle assembly",
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            {
                "name": "maintenance of sister chromatid cohesion",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034086",
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                    {
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                "pmid": ""
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        ],
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                "name": "nucleoplasm",
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            {
                "name": "protein phosphatase type 2A complex",
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            {
                "name": "neurotransmitter secretion",
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                "name": "regulation of synaptic vesicle fusion to presynaptic active zone membrane",
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                "evidence": [
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                "pmid": ""
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            {
                "name": "presynaptic active zone assembly",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K7K9"
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                "pmid": ""
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                "name": "synapse maturation",
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                "pmid": ""
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            {
                "name": "anesthesia-resistant memory",
                "id": "GO:0007615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4K7K9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K7K9"
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                ],
                "pmid": ""
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            {
                "name": "synaptic vesicle tethering involved in synaptic vesicle exocytosis",
                "id": "GO:0099069",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0099069",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4K7K9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K7K9"
                    }
                ],
                "pmid": ""
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            {
                "name": "regulation of calcium-dependent activation of synaptic vesicle fusion",
                "id": "GO:0150037",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0150037",
                "evidence": [
                    {
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LHY5",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "triglyceride homeostasis",
                "id": "GO:0070328",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070328",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LHY5",
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                "pmid": ""
            }
        ],
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            {
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                "id": "GO:0035591",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmembrane receptor protein tyrosine kinase adaptor activity",
                "id": "GO:0005068",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005068",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LHY5",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LHY5",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell cortex",
                "id": "GO:0005938",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005938",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LHY5",
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                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A0B4LHY5-1",
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                "end_pos": "22",
                "site_lbl": "Thr22",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
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                        "site_category_dict": {
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                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
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                        "end_aa": "Thr",
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                        "evidence": [
                            {
                                "id": "GLY_001163",
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                            }
                        ]
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            {
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                "end_pos": "400",
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                        "subtype": "",
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                            {
                                "label": "isoglyp",
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                        ],
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                        "site_category_dict": {
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                        },
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                        "icn3d_view": {},
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    },
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                ],
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 218,
        "chemical_mass": 24511.0,
        "gene_names": "Ptth;CG13687;Dmel\\CG13687;Dmel_CG13687;PTTH;Ptth;ptth",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "varicosity",
                "id": "GO:0043196",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043196",
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                    {
                        "database": "UniProtKB",
                        "id": "X2JCX9",
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                ],
                "pmid": ""
            }
        ],
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            {
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                "id": "GO:0018445",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "negative phototaxis",
                "id": "GO:0046957",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046957",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCX9",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "metamorphosis",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007552",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/X2JCX9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "torso signaling pathway",
                "id": "GO:0008293",
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                        "id": "X2JCX9",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of ecdysteroid biosynthetic process",
                "id": "GO:0045998",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045998",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCX9",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCX9"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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        "species": [
            {
                "name": "Drosophila melanogaster",
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                        "id": "A0A0B4KFE4",
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                    }
                ],
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 81815.0,
        "gene_names": "Acsl;4;7447;ACSL1;ACSL3/4;ACSL3;ACS;Acsl;CG8732;Dmel\\CG8732;Dmel_CG8732;FACS;FCS;acsl;anon-WO0172774.173;dAcsl;dFAC;l(2)05847;l(2)44DEa;l(2)7447;l(2)SH0465;l(2)SH2 0465;l(2)k05304",
        "protein_name": "long-chain-fatty-acid--CoA ligase",
        "disease": [
            {
                "disease_id": "DOID:0050776",
                "name": "non-syndromic X-linked intellectual disability",
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                "url": "https://disease-ontology.org/term/DOID:0050776",
                "evidence": [
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                        "id": "0050776",
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                    }
                ],
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            },
            {
                "disease_id": "DOID:0112050",
                "name": "non-syndromic X-linked intellectual disability 63",
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                "url": "https://disease-ontology.org/term/DOID:0112050",
                "evidence": [
                    {
                        "id": "0112050",
                        "database": "AGR",
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                    }
                ],
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            },
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
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                        "id": "10283",
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                    }
                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:1059",
                "evidence": [
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                ],
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            },
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                "name": "lung cancer",
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                ],
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                "url": "https://disease-ontology.org/term/DOID:14501",
                "evidence": [
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                        "id": "14501",
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                        "url": "https://www.alliancegenome.org/disease/DOID:14501"
                    }
                ],
                "weight": 0.0
            },
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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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                ],
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                ],
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            },
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                    }
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        ],
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                ],
                "pmid": ""
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                    }
                ],
                "pmid": ""
            },
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                ],
                "pmid": ""
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            {
                "name": "neuron differentiation",
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                ],
                "pmid": ""
            },
            {
                "name": "long-chain fatty-acyl-CoA metabolic process",
                "id": "GO:0035336",
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                "evidence": [
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "phosphatidylglycerol biosynthetic process",
                "id": "GO:0006655",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006655",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFE4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "A0A0B4KFE4-1"
    },
    {
        "uniprot_canonical_ac": "A1ZBW0-1",
        "species": [
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                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "A1ZBW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBW0"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "HnRNP-K;BL;Bancal;Bl;CG13425;Dmel\\CG13425;Dmel_CG13425;HnRNP-K;Hrb57A;Q18;bl;dhnRNP K;hnRNP K;hnRNP-A1L;hrb57a;l(2)k08305",
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                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
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                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
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            },
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                "disease_id": "DOID:10300",
                "name": "Raynaud disease",
                "description": "A peripheral vascular disease that is characterized by bilateral Raynaud phenomenon, the abrupt onset of digital paleness or cyanosis in response to cold exposure or stress.",
                "url": "https://disease-ontology.org/term/DOID:10300",
                "evidence": [
                    {
                        "id": "10300",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10300"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
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            }
        ],
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            {
                "name": "mRNA binding",
                "id": "GO:0003729",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003729",
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                    {
                        "database": "UniProtKB",
                        "id": "A1ZBW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBW0"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "nucleus",
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                    {
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                    }
                ],
                "pmid": ""
            },
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                    {
                        "database": "UniProtKB",
                        "id": "A1ZBW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chromatin",
                "id": "GO:0000785",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000785",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBW0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ribonucleoprotein complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990904",
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                    {
                        "database": "UniProtKB",
                        "id": "A1ZBW0",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "omega speckle",
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                    {
                        "database": "UniProtKB",
                        "id": "A1ZBW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBW0"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "regulation of alternative mRNA splicing, via spliceosome",
                "id": "GO:0000381",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000381",
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                    {
                        "database": "UniProtKB",
                        "id": "A1ZBW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBW0"
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                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
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                    {
                        "database": "UniProtKB",
                        "id": "A1ZBW0",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of mRNA splicing, via spliceosome",
                "id": "GO:0048024",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048024",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBW0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBW0"
                    }
                ],
                "pmid": ""
            }
        ],
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    {
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                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                        "id": "X2JEJ0",
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            }
        ],
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        "protein_name": "Bleomycin hydrolase",
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            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                    {
                        "database": "UniProtKB",
                        "id": "X2JEJ0",
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                    }
                ],
                "pmid": ""
            },
            {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JEJ0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JEJ0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to toxic substance",
                "id": "GO:0009636",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009636",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/X2JEJ0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "homocysteine catabolic process",
                "id": "GO:0043418",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043418",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JEJ0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JEJ0"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cysteine-type endopeptidase activity",
                "id": "GO:0004197",
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                    {
                        "database": "UniProtKB",
                        "id": "X2JEJ0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JEJ0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cysteine-type aminopeptidase activity",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "aminopeptidase activity",
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                    {
                        "database": "UniProtKB",
                        "id": "X2JEJ0",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cysteine-type peptidase activity",
                "id": "GO:0008234",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008234",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JEJ0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JEJ0"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "Q9VYF5-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VYF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VYF5"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 23669.0,
        "gene_names": "Dmel\\CG15742;CG15742;Dmel\\CG15742;Dmel_CG15742",
        "protein_name": "CG15742-PA",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "Q9VYF5-1"
    },
    {
        "uniprot_canonical_ac": "Q9W2H8-1",
        "species": [
            {
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                "evidence": [
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                        "database": "UniProtKB",
                        "id": "Q9W2H8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2H8"
                    }
                ],
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            }
        ],
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        "gene_names": "Agl;BEST:GH22856;CG9485;Dmel\\CG9485;Dmel_CG9485",
        "protein_name": "Glycogen debranching enzyme",
        "disease": [
            {
                "disease_id": "DOID:2748",
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                "url": "https://disease-ontology.org/term/DOID:2748",
                "evidence": [
                    {
                        "id": "2748",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2748"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4676",
                "name": "uremia",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:4676",
                "evidence": [
                    {
                        "id": "4676",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4676"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5212",
                "name": "congenital disorder of glycosylation",
                "description": "A carbohydrate metabolic disorder that involves deficient or defective glycosylation of a variety of tissue proteins and/or lipids.",
                "url": "https://disease-ontology.org/term/DOID:5212",
                "evidence": [
                    {
                        "id": "5212",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5212"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "4-alpha-glucanotransferase activity",
                "id": "GO:0004134",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W2H8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2H8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "amylo-alpha-1,6-glucosidase activity",
                "id": "GO:0004135",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004135",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W2H8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2H8"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W2H8",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9W2H8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2H8"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "glycogen biosynthetic process",
                "id": "GO:0005978",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005978",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W2H8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2H8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glycogen catabolic process",
                "id": "GO:0005980",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005980",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W2H8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2H8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "record_id": "Q9W2H8-1"
    },
    {
        "uniprot_canonical_ac": "Q9VVE0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 145,
        "chemical_mass": 17055.0,
        "gene_names": "Pop5;CG14057;Dmel\\CG14057;Dmel_CG14057;Pop5",
        "protein_name": "Ribonuclease P/MRP protein subunit POP5",
        "disease": [],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ribonuclease P complex",
                "id": "GO:0030677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleolar ribonuclease P complex",
                "id": "GO:0005655",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005655",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "multimeric ribonuclease P complex",
                "id": "GO:0030681",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030681",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ribonuclease MRP complex",
                "id": "GO:0000172",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000172",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "rRNA processing",
                "id": "GO:0006364",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006364",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tRNA 5'-leader removal",
                "id": "GO:0001682",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001682",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA processing",
                "id": "GO:0006396",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006396",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tRNA processing",
                "id": "GO:0008033",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008033",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "ribonuclease P RNA binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033204",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA binding",
                "id": "GO:0003723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVE0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVE0"
                    }
                ],
                "pmid": ""
            }
        ],
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        "record_id": "Q9VVE0-1"
    },
    {
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JAR4",
                        "url": "https://www.uniprot.org/uniprotkb/X2JAR4"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "Dmel\\CG42780;CG42780;Dmel\\CG42780;Dmel_CG42780",
        "protein_name": "SCP domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JAR4",
                        "url": "https://www.uniprot.org/uniprotkb/X2JAR4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JAR4",
                        "url": "https://www.uniprot.org/uniprotkb/X2JAR4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "X2JAR4-1"
    },
    {
        "uniprot_canonical_ac": "Q9VT40-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                    {
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                        "id": "Q9VT40",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VT40"
                    }
                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "chemical_mass": 91503.0,
        "gene_names": "nbs;6754;CG6754;Dmel\\CG6754;Dmel_CG6754;Dnbs1;NBS1;NBS;Nbs1;Nbs;dNbs1;l(3)67BDp;l(3)67BDr;l(3)e77A1;nbs1;nbs",
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                "disease_id": "DOID:0014667",
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                "evidence": [
                    {
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                        "database": "AGR",
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                ],
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            },
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                "disease_id": "DOID:10283",
                "name": "prostate cancer",
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                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:10652",
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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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                    }
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            {
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                ],
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            },
            {
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            }
        ],
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                    }
                ],
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            },
            {
                "name": "dynein light intermediate chain binding",
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                    }
                ],
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            }
        ],
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
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                        "subtype": "",
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                        ],
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                        "site_category_dict": {
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                        },
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                        "relation": "attached",
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                        "start_aa": "Thr",
                        "end_pos": 1280,
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                                "id": "GLY_001163",
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                            }
                        ]
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                ]
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                        ]
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                ]
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                "name": "chromosome, telomeric region",
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        ],
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                ],
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            }
        ],
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            },
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                "name": "basolateral plasma membrane",
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                    {
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                ]
            }
        ],
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        ],
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        "protein_name": "Bifunctional coenzyme A synthase",
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                "disease_id": "DOID:0110740",
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                        "id": "0110740",
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                ],
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                        "id": "0112327",
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                ],
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                ],
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                        "id": "162",
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                ],
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            }
        ],
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                "name": "dephospho-CoA kinase activity",
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                ],
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            },
            {
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                    {
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                ],
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            },
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                "name": "ATP binding",
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                ],
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            }
        ],
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            {
                "name": "mitochondrion",
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                ],
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            },
            {
                "name": "mitochondrial matrix",
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                ],
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            }
        ],
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            {
                "name": "triglyceride homeostasis",
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                    {
                        "database": "UniProtKB",
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                ],
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            },
            {
                "name": "coenzyme A biosynthetic process",
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                    {
                        "database": "UniProtKB",
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                ],
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                        ],
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                "url": "https://disease-ontology.org/term/DOID:2841",
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                    {
                        "id": "2841",
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                ],
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                "disease_id": "DOID:3021",
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                ],
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            }
        ],
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                ],
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        ],
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                "name": "transmembrane transporter activity",
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        ],
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        "uniprot_canonical_ac": "Q9VS65-1",
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                "url": "https://disease-ontology.org/term/DOID:0111308",
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                        "id": "0111308",
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                ],
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                "url": "https://disease-ontology.org/term/DOID:1184",
                "evidence": [
                    {
                        "id": "1184",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1184"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13241",
                "name": "Behcet's disease",
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                "url": "https://disease-ontology.org/term/DOID:13241",
                "evidence": [
                    {
                        "id": "13241",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13241"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2228",
                "name": "thrombocytosis",
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                "url": "https://disease-ontology.org/term/DOID:2228",
                "evidence": [
                    {
                        "id": "2228",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2228"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4989",
                "name": "pancreatitis",
                "description": "A pancreas disease that is characterized by inflammation of the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:4989",
                "evidence": [
                    {
                        "id": "4989",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4989"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:784",
                "name": "chronic kidney disease",
                "description": "A kidney failure that is characterized by the gradual loss of kidney function, present for a minimum of 3 months. CKD is classified based on cause, glomerular filtration rate (GFR) category (G2-G5), and albuminuria category (A1-A3).",
                "url": "https://disease-ontology.org/term/DOID:784",
                "evidence": [
                    {
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            },
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            },
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                ],
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        ],
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                "url": "https://disease-ontology.org/term/DOID:0080874",
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                "url": "https://disease-ontology.org/term/DOID:0111085",
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                "url": "https://disease-ontology.org/term/DOID:0112272",
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                ],
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            },
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                            {
                                "id": "40245499",
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                            },
                            {
                                "id": "X2JCF3",
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                ]
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        ],
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        ],
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        ],
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                "name": "regulation of mitotic cell cycle",
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            {
                "name": "protein ubiquitination",
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            {
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        ],
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                "description": "A male infertility disease characterized by the absence of any measurable level of sperm in semen.",
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        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "X2JA25-1"
    },
    {
        "uniprot_canonical_ac": "X2JB67-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JB67",
                        "url": "https://www.uniprot.org/uniprotkb/X2JB67"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 72,
        "chemical_mass": 7957.0,
        "gene_names": "Dmel\\CG34250;CG34250;Dmel\\CG34250;Dmel_CG34250",
        "protein_name": "Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit KCP2",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "X2JB67-1"
    },
    {
        "uniprot_canonical_ac": "X2JBD0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
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                        "id": "X2JBD0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JBD0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1552,
        "chemical_mass": 142914.0,
        "gene_names": "Muc11A;CG2779;CG32656;Dmel\\CG32656;Dmel_CG32656;Muc11A",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050156",
                "name": "idiopathic pulmonary fibrosis",
                "description": "A pulmonary fibrosis that is characterized by scarring of the lung characterized by stiffness in the lungs and makes it difficult to breathe.",
                "url": "https://disease-ontology.org/term/DOID:0050156",
                "evidence": [
                    {
                        "id": "0050156",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050156"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050625",
                "name": "biliary tract benign neoplasm",
                "description": "A hepatobiliary benign neoplasm located_in the biliary tract.",
                "url": "https://disease-ontology.org/term/DOID:0050625",
                "evidence": [
                    {
                        "id": "0050625",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050625"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050848",
                "name": "obstructive sleep apnea",
                "description": "A sleep apnea that is characterized by repeated collapse and obstruction of the upper airway during sleep, which results in reduced airflow (hypopnea) or complete airflow cessation (apnea), oxygen desaturation, and arousals from sleep.",
                "url": "https://disease-ontology.org/term/DOID:0050848",
                "evidence": [
                    {
                        "id": "0050848",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050848"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0061118",
                "name": "autosomal dominant tubulointerstitial kidney disease 2",
                "description": "An autosomal dominant tubulointerstitial kidney disease characterized by adult onset of impaired renal function and salt wasting resulting in chronic renal insufficiency and end-stage renal failure by the sixth decade that has_material_basis_in eterozygous mutation in the MUC1 gene on chromosome 1q22.",
                "url": "https://disease-ontology.org/term/DOID:0061118",
                "evidence": [
                    {
                        "id": "0061118",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0061118"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10140",
                "name": "dry eye syndrome",
                "description": "A lacrimal apparatus disease that is characterized by persistent irritation or burning of the coreneal surface.",
                "url": "https://disease-ontology.org/term/DOID:10140",
                "evidence": [
                    {
                        "id": "10140",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10140"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11054",
                "name": "urinary bladder cancer",
                "description": "An urinary system cancer that results_in malignant growth located_in the urinary bladder.",
                "url": "https://disease-ontology.org/term/DOID:11054",
                "evidence": [
                    {
                        "id": "11054",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11054"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11204",
                "name": "allergic conjunctivitis",
                "description": "A chronic conjunctivitis that is an inflammation of the conjunctiva involing red, itchy, and watery eyes a resulting from an exposure to an allergen or an irritant.",
                "url": "https://disease-ontology.org/term/DOID:11204",
                "evidence": [
                    {
                        "id": "11204",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11204"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11339",
                "name": "pneumocystosis",
                "description": "An opportunistic mycosis that is located in lungs, but can also occur in eyes, ears, skin, thyroid, pituitary, palate, parathyroid, esophagus, pleura, heart, liver, spleen, small intestine, adrenals, kidneys, bone marrow, and lymph nodes, has_material_basis_in Pneumocystis jirovecii that effects interstitial and alveolar tissues and has symptom nonproductive cough, has symptom shortness of breath, and has symptom fever.",
                "url": "https://disease-ontology.org/term/DOID:11339",
                "evidence": [
                    {
                        "id": "11339",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11339"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11394",
                "name": "adult respiratory distress syndrome",
                "description": "A respiratory failure that results from diffuse injury to the endothelium of the lung (as in sepsis, chest trauma, massive blood transfusion, aspiration of the gastric contents, or pneumonia) and is characterized by pulmonary edema with an abnormally high amount of protein in the edematous fluid and by difficult rapid breathing and hypoxemia.",
                "url": "https://disease-ontology.org/term/DOID:11394",
                "evidence": [
                    {
                        "id": "11394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:114",
                "name": "heart disease",
                "description": "A cardiovascular system disease that involves the heart.",
                "url": "https://disease-ontology.org/term/DOID:114",
                "evidence": [
                    {
                        "id": "114",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:114"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11650",
                "name": "bronchopulmonary dysplasia",
                "description": "A lung disease that is characterized by underdeveloped lungs in newborns that can be easily irritated or inflamed after birth resulting in damage to the alveoli of the lungs and bronchi. Most newborns who develop BPD are born more than 10 weeks before their due dates, weigh less than 2 pounds at birth, and have breathing problems.",
                "url": "https://disease-ontology.org/term/DOID:11650",
                "evidence": [
                    {
                        "id": "11650",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11650"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13406",
                "name": "pulmonary sarcoidosis",
                "description": "A sarcoidosis that is characterized by noncaseating granulomatous infiltration of the lungs and supporting lymph nodes, bilateral hilar adenopathy, and pulmonary issues, has_symptom shortness of breath, fatigue, wheezing, and chronic cough, and develops_from a type IV hypersensitivity reaction.",
                "url": "https://disease-ontology.org/term/DOID:13406",
                "evidence": [
                    {
                        "id": "13406",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13406"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13891",
                "name": "bird fancier's lung",
                "description": "An extrinsic allergic alveolitis which is caused by inhalation of antigens from avian excreta. The disease has_symptom abrupt onset of dyspnea, has_symptom cough, has_symptom malaise, and has_symptom fever, after exposure to antigen.",
                "url": "https://disease-ontology.org/term/DOID:13891",
                "evidence": [
                    {
                        "id": "13891",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13891"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1485",
                "name": "cystic fibrosis",
                "description": "A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs.",
                "url": "https://disease-ontology.org/term/DOID:1485",
                "evidence": [
                    {
                        "id": "1485",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1485"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2799",
                "name": "bronchiolitis obliterans",
                "description": "A obstructive lung disease involving obstruction of the bronchioles due to inflammation and fibrosis which occurs as a complication of various lung conditions or physiological insults.",
                "url": "https://disease-ontology.org/term/DOID:2799",
                "evidence": [
                    {
                        "id": "2799",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2799"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing.",
                "url": "https://disease-ontology.org/term/DOID:2841",
                "evidence": [
                    {
                        "id": "2841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3030",
                "name": "mucinous adenocarcinoma",
                "description": "An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which produce mucin.",
                "url": "https://disease-ontology.org/term/DOID:3030",
                "evidence": [
                    {
                        "id": "3030",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3030"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3082",
                "name": "interstitial lung disease",
                "description": "A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough.",
                "url": "https://disease-ontology.org/term/DOID:3082",
                "evidence": [
                    {
                        "id": "3082",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3082"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3458",
                "name": "breast adenocarcinoma",
                "description": "A breast carcinoma that originates in the milk ducts and/or lobules (glandular tissue) of the breast.",
                "url": "https://disease-ontology.org/term/DOID:3458",
                "evidence": [
                    {
                        "id": "3458",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3458"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3587",
                "name": "pancreatic ductal carcinoma",
                "description": "A pancreatic carcinoma located_in the pancreatic duct.",
                "url": "https://disease-ontology.org/term/DOID:3587",
                "evidence": [
                    {
                        "id": "3587",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3587"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3910",
                "name": "lung adenocarcinoma",
                "description": "A lung non-small cell carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3910",
                "evidence": [
                    {
                        "id": "3910",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3910"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:418",
                "name": "systemic scleroderma",
                "description": "A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies.",
                "url": "https://disease-ontology.org/term/DOID:418",
                "evidence": [
                    {
                        "id": "418",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:418"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4450",
                "name": "renal cell carcinoma",
                "description": "A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney.",
                "url": "https://disease-ontology.org/term/DOID:4450",
                "evidence": [
                    {
                        "id": "4450",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4450"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4481",
                "name": "allergic rhinitis",
                "description": "A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites.",
                "url": "https://disease-ontology.org/term/DOID:4481",
                "evidence": [
                    {
                        "id": "4481",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4481"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4608",
                "name": "common bile duct neoplasm",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:4608",
                "evidence": [
                    {
                        "id": "4608",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4608"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4947",
                "name": "cholangiocarcinoma",
                "description": "A bile duct adenocarcinoma that has_material_basis_in bile duct epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:4947",
                "evidence": [
                    {
                        "id": "4947",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4947"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:552",
                "name": "pneumonia",
                "description": "A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing.",
                "url": "https://disease-ontology.org/term/DOID:552",
                "evidence": [
                    {
                        "id": "552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:552"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:850",
                "name": "lung disease",
                "description": "A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide.",
                "url": "https://disease-ontology.org/term/DOID:850",
                "evidence": [
                    {
                        "id": "850",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:850"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8622",
                "name": "measles",
                "description": "A viral infectious disease that results_in infection located_in skin, has_material_basis_in Measles virus (Morbillivirus hominis), which is transmitted_by contact with oronasal secretions, or semen of an infected person. The infection has_symptom fever, has_symptom cough, has_symptom coryza, has_symptom conjunctivitis, and has_symptom maculopapular, erythematous rash.",
                "url": "https://disease-ontology.org/term/DOID:8622",
                "evidence": [
                    {
                        "id": "8622",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8622"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JBD0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JBD0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular matrix",
                "id": "GO:0031012",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031012",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JBD0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JBD0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "extracellular matrix structural constituent",
                "id": "GO:0005201",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005201",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JBD0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JBD0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chitin binding",
                "id": "GO:0008061",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008061",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JBD0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JBD0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "X2JBD0-1",
                "start_pos": "292",
                "end_pos": "292",
                "site_lbl": "Thr292",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 292,
                        "start_aa": "Thr",
                        "end_pos": 292,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr292",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "X2JBD0-1",
                "start_pos": "86",
                "end_pos": "86",
                "site_lbl": "Thr86",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
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                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
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                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
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                        },
                        "site_seq": "",
                        "relation": "attached",
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                        "icn3d_view": {},
                        "start_pos": 86,
                        "start_aa": "Thr",
                        "end_pos": 86,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr86",
                        "evidence": [
                            {
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                "name": "positive regulation of ER to Golgi vesicle-mediated transport",
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            {
                "name": "COPII-coated ER to Golgi transport vesicle",
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            {
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                "name": "dendrite",
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                "name": "neuronal cell body",
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            {
                "name": "basal cortex",
                "id": "GO:0045180",
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                "name": "lamellipodium",
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                "name": "basal part of cell",
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            {
                "name": "perinuclear region of cytoplasm",
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                "name": "SCAR complex",
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                "name": "lamellipodium membrane",
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                "name": "positive regulation of cytoskeleton organization",
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                "name": "establishment of planar polarity of follicular epithelium",
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                "name": "cell adhesion",
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            {
                "name": "hindgut morphogenesis",
                "id": "GO:0007442",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007442",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell migration",
                "id": "GO:0016477",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016477",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of DNA-templated transcription",
                "id": "GO:0006355",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006355",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane organization",
                "id": "GO:0061024",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061024",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "central nervous system development",
                "id": "GO:0007417",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007417",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoskeleton organization",
                "id": "GO:0007010",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007010",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of cell shape",
                "id": "GO:0008360",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008360",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular protein localization",
                "id": "GO:0008104",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008104",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "salivary gland development",
                "id": "GO:0007431",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007431",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "salivary gland morphogenesis",
                "id": "GO:0007435",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007435",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "gonad development",
                "id": "GO:0008406",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008406",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "establishment or maintenance of epithelial cell apical/basal polarity",
                "id": "GO:0045197",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045197",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dorsal closure",
                "id": "GO:0007391",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007391",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "open tracheal system development",
                "id": "GO:0007424",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007424",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tracheal outgrowth, open tracheal system",
                "id": "GO:0007426",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007426",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "epithelial cell migration, open tracheal system",
                "id": "GO:0007427",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007427",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Malpighian tubule morphogenesis",
                "id": "GO:0007443",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007443",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "head involution",
                "id": "GO:0008258",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008258",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of Malpighian tubule diameter",
                "id": "GO:0035297",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035297",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-binding transcription factor activity",
                "id": "GO:0003700",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003700",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A0B4KFC4-1",
                "start_pos": "141",
                "end_pos": "141",
                "site_lbl": "Thr141",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 141,
                        "start_aa": "Thr",
                        "end_pos": 141,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr141",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A0A0B4KFC4-1",
                "start_pos": "5",
                "end_pos": "5",
                "site_lbl": "Thr5",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 5,
                        "start_aa": "Thr",
                        "end_pos": 5,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr5",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "A0A0B4KFC4-1"
    },
    {
        "uniprot_canonical_ac": "A0A0B4KFK6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFK6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFK6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 582,
        "chemical_mass": 64311.0,
        "gene_names": "Dmel\\CG4630;CG4630;Dmel\\CG4630;Dmel_CG4630",
        "protein_name": "Major facilitator superfamily (MFS) profile domain-containing protein",
        "disease": [
            {
                "disease_id": "DOID:0050700",
                "name": "cardiomyopathy",
                "description": "A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle.",
                "url": "https://disease-ontology.org/term/DOID:0050700",
                "evidence": [
                    {
                        "id": "0050700",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050700"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050908",
                "name": "myelodysplastic syndrome",
                "description": "A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets.",
                "url": "https://disease-ontology.org/term/DOID:0050908",
                "evidence": [
                    {
                        "id": "0050908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080208",
                "name": "metabolic dysfunction-associated steatotic liver disease",
                "description": "A steatotic liver disease characterized by at least one of five specified cardiometabolic risk factors and no other discernible cause with normal to no alcohol use. The five cardiometabolic risk factors are: (1) higher than normal body mass index or waist circumference; (2) higher than normal serum glucose or glycated hemoglobin level, or type 2 diabetes; (3) higher than normal blood pressure or hypertensive treatment; (4) higher than normal plasma triglycerides or lipid lowering treatment; and (5) lower than normal plasma high-density lipoprotein cholesterol.",
                "url": "https://disease-ontology.org/term/DOID:0080208",
                "evidence": [
                    {
                        "id": "0080208",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080208"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14365",
                "name": "systemic primary carnitine deficiency disease",
                "description": "An amino acid metabolic disorder that involves defective proteins called carnitine transporters, which bring carnitine into cells and prevent its escape from the body preventing the body cannot utilize fats for energy.",
                "url": "https://disease-ontology.org/term/DOID:14365",
                "evidence": [
                    {
                        "id": "14365",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14365"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6000",
                "name": "congestive heart failure",
                "description": "A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body.",
                "url": "https://disease-ontology.org/term/DOID:6000",
                "evidence": [
                    {
                        "id": "6000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6000"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:655",
                "name": "inherited metabolic disorder",
                "description": "A disease of metabolism that is characterized by enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to inherited enzyme abnormality.",
                "url": "https://disease-ontology.org/term/DOID:655",
                "evidence": [
                    {
                        "id": "655",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:655"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7148",
                "name": "rheumatoid arthritis",
                "description": "An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint.",
                "url": "https://disease-ontology.org/term/DOID:7148",
                "evidence": [
                    {
                        "id": "7148",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7148"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8778",
                "name": "Crohn's disease",
                "description": "An intestinal disease that involves inflammation located_in intestine.",
                "url": "https://disease-ontology.org/term/DOID:8778",
                "evidence": [
                    {
                        "id": "8778",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8778"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFK6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFK6"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane transporter activity",
                "id": "GO:0022857",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022857",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFK6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFK6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A0B4KFK6-1"
    },
    {
        "uniprot_canonical_ac": "A0A0B4KFW6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFW6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFW6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 154,
        "chemical_mass": 17817.0,
        "gene_names": "Dmel\\CG43709;CG43709;Dmel\\CG43709;Dmel_CG43709",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A0B4KFW6-1"
    },
    {
        "uniprot_canonical_ac": "A0A0B4KG18-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG18",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG18"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 72,
        "chemical_mass": 8526.0,
        "gene_names": "Dmel\\CG43829;CG43829;Dmel\\CG43829;Dmel_CG43829",
        "protein_name": "Seminal fluid protein",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A0B4KG18-1"
    },
    {
        "uniprot_canonical_ac": "A0A0B4KG96-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 827,
        "chemical_mass": 92360.0,
        "gene_names": "hrg;CG9854;Dmel\\CG9854;Dmel_CG9854;Hiiragi;PAP;Pap;dHrg;hrg;l(2)07619;l(2)k07619",
        "protein_name": "polynucleotide adenylyltransferase",
        "disease": [],
        "molecular_function": [
            {
                "name": "RNA binding",
                "id": "GO:0003723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "poly(A) RNA polymerase activity",
                "id": "GO:1990817",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990817",
                "evidence": [
                    {
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                "name": "nucleus",
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            {
                "name": "actin filament organization",
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                "pmid": ""
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            {
                "name": "cell migration",
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                ],
                "pmid": ""
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            {
                "name": "intracellular signal transduction",
                "id": "GO:0035556",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035556",
                "evidence": [
                    {
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                "pmid": ""
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                "name": "positive regulation of synapse assembly",
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                    {
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                "pmid": ""
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                "name": "myoblast fusion",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007520",
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            {
                "name": "cellular response to starvation",
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                ],
                "pmid": ""
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            {
                "name": "cell projection organization",
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            {
                "name": "regulation of MAPK cascade",
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                "name": "ecdysteroid 22-kinase activity",
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            {
                "name": "membrane",
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            {
                "name": "transmembrane transporter activity",
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                "name": "axonemal dynein complex assembly",
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                "name": "ubiquitin-like ligase-substrate adaptor activity",
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                "disease_id": "DOID:0050848",
                "name": "obstructive sleep apnea",
                "description": "A sleep apnea that is characterized by repeated collapse and obstruction of the upper airway during sleep, which results in reduced airflow (hypopnea) or complete airflow cessation (apnea), oxygen desaturation, and arousals from sleep.",
                "url": "https://disease-ontology.org/term/DOID:0050848",
                "evidence": [
                    {
                        "id": "0050848",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050848"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050855",
                "name": "renal fibrosis",
                "description": "A kidney disease that is characterized by progressive detrimental connective tissue deposition of the kidney parenchyma leading to deterioration of renal function.",
                "url": "https://disease-ontology.org/term/DOID:0050855",
                "evidence": [
                    {
                        "id": "0050855",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050855"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050864",
                "name": "non-arteritic anterior ischemic optic neuropathy",
                "description": "An anterior ischemic optic neuropathy that is characterized by near-complete vision loss caused by acute ischemic damage to the optic nerve due to non-inflammatory small vessel disease.",
                "url": "https://disease-ontology.org/term/DOID:0050864",
                "evidence": [
                    {
                        "id": "0050864",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050864"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0051061",
                "name": "stroke",
                "description": "A cerebrovascular disease that is characterized by disruption of blood flow to the brain resulting in damage to brain cells due to a lack of oxygen.",
                "url": "https://disease-ontology.org/term/DOID:0051061",
                "evidence": [
                    {
                        "id": "0051061",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0051061"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060224",
                "name": "atrial fibrillation",
                "description": "A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain.",
                "url": "https://disease-ontology.org/term/DOID:0060224",
                "evidence": [
                    {
                        "id": "0060224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070658",
                "name": "alcohol-associated liver disease",
                "description": "A liver disease resulting from excessive alcohol intake.",
                "url": "https://disease-ontology.org/term/DOID:0070658",
                "evidence": [
                    {
                        "id": "0070658",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070658"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080599",
                "name": "Coronavirus infectious disease",
                "description": "A viral infectious disease that has_material_basis_in Coronavirus.",
                "url": "https://disease-ontology.org/term/DOID:0080599",
                "evidence": [
                    {
                        "id": "0080599",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080599"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080600",
                "name": "COVID-19",
                "description": "A Coronavirus infectious disease that is characterized by fever, cough and shortness of breath and that has_material_basis_in Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a subtype of Betacoronavirus pandemicum.",
                "url": "https://disease-ontology.org/term/DOID:0080600",
                "evidence": [
                    {
                        "id": "0080600",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080600"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "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.",
                "url": "https://disease-ontology.org/term/DOID:10591",
                "evidence": [
                    {
                        "id": "10591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10591"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10952",
                "name": "nephritis",
                "description": "A kidney disease that is characterized by an inflammation of the kidneys.",
                "url": "https://disease-ontology.org/term/DOID:10952",
                "evidence": [
                    {
                        "id": "10952",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10952"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11123",
                "name": "IgA vasculitis",
                "description": "A hypersensitivity vasculitis that is characterized by purpura (purplish plaques), arthralgia, gastrointestinal upset, and/or glomerulonephritis, and may be related to increased immune response following an infection.",
                "url": "https://disease-ontology.org/term/DOID:11123",
                "evidence": [
                    {
                        "id": "11123",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11123"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11335",
                "name": "sarcoidosis",
                "description": "A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs.",
                "url": "https://disease-ontology.org/term/DOID:11335",
                "evidence": [
                    {
                        "id": "11335",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11335"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11400",
                "name": "pyelonephritis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11400",
                "evidence": [
                    {
                        "id": "11400",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11400"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11713",
                "name": "diabetic angiopathy",
                "description": "A peripheral vascular disease that is characterized by narrowing of the arteries as a complication arising from chronic diabetes.",
                "url": "https://disease-ontology.org/term/DOID:11713",
                "evidence": [
                    {
                        "id": "11713",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11713"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1205",
                "name": "allergic disease",
                "description": "An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods.",
                "url": "https://disease-ontology.org/term/DOID:1205",
                "evidence": [
                    {
                        "id": "1205",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1205"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1240",
                "name": "leukemia",
                "description": "A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells.",
                "url": "https://disease-ontology.org/term/DOID:1240",
                "evidence": [
                    {
                        "id": "1240",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1240"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12549",
                "name": "hepatitis A",
                "description": "A viral hepatitis that results_in inflammation located_in liver, has_material_basis_in Hepatitis A virus (Hepatovirus ahepa), which is transmitted_by ingestion of contaminated food or water, or transmitted_by direct contact with an infected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice.",
                "url": "https://disease-ontology.org/term/DOID:12549",
                "evidence": [
                    {
                        "id": "12549",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12549"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13141",
                "name": "uveitis",
                "description": "An uveal disease is characterized by inflammation of any of the layers of the uvea of the eye, which includes the iris, ciliary body, and choroid.",
                "url": "https://disease-ontology.org/term/DOID:13141",
                "evidence": [
                    {
                        "id": "13141",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13141"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13241",
                "name": "Behcet's disease",
                "description": "An autoimmune disease that is characterized by mucocutaneous manifestations, including recurrent oral and genital ulcerations, ocular manifestations, especially chronic relapsing uveitis, and systemic vasculitis involving arteries and veins of all sizes.",
                "url": "https://disease-ontology.org/term/DOID:13241",
                "evidence": [
                    {
                        "id": "13241",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13241"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14115",
                "name": "toxic shock syndrome",
                "description": "A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus, which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities.",
                "url": "https://disease-ontology.org/term/DOID:14115",
                "evidence": [
                    {
                        "id": "14115",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14115"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14499",
                "name": "Fabry disease",
                "description": "A sphingolipidosis that is characterized by the buildup of globotriaosylceramide in the body's cells and has_material_basis_in X-linked inherited mutations in the GLA gene, encoding alpha-galactosidase A, on chromosome Xq22.",
                "url": "https://disease-ontology.org/term/DOID:14499",
                "evidence": [
                    {
                        "id": "14499",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14499"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2355",
                "name": "anemia",
                "description": "A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells.",
                "url": "https://disease-ontology.org/term/DOID:2355",
                "evidence": [
                    {
                        "id": "2355",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2355"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing.",
                "url": "https://disease-ontology.org/term/DOID:2841",
                "evidence": [
                    {
                        "id": "2841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2986",
                "name": "IgA glomerulonephritis",
                "description": "A glomerulonephritis characterized by build up of IgA antibody in the glomerulus.",
                "url": "https://disease-ontology.org/term/DOID:2986",
                "evidence": [
                    {
                        "id": "2986",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2986"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2987",
                "name": "familial Mediterranean fever",
                "description": "An autoinflammatory disease characterized by recurrent episodes of fever and acute inflammation of the membranes lining the abdomen, joints and lungs; that has_material_basis_in mutations in the MEFV gene, which encodes the protein pyrin.",
                "url": "https://disease-ontology.org/term/DOID:2987",
                "evidence": [
                    {
                        "id": "2987",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2987"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3393",
                "name": "coronary artery disease",
                "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles.",
                "url": "https://disease-ontology.org/term/DOID:3393",
                "evidence": [
                    {
                        "id": "3393",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3393"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3500",
                "name": "gallbladder adenocarcinoma",
                "description": "A gallbladder carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3500",
                "evidence": [
                    {
                        "id": "3500",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3500"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3526",
                "name": "cerebral infarction",
                "description": "A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain.",
                "url": "https://disease-ontology.org/term/DOID:3526",
                "evidence": [
                    {
                        "id": "3526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3526"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3587",
                "name": "pancreatic ductal carcinoma",
                "description": "A pancreatic carcinoma located_in the pancreatic duct.",
                "url": "https://disease-ontology.org/term/DOID:3587",
                "evidence": [
                    {
                        "id": "3587",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3587"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3905",
                "name": "lung carcinoma",
                "description": "A lung cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells and is located_in the lungs and has_symptom cough and has_symptom chest discomfort or pain and has_symptom weight loss and has_symptom hemoptysis.",
                "url": "https://disease-ontology.org/term/DOID:3905",
                "evidence": [
                    {
                        "id": "3905",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3905"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4079",
                "name": "heart valve disease",
                "description": "A heart disease involving one or more of the four valves of the heart (the aortic and mitral valves on the left and the pulmonary and tricuspid valves on the right).",
                "url": "https://disease-ontology.org/term/DOID:4079",
                "evidence": [
                    {
                        "id": "4079",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4079"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:418",
                "name": "systemic scleroderma",
                "description": "A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies.",
                "url": "https://disease-ontology.org/term/DOID:418",
                "evidence": [
                    {
                        "id": "418",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:418"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5082",
                "name": "liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:5082",
                "evidence": [
                    {
                        "id": "5082",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5082"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.",
                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:552",
                "name": "pneumonia",
                "description": "A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing.",
                "url": "https://disease-ontology.org/term/DOID:552",
                "evidence": [
                    {
                        "id": "552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:552"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:576",
                "name": "proteinuria",
                "description": "A kidney disease that is characterized by the presence of excess proteins in the urine.",
                "url": "https://disease-ontology.org/term/DOID:576",
                "evidence": [
                    {
                        "id": "576",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:576"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:61",
                "name": "mitral valve disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:61",
                "evidence": [
                    {
                        "id": "61",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:61"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7147",
                "name": "ankylosing spondylitis",
                "description": "An arthritis that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage.",
                "url": "https://disease-ontology.org/term/DOID:7147",
                "evidence": [
                    {
                        "id": "7147",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7147"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:783",
                "name": "end stage renal disease",
                "description": "A chronic kidney disease is characterized by non-functioning kidneys, as the final stage in chronic kidney disease.",
                "url": "https://disease-ontology.org/term/DOID:783",
                "evidence": [
                    {
                        "id": "783",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:783"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:841",
                "name": "extrinsic allergic alveolitis",
                "description": "An interstitial lung disease involving inflammation of alveoli and smallest airways (bronchioles) of the lung caused by an allergic reaction to inhaled organic dusts containing microorganisms or proteins, and chemicals. Symptoms include chills, cough, fever, malaise, shortness of breath, loss of appetite and weight loss.",
                "url": "https://disease-ontology.org/term/DOID:841",
                "evidence": [
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                        "id": "841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:841"
                    }
                ],
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            {
                "disease_id": "DOID:8432",
                "name": "polycythemia",
                "description": "A bone marrow disease characterized by an increased number of red blood cells in the bloodstream resulting in thicker blood and reduced blood flow.",
                "url": "https://disease-ontology.org/term/DOID:8432",
                "evidence": [
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                        "id": "8432",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8432"
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                "name": "chronic myeloid leukemia",
                "description": "A myeloid leukemia that is characterized by over production of white blood cells.",
                "url": "https://disease-ontology.org/term/DOID:8552",
                "evidence": [
                    {
                        "id": "8552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8552"
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                ],
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                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8805",
                "evidence": [
                    {
                        "id": "8805",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8805"
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                ],
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                "name": "diabetic retinopathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8947",
                "evidence": [
                    {
                        "id": "8947",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8947"
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                ],
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            },
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                        "url": "https://www.alliancegenome.org/disease/DOID:8970"
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                "evidence": [
                    {
                        "id": "9538",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9538"
                    }
                ],
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            },
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                "evidence": [
                    {
                        "id": "9744",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9744"
                    }
                ],
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            },
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                "disease_id": "DOID:9775",
                "name": "diastolic heart failure",
                "description": "",
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                        "id": "9775",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9775"
                    }
                ],
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                "description": "A mitral valve disease where one or both of the cusps of the mitral valve bulge or collapse backward in the left atrium during systole.",
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                "evidence": [
                    {
                        "id": "988",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:988"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "membrane",
                "id": "GO:0016020",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A1Z7M8"
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            },
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                "name": "extracellular space",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z7M8",
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                "pmid": ""
            }
        ],
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            {
                "name": "hydrolase activity",
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                    {
                        "database": "UniProtKB",
                        "id": "A1Z7M8",
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                    }
                ],
                "pmid": ""
            },
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A1Z7M8"
                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
        "sites": [],
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    {
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            {
                "name": "Drosophila melanogaster",
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                ],
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        ],
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        "chemical_mass": 99091.0,
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        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A1ZAP1-1",
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                "end_pos": "440",
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                        "glytoucan_ac": "",
                        "type": "O-linked",
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                        ],
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                        "site_category_dict": {
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                        },
                        "site_seq": "",
                        "relation": "attached",
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                        "icn3d_view": {},
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        ],
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        "binding_glycans": [],
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        "record_id": "A0A0B4LFY7-1"
    },
    {
        "uniprot_canonical_ac": "A0A0B4LGL7-1",
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                ],
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        ],
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        "protein_name": "",
        "disease": [],
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        "biomarkers": [],
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        "record_id": "A0A0B4LGL7-1"
    },
    {
        "uniprot_canonical_ac": "A0A0B4LH86-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
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        ],
        "length": 292,
        "chemical_mass": 32579.0,
        "gene_names": "Dmel\\CG13527;SPH182;CG13527;Dmel\\CG13527;Dmel_CG13527;SPH182",
        "protein_name": "Peptidase S1 domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
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                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "proteolysis",
                "id": "GO:0006508",
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                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4LH86"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "innate immune response",
                "id": "GO:0045087",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045087",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                "pmid": ""
            }
        ],
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            {
                "name": "hydrolase activity",
                "id": "GO:0016787",
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                ],
                "pmid": ""
            },
            {
                "name": "serine-type peptidase activity",
                "id": "GO:0008236",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008236",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "A0A0B4LHE5-1",
        "species": [
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                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4LHE5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "pre-mod(mdg4)-P;CG44881;Dmel\\CG44881;Dmel_CG44881;pre-mod(mdg4)-P",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LHE5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4LHE5"
                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
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        "record_id": "A0A0B4LHE5-1"
    },
    {
        "uniprot_canonical_ac": "A0A0B4LID7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LID7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4LID7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 71652.0,
        "gene_names": "ClpX;CG4538;ClpX;Clpx;Dmel\\CG4538;Dmel_CG4538",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:13270",
                "name": "erythropoietic protoporphyria",
                "description": "An acute porphyria characterized by a deficiency in the enzyme ferrochelatase, leading to abnormally high levels of protoporphyrin in the tissue.",
                "url": "https://disease-ontology.org/term/DOID:13270",
                "evidence": [
                    {
                        "id": "13270",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13270"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LID7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4LID7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LID7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4LID7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "unfolded protein binding",
                "id": "GO:0051082",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051082",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LID7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4LID7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP hydrolysis activity",
                "id": "GO:0016887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LID7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4LID7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "peptidase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008233",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4LID7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP-dependent protein folding chaperone",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LID7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4LID7"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "mitochondrial matrix",
                "id": "GO:0005759",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005759",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4LID7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial endopeptidase Clp complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009841",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "proteolysis involved in protein catabolic process",
                "id": "GO:0051603",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051603",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial protein quality control",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0141164",
                "evidence": [
                    {
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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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    {
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        ],
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            {
                "disease_id": "DOID:0090030",
                "name": "corticosteroid-binding globulin deficiency",
                "description": "An adrenal gland disease characterized by decreased levels of serum corticosteroid-binding globulin and cortisol, and in some cases hypo- or hypertension, and muscle fatigue that has_material_basis_in heterozygous or homozygous mutation in the SERPINA6 gene on chromosome 14q32.",
                "url": "https://disease-ontology.org/term/DOID:0090030",
                "evidence": [
                    {
                        "id": "0090030",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0090030"
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                ],
                "weight": 0.0
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            {
                "disease_id": "DOID:0110350",
                "name": "osteogenesis imperfecta type 6",
                "description": "An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINF1 gene on chromosome 17p13.3.",
                "url": "https://disease-ontology.org/term/DOID:0110350",
                "evidence": [
                    {
                        "id": "0110350",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110350"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111901",
                "name": "heparin cofactor II deficiency",
                "description": "A thrombophilia characterized by increased risk of thromboembolism that has_material_basis_in heterozygous mutation in the HCF2 gene on chromosome 22q11.21.",
                "url": "https://disease-ontology.org/term/DOID:0111901",
                "evidence": [
                    {
                        "id": "0111901",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111901"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10584",
                "name": "retinitis pigmentosa",
                "description": "A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss.",
                "url": "https://disease-ontology.org/term/DOID:10584",
                "evidence": [
                    {
                        "id": "10584",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10584"
                    }
                ],
                "weight": 0.0
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            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:1074",
                "name": "kidney failure",
                "description": "A kidney disease characterized by the failure of the kidneys to adequately filter waste products from the blood.",
                "url": "https://disease-ontology.org/term/DOID:1074",
                "evidence": [
                    {
                        "id": "1074",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1074"
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                ],
                "weight": 0.0
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                "disease_id": "DOID:11168",
                "name": "anogenital venereal wart",
                "description": "A viral infectious disease that results_in infection located_in skin of vagina, cervix, uterus, anus, penis, scrotum, mouth, or throat, has_material_basis_in human papillomaviruses (types 6 and 11), which are transmitted_by direct contact with the skin during oral, genital, or anal sex with an infected partner. The infection has_symptom anogenital warts.",
                "url": "https://disease-ontology.org/term/DOID:11168",
                "evidence": [
                    {
                        "id": "11168",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11168"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:11382",
                "name": "corneal neovascularization",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11382",
                "evidence": [
                    {
                        "id": "11382",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11382"
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                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:11446",
                "name": "sciatic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11446",
                "evidence": [
                    {
                        "id": "11446",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11446"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:12986",
                "name": "leukostasis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:12986",
                "evidence": [
                    {
                        "id": "12986",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12986"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:13141",
                "name": "uveitis",
                "description": "An uveal disease is characterized by inflammation of any of the layers of the uvea of the eye, which includes the iris, ciliary body, and choroid.",
                "url": "https://disease-ontology.org/term/DOID:13141",
                "evidence": [
                    {
                        "id": "13141",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13141"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:13207",
                "name": "proliferative diabetic retinopathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:13207",
                "evidence": [
                    {
                        "id": "13207",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13207"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13514",
                "name": "venous tributary occlusion of retina",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:13514",
                "evidence": [
                    {
                        "id": "13514",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13514"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14018",
                "name": "alcoholic liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:14018",
                "evidence": [
                    {
                        "id": "14018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14018"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14115",
                "name": "toxic shock syndrome",
                "description": "A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus, which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities.",
                "url": "https://disease-ontology.org/term/DOID:14115",
                "evidence": [
                    {
                        "id": "14115",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14115"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14330",
                "name": "Parkinson's disease",
                "description": "A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions.",
                "url": "https://disease-ontology.org/term/DOID:14330",
                "evidence": [
                    {
                        "id": "14330",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14330"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1459",
                "name": "hypothyroidism",
                "description": "A thyroid gland disease which involves an underproduction of thyroid hormone.",
                "url": "https://disease-ontology.org/term/DOID:1459",
                "evidence": [
                    {
                        "id": "1459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1727",
                "name": "retinal vein occlusion",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1727",
                "evidence": [
                    {
                        "id": "1727",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1727"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2154",
                "name": "nephroblastoma",
                "description": "A kidney cancer that affects the kidneys and typically occuring in children.",
                "url": "https://disease-ontology.org/term/DOID:2154",
                "evidence": [
                    {
                        "id": "2154",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2154"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
                "description": "A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.",
                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:289",
                "name": "endometriosis",
                "description": "A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body.",
                "url": "https://disease-ontology.org/term/DOID:289",
                "evidence": [
                    {
                        "id": "289",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:289"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:332",
                "name": "amyotrophic lateral sclerosis",
                "description": "A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.",
                "url": "https://disease-ontology.org/term/DOID:332",
                "evidence": [
                    {
                        "id": "332",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:332"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3347",
                "name": "osteosarcoma",
                "description": "A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. It usually involves bones and less frequently extraosseous sites. It often involves the long bones (particularly distal femur, proximal tibia, and proximal humerus).",
                "url": "https://disease-ontology.org/term/DOID:3347",
                "evidence": [
                    {
                        "id": "3347",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3347"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4448",
                "name": "macular degeneration",
                "description": "A retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye and has_symptom vision loss.",
                "url": "https://disease-ontology.org/term/DOID:4448",
                "evidence": [
                    {
                        "id": "4448",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4448"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4449",
                "name": "macular retinal edema",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:4449",
                "evidence": [
                    {
                        "id": "4449",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4449"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4724",
                "name": "brain edema",
                "description": "A brain disease that is characterized by excess accumulation of fluid in the intracellular and/or extracellular spaces of the brain, has_symptom nausea, has_symptom vomiting, has_symptom blurred vision, has_symptom seizure, has_symptom coma.",
                "url": "https://disease-ontology.org/term/DOID:4724",
                "evidence": [
                    {
                        "id": "4724",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4724"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5052",
                "name": "melioidosis",
                "description": "A primary bacterial infectious disease that results_in infection, has_material_basis_in Burkholderia pseudomallei, which is transmitted_by contact with the contaminated water or soil. The infection has_symptom fever, has_symptom respiratory distress, has_symptom chest pain, and has_symptom stomach pain.",
                "url": "https://disease-ontology.org/term/DOID:5052",
                "evidence": [
                    {
                        "id": "5052",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5052"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5425",
                "name": "ovarian hyperstimulation syndrome",
                "description": "An ovarian disease that is characterized by cystic enlargement of the ovaries and a fluid shift from the intravascular to the third space and has_symptom abdominal pain, has_symptom nausea and has_symptom vomiting. This disease is an iatrogenic complication of assisted reproduction technology.",
                "url": "https://disease-ontology.org/term/DOID:5425",
                "evidence": [
                    {
                        "id": "5425",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5425"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:768",
                "name": "retinoblastoma",
                "description": "A retinal cell cancer and malignant neoplasm of retina and neuroblastoma and neuroendocrine tumors that derives_from the tissues of the retina.",
                "url": "https://disease-ontology.org/term/DOID:768",
                "evidence": [
                    {
                        "id": "768",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:768"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7998",
                "name": "hyperthyroidism",
                "description": "A thyroid gland disease that involves an over production of thyroid hormone.",
                "url": "https://disease-ontology.org/term/DOID:7998",
                "evidence": [
                    {
                        "id": "7998",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7998"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8466",
                "name": "retinal degeneration",
                "description": "A retinal disease that is characterized by deterioration of the retina caused by the progressive and eventual death of the cells of the retina.",
                "url": "https://disease-ontology.org/term/DOID:8466",
                "evidence": [
                    {
                        "id": "8466",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8466"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8544",
                "name": "chronic fatigue syndrome",
                "description": "A syndrome that involves prolonged and severe tiredness or weariness that is unrelated to exertion, is not relieved by rest and for a minimum of six months and is not directly caused by other conditions.",
                "url": "https://disease-ontology.org/term/DOID:8544",
                "evidence": [
                    {
                        "id": "8544",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8544"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8947",
                "name": "diabetic retinopathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8947",
                "evidence": [
                    {
                        "id": "8947",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8947"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9719",
                "name": "neovascular inflammatory vitreoretinopathy",
                "description": "A retinal and vitreous disease characterized by ocular inflammation, vascular dropout, large spots of hyperpigmentation, neovascularization of the peripheral and posterior retina, vitreous hemorrhage, and retinal detachment that has_material_basis_in heterozygous mutation in the CAPN5 gene on chromosome 11q13.5.",
                "url": "https://disease-ontology.org/term/DOID:9719",
                "evidence": [
                    {
                        "id": "9719",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9719"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9744",
                "name": "type 1 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by destruction of pancreatic beta cells resulting in absent or extremely low insulin production.",
                "url": "https://disease-ontology.org/term/DOID:9744",
                "evidence": [
                    {
                        "id": "9744",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9744"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:9970",
                "name": "obesity",
                "description": "An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness.",
                "url": "https://disease-ontology.org/term/DOID:9970",
                "evidence": [
                    {
                        "id": "9970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9970"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6I3",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6I3"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "peptidase inhibitor activity",
                "id": "GO:0030414",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030414",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6I3",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6I3"
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                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of immune response",
                "id": "GO:0050776",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050776",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A1Z6I3-1",
                "start_pos": "20",
                "end_pos": "20",
                "site_lbl": "Thr20",
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                "glycosylation": [
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                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
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                                "label": "isoglyp",
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                        "site_category_dict": {
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                        },
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                        "icn3d_view": {},
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                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr20",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
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                    }
                ]
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                "uniprot_canonical_ac": "A1Z6I3-1",
                "start_pos": "313",
                "end_pos": "313",
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                        "url": "https://www.alliancegenome.org/disease/DOID:127"
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                "name": "malignant mesothelioma",
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                "disease_id": "DOID:1793",
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                ],
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                "name": "osteochondrodysplasia",
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                ],
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                    {
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                ],
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                "description": "",
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                        "sequence_mut": "D",
                        "comment": "Constitutively active kinase. Phosphorylates Smox/SMAD2 and Mad in the absence of activin or BMP signaling. Even in the absence of a type II receptor can weakly phosphorylate Smox/SMAD2.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1Z7L8",
                                "url": "https://www.uniprot.org/uniprotkb/A1Z7L8"
                            },
                            {
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                                "id": "10320478",
                                "url": "https://glygen.org/publication/PubMed/10320478"
                            },
                            {
                                "database": "PubMed",
                                "id": "22563507",
                                "url": "https://glygen.org/publication/PubMed/22563507"
                            }
                        ]
                    }
                ]
            },
            {
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                "start_pos": "351",
                "end_pos": "351",
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                    {
                        "sequence_org": "K",
                        "sequence_mut": "R",
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                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A1Z7L8",
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                            },
                            {
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                                "id": "10320478",
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                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
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            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z7R9",
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                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 19781.0,
        "gene_names": "Dmel\\CG42382;CG42382;CG8016;Dmel\\CG42382;Dmel_CG42382",
        "protein_name": "C3H1-type domain-containing protein",
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            {
                "name": "nucleus",
                "id": "GO:0005634",
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                    {
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                        "id": "A1Z7R9",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z7U1",
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                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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        "chemical_mass": 85491.0,
        "gene_names": "Dmel\\CG13954;CG13954;Dmel\\CG13954;Dmel_CG13954",
        "protein_name": "Pneumococcal serine-rich repeat protein",
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        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A1Z7U1-1"
    },
    {
        "uniprot_canonical_ac": "A1Z892-1",
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            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z892",
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                    }
                ],
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            }
        ],
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        "chemical_mass": 24784.0,
        "gene_names": "Prx6b;1-cys peroxiredoxin DPx- 2540-1;BEST:LD11278;CG12405;DPx-2540-1;DPx2540;Dmel\\CG12405;Dmel_CG12405;Prx2540-1;Prx2540;Prx6b;dPRDX6-2;dPrx6a",
        "protein_name": "1-Cys peroxiredoxin",
        "disease": [],
        "cellular_component": [
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                    {
                        "database": "UniProtKB",
                        "id": "A1Z892",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cell redox homeostasis",
                "id": "GO:0045454",
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                    {
                        "database": "UniProtKB",
                        "id": "A1Z892",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z892"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "hydrogen peroxide catabolic process",
                "id": "GO:0042744",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042744",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z892",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z892"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "peroxiredoxin activity",
                "id": "GO:0051920",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051920",
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                    {
                        "database": "UniProtKB",
                        "id": "A1Z892",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z892"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "peroxidase activity",
                "id": "GO:0004601",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004601",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z892",
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                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A1Z892-1"
    },
    {
        "uniprot_canonical_ac": "A1Z898-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z898",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z898"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 83395.0,
        "gene_names": "Caf1-105;75;CAF p105;CAF-1 p105;CAF1-105;CAF1-p105;CAF1-p75/p105;CAF1-p75;CAF105/75;CAF1p105;CAF1p75;CAF1;CG12892;Caf-105;Caf1-105;Caf1-10;Caf1-p105;Caf1;Dmel\\CG12892;Dmel_CG12892;P105;caf1-105;dCAF-1-p105;dCAF1-p105;dCAF1-p75;p105/p75;p105;p75/p105;p75",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050866",
                "name": "oral squamous cell carcinoma",
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                "evidence": [
                    {
                        "id": "0050866",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050866"
                    }
                ],
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            },
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
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                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
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                    }
                ],
                "weight": 0.0
            },
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                "url": "https://disease-ontology.org/term/DOID:3068",
                "evidence": [
                    {
                        "id": "3068",
                        "database": "AGR",
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                    }
                ],
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            },
            {
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                "evidence": [
                    {
                        "id": "3070",
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                    }
                ],
                "weight": 0.0
            },
            {
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                "evidence": [
                    {
                        "id": "8923",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8923"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
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                    {
                        "database": "UniProtKB",
                        "id": "A1Z898",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "chromatin",
                "id": "GO:0000785",
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                    {
                        "database": "UniProtKB",
                        "id": "A1Z898",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "CAF-1 complex",
                "id": "GO:0033186",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "DNA repair",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleosome assembly",
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                    }
                ],
                "pmid": ""
            },
            {
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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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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                "evidence": [
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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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                "name": "metal ion binding",
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                    }
                ],
                "pmid": ""
            },
            {
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                    {
                        "database": "UniProtKB",
                        "id": "A1Z8V9",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8V9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "amino acid:monoatomic cation symporter activity",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z8V9",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8V9"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z8V9",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8V9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
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                    {
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                        "id": "A1Z8V9",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8V9"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "sodium ion transmembrane transport",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
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                        "url": "https://www.uniprot.org/uniprotkb/A1Z8V9"
                    }
                ],
                "pmid": ""
            },
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                    }
                ],
                "pmid": ""
            },
            {
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                    }
                ],
                "pmid": ""
            },
            {
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "A1Z8X5-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                    }
                ],
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "CG30049-PA;CG30049-PA;CG30049;Dmel\\CG30049;Dmel_CG30049",
        "protein_name": "FXNA-like protease",
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            {
                "disease_id": "DOID:784",
                "name": "chronic kidney disease",
                "description": "A kidney failure that is characterized by the gradual loss of kidney function, present for a minimum of 3 months. CKD is classified based on cause, glomerular filtration rate (GFR) category (G2-G5), and albuminuria category (A1-A3).",
                "url": "https://disease-ontology.org/term/DOID:784",
                "evidence": [
                    {
                        "id": "784",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:784"
                    }
                ],
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            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z8X5",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8X5"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z8X5",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8X5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metalloexopeptidase activity",
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                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 850,
                        "start_aa": "Thr",
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                        "end_aa": "Thr",
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                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
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            {
                "name": "Drosophila melanogaster",
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                        "id": "A1Z9Q4",
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                ],
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "Obp50c;CG30072;DmelObp50c;Dmel\\CG30072;Dmel_CG30072;Obp50c",
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            {
                "name": "extracellular region",
                "id": "GO:0005576",
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                        "url": "https://www.uniprot.org/uniprotkb/A1Z9Q4"
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "sensory perception of chemical stimulus",
                "id": "GO:0007606",
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                ],
                "pmid": ""
            }
        ],
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                ],
                "pmid": ""
            }
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                        "id": "A1Z9W8",
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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    {
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                "name": "Drosophila melanogaster",
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                ],
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        ],
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            {
                "disease_id": "DOID:0080539",
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                "url": "https://disease-ontology.org/term/DOID:0080539",
                "evidence": [
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        ],
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            {
                "name": "nucleus",
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                ],
                "pmid": ""
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            {
                "name": "pre-snoRNP complex",
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        ],
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                "name": "box C/D snoRNP assembly",
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                ],
                "pmid": ""
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            {
                "name": "maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)",
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                ],
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            {
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        ],
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        ],
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                "name": "innate immune response",
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            {
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        ],
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                ],
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                ],
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                "name": "plasma membrane",
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            {
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            {
                "name": "muscle cell cellular homeostasis",
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            {
                "name": "defense response to Gram-negative bacterium",
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
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            {
                "name": "negative regulation of innate immune response",
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                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZA87"
                    }
                ],
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                "name": "rhabdomere development",
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                        "id": "A1ZA87",
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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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                ],
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        ],
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            {
                "name": "insemination",
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                "name": "extracellular space",
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                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VGX7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VGX7"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane transporter activity",
                "id": "GO:0022857",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022857",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VGX7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VGX7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "transmembrane transport",
                "id": "GO:0055085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055085",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VGX7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VGX7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VGX7-1"
    },
    {
        "uniprot_canonical_ac": "Q9VAF2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAF2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAF2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 35405.0,
        "gene_names": "Dmel\\CG15514;CC30;CG15514;Dmel\\CG15514;Dmel_CG15514",
        "protein_name": "BED-type domain-containing protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAF2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAF2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAF2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAF2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "identical protein binding",
                "id": "GO:0042802",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042802",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAF2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAF2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VAF2-1"
    },
    {
        "uniprot_canonical_ac": "B7Z0M0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0M0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0M0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 122,
        "chemical_mass": 13757.0,
        "gene_names": "Vti1b;CG31232;CG44009;CG7682;Dmel\\CG44009;Dmel_CG44009;EP(3)1037;Vti1b;koko",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "Golgi apparatus",
                "id": "GO:0005794",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005794",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0M0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0M0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "SNARE complex",
                "id": "GO:0031201",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031201",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0M0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0M0"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein transport",
                "id": "GO:0015031",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015031",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0M0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0M0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "vesicle-mediated transport",
                "id": "GO:0016192",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016192",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0M0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0M0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "SNAP receptor activity",
                "id": "GO:0005484",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005484",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0M0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0M0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "B7Z0M0-1"
    },
    {
        "uniprot_canonical_ac": "Q9VBJ2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 2802,
        "chemical_mass": 317249.0,
        "gene_names": "Nf1;CG8318;Dmel\\CG8318;Dmel_CG8318;FBpp0084326;NF-1;NF1;Nf-1;Nf1;dNF1;dNf1;nf1",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050458",
                "name": "juvenile myelomonocytic leukemia",
                "description": "A myelodysplastic/myeloproliferative neoplasm that is characterized by the uncontrolled growth of monocytes.",
                "url": "https://disease-ontology.org/term/DOID:0050458",
                "evidence": [
                    {
                        "id": "0050458",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050458"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070482",
                "name": "spinal neurofibromatosis",
                "description": "A neurofibromatosis 1 characterized by bilateral neurofibromas of all spinal roots.",
                "url": "https://disease-ontology.org/term/DOID:0070482",
                "evidence": [
                    {
                        "id": "0070482",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070482"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070483",
                "name": "Watson syndrome",
                "description": "A RASopathy characterized by pulmonic stenosis, cafe-au-lait macules, decreased intellectual ability, and short stature that has_material_basis_in heterozygous mutation in the NF1 gene on chromosome 17q11.2.",
                "url": "https://disease-ontology.org/term/DOID:0070483",
                "evidence": [
                    {
                        "id": "0070483",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070483"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080199",
                "name": "colorectal carcinoma",
                "description": "A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa.",
                "url": "https://disease-ontology.org/term/DOID:0080199",
                "evidence": [
                    {
                        "id": "0080199",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080199"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111253",
                "name": "neurofibromatosis 1",
                "description": "A neurofibromatosis characterized by multiple cafe-au-lait macules, skin fold freckling, neurofibromas, optic gliomas, Lisch nodules or choroidal abnormalities in the eye, or a specific bone abnormality that has_material_basis_in the NF1 gene on chromosome 17q11.2. Bone abnormalities include a distinctive osseous lesion such as sphenoid dysplasia, anterolateral bowing of the tibia, or pseudarthrosis of a long bone.",
                "url": "https://disease-ontology.org/term/DOID:0111253",
                "evidence": [
                    {
                        "id": "0111253",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111253"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111683",
                "name": "neurofibromatosis-Noonan syndrome",
                "description": "A RASopathy characterized by neurofibromatosis and manifestations of Noonan syndrome including short stature, ptosis, midface hypoplasia, webbed neck, learning disabilities, and muscle weakness that has_material_basis_in heterozygous mutation in NF1 on chromosome 17q11.2.",
                "url": "https://disease-ontology.org/term/DOID:0111683",
                "evidence": [
                    {
                        "id": "0111683",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111683"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1094",
                "name": "attention deficit hyperactivity disorder",
                "description": "A specific developmental disorder that is characterized by co-existence of attentional problems and hyperactivity, with each behavior occurring infrequently alone and symptoms starting before seven years of age.",
                "url": "https://disease-ontology.org/term/DOID:1094",
                "evidence": [
                    {
                        "id": "1094",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1094"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11446",
                "name": "sciatic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11446",
                "evidence": [
                    {
                        "id": "11446",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11446"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12849",
                "name": "autistic disorder",
                "description": "An autism spectrum disorder that is characterized by symptoms across all three symptom domains (communication, social, restricted repetitive interests and behaviors), delayed language development, and symptom onset prior to age 3 years.",
                "url": "https://disease-ontology.org/term/DOID:12849",
                "evidence": [
                    {
                        "id": "12849",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12849"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:219",
                "name": "colon cancer",
                "description": "A colorectal cancer that is located_in the colon.",
                "url": "https://disease-ontology.org/term/DOID:219",
                "evidence": [
                    {
                        "id": "219",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:219"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
                "description": "A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.",
                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3069",
                "name": "malignant astrocytoma",
                "description": "A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord.",
                "url": "https://disease-ontology.org/term/DOID:3069",
                "evidence": [
                    {
                        "id": "3069",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3069"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3070",
                "name": "high grade glioma",
                "description": "A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine.",
                "url": "https://disease-ontology.org/term/DOID:3070",
                "evidence": [
                    {
                        "id": "3070",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3070"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4992",
                "name": "optic nerve glioma",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:4992",
                "evidence": [
                    {
                        "id": "4992",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4992"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5151",
                "name": "plexiform neurofibroma",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:5151",
                "evidence": [
                    {
                        "id": "5151",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5151"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:535",
                "name": "sleep disorder",
                "description": "A disease of mental health that involves disruption of sleep patterns.",
                "url": "https://disease-ontology.org/term/DOID:535",
                "evidence": [
                    {
                        "id": "535",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:535"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8712",
                "name": "neurofibromatosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8712",
                "evidence": [
                    {
                        "id": "8712",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8712"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9119",
                "name": "acute myeloid leukemia",
                "description": "A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells.",
                "url": "https://disease-ontology.org/term/DOID:9119",
                "evidence": [
                    {
                        "id": "9119",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9119"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "GTPase activator activity",
                "id": "GO:0005096",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005096",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "response to oxidative stress",
                "id": "GO:0006979",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006979",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "adult locomotory behavior",
                "id": "GO:0008344",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008344",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of multicellular organism growth",
                "id": "GO:0040014",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040014",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "short-term memory",
                "id": "GO:0007614",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007614",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Ras protein signal transduction",
                "id": "GO:0007265",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007265",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "long-term memory",
                "id": "GO:0007616",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007616",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "olfactory learning",
                "id": "GO:0008355",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008355",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "locomotor rhythm",
                "id": "GO:0045475",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045475",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to heat",
                "id": "GO:0009408",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009408",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of multicellular organism growth",
                "id": "GO:0040018",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040018",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of Ras protein signal transduction",
                "id": "GO:0046578",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046578",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "determination of adult lifespan",
                "id": "GO:0008340",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008340",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "perineurial glial growth",
                "id": "GO:0042066",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042066",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of synaptic assembly at neuromuscular junction",
                "id": "GO:0045886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of circadian rhythm",
                "id": "GO:0042752",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042752",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of intracellular signal transduction",
                "id": "GO:1902531",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1902531",
                "evidence": [
                    {
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                        "end_aa": "Thr",
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                            {
                                "id": "H9XVM9",
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                            },
                            {
                                "id": "H9XVM9",
                                "database": "O-GlcNAc Database",
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                            }
                        ]
                    }
                ]
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                    {
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                            },
                            {
                                "id": "H9XVM9",
                                "database": "O-GlcNAc Database",
                                "url": "https://www.oglcnac.mcw.edu/search/?query_protein=H9XVM9"
                            }
                        ]
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                ]
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        ],
        "record_id": "H9XVM9-1"
    },
    {
        "uniprot_canonical_ac": "M9NGY4-1",
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            {
                "name": "Drosophila melanogaster",
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                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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            {
                "name": "nucleus",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear speck",
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            }
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                "name": "protein phosphatase 1 binding",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            }
        ],
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                "name": "DNA-templated transcription",
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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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        ],
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                "name": "Drosophila melanogaster",
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        ],
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        "gene_names": "nAChRalpha6;AChRalpha6;BcDNA:GH01410;CG4128;CT13662;Dalpha6;Dmel\\CG4128;Dmel_CG4128;alpha6;dalpha6;das;nACRalpha-30D;nAChR alpha 6;nAChR-alpha30D;nAChRAlpha-30D;nAChRalpha-30D;nAChRalpha6;nAChRalpha;nAChR;nAChralpha6;nAcR-alpha-30D;nAcRalpha-30D;nAchR_alpha6;rsn",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050742",
                "name": "nicotine dependence",
                "description": "A substance dependence that is characterized by a physical dependence on nicotine.",
                "url": "https://disease-ontology.org/term/DOID:0050742",
                "evidence": [
                    {
                        "id": "0050742",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050742"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
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                    }
                ],
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            },
            {
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                "name": "Lewy body dementia",
                "description": "A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities that has_material_basis_in accumulation of alpha-synuclein, SCNA, (protein). The causal mutation might be in SCNA or SCNB or some other gene(s) but the end result is always accumulation of SCNA in Lewy bodies.",
                "url": "https://disease-ontology.org/term/DOID:12217",
                "evidence": [
                    {
                        "id": "12217",
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                        "url": "https://www.alliancegenome.org/disease/DOID:12217"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1561",
                "name": "cognitive disorder",
                "description": "A disease of mental health that affects cognitive functions including memory processing, perception and problem solving.",
                "url": "https://disease-ontology.org/term/DOID:1561",
                "evidence": [
                    {
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1561"
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                ],
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            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3748",
                "name": "esophagus squamous cell carcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus.",
                "url": "https://disease-ontology.org/term/DOID:3748",
                "evidence": [
                    {
                        "id": "3748",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3748"
                    }
                ],
                "weight": 0.0
            },
            {
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                "name": "lung non-small cell carcinoma",
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                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
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                "evidence": [
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                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7148",
                "name": "rheumatoid arthritis",
                "description": "An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint.",
                "url": "https://disease-ontology.org/term/DOID:7148",
                "evidence": [
                    {
                        "id": "7148",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7148"
                    }
                ],
                "weight": 0.0
            },
            {
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                "name": "malignant pleural mesothelioma",
                "description": "A pleural cancer that has_material_basis_in mesothelium cells.",
                "url": "https://disease-ontology.org/term/DOID:7474",
                "evidence": [
                    {
                        "id": "7474",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7474"
                    }
                ],
                "weight": 0.0
            },
            {
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                "description": "A colitis that is predominantly confined to the mucosa located_in colon and includes characteristic ulcers, or open sores.",
                "url": "https://disease-ontology.org/term/DOID:8577",
                "evidence": [
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                        "id": "8577",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8577"
                    }
                ],
                "weight": 0.0
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                "disease_id": "DOID:8778",
                "name": "Crohn's disease",
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                "url": "https://disease-ontology.org/term/DOID:8778",
                "evidence": [
                    {
                        "id": "8778",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8778"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "transmembrane signaling receptor activity",
                "id": "GO:0004888",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004888",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "acetylcholine-gated monoatomic cation-selective channel activity",
                "id": "GO:0022848",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022848",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "excitatory extracellular ligand-gated monoatomic ion channel activity",
                "id": "GO:0005231",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005231",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "acetylcholine-gated channel complex",
                "id": "GO:0005892",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005892",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
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                        "id": "A8JUP5",
                        "url": "https://www.uniprot.org/uniprotkb/A8JUP5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 206,
        "chemical_mass": 23638.0,
        "gene_names": "Dmel\\CG12645;CG12645;Dmel\\CG12645;Dmel_CG12645",
        "protein_name": "LITAF domain-containing protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JUP5",
                        "url": "https://www.uniprot.org/uniprotkb/A8JUP5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JUP5",
                        "url": "https://www.uniprot.org/uniprotkb/A8JUP5"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "lysosomal membrane",
                "id": "GO:0005765",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005765",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JUP5",
                        "url": "https://www.uniprot.org/uniprotkb/A8JUP5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "late endosome membrane",
                "id": "GO:0031902",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031902",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JUP5",
                        "url": "https://www.uniprot.org/uniprotkb/A8JUP5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A8JUP5-1"
    },
    {
        "uniprot_canonical_ac": "Q2PE08-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q2PE08",
                        "url": "https://www.uniprot.org/uniprotkb/Q2PE08"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 355,
        "chemical_mass": 41231.0,
        "gene_names": "CG13904;CG13904;CG34057;Dmel\\CG34057;Dmel_CG34057;dC1GalT6",
        "protein_name": "Glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1",
        "disease": [],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q2PE08",
                        "url": "https://www.uniprot.org/uniprotkb/Q2PE08"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "manganese ion binding",
                "id": "GO:0030145",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030145",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q2PE08",
                        "url": "https://www.uniprot.org/uniprotkb/Q2PE08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleotide binding",
                "id": "GO:0000166",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000166",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q2PE08",
                        "url": "https://www.uniprot.org/uniprotkb/Q2PE08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase activity",
                "id": "GO:0016263",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016263",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q2PE08",
                        "url": "https://www.uniprot.org/uniprotkb/Q2PE08"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q2PE08-1"
    },
    {
        "uniprot_canonical_ac": "Q9V4E5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1096,
        "chemical_mass": 123282.0,
        "gene_names": "Eph;CG1511;CT3831;DEK;Dek7;Dek;Deph;Dmel\\CG1511;Dmel_CG1511;EPH;Ek7;Eph;RPTK Dek7;dek;eph;lincRNA.923",
        "protein_name": "receptor protein-tyrosine kinase",
        "disease": [
            {
                "disease_id": "DOID:0070611",
                "name": "autosomal dominant nonsyndromic deafness 88",
                "description": "An autosomal dominant nonsyndromic deafness characterized by postlingual progressive severe sensorineural hearing loss with tinnitus that has_material_basis_in heterozygous mutation in the EPHA10 gene on chromosome 1p34.",
                "url": "https://disease-ontology.org/term/DOID:0070611",
                "evidence": [
                    {
                        "id": "0070611",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070611"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080685",
                "name": "aortic dissection",
                "description": "An aortic disease that is characterized by tearing of the intimal layer of the aorta resulting in separation of the layers of the aortic wall.",
                "url": "https://disease-ontology.org/term/DOID:0080685",
                "evidence": [
                    {
                        "id": "0080685",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080685"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081030",
                "name": "central conducting lymphatic anomaly",
                "description": "A lymphatic system disease that is characterized by dysfunction of the thoracic duct or cisterna chyli, leading to a retrograde flux of lymphatic fluid or abnormal drainage of lymphatic fluid and that has_material_basis_in heterozygous mutation in the EPHB4 gene on chromosome 7q22.",
                "url": "https://disease-ontology.org/term/DOID:0081030",
                "evidence": [
                    {
                        "id": "0081030",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081030"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110229",
                "name": "cataract 6 multiple types",
                "description": "A cataract that has_material_basis_in heterozygous mutation in the EPHA2 gene on chromosome 1p36.",
                "url": "https://disease-ontology.org/term/DOID:0110229",
                "evidence": [
                    {
                        "id": "0110229",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110229"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12365",
                "name": "malaria",
                "description": "A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle.",
                "url": "https://disease-ontology.org/term/DOID:12365",
                "evidence": [
                    {
                        "id": "12365",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12365"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1561",
                "name": "cognitive disorder",
                "description": "A disease of mental health that affects cognitive functions including memory processing, perception and problem solving.",
                "url": "https://disease-ontology.org/term/DOID:1561",
                "evidence": [
                    {
                        "id": "1561",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1561"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2218",
                "name": "blood platelet disease",
                "description": "A blood coagulation disease that is characterized by an abnormal increase or decrease in platelets or platelet dysfunction.",
                "url": "https://disease-ontology.org/term/DOID:2218",
                "evidence": [
                    {
                        "id": "2218",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2218"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:264",
                "name": "hemangiopericytoma",
                "description": "A hemangiopericytic tumor that is a soft tissue sarcoma and originates in the pericytes in the walls of capillaries.",
                "url": "https://disease-ontology.org/term/DOID:264",
                "evidence": [
                    {
                        "id": "264",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:264"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2975",
                "name": "cystic kidney disease",
                "description": "A kidney disease that is characterized by the formation of cysts (fluid-filled sacs) in and around the kidney.",
                "url": "https://disease-ontology.org/term/DOID:2975",
                "evidence": [
                    {
                        "id": "2975",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2975"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3525",
                "name": "middle cerebral artery infarction",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3525",
                "evidence": [
                    {
                        "id": "3525",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3525"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3602",
                "name": "toxic encephalopathy",
                "description": "A nervous system disease that results from exposure to neurotoxicants and is characterized by an altered mental status, memory loss, and visual problems.",
                "url": "https://disease-ontology.org/term/DOID:3602",
                "evidence": [
                    {
                        "id": "3602",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3602"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3748",
                "name": "esophagus squamous cell carcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus.",
                "url": "https://disease-ontology.org/term/DOID:3748",
                "evidence": [
                    {
                        "id": "3748",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3748"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:526",
                "name": "human immunodeficiency virus infectious disease",
                "description": "A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 (Lentivirus humimdef1) or Human immunodeficiency virus 2 (Lentivirus humimdef2), which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands.",
                "url": "https://disease-ontology.org/term/DOID:526",
                "evidence": [
                    {
                        "id": "526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:526"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:75",
                "name": "lymphatic system disease",
                "description": "An immune system disease that is located_in the lymphatic system.",
                "url": "https://disease-ontology.org/term/DOID:75",
                "evidence": [
                    {
                        "id": "75",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:75"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8577",
                "name": "ulcerative colitis",
                "description": "A colitis that is predominantly confined to the mucosa located_in colon and includes characteristic ulcers, or open sores.",
                "url": "https://disease-ontology.org/term/DOID:8577",
                "evidence": [
                    {
                        "id": "8577",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8577"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9778",
                "name": "irritable bowel syndrome",
                "description": "An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause.",
                "url": "https://disease-ontology.org/term/DOID:9778",
                "evidence": [
                    {
                        "id": "9778",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9778"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmembrane-ephrin receptor activity",
                "id": "GO:0005005",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005005",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmembrane receptor protein tyrosine kinase activity",
                "id": "GO:0004714",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004714",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "receptor complex",
                "id": "GO:0043235",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043235",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cell differentiation",
                "id": "GO:0030154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ephrin receptor signaling pathway",
                "id": "GO:0048013",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048013",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "peripheral nervous system development",
                "id": "GO:0007422",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007422",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "anatomical structure morphogenesis",
                "id": "GO:0009653",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009653",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mushroom body development",
                "id": "GO:0016319",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016319",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "melanotic encapsulation of foreign target",
                "id": "GO:0035011",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035011",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell surface receptor protein tyrosine kinase signaling pathway",
                "id": "GO:0007169",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007169",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9V4E5-1"
    },
    {
        "uniprot_canonical_ac": "Q8IPH8-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 2122,
        "chemical_mass": 243303.0,
        "gene_names": "Myo28B1;28B;CG6976;DmVIIB;Dmel\\CG6976;Dmel_CG6976;Myo18;Myo28B1;Myo28B;VIIb 28B;myo 28B1;myo28B",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "system development",
                "id": "GO:0048731",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048731",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin filament-based movement",
                "id": "GO:0030048",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030048",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
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                        "id": "Q9VC75",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC75"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 231,
        "chemical_mass": 26065.0,
        "gene_names": "Dmel\\CG13616;CG13616;Dmel\\CG13616;Dmel_CG13616",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VC75-1"
    },
    {
        "uniprot_canonical_ac": "M9PHV5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1182,
        "chemical_mass": 129788.0,
        "gene_names": "GluRIB;CG42509;CG43743;CG4481;DGluR-IB;Dm_3L:43677;DmelGlu-R1B;Dmel\\CG43743;Dmel_CG43743;Glu-R1B;Glu-RIB;GluR1B;GluRIB;GluRIb;dglur-IB",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0060001",
                "name": "withdrawal disorder",
                "description": "A substance-related disorder that occurs upon the abrupt discontinuation/separation or a decrease in dosage of the intake of medications, recreational drugs, and alcohol.",
                "url": "https://disease-ontology.org/term/DOID:0060001",
                "evidence": [
                    {
                        "id": "0060001",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060001"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060823",
                "name": "syndromic X-linked intellectual disability 94",
                "description": "A syndromic X-linked intellectual disability characterized by moderate intellectual disability with variable occurrence of asthenic body habitus, dysmorphic features, autistic features, macrocephaly, seizures, myoclonic jerks, and hyporeflexia that has_material_basis_in mutation in the GRIA3 gene on chromosome Xq25.",
                "url": "https://disease-ontology.org/term/DOID:0060823",
                "evidence": [
                    {
                        "id": "0060823",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060823"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0061040",
                "name": "autosomal dominant intellectual developmental disorder 67",
                "description": "An autosomal dominant intellectual developmental disorder characterized by global developmental delay with variably impaired intellectual development apparent from infancy or early childhood that has_material_basis_in heterozygous mutation in the GRIA1 gene on chromosome 5q33.",
                "url": "https://disease-ontology.org/term/DOID:0061040",
                "evidence": [
                    {
                        "id": "0061040",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0061040"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081235",
                "name": "autosomal recessive intellectual developmental disorder 76",
                "description": "An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the GRIA1 gene on chromosome 5q33.",
                "url": "https://disease-ontology.org/term/DOID:0081235",
                "evidence": [
                    {
                        "id": "0081235",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081235"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081292",
                "name": "traumatic brain injury",
                "description": "A brain disease that is characterized by brain dysfunction caused by an outside force, usually a violent blow to the head.",
                "url": "https://disease-ontology.org/term/DOID:0081292",
                "evidence": [
                    {
                        "id": "0081292",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081292"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1289",
                "name": "neurodegenerative disease",
                "description": "A central nervous system disease that results in the progressive deterioration of function or structure of neurons.",
                "url": "https://disease-ontology.org/term/DOID:1289",
                "evidence": [
                    {
                        "id": "1289",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1289"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13413",
                "name": "hepatic encephalopathy",
                "description": "A brain disease that is characterized by loss of brain function, the occurrence of confusion, altered level of consciousness, and coma that results when the liver is unable to remove toxins from the blood.",
                "url": "https://disease-ontology.org/term/DOID:13413",
                "evidence": [
                    {
                        "id": "13413",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13413"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1574",
                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:1574",
                "evidence": [
                    {
                        "id": "1574",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1574"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1596",
                "name": "depressive disorder",
                "description": "A mood disorder characterized by persistent sadness, emptiness, or irritability and decreased ability to function.",
                "url": "https://disease-ontology.org/term/DOID:1596",
                "evidence": [
                    {
                        "id": "1596",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1596"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1824",
                "name": "status epilepticus",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1824",
                "evidence": [
                    {
                        "id": "1824",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1824"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1826",
                "name": "epilepsy",
                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.",
                "url": "https://disease-ontology.org/term/DOID:1826",
                "evidence": [
                    {
                        "id": "1826",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1826"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2560",
                "name": "morphine dependence",
                "description": "An opiate dependence that involves the continued use of morphine despite despite problems related to use of the substance.",
                "url": "https://disease-ontology.org/term/DOID:2560",
                "evidence": [
                    {
                        "id": "2560",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2560"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5418",
                "name": "schizoaffective disorder",
                "description": "A psychotic disorder that is characterized by recurring episodes of mood fluctuations and a loss of contact with reality.",
                "url": "https://disease-ontology.org/term/DOID:5418",
                "evidence": [
                    {
                        "id": "5418",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5418"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.",
                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:670",
                "name": "amphetamine abuse",
                "description": "A substance abuse that involves the recurring use of amphetamines despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:670",
                "evidence": [
                    {
                        "id": "670",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:670"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:809",
                "name": "cocaine abuse",
                "description": "A substance abuse that involves the recurring use of cocaine despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:809",
                "evidence": [
                    {
                        "id": "809",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:809"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9279",
                "name": "hyperhomocysteinemia",
                "description": "An amino acid metabolic disorder that involves an abnormally large level of homocysteine in the blood.",
                "url": "https://disease-ontology.org/term/DOID:9279",
                "evidence": [
                    {
                        "id": "9279",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9279"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9505",
                "name": "cannabis abuse",
                "description": "A substance abuse that involves the recurring use of cannabis despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:9505",
                "evidence": [
                    {
                        "id": "9505",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9505"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9975",
                "name": "cocaine dependence",
                "description": "A drug dependence that is a psychological dependency on the regular use of cocaine.",
                "url": "https://disease-ontology.org/term/DOID:9975",
                "evidence": [
                    {
                        "id": "9975",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9975"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9976",
                "name": "heroin dependence",
                "description": "An opiate dependence that involves the continued use of heroin despite problems related to use of the substance.",
                "url": "https://disease-ontology.org/term/DOID:9976",
                "evidence": [
                    {
                        "id": "9976",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9976"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "transmitter-gated monoatomic ion channel activity",
                "id": "GO:0022824",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022824",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular ligand-gated monoatomic ion channel activity",
                "id": "GO:0005230",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005230",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential",
                "id": "GO:1904315",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1904315",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glutamate receptor activity",
                "id": "GO:0008066",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008066",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "ionotropic glutamate receptor complex",
                "id": "GO:0008328",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008328",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "postsynaptic membrane",
                "id": "GO:0045211",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045211",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "postsynaptic density membrane",
                "id": "GO:0098839",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098839",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cell surface receptor signaling pathway",
                "id": "GO:0007166",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007166",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoatomic cation transport",
                "id": "GO:0006812",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006812",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synaptic transmission, glutamatergic",
                "id": "GO:0035249",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035249",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "modulation of chemical synaptic transmission",
                "id": "GO:0050804",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050804",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "M9PHV5-1",
                "start_pos": "703",
                "end_pos": "703",
                "site_lbl": "Thr703",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 703,
                        "start_aa": "Thr",
                        "end_pos": 703,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr703",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "M9PHV5-1"
    },
    {
        "uniprot_canonical_ac": "Q8IQE6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1076,
        "chemical_mass": 120321.0,
        "gene_names": "IRSp53;CG32082;CG7624;Dmel\\CG32082;Dmel_CG32082;IRSp53;IRS;anon-WO0118547.199",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0060041",
                "name": "autism spectrum disorder",
                "description": "A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior.",
                "url": "https://disease-ontology.org/term/DOID:0060041",
                "evidence": [
                    {
                        "id": "0060041",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060041"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1094",
                "name": "attention deficit hyperactivity disorder",
                "description": "A specific developmental disorder that is characterized by co-existence of attentional problems and hyperactivity, with each behavior occurring infrequently alone and symptoms starting before seven years of age.",
                "url": "https://disease-ontology.org/term/DOID:1094",
                "evidence": [
                    {
                        "id": "1094",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1094"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11119",
                "name": "Gilles de la Tourette syndrome",
                "description": "A tic disorder that is characterized by multiple physical (motor) tics and at least one vocal (phonic) tic present for more than a year.",
                "url": "https://disease-ontology.org/term/DOID:11119",
                "evidence": [
                    {
                        "id": "11119",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11119"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "phospholipid binding",
                "id": "GO:0005543",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005543",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "plasma membrane organization",
                "id": "GO:0007009",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007009",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "filopodium assembly",
                "id": "GO:0046847",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046847",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane organization",
                "id": "GO:0061024",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061024",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin filament bundle assembly",
                "id": "GO:0051017",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051017",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin crosslink formation",
                "id": "GO:0051764",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051764",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of actin filament polymerization",
                "id": "GO:0030838",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030838",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
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        ],
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                "name": "plasma membrane",
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                "name": "side of membrane",
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            }
        ],
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            {
                "name": "proteolysis",
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                ],
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        ],
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            },
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                "name": "chorion-containing eggshell formation",
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                "name": "protein transport",
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                ],
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            }
        ],
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                "name": "cytoplasm",
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                ],
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                "url": "https://disease-ontology.org/term/DOID:0070595",
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                ],
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            },
            {
                "name": "P granule",
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                "name": "DNA topoisomerase binding",
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                    }
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            },
            {
                "name": "intracellular calcium ion homeostasis",
                "id": "GO:0006874",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006874",
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                    {
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            },
            {
                "name": "calcium ion transmembrane transport",
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                "pmid": ""
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        ],
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                ],
                "pmid": ""
            },
            {
                "name": "calcium channel activity",
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                ],
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            },
            {
                "name": "calcium, potassium:sodium antiporter activity",
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
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            {
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                ],
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            {
                "name": "lipid metabolic process",
                "id": "GO:0006629",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PGQ5",
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
        "uniprot_canonical_ac": "M9NDP9-1",
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                ],
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                    {
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            }
        ],
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        "chemical_mass": 112143.0,
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        "protein_name": "Nose resistant-to-fluoxetine protein N-terminal domain-containing protein",
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            {
                "name": "acyltransferase activity, transferring groups other than amino-acyl groups",
                "id": "GO:0016747",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016747",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JUS7",
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
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                "name": "Drosophila melanogaster",
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                    {
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                        "id": "Q5LJX8",
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                ],
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            }
        ],
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        "chemical_mass": 58408.0,
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        "protein_name": "",
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                "disease_id": "DOID:0110063",
                "name": "amelogenesis imperfecta hypomaturation type 2A5",
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                "url": "https://disease-ontology.org/term/DOID:0110063",
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                    }
                ],
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            },
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                "evidence": [
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                    }
                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:1826",
                "evidence": [
                    {
                        "id": "1826",
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                    }
                ],
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            }
        ],
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            {
                "name": "Golgi apparatus",
                "id": "GO:0005794",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005794",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
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                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "calcium ion transport",
                "id": "GO:0006816",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006816",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "potassium ion transport",
                "id": "GO:0006813",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006813",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sodium ion transport",
                "id": "GO:0006814",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006814",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium-mediated signaling",
                "id": "GO:0019722",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019722",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
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            },
            {
                "name": "intracellular calcium ion homeostasis",
                "id": "GO:0006874",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006874",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium ion transmembrane transport",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070588",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "symporter activity",
                "id": "GO:0015293",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015293",
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                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "antiporter activity",
                "id": "GO:0015297",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
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                ],
                "pmid": ""
            },
            {
                "name": "calcium channel activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005262",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium, potassium:sodium antiporter activity",
                "id": "GO:0008273",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008273",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
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                ],
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            }
        ],
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            {
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                "end_pos": "158",
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                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
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                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
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                        ],
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                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
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                                "id": "GLY_001163",
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                        ]
                    }
                ]
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    {
        "uniprot_canonical_ac": "Q9VAJ0-1",
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                "name": "Drosophila melanogaster",
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                        "database": "UniProtKB",
                        "id": "Q9VAJ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAJ0"
                    }
                ],
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                "reference_species": "Drosophila melanogaster [7227]"
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        ],
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        "chemical_mass": 28582.0,
        "gene_names": "Dmel\\CG7582;CG7582;Dmel\\CG7582;Dmel_CG7582",
        "protein_name": "lysoplasmalogenase",
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            {
                "name": "alkenylglycerophosphocholine hydrolase activity",
                "id": "GO:0047408",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0047408",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAJ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAJ0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "hydrolase activity",
                "id": "GO:0016787",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016787",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAJ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAJ0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAJ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAJ0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
        "uniprot_canonical_ac": "Q3KN41-1",
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            {
                "name": "Drosophila melanogaster",
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                    {
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                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
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                ],
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                "reference_species": "Drosophila melanogaster [7227]"
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        ],
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        "chemical_mass": 199615.0,
        "gene_names": "Nrx-1;CG7050;CT21808;DNrx;Dmel\\CG7050;Dmel_CG7050;Dnrx;Nrx-1;Nrx-I;Nrx1;Nrx;dNRXN3;dNrx;dnrx-1;dnrx1;dnrx;neurexin;nrx-1;nrx1;nrx",
        "protein_name": "Neurexin 1",
        "disease": [
            {
                "disease_id": "DOID:0050741",
                "name": "alcohol dependence",
                "description": "A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol.",
                "url": "https://disease-ontology.org/term/DOID:0050741",
                "evidence": [
                    {
                        "id": "0050741",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050741"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050742",
                "name": "nicotine dependence",
                "description": "A substance dependence that is characterized by a physical dependence on nicotine.",
                "url": "https://disease-ontology.org/term/DOID:0050742",
                "evidence": [
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                        "id": "0050742",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050742"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060041",
                "name": "autism spectrum disorder",
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                "url": "https://disease-ontology.org/term/DOID:0060041",
                "evidence": [
                    {
                        "id": "0060041",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060041"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111332",
                "name": "Pitt-Hopkins-like syndrome 2",
                "description": "A syndromic intellectual disability characterized by developmental delay and intellectual disability with many patients also displaying infantile hypotonia and autistic features that has_material_basis_in compound heterozygous or homozygous mutation in the NRXN1 gene on chromosome 2p16.3.",
                "url": "https://disease-ontology.org/term/DOID:0111332",
                "evidence": [
                    {
                        "id": "0111332",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111332"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
                "description": "A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.",
                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
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            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
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                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "neuromuscular synaptic transmission",
                "id": "GO:0007274",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007274",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "associative learning",
                "id": "GO:0008306",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008306",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synapse organization",
                "id": "GO:0050808",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050808",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synaptic assembly at neuromuscular junction",
                "id": "GO:0051124",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051124",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chemical synaptic transmission",
                "id": "GO:0007268",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007268",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synapse assembly",
                "id": "GO:0007416",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007416",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "locomotion",
                "id": "GO:0040011",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040011",
                "evidence": [
                    {
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                "name": "mesodermal cell fate specification",
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                "name": "mesodermal cell fate commitment",
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                "name": "positive regulation of glial cell proliferation",
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                "name": "mesodermal cell migration",
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                "pmid": ""
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            {
                "name": "mesoderm development",
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                "pmid": ""
            },
            {
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                "pmid": ""
            },
            {
                "name": "mesoderm migration involved in gastrulation",
                "id": "GO:0007509",
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                    {
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                "pmid": ""
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                "pmid": ""
            },
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                "name": "glial cell projection elongation",
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            },
            {
                "name": "lymph gland crystal cell differentiation",
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                "name": "myotube cell migration",
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                "pmid": ""
            },
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                "name": "larval somatic muscle development",
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            {
                "name": "pericardial nephrocyte differentiation",
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                "pmid": ""
            }
        ],
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                "name": "extracellular space",
                "id": "GO:0005615",
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            }
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                "name": "growth factor activity",
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            },
            {
                "name": "receptor ligand activity",
                "id": "GO:0048018",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048018",
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                "name": "fibroblast growth factor receptor binding",
                "id": "GO:0005104",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005104",
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                        "id": "B9ZW35",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
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                "name": "Drosophila melanogaster",
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                        "id": "Q0E910",
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        ],
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                "disease_id": "DOID:0110247",
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                        "id": "0110247",
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            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                    {
                        "database": "UniProtKB",
                        "id": "Q0E910",
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                    }
                ],
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            },
            {
                "name": "perinuclear region of cytoplasm",
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                    {
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                        "id": "Q0E910",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "P granule",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043186",
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                        "database": "UniProtKB",
                        "id": "Q0E910",
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                    }
                ],
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            }
        ],
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            {
                "name": "spermatogenesis",
                "id": "GO:0007283",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            },
            {
                "name": "cell differentiation",
                "id": "GO:0030154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030154",
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                        "database": "UniProtKB",
                        "id": "Q0E910",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E910"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "secondary piRNA processing",
                "id": "GO:0140965",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140965",
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                    {
                        "database": "UniProtKB",
                        "id": "Q0E910",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "transposable element silencing by piRNA-mediated mRNA destabilization",
                "id": "GO:0141009",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0141009",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E910",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E910"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "uniprot_canonical_ac": "Q0E910-1",
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                "end_pos": "328",
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                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
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                            {
                                "label": "isoglyp",
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                        ],
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                        "site_category_dict": {
                            "predicted": true
                        },
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                        "comment": "",
                        "icn3d_view": {},
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                        "end_aa": "Thr",
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                            {
                                "id": "GLY_001163",
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                            }
                        ]
                    }
                ]
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            {
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                        "glytoucan_ac": "",
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                        ],
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                                "id": "GLY_001163",
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                        ]
                    }
                ]
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        ],
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    {
        "uniprot_canonical_ac": "E1JGT2-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JGT2",
                        "url": "https://www.uniprot.org/uniprotkb/E1JGT2"
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "chemical_mass": 8757.0,
        "gene_names": "Dmel\\CG44253;CG30194;CG44253;Dmel\\CG44253;Dmel_CG44253",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "E1JGT2-1"
    },
    {
        "uniprot_canonical_ac": "Q59DZ7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q59DZ7",
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                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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        "chemical_mass": 116547.0,
        "gene_names": "Ddr;CG11573;CG13985;CG33531;CG9488;CG9490;CT33540;DDR;Ddr;Dmel\\CG33531;Dmel_CG33531;ddr",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050156",
                "name": "idiopathic pulmonary fibrosis",
                "description": "A pulmonary fibrosis that is characterized by scarring of the lung characterized by stiffness in the lungs and makes it difficult to breathe.",
                "url": "https://disease-ontology.org/term/DOID:0050156",
                "evidence": [
                    {
                        "id": "0050156",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050156"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050866",
                "name": "oral squamous cell carcinoma",
                "description": "An oral cavity cancer that has_material_basis_in squamous cells.",
                "url": "https://disease-ontology.org/term/DOID:0050866",
                "evidence": [
                    {
                        "id": "0050866",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050866"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0112196",
                "name": "spondylometaepiphyseal dysplasia, short limb-hand type",
                "description": "A spondyloepimetaphyseal dysplasia characterized by short stature, short limbs and hands, and typical radiological features which include platyspondyly, metaphyseal, and epiphyseal involvement, short tubular bones of the limbs, and abnormal calcification of cartilage that has_material_basis_in homozygous or compound heterozygous mutation in the DDR2 gene on chromosome 1q23.3.",
                "url": "https://disease-ontology.org/term/DOID:0112196",
                "evidence": [
                    {
                        "id": "0112196",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112196"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
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                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
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            },
            {
                "disease_id": "DOID:12351",
                "name": "alcoholic hepatitis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:12351",
                "evidence": [
                    {
                        "id": "12351",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12351"
                    }
                ],
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                "disease_id": "DOID:14018",
                "name": "alcoholic liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:14018",
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                    {
                        "id": "14018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14018"
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                ],
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                        "id": "1612",
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                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
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            },
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                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
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                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
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            },
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                "evidence": [
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                        "url": "https://www.alliancegenome.org/disease/DOID:3070"
                    }
                ],
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                "name": "osteosarcoma",
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                "url": "https://disease-ontology.org/term/DOID:3347",
                "evidence": [
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                        "id": "3347",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3347"
                    }
                ],
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            },
            {
                "disease_id": "DOID:3459",
                "name": "breast carcinoma",
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                "url": "https://disease-ontology.org/term/DOID:3459",
                "evidence": [
                    {
                        "id": "3459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3500",
                "name": "gallbladder adenocarcinoma",
                "description": "A gallbladder carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3500",
                "evidence": [
                    {
                        "id": "3500",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3500"
                    }
                ],
                "weight": 0.0
            },
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                "name": "lung squamous cell carcinoma",
                "description": "A non-small cell lung carcinoma that has_material_basis_in the squamous cell.",
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                "evidence": [
                    {
                        "id": "3907",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3907"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4467",
                "name": "clear cell renal cell carcinoma",
                "description": "A renal cell carcinoma that has_material_basis_in cells that appear very pale or clear when examined under microscope.",
                "url": "https://disease-ontology.org/term/DOID:4467",
                "evidence": [
                    {
                        "id": "4467",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4467"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5520",
                "name": "head and neck squamous cell carcinoma",
                "description": "A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck.",
                "url": "https://disease-ontology.org/term/DOID:5520",
                "evidence": [
                    {
                        "id": "5520",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5520"
                    }
                ],
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                "description": "A gallbladder carcinoma that derives_from squamous cells and gland-like cells.",
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                    {
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                    {
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        ],
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            {
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                        "id": "0070263",
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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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                    }
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            },
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
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        ],
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        "protein_name": "Protein I'm not dead yet 2",
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                "url": "https://disease-ontology.org/term/DOID:0080453",
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                    {
                        "id": "0080453",
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                    }
                ],
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        ],
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                "name": "plasma membrane",
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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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            },
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        ],
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            },
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                "name": "C4-dicarboxylate transmembrane transporter activity",
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        "gene_names": "Sfp93F;CG42608;Dmel\\CG42608;Dmel_CG42608;Sfp93F",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "insemination",
                "id": "GO:0007320",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007320",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIS3",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIS3"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIS3",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIS3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "E1JIS3-1"
    },
    {
        "uniprot_canonical_ac": "Q9VHR7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHR7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHR7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 466,
        "chemical_mass": 56065.0,
        "gene_names": "Dmel\\CG7352;CG7352;Dmel\\CG7352;Dmel_CG7352",
        "protein_name": "Meiosis-specific nuclear structural protein 1",
        "disease": [
            {
                "disease_id": "DOID:0051023",
                "name": "visceral heterotaxy 9",
                "description": "A visceral heterotaxy that is characterized by randomization of organ laterality, resulting in defects such as situs inversus and dextrocardia and that has_material_basis_in homozygous mutation in the MNS1 gene on chromosome 15q21.",
                "url": "https://disease-ontology.org/term/DOID:0051023",
                "evidence": [
                    {
                        "id": "0051023",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0051023"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHR7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHR7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "motile cilium",
                "id": "GO:0031514",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031514",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHR7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHR7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "meiotic cell cycle",
                "id": "GO:0051321",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051321",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHR7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHR7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cilium organization",
                "id": "GO:0044782",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0044782",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHR7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHR7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VHR7-1"
    },
    {
        "uniprot_canonical_ac": "E1JJ97-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JJ97",
                        "url": "https://www.uniprot.org/uniprotkb/E1JJ97"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 92,
        "chemical_mass": 10575.0,
        "gene_names": "Dmel\\CG42577;CG42577;Dmel\\CG42577;Dmel_CG42577",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "E1JJ97-1"
    },
    {
        "uniprot_canonical_ac": "E1JJF2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JJF2",
                        "url": "https://www.uniprot.org/uniprotkb/E1JJF2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 385,
        "chemical_mass": 44985.0,
        "gene_names": "Dmel\\CG4558;CG4558;Dmel\\CG4558;Dmel_CG4558",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "Golgi membrane",
                "id": "GO:0000139",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000139",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JJF2",
                        "url": "https://www.uniprot.org/uniprotkb/E1JJF2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "E1JJF2-1"
    },
    {
        "uniprot_canonical_ac": "E2QCM9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 476,
        "chemical_mass": 54061.0,
        "gene_names": "Dh44-R2;CG12370;CG13156;DH-R;DH44-R2;DH44R2;DH[[44]]-R2;Dh44-R2;Dh442;Dh44R2;Dmel\\CG12370;Dmel_CG12370;anon-WO0170980.103;anon-WO0170980.104",
        "protein_name": "Diuretic hormone receptor",
        "disease": [
            {
                "disease_id": "DOID:0050696",
                "name": "fetal alcohol spectrum disorder",
                "description": "A specific developmental disorder and physical disorder that is characterized by physical, behavioral and learning birth defects resulting from maternal ingestion of alcohol during pregnancy.",
                "url": "https://disease-ontology.org/term/DOID:0050696",
                "evidence": [
                    {
                        "id": "0050696",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050696"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12918",
                "name": "thromboangiitis obliterans",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:12918",
                "evidence": [
                    {
                        "id": "12918",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12918"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1574",
                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:1574",
                "evidence": [
                    {
                        "id": "1574",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1574"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1596",
                "name": "depressive disorder",
                "description": "A mood disorder characterized by persistent sadness, emptiness, or irritability and decreased ability to function.",
                "url": "https://disease-ontology.org/term/DOID:1596",
                "evidence": [
                    {
                        "id": "1596",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1596"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing.",
                "url": "https://disease-ontology.org/term/DOID:2841",
                "evidence": [
                    {
                        "id": "2841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3877",
                "name": "functional colonic disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3877",
                "evidence": [
                    {
                        "id": "3877",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3877"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4483",
                "name": "rhinitis",
                "description": "A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip.",
                "url": "https://disease-ontology.org/term/DOID:4483",
                "evidence": [
                    {
                        "id": "4483",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4483"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9778",
                "name": "irritable bowel syndrome",
                "description": "An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause.",
                "url": "https://disease-ontology.org/term/DOID:9778",
                "evidence": [
                    {
                        "id": "9778",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9778"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9970",
                "name": "obesity",
                "description": "An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness.",
                "url": "https://disease-ontology.org/term/DOID:9970",
                "evidence": [
                    {
                        "id": "9970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9970"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9976",
                "name": "heroin dependence",
                "description": "An opiate dependence that involves the continued use of heroin despite problems related to use of the substance.",
                "url": "https://disease-ontology.org/term/DOID:9976",
                "evidence": [
                    {
                        "id": "9976",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9976"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cell surface receptor signaling pathway",
                "id": "GO:0007166",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007166",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "G protein-coupled receptor signaling pathway",
                "id": "GO:0007186",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007186",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "adenylate cyclase-modulating G protein-coupled receptor signaling pathway",
                "id": "GO:0007188",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007188",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "hormone-mediated signaling pathway",
                "id": "GO:0009755",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009755",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to salt stress",
                "id": "GO:0009651",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009651",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "peptide hormone binding",
                "id": "GO:0017046",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0017046",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "G protein-coupled peptide receptor activity",
                "id": "GO:0008528",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008528",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcitonin receptor activity",
                "id": "GO:0004948",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004948",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuropeptide receptor activity",
                "id": "GO:0008188",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008188",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "diuretic hormone receptor activity",
                "id": "GO:0008036",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008036",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "E2QCM9-1"
    },
    {
        "uniprot_canonical_ac": "Q9V491-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1945,
        "chemical_mass": 218358.0,
        "gene_names": "PlexA;BcDNA:GM05237;CG11081;D-Plex A;DPlexA;Dmel\\CG11081;Dmel_CG11081;Plex1;PlexA1;PlexA;Plexa;PlexinA;lincRNA.927;plex A;plexA;plex",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "GTPase activator activity",
                "id": "GO:0005096",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005096",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "heparin binding",
                "id": "GO:0008201",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008201",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "14-3-3 protein binding",
                "id": "GO:0071889",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071889",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "semaphorin receptor activity",
                "id": "GO:0017154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0017154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "guanylate cyclase activator activity",
                "id": "GO:0030250",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030250",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "semaphorin receptor complex",
                "id": "GO:0002116",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002116",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "axon midline choice point recognition",
                "id": "GO:0016199",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016199",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
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                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein dimerization activity",
                "id": "GO:0046983",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046983",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear receptor binding",
                "id": "GO:0016922",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016922",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription coactivator binding",
                "id": "GO:0001223",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001223",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription regulator inhibitor activity",
                "id": "GO:0140416",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140416",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "positive regulation of transcription by RNA polymerase II",
                "id": "GO:0045944",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045944",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of DNA-templated transcription",
                "id": "GO:0006355",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006355",
                "evidence": [
                    {
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                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
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                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of growth",
                "id": "GO:0045927",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045927",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "border follicle cell migration",
                "id": "GO:0007298",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007298",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "germ-line stem-cell niche homeostasis",
                "id": "GO:0060250",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060250",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of border follicle cell migration",
                "id": "GO:1903688",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1903688",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellular response to hormone stimulus",
                "id": "GO:0032870",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032870",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of smoothened signaling pathway",
                "id": "GO:0045879",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045879",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "uniprot_canonical_ac": "M9ND53-1",
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                "end_pos": "1492",
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                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
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                        "site_lbl": "Thr1492",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "M9MRI7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9MRI7",
                        "url": "https://www.uniprot.org/uniprotkb/M9MRI7"
                    }
                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "gene_names": "Dmel\\CG42751;CG42751;Dmel\\CG42751;Dmel_CG42751",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
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        "record_id": "M9MRI7-1"
    },
    {
        "uniprot_canonical_ac": "Q8IP51-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
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                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "wb;2Lan;2]];2;A1;BEST:CK02229;BG:DS03792.1;BG:DS03792.2;CG15288;CG32970;CG42677;CK02229;CT35236;DLAM;Dmel\\CG42677;Dmel_CG42677;LM-A/alpha2;LanA1;LanWb;Wb;alpha1;alpha2;alpha[[1;fus5;l(2)09437;l(2)34Fb;l(2)br1;l34Fb;wb",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0061132",
                "name": "autosomal recessive limb-girdle muscular dystrophy type 23",
                "description": "An autosomal recessive limb-girdle muscular dystrophy characterized by slowly progressive proximal muscle weakness primarily affecting the lower limbs and resulting in gait difficulties that has_material_basis_in y homozygous or compound heterozygous mutation in the LAMA2 gene on chromosome 6q22.",
                "url": "https://disease-ontology.org/term/DOID:0061132",
                "evidence": [
                    {
                        "id": "0061132",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0061132"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0110636",
                "name": "congenital merosin-deficient muscular dystrophy 1A",
                "description": "A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscle weakness that is apparent at birth or in the first 6 months of life and frequent development of periventricular white matter abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the LAMA2 gene on chromosome 6q22.",
                "url": "https://disease-ontology.org/term/DOID:0110636",
                "evidence": [
                    {
                        "id": "0110636",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110636"
                    }
                ],
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            },
            {
                "disease_id": "DOID:11830",
                "name": "myopia",
                "description": "A refractive error characterized by the inability to see farther objects clearly.",
                "url": "https://disease-ontology.org/term/DOID:11830",
                "evidence": [
                    {
                        "id": "11830",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11830"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1591",
                "name": "renovascular hypertension",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1591",
                "evidence": [
                    {
                        "id": "1591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1591"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9884",
                "name": "muscular dystrophy",
                "description": "A myopathy is characterized by progressive skeletal muscle weakness degeneration.",
                "url": "https://disease-ontology.org/term/DOID:9884",
                "evidence": [
                    {
                        "id": "9884",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9884"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "cell adhesion",
                "id": "GO:0007155",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007155",
                "evidence": [
                    {
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                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
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                ],
                "pmid": ""
            },
            {
                "name": "gonad development",
                "id": "GO:0008406",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008406",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "digestive tract mesoderm development",
                "id": "GO:0007502",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007502",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "animal organ morphogenesis",
                "id": "GO:0009887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axon guidance",
                "id": "GO:0007411",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007411",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tissue development",
                "id": "GO:0009888",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009888",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "epithelial structure maintenance",
                "id": "GO:0010669",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010669",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "anatomical structure morphogenesis",
                "id": "GO:0009653",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009653",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
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                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "basement membrane",
                "id": "GO:0005604",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005604",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
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                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "extracellular matrix structural constituent",
                "id": "GO:0005201",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005201",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            }
        ],
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    {
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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                "disease_id": "DOID:0060870",
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                "description": "A hypopituitarism characterized by abnormally low levels, absence or impaired function of growth hormone in the absence of abnormalities in other pituitary hormones.",
                "url": "https://disease-ontology.org/term/DOID:0060870",
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                    {
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                        "url": "https://www.alliancegenome.org/disease/DOID:0060870"
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                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:0080552",
                "evidence": [
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080552"
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                ],
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            },
            {
                "disease_id": "DOID:1184",
                "name": "nephrotic syndrome",
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                "url": "https://disease-ontology.org/term/DOID:1184",
                "evidence": [
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                        "id": "1184",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1184"
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                ],
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            },
            {
                "disease_id": "DOID:3490",
                "name": "Noonan syndrome",
                "description": "A RASopathy that is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms.",
                "url": "https://disease-ontology.org/term/DOID:3490",
                "evidence": [
                    {
                        "id": "3490",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3490"
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                ],
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            },
            {
                "disease_id": "DOID:8689",
                "name": "anorexia nervosa",
                "description": "An eating disorder characterized by refusal to maintain a healthy body weight, and an obsessive fear of gaining weight due to a distorted self image.",
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                "evidence": [
                    {
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8689"
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                ],
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        ],
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            {
                "name": "extracellular space",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
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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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    {
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                ],
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        ],
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        "protein_name": "BPTI/Kunitz inhibitor domain-containing protein",
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            {
                "name": "serine-type endopeptidase inhibitor activity",
                "id": "GO:0004867",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004867",
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                ],
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        ],
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    {
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                ],
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        "protein_name": "Secreted protein",
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            {
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                ],
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        ],
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        "chemical_mass": 20946.0,
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        "biomarkers": [],
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    },
    {
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        ],
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        "protein_name": "",
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    },
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        "species": [
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        "gene_names": "HDAC6;CG6170;DHDAC2;DmHDAC2;Dmel\\CG6170;Dmel_CG6170;HDAC2;HDAC6;HDAC;Hdac6;dHDAC2;dHDAC6;dmHDA404;hDAC6;hdac6",
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                "url": "https://disease-ontology.org/term/DOID:0060980",
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                "url": "https://disease-ontology.org/term/DOID:0080322",
                "evidence": [
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                "url": "https://disease-ontology.org/term/DOID:0112106",
                "evidence": [
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                    }
                ],
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            },
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                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:9970",
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                    }
                ],
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            }
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            {
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                    }
                ],
                "pmid": ""
            },
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                "pmid": ""
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                    }
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                    }
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                "pmid": ""
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                        "url": "https://www.uniprot.org/uniprotkb/M9PJN5"
                    }
                ],
                "pmid": ""
            },
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                "name": "protein lysine deacetylase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033558",
                "evidence": [
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H4K16 deacetylase activity, hydrolytic mechanism",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034739",
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                    {
                        "database": "UniProtKB",
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                    }
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                "pmid": ""
            },
            {
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/M9PJN5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H4K8 deacetylase activity, hydrolytic mechanism",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0180033",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H4K12 deacetylase activity, hydrolytic mechanism",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140937",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/M9PJN5"
                    }
                ],
                "pmid": ""
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        ],
        "binding_glycans": [],
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        "sites": [
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                "glycosylation": [
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                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
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                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
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                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
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                        "residue": "Thr",
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        ],
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    },
    {
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                "name": "Drosophila melanogaster",
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "Dmel\\CG43052;CG43052;Dmel\\CG43052;Dmel_CG43052;MB6.chr2L.pasa.1468",
        "protein_name": "",
        "disease": [],
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        "biomarkers": [],
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    },
    {
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        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
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                        "id": "M9NFE3",
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                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 97,
        "chemical_mass": 10989.0,
        "gene_names": "Dmel\\CG43082;CG43082;Dmel\\CG43082;Dmel_CG43082",
        "protein_name": "DUF19 domain-containing protein",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "M9NFE3-1"
    },
    {
        "uniprot_canonical_ac": "M9PBB4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PBB4",
                        "url": "https://www.uniprot.org/uniprotkb/M9PBB4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 622,
        "chemical_mass": 67904.0,
        "gene_names": "NimC1;BG:DS00180.10;CG8942;CT25688;Dmel\\CG8942;Dmel_CG8942;NimC1;NimC;Nim;P1;nimC1;nimrod C1;nimrod",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PBB4",
                        "url": "https://www.uniprot.org/uniprotkb/M9PBB4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PBB4",
                        "url": "https://www.uniprot.org/uniprotkb/M9PBB4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "immune response",
                "id": "GO:0006955",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006955",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PBB4",
                        "url": "https://www.uniprot.org/uniprotkb/M9PBB4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phagocytosis",
                "id": "GO:0006909",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006909",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PBB4",
                        "url": "https://www.uniprot.org/uniprotkb/M9PBB4"
                    }
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                "pmid": ""
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                "name": "defense response to bacterium",
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                            {
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                "name": "insemination",
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                ],
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        ],
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            {
                "name": "extracellular space",
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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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                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histidine-tRNA ligase activity",
                "id": "GO:0004821",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004821",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA binding",
                "id": "GO:0003723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQX8"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQX8"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "histidyl-tRNA aminoacylation",
                "id": "GO:0006427",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006427",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial translation",
                "id": "GO:0032543",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032543",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQX8"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
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                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "Ada3;ADA3;Ada3;CG7098;DADA3;Dmel\\CG7098;Dmel_CG7098;HL-XIV;ada3;dADA3;dAda3;dik",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "chromatin binding",
                "id": "GO:0003682",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003682",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription coactivator activity",
                "id": "GO:0003713",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003713",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone acetyltransferase complex",
                "id": "GO:0000123",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000123",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "SAGA complex",
                "id": "GO:0000124",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000124",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "H3 histone acetyltransferase complex",
                "id": "GO:0070775",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070775",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "polytene chromosome",
                "id": "GO:0005700",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005700",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "polytene chromosome puff",
                "id": "GO:0005703",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005703",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATAC complex",
                "id": "GO:0140672",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140672",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "chromatin remodeling",
                "id": "GO:0006338",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006338",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of DNA-templated transcription",
                "id": "GO:0006355",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006355",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of DNA-templated transcription",
                "id": "GO:0045893",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045893",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription initiation-coupled chromatin remodeling",
                "id": "GO:0045815",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045815",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "sites": [],
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    },
    {
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        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
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                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
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                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "protein_name": "N-alpha-acetyltransferase 20",
        "disease": [
            {
                "disease_id": "DOID:0081233",
                "name": "autosomal recessive intellectual developmental disorder 73",
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                "url": "https://disease-ontology.org/term/DOID:0081233",
                "evidence": [
                    {
                        "id": "0081233",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081233"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "NatB complex",
                "id": "GO:0031416",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031416",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of actin cytoskeleton organization",
                "id": "GO:0032956",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032956",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of neuron apoptotic process",
                "id": "GO:0043524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "protein-N-terminal amino-acid acetyltransferase activity",
                "id": "GO:0004596",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004596",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein N-terminal-methionine acetyltransferase activity",
                "id": "GO:0120518",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0120518",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            }
        ],
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        "sites": [],
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    },
    {
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                "name": "Drosophila melanogaster",
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                "evidence": [
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                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
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            }
        ],
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        "protein_name": "",
        "disease": [],
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            {
                "name": "negative regulation of transcription by RNA polymerase II",
                "id": "GO:0000122",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000122",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
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                "id": "GO:0006357",
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                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of DNA-templated transcription",
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                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron differentiation",
                "id": "GO:0030182",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030182",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "peripheral nervous system development",
                "id": "GO:0007422",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007422",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell development",
                "id": "GO:0048468",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048468",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sensory neuron axon guidance",
                "id": "GO:0097374",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097374",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of growth",
                "id": "GO:0045926",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045926",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "muscle cell fate commitment",
                "id": "GO:0042693",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042693",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "embryonic development via the syncytial blastoderm",
                "id": "GO:0001700",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001700",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "compound eye morphogenesis",
                "id": "GO:0001745",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001745",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc-derived wing vein specification",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007474",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc-derived wing morphogenesis",
                "id": "GO:0007476",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007476",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "equator specification",
                "id": "GO:0045317",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045317",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dorsal appendage formation",
                "id": "GO:0046843",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046843",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "protein homodimerization activity",
                "id": "GO:0042803",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042803",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
                "id": "GO:0000978",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000978",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-binding transcription factor activity, RNA polymerase II-specific",
                "id": "GO:0000981",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000981",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "M9PI45-1"
    },
    {
        "uniprot_canonical_ac": "M9PI57-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 834,
        "chemical_mass": 96325.0,
        "gene_names": "nan;CG5842;CT18317;DmNan;Dmel\\CG5842;Dmel_CG5842;Iav;NAN;Nan;OCR;TRPV;nan",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050534",
                "name": "congenital stationary night blindness",
                "description": "A hereditary night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves.",
                "url": "https://disease-ontology.org/term/DOID:0050534",
                "evidence": [
                    {
                        "id": "0050534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070355",
                "name": "overactive bladder syndrome",
                "description": "A bladder disease characterized by urinary urgency without urinary tract infection or obvious pathology, usually accompanied by urinary frequency and nocturia.",
                "url": "https://disease-ontology.org/term/DOID:0070355",
                "evidence": [
                    {
                        "id": "0070355",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070355"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110182",
                "name": "Charcot-Marie-Tooth disease axonal type 2C",
                "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.",
                "url": "https://disease-ontology.org/term/DOID:0110182",
                "evidence": [
                    {
                        "id": "0110182",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110182"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110555",
                "name": "autosomal dominant nonsyndromic deafness 25",
                "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second-sixth decade of life with high frequency progressive hearing loss and has_material_basis_in mutation in the SLC17A8 gene on chromosome 12q23.",
                "url": "https://disease-ontology.org/term/DOID:0110555",
                "evidence": [
                    {
                        "id": "0110555",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110555"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111215",
                "name": "autosomal dominant distal hereditary motor neuronopathy 8",
                "description": "An autosomal dominant distal hereditary motor neuronopathy that is characterized by congenital, non-progressive, predominantly distal, lower limb muscle weakness and atrophy with variable severity that has_material_basis_in heterozygous mutation in the TRPV4 gene on 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111215",
                "evidence": [
                    {
                        "id": "0111215",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111215"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111514",
                "name": "metatropic dysplasia",
                "description": "A spondyloepimetaphyseal dysplasia characterized by short limbs with limitation and enlargement of joints, usually severe and progressive kyphoscoliosis, severe platyspondyly, and severe metaphyseal enlargement that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111514",
                "evidence": [
                    {
                        "id": "0111514",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111514"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111539",
                "name": "parastremmatic dwarfism",
                "description": "An osteochondrodysplasia characterized by severe dwarfism, kyphoscoliosis, stiffness of large joints and bowing and twisting of lower limbs that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111539",
                "evidence": [
                    {
                        "id": "0111539",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111539"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111552",
                "name": "scapuloperoneal spinal muscular atrophy",
                "description": "A motor neuron disease characterized by progressive scapuloperoneal atrophy and weakness, laryngeal palsy, congenital absence of muscles and in some cases developmental abnormalities of the bones that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111552",
                "evidence": [
                    {
                        "id": "0111552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111552"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111553",
                "name": "spondyloepiphyseal dysplasia Maroteaux type",
                "description": "An osteochondrodysplasia characterized by dysplastic epiphyses, short stature appearing in infancy, short neck, short and stubby hands and feet, platyspondyly, severe brachydactyly, and pelvic abnormalities that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111553",
                "evidence": [
                    {
                        "id": "0111553",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111553"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111554",
                "name": "spondylometaphyseal dysplasia Kozlowski type",
                "description": "A spondylometaphyseal dysplasia characterized by vetebral platyspondyly and overfaced pedicles, scoliosis, and mild metaphyseal abnormalities in the pelvis that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111554",
                "evidence": [
                    {
                        "id": "0111554",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111554"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111711",
                "name": "focal nonepidermolytic palmoplantar keratoderma 2",
                "description": "A focal nonepidermolytic palmoplantar keratoderma that has_material_basis_in heterozygous mutation in the TRPV3 gene on chromosome 17p13.2.",
                "url": "https://disease-ontology.org/term/DOID:0111711",
                "evidence": [
                    {
                        "id": "0111711",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111711"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0112013",
                "name": "autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques",
                "description": "A mutilating palmoplantar keratoderma with periorificial keratotic plaques that has_material_basis_in heterozygous mutation in the TRPV3 gene on chromosome 17p13.2.",
                "url": "https://disease-ontology.org/term/DOID:0112013",
                "evidence": [
                    {
                        "id": "0112013",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112013"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10024",
                "name": "migraine with aura",
                "description": "A migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon.",
                "url": "https://disease-ontology.org/term/DOID:10024",
                "evidence": [
                    {
                        "id": "10024",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10024"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10159",
                "name": "osteonecrosis",
                "description": "An ischemic bone disease that results_in necrosis located_in bone.",
                "url": "https://disease-ontology.org/term/DOID:10159",
                "evidence": [
                    {
                        "id": "10159",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10159"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "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.",
                "url": "https://disease-ontology.org/term/DOID:10591",
                "evidence": [
                    {
                        "id": "10591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10591"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10808",
                "name": "gastric ulcer",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:10808",
                "evidence": [
                    {
                        "id": "10808",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10808"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11446",
                "name": "sciatic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11446",
                "evidence": [
                    {
                        "id": "11446",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11446"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11714",
                "name": "gestational diabetes",
                "description": "A diabetes mellitus that manifests during pregnancy.",
                "url": "https://disease-ontology.org/term/DOID:11714",
                "evidence": [
                    {
                        "id": "11714",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11714"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13543",
                "name": "hyperparathyroidism",
                "description": "A parathyroid gland disease characterized by an overactivity of the parathyroid glands, leading to an excess of parathyroid hormone in the body.",
                "url": "https://disease-ontology.org/term/DOID:13543",
                "evidence": [
                    {
                        "id": "13543",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13543"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2548",
                "name": "reflex epilepsy",
                "description": "A variable age at onset electroclinical syndrome that is consistently induced by identifiable and objective-specific triggers, which may be an afferent stimulus or by the patient's own activity.",
                "url": "https://disease-ontology.org/term/DOID:2548",
                "evidence": [
                    {
                        "id": "2548",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2548"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2723",
                "name": "dermatitis",
                "description": "A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin.",
                "url": "https://disease-ontology.org/term/DOID:2723",
                "evidence": [
                    {
                        "id": "2723",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2723"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3310",
                "name": "atopic dermatitis",
                "description": "An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking.",
                "url": "https://disease-ontology.org/term/DOID:3310",
                "evidence": [
                    {
                        "id": "3310",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3310"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.",
                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6364",
                "name": "migraine",
                "description": "A brain disease that is characterized by moderate to severe headaches, nausea, extreme sensitivity to light and sound and intense unilaterial throbbing or pulsing.",
                "url": "https://disease-ontology.org/term/DOID:6364",
                "evidence": [
                    {
                        "id": "6364",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6364"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6432",
                "name": "pulmonary hypertension",
                "description": "A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries.",
                "url": "https://disease-ontology.org/term/DOID:6432",
                "evidence": [
                    {
                        "id": "6432",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6432"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:809",
                "name": "cocaine abuse",
                "description": "A substance abuse that involves the recurring use of cocaine despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:809",
                "evidence": [
                    {
                        "id": "809",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:809"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8881",
                "name": "rosacea",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8881",
                "evidence": [
                    {
                        "id": "8881",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8881"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9743",
                "name": "diabetic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:9743",
                "evidence": [
                    {
                        "id": "9743",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9743"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:987",
                "name": "alopecia",
                "description": "A hypotrichosis that is characterized by a loss of hair from the head or body.",
                "url": "https://disease-ontology.org/term/DOID:987",
                "evidence": [
                    {
                        "id": "987",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:987"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9975",
                "name": "cocaine dependence",
                "description": "A drug dependence that is a psychological dependency on the regular use of cocaine.",
                "url": "https://disease-ontology.org/term/DOID:9975",
                "evidence": [
                    {
                        "id": "9975",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9975"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "startle response",
                "id": "GO:0001964",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001964",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mechanosensory behavior",
                "id": "GO:0007638",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007638",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "detection of mechanical stimulus involved in sensory perception of touch",
                "id": "GO:0050976",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050976",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "detection of mechanical stimulus involved in sensory perception of sound",
                "id": "GO:0050910",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050910",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium ion transport",
                "id": "GO:0006816",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006816",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoatomic ion transmembrane transport",
                "id": "GO:0034220",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034220",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoatomic cation transport",
                "id": "GO:0006812",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006812",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "adult walking behavior",
                "id": "GO:0007628",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007628",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to auditory stimulus",
                "id": "GO:0010996",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010996",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sensory perception of sound",
                "id": "GO:0007605",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007605",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium ion transmembrane transport",
                "id": "GO:0070588",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070588",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "detection of mechanical stimulus involved in sensory perception",
                "id": "GO:0050974",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050974",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuromuscular process controlling posture",
                "id": "GO:0050884",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050884",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium ion import across plasma membrane",
                "id": "GO:0098703",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098703",
                "evidence": [
                    {
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                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to humidity",
                "id": "GO:0009270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative gravitaxis",
                "id": "GO:0048060",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048060",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of mechanosensory behavior",
                "id": "GO:1905790",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905790",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cation channel complex",
                "id": "GO:0034703",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034703",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium channel complex",
                "id": "GO:0034704",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034704",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "monoatomic ion channel activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005216",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium channel activity",
                "id": "GO:0005262",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005262",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoatomic cation channel activity",
                "id": "GO:0005261",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005261",
                "evidence": [
                    {
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                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mechanosensitive monoatomic ion channel activity",
                "id": "GO:0008381",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008381",
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                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mechanosensitive monoatomic cation channel activity",
                "id": "GO:0140135",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140135",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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            {
                "name": "Drosophila melanogaster",
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                    {
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                        "id": "M9PIC9",
                        "url": "https://www.uniprot.org/uniprotkb/M9PIC9"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 223190.0,
        "gene_names": "Spc105R;CG11451;DmSpc105;Dmel\\CG11451;Dmel_CG11451;KNL1;Spc105-R;Spc105R;Spc105r;Spc105;dmKNL-1;dmSpc105R;spc105R;spc105r",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "kinetochore assembly",
                "id": "GO:0051382",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051382",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PIC9",
                        "url": "https://www.uniprot.org/uniprotkb/M9PIC9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "attachment of spindle microtubules to kinetochore",
                "id": "GO:0008608",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008608",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PIC9",
                        "url": "https://www.uniprot.org/uniprotkb/M9PIC9"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "outer kinetochore",
                "id": "GO:0000940",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000940",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PIC9",
                        "url": "https://www.uniprot.org/uniprotkb/M9PIC9"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "uniprot_canonical_ac": "M9PIC9-1",
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                "end_pos": "1349",
                "site_lbl": "Thr1349",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1349,
                        "start_aa": "Thr",
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                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1349",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
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                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "M9PIM3-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PIM3",
                        "url": "https://www.uniprot.org/uniprotkb/M9PIM3"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 118749.0,
        "gene_names": "Dmel\\CG43968;CG43968;Dmel\\CG43968;Dmel_CG43968;lincRNA.665",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "M9PIM3-1"
    },
    {
        "uniprot_canonical_ac": "O16043-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 183,
        "chemical_mass": 18823.0,
        "gene_names": "Df31;BEST:LD04967;CG2207;DF 31;DF31;Df31;Dmel\\CG2207;Dmel_CG2207;LD04967;anon-EST:Liang-1.46;anon-EST:Posey126;anon-EST:fe1A4;anon-WO0153538.53;anon1A4;clone 1.46;l(2)k05815",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chromatin",
                "id": "GO:0000785",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000785",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "chromatin organization",
                "id": "GO:0006325",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006325",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleosome assembly",
                "id": "GO:0006334",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006334",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "histone binding",
                "id": "GO:0042393",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042393",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
        "uniprot_canonical_ac": "O17452-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O17452",
                        "url": "https://www.uniprot.org/uniprotkb/O17452"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 230,
        "chemical_mass": 25492.0,
        "gene_names": "PeriA;CG17058;CG31559;Dmel\\CG17058;Dmel_CG17058;PeriA;Peritrophin-A;obst-D",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "insemination",
                "id": "GO:0007320",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007320",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O17452",
                        "url": "https://www.uniprot.org/uniprotkb/O17452"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chitin-based cuticle development",
                "id": "GO:0040003",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040003",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O17452",
                        "url": "https://www.uniprot.org/uniprotkb/O17452"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O17452",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "external encapsulating structure",
                "id": "GO:0030312",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030312",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O17452",
                        "url": "https://www.uniprot.org/uniprotkb/O17452"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "chitin binding",
                "id": "GO:0008061",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008061",
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                    {
                        "database": "UniProtKB",
                        "id": "O17452",
                        "url": "https://www.uniprot.org/uniprotkb/O17452"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "structural constituent of chitin-based cuticle",
                "id": "GO:0005214",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005214",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O17452",
                        "url": "https://www.uniprot.org/uniprotkb/O17452"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "O62526-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O62526",
                        "url": "https://www.uniprot.org/uniprotkb/O62526"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
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        ],
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        "gene_names": "Ant2;ANT2;Ant2;CG1683;Dmel\\CG1683;Dmel_CG1683;FBgn0025111;l(1)G0126;l(1)G0247;l(1)G0386",
        "protein_name": "ADP/ATP translocase",
        "disease": [
            {
                "disease_id": "DOID:0080130",
                "name": "mitochondrial DNA depletion syndrome 12a",
                "description": "A mitochondrial DNA depletion syndrome that is characterized by severe hypotonia due to mitochondrial dysfunction apparent at birth and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 25 member 4 gene on chromosome 4q35.",
                "url": "https://disease-ontology.org/term/DOID:0080130",
                "evidence": [
                    {
                        "id": "0080130",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0080130"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0080335",
                "name": "mitochondrial DNA depletion syndrome 12b",
                "description": "A mitochondrial DNA depletion syndrome that is characterized by childhood onset of slowly progressive hypertrophic cardiomyopathy and generalized skeletal myopathy resulting in exercise intolerance, muscle weakness, and atrophy, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the the solute carrier family 25 member 4 on chromosome 4q35.",
                "url": "https://disease-ontology.org/term/DOID:0080335",
                "evidence": [
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                        "id": "0080335",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080335"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0110429",
                "name": "dilated cardiomyopathy 1H",
                "description": "A dilated cardiomyopathy that has_material_basis_in variation in the chromosome region 2q14-q22.",
                "url": "https://disease-ontology.org/term/DOID:0110429",
                "evidence": [
                    {
                        "id": "0110429",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0110429"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0111517",
                "name": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2",
                "description": "A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the SLC25A4 gene on chromosome 4q35.1.",
                "url": "https://disease-ontology.org/term/DOID:0111517",
                "evidence": [
                    {
                        "id": "0111517",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0111517"
                    }
                ],
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            },
            {
                "disease_id": "DOID:10652",
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                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
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                ],
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            },
            {
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                "description": "",
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                "evidence": [
                    {
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                    }
                ],
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            },
            {
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                        "url": "https://www.alliancegenome.org/disease/DOID:11984"
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                ],
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            },
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                "evidence": [
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                        "id": "12558",
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                    }
                ],
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            },
            {
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                "name": "alcoholic cardiomyopathy",
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                "evidence": [
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                    }
                ],
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            },
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                "evidence": [
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                    }
                ],
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            },
            {
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                    {
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                    }
                ],
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            }
        ],
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            {
                "name": "mitochondrial inner membrane",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial permeability transition pore complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005757",
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "mitochondrial transport",
                "id": "GO:0006839",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006839",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O62526",
                        "url": "https://www.uniprot.org/uniprotkb/O62526"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of mitochondrial membrane permeability",
                "id": "GO:0046902",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046902",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O62526",
                        "url": "https://www.uniprot.org/uniprotkb/O62526"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial ADP transmembrane transport",
                "id": "GO:0140021",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140021",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O62526",
                        "url": "https://www.uniprot.org/uniprotkb/O62526"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial ATP transmembrane transport",
                "id": "GO:1990544",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990544",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O62526",
                        "url": "https://www.uniprot.org/uniprotkb/O62526"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "ATP:ADP antiporter activity",
                "id": "GO:0005471",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005471",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O62526",
                        "url": "https://www.uniprot.org/uniprotkb/O62526"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
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    },
    {
        "uniprot_canonical_ac": "O76861-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "O76861",
                        "url": "https://www.uniprot.org/uniprotkb/O76861"
                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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        "chemical_mass": 60969.0,
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        "protein_name": "Wbp11/ELF5/Saf1 N-terminal domain-containing protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "RNA binding",
                "id": "GO:0003723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76861",
                        "url": "https://www.uniprot.org/uniprotkb/O76861"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein phosphatase regulator activity",
                "id": "GO:0019888",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019888",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76861",
                        "url": "https://www.uniprot.org/uniprotkb/O76861"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "RNA splicing",
                "id": "GO:0008380",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008380",
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                    {
                        "database": "UniProtKB",
                        "id": "O76861",
                        "url": "https://www.uniprot.org/uniprotkb/O76861"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mRNA splicing, via spliceosome",
                "id": "GO:0000398",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000398",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76861",
                        "url": "https://www.uniprot.org/uniprotkb/O76861"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "catalytic step 2 spliceosome",
                "id": "GO:0071013",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071013",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76861",
                        "url": "https://www.uniprot.org/uniprotkb/O76861"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "precatalytic spliceosome",
                "id": "GO:0071011",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071011",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76861",
                        "url": "https://www.uniprot.org/uniprotkb/O76861"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "O76861-1",
                "start_pos": "361",
                "end_pos": "361",
                "site_lbl": "Thr361",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 361,
                        "start_aa": "Thr",
                        "end_pos": 361,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr361",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "O76861-1",
                "start_pos": "368",
                "end_pos": "368",
                "site_lbl": "Thr368",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 368,
                        "start_aa": "Thr",
                        "end_pos": 368,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr368",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "O76861-1"
    },
    {
        "uniprot_canonical_ac": "O96660-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 486,
        "chemical_mass": 53677.0,
        "gene_names": "Smox;3;CG2262;DSMAD2;DSmad2;Dmel\\CG2262;SMAD2;SMOX;Sad;Smad2/3;Smad2;Smad;SmoX;Smox;dSMAD2;dSmad2;dSmad;dsmad2;l(1)G0348;sad;smad2;smox;ted;tmp",
        "protein_name": "SMAD family member 2",
        "disease": [
            {
                "disease_id": "DOID:0050156",
                "name": "idiopathic pulmonary fibrosis",
                "description": "A pulmonary fibrosis that is characterized by scarring of the lung characterized by stiffness in the lungs and makes it difficult to breathe.",
                "url": "https://disease-ontology.org/term/DOID:0050156",
                "evidence": [
                    {
                        "id": "0050156",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050156"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060071",
                "name": "pre-malignant neoplasm",
                "description": "A disease of cellular proliferation that results in abnormal growths in the body, which do not invade or destroy the surrounding tissue but, given enough time, will transform into a cancer.",
                "url": "https://disease-ontology.org/term/DOID:0060071",
                "evidence": [
                    {
                        "id": "0060071",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060071"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060964",
                "name": "Loeys-Dietz syndrome 6",
                "description": "A Loeys-Dietz syndrome characterized by aortic/arterial aneurysm and dissection in association with connective tissue findings that has_material_basis_in heterozygous mutation in the SMAD2 gene (601366) on chromosome 18q21.",
                "url": "https://disease-ontology.org/term/DOID:0060964",
                "evidence": [
                    {
                        "id": "0060964",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060964"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070237",
                "name": "Loeys-Dietz syndrome 3",
                "description": "A Loeys-Dietz syndrome that has_material_basis_in heterozygous mutation in the SMAD3 gene on chromosome 15q.",
                "url": "https://disease-ontology.org/term/DOID:0070237",
                "evidence": [
                    {
                        "id": "0070237",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070237"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10892",
                "name": "hypospadias",
                "description": "A physical disorder characterized by an abnormally placed urethral opening on the underside of the penis or on the perineum.",
                "url": "https://disease-ontology.org/term/DOID:10892",
                "evidence": [
                    {
                        "id": "10892",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10892"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12935",
                "name": "alcoholic cardiomyopathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:12935",
                "evidence": [
                    {
                        "id": "12935",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12935"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1380",
                "name": "endometrial cancer",
                "description": "A uterine cancer that is located_in tissues lining the uterus.",
                "url": "https://disease-ontology.org/term/DOID:1380",
                "evidence": [
                    {
                        "id": "1380",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1380"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14018",
                "name": "alcoholic liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:14018",
                "evidence": [
                    {
                        "id": "14018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14018"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:219",
                "name": "colon cancer",
                "description": "A colorectal cancer that is located_in the colon.",
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                "evidence": [
                    {
                        "id": "219",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:219"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
                "url": "https://disease-ontology.org/term/DOID:2394",
                "evidence": [
                    {
                        "id": "2394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3459",
                "name": "breast carcinoma",
                "description": "A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:3459",
                "evidence": [
                    {
                        "id": "3459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3498",
                "name": "pancreatic ductal adenocarcinoma",
                "description": "A pancreatic adenocarcinoma that derives_from pancreatic duct cells.",
                "url": "https://disease-ontology.org/term/DOID:3498",
                "evidence": [
                    {
                        "id": "3498",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3498"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3744",
                "name": "cervical squamous cell carcinoma",
                "description": "A cervix carcinoma that has_material_basis_in squamous cells of the cervix.",
                "url": "https://disease-ontology.org/term/DOID:3744",
                "evidence": [
                    {
                        "id": "3744",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3744"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "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.",
                "url": "https://disease-ontology.org/term/DOID:3883",
                "evidence": [
                    {
                        "id": "3883",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3883"
                    }
                ],
                "weight": 0.0
            },
            {
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                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4001",
                "name": "ovarian carcinoma",
                "description": "An ovarian cancer that has_material_basis_in epithelial tissue and is located_in the ovary.",
                "url": "https://disease-ontology.org/term/DOID:4001",
                "evidence": [
                    {
                        "id": "4001",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4001"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4362",
                "name": "cervical cancer",
                "description": "A female reproductive organ cancer that is located_in the cervix.",
                "url": "https://disease-ontology.org/term/DOID:4362",
                "evidence": [
                    {
                        "id": "4362",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4362"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4450",
                "name": "renal cell carcinoma",
                "description": "A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney.",
                "url": "https://disease-ontology.org/term/DOID:4450",
                "evidence": [
                    {
                        "id": "4450",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4450"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8398",
                "name": "osteoarthritis",
                "description": "An arthritis that has_material_basis_in worn out cartilage located_in joint.",
                "url": "https://disease-ontology.org/term/DOID:8398",
                "evidence": [
                    {
                        "id": "8398",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8398"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9975",
                "name": "cocaine dependence",
                "description": "A drug dependence that is a psychological dependency on the regular use of cocaine.",
                "url": "https://disease-ontology.org/term/DOID:9975",
                "evidence": [
                    {
                        "id": "9975",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9975"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "positive regulation of glycogen catabolic process",
                "id": "GO:0045819",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045819",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell differentiation",
                "id": "GO:0030154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of transcription by RNA polymerase II",
                "id": "GO:0045944",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045944",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of synapse structure or activity",
                "id": "GO:0050803",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050803",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellular response to glucose stimulus",
                "id": "GO:0071333",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071333",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glucose homeostasis",
                "id": "GO:0042593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042593",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of autophagy",
                "id": "GO:0010507",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010507",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "SMAD protein signal transduction",
                "id": "GO:0060395",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060395",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "activin receptor signaling pathway",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032924",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/O96660"
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                ],
                "pmid": ""
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            {
                "name": "dendrite morphogenesis",
                "id": "GO:0048813",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048813",
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                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron development",
                "id": "GO:0048666",
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                    }
                ],
                "pmid": ""
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            {
                "name": "axon guidance",
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                        "database": "UniProtKB",
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                ],
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            {
                "name": "positive regulation of neuroblast proliferation",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002052",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/O96660"
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                ],
                "pmid": ""
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            {
                "name": "determination of adult lifespan",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008340",
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                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "anatomical structure morphogenesis",
                "id": "GO:0009653",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009653",
                "evidence": [
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                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/O96660"
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                ],
                "pmid": ""
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            {
                "name": "regulation of cell proliferation involved in imaginal disc-derived wing morphogenesis",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090256",
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                    {
                        "database": "UniProtKB",
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                "pmid": ""
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            {
                "name": "imaginal disc growth",
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                ],
                "pmid": ""
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            {
                "name": "imaginal disc-derived wing morphogenesis",
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                        "url": "https://www.uniprot.org/uniprotkb/O96660"
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                "pmid": ""
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                "name": "mushroom body development",
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                        "url": "https://www.uniprot.org/uniprotkb/O96660"
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                ],
                "pmid": ""
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            {
                "name": "regulation of imaginal disc-derived wing size",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0044719",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/O96660"
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                ],
                "pmid": ""
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            {
                "name": "R8 cell fate specification",
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                ],
                "pmid": ""
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            {
                "name": "positive regulation of imaginal disc growth",
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                "pmid": ""
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                "name": "metal ion binding",
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                ],
                "pmid": ""
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                "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
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                ],
                "pmid": ""
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            {
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                ],
                "pmid": ""
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            {
                "name": "chromatin DNA binding",
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                "pmid": ""
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            {
                "name": "I-SMAD binding",
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                "pmid": ""
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                ],
                "pmid": ""
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            {
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                ],
                "pmid": ""
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            {
                "name": "cytosol",
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                "pmid": ""
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                        ],
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                        "site_category_dict": {
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                        },
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                        "relation": "attached",
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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_org": "E",
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                        "comment": "Reduces phosphorylation by babo and reduces the inhibitory effect on phosphorylation of R-SMADMad by babo.",
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                            {
                                "database": "UniProtKB",
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                            {
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                        ]
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    {
        "uniprot_canonical_ac": "P83262-1",
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                "name": "Drosophila melanogaster",
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                ],
                "common_name": "Fruit fly",
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        ],
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            {
                "name": "cell fate specification",
                "id": "GO:0001708",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001708",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/P83262"
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                ],
                "pmid": ""
            },
            {
                "name": "defense response to bacterium",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042742",
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                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of Notch signaling pathway",
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
            },
            {
                "name": "sensory organ precursor cell fate determination",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/P83262"
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                ],
                "pmid": ""
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        ],
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            {
                "name": "ubiquitin protein ligase binding",
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        ],
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    {
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                "name": "Drosophila melanogaster",
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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    {
        "uniprot_canonical_ac": "Q0E8P5-1",
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                "name": "Drosophila melanogaster",
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                "evidence": [
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                        "database": "UniProtKB",
                        "id": "Q0E8P5",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8P5"
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
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        ],
        "length": 625,
        "chemical_mass": 70527.0,
        "gene_names": "Dmel\\CG5758;CG5758;Dmel\\CG5758;Dmel_CG5758",
        "protein_name": "FAS1 domain-containing protein",
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            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "extracellular matrix",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031012",
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        ],
        "biological_process": [
            {
                "name": "cell adhesion",
                "id": "GO:0007155",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007155",
                "evidence": [
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                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q0E8P5"
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                ],
                "pmid": ""
            },
            {
                "name": "extracellular matrix organization",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030198",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8P5",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8P5"
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                ],
                "pmid": ""
            },
            {
                "name": "synaptic target recognition",
                "id": "GO:0008039",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008039",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8P5",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8P5"
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                ],
                "pmid": ""
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        ],
        "molecular_function": [
            {
                "name": "cell adhesion molecule binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050839",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        ],
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    {
        "uniprot_canonical_ac": "Q0E8Q6-1",
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                "name": "Drosophila melanogaster",
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                        "id": "Q0E8Q6",
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
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        ],
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        "protein_name": "BED-type domain-containing protein",
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            {
                "name": "DNA binding",
                "id": "GO:0003677",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8Q6",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8Q6"
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                ],
                "pmid": ""
            },
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E8Q6",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8Q6"
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                ],
                "pmid": ""
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        ],
        "cellular_component": [
            {
                "name": "nucleus",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q0E8Q6"
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                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        ],
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    {
        "uniprot_canonical_ac": "Q0E9N0-1",
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                ],
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        ],
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            {
                "name": "mRNA regulatory element binding translation repressor activity",
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                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "negative regulation of translational initiation",
                "id": "GO:0045947",
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                    {
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                ],
                "pmid": ""
            }
        ],
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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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        ],
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    {
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                ],
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        ],
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        "gene_names": "VhaAC45RP;BcDNA:RH09162;CG2176;CG31030;Dmel\\CG31030;Dmel_CG31030;VhaAC45RP;anon-EST:Posey81",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "proton-transporting V-type ATPase complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033176",
                "evidence": [
                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "presynaptic membrane",
                "id": "GO:0042734",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042734",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHY8",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "regulation of cellular pH",
                "id": "GO:0030641",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030641",
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                    {
                        "database": "UniProtKB",
                        "id": "Q0KHY8",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHY8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synaptic vesicle lumen acidification",
                "id": "GO:0097401",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097401",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHY8",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "ATPase regulator activity",
                "id": "GO:0060590",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060590",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
        "uniprot_canonical_ac": "Q9VDI5-1",
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                "name": "Drosophila melanogaster",
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                    {
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                        "id": "Q9VDI5",
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                ],
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            }
        ],
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        "gene_names": "Dm_3R:88623;Dmel\\CG17271;CG17271;Dm_3R:88623;Dmel\\CG17271;Dmel_CG17271",
        "protein_name": "EF-hand domain-containing protein",
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                "disease_id": "DOID:224",
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                ],
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            }
        ],
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            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "endoplasmic reticulum",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "Golgi apparatus",
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                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "calcium ion binding",
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                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "mating",
                "id": "GO:0007618",
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                    {
                        "database": "UniProtKB",
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                ],
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            },
            {
                "name": "protein transport",
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                ],
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        ],
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    {
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            {
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                "url": "https://disease-ontology.org/term/DOID:0050824",
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                        "id": "0050824",
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                "url": "https://disease-ontology.org/term/DOID:0060224",
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                        "id": "0060224",
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                ],
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                "description": "A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the ANK1 gene on chromosome 8p11.21.",
                "url": "https://disease-ontology.org/term/DOID:0110916",
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                "url": "https://disease-ontology.org/term/DOID:0111700",
                "evidence": [
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                        "id": "0111700",
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                ],
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                "url": "https://disease-ontology.org/term/DOID:12365",
                "evidence": [
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                        "id": "12365",
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                ],
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            },
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                        "id": "12849",
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                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:12971",
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                    {
                        "id": "12971",
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                        "url": "https://www.alliancegenome.org/disease/DOID:12971"
                    }
                ],
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            },
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                "evidence": [
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                        "id": "13884",
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                ],
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                        "id": "1824",
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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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                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
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                        "id": "5419",
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                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
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            }
        ],
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            {
                "name": "cytoskeleton",
                "id": "GO:0005856",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005856",
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                ],
                "pmid": ""
            },
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                "name": "plasma membrane",
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                        "database": "UniProtKB",
                        "id": "Q0KIE7",
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                    }
                ],
                "pmid": ""
            },
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                "name": "neuron projection",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043005",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "spectrosome",
                "id": "GO:0045170",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045170",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KIE7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KIE7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "signal transduction",
                "id": "GO:0007165",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007165",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein localization to plasma membrane",
                "id": "GO:0072659",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072659",
                "evidence": [
                    {
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        "protein_name": "Syntaxin interacting protein 3",
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                ],
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        ],
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "extracellular space",
                "id": "GO:0005615",
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                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "proteolysis",
                "id": "GO:0006508",
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                    {
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                    {
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        ],
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            {
                "name": "nucleus",
                "id": "GO:0005634",
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                    {
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                "pmid": ""
            }
        ],
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            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
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                    {
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                "name": "regulation of transcription by RNA polymerase II",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8INE2",
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                ],
                "pmid": ""
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        ],
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            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            },
            {
                "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000978",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INE2",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-binding transcription factor activity, RNA polymerase II-specific",
                "id": "GO:0000981",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000981",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INE2",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "Q8INH7-1",
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            {
                "name": "Drosophila melanogaster",
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                    {
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                ],
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        ],
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                "disease_id": "DOID:0061006",
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                        "id": "0061006",
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                    {
                        "id": "1574",
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                ],
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            }
        ],
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            {
                "name": "DNA replication checkpoint signaling",
                "id": "GO:0000076",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000076",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA repair",
                "id": "GO:0006281",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006281",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "entrainment of circadian clock",
                "id": "GO:0009649",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009649",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA damage checkpoint signaling",
                "id": "GO:0000077",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000077",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "replication fork arrest",
                "id": "GO:0043111",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043111",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INH7"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "replication fork protection complex",
                "id": "GO:0031298",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031298",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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            {
                "name": "Drosophila melanogaster",
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                        "database": "UniProtKB",
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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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                "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.",
                "url": "https://disease-ontology.org/term/DOID:10591",
                "evidence": [
                    {
                        "id": "10591",
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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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                "name": "Down syndrome",
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                ],
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                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:1875",
                "evidence": [
                    {
                        "id": "1875",
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                ],
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                "name": "glioblastoma",
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                "url": "https://disease-ontology.org/term/DOID:3068",
                "evidence": [
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                        "database": "AGR",
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                ],
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                ],
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                ],
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                "evidence": [
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                        "id": "8893",
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                ],
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            },
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                ],
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                        "id": "9970",
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                ],
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                "name": "fatty acid binding",
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                    {
                        "database": "UniProtKB",
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        ],
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                    {
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                ],
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            },
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                ],
                "pmid": ""
            },
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                "name": "nucleus",
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "long-term memory",
                "id": "GO:0007616",
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                    {
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                    }
                ],
                "pmid": ""
            },
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                ],
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                "name": "chitin-based cuticle development",
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                    {
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                ],
                "pmid": ""
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        ],
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    {
        "uniprot_canonical_ac": "Q8INM2-1",
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                "name": "Drosophila melanogaster",
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                ],
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        ],
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        "protein_name": "",
        "disease": [],
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            {
                "name": "notum morphogenesis",
                "id": "GO:0048802",
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                ],
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            }
        ],
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    {
        "uniprot_canonical_ac": "Q8INX1-1",
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                ],
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        ],
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        "chemical_mass": 21029.0,
        "gene_names": "Dmel\\CG31800;CG31800;Dmel\\CG31800;Dmel_CG31800",
        "protein_name": "",
        "disease": [],
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        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "Q8INX4-1",
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                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                ],
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                "name": "serine-type endopeptidase activity",
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                "name": "proteolysis",
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            {
                "name": "cytoplasmic side of membrane",
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                    }
                ],
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        ],
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            {
                "name": "regulation of DNA biosynthetic process",
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                ],
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            {
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                    }
                ],
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            {
                "name": "protein phosphorylation",
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                ],
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            },
            {
                "name": "positive regulation of gene expression",
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                ],
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            {
                "name": "positive regulation of DNA-templated transcription",
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                "name": "protein autophosphorylation",
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                "name": "dendrite morphogenesis",
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            {
                "name": "chaeta development",
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            {
                "name": "sensory organ precursor cell division",
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
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            {
                "name": "regulation of cell proliferation involved in compound eye morphogenesis",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:2000495",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q94883"
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            {
                "name": "identical protein binding",
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                        "database": "UniProtKB",
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                "pmid": ""
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            {
                "name": "calcium ion binding",
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                "name": "transcription cis-regulatory region binding",
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                        "database": "UniProtKB",
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                "name": "nucleus",
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            {
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                "pmid": ""
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            {
                "name": "polytene chromosome",
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                ],
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        ],
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    {
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                        "id": "Q9I7H4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9I7H4"
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                ],
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        "protein_name": "Sodium-independent sulfate anion transporter",
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        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                        "id": "Q9I7H4",
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                ],
                "pmid": ""
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        ],
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                "name": "chloride transmembrane transport",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1902476",
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            {
                "name": "sulfate transmembrane transport",
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                        "id": "Q9I7H4",
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        ],
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            {
                "name": "sulfate transmembrane transporter activity",
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                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
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                                "label": "isoglyp",
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                        ],
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                        "relation": "attached",
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    {
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                        "id": "Q9I7K8",
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                ],
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        ],
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        "protein_name": "Arrestin C-terminal-like domain-containing protein",
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                "disease_id": "DOID:10534",
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                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
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                        "id": "10534",
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                ],
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            },
            {
                "disease_id": "DOID:14525",
                "name": "Reye syndrome",
                "description": "A syndrome characterized by acute brain damage and liver function problems. It has been associated with aspirin consumption by children with viral illness, although it also occurs in the absence of aspirin use.",
                "url": "https://disease-ontology.org/term/DOID:14525",
                "evidence": [
                    {
                        "id": "14525",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14525"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1686",
                "name": "glaucoma",
                "description": "An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function.",
                "url": "https://disease-ontology.org/term/DOID:1686",
                "evidence": [
                    {
                        "id": "1686",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1686"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4450",
                "name": "renal cell carcinoma",
                "description": "A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney.",
                "url": "https://disease-ontology.org/term/DOID:4450",
                "evidence": [
                    {
                        "id": "4450",
                        "database": "AGR",
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                "name": "GTPase activity",
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                "url": "https://disease-ontology.org/term/DOID:0060041",
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            },
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                ],
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        ],
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                ],
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                                "label": "isoglyp",
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                        ],
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                        "relation": "attached",
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                                "id": "GLY_001163",
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                            }
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                ],
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                "name": "mRNA binding",
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                "name": "double-stranded DNA binding",
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            {
                "name": "uracil DNA N-glycosylase activity",
                "id": "GO:0004844",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004844",
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                    {
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                        "id": "Q9V4D8",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "SUMO binding",
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                    }
                ],
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            },
            {
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "G/T mismatch-specific thymine-DNA glycosylase activity",
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                    {
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                        "id": "Q9V4D8",
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                    }
                ],
                "pmid": ""
            }
        ],
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                    {
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                ],
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            },
            {
                "name": "nucleoplasm",
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            }
        ],
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            {
                "name": "DNA-templated transcription",
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                ],
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            },
            {
                "name": "mismatch repair",
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                    {
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                ],
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            {
                "name": "epigenetic regulation of gene expression",
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                ],
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            },
            {
                "name": "base-excision repair, AP site formation",
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                    {
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                        "id": "Q9V4D8",
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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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            {
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                ],
                "pmid": ""
            },
            {
                "name": "nucleolus",
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                    {
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                        "id": "Q9V9M6",
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "determination of adult lifespan",
                "id": "GO:0008340",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008340",
                "evidence": [
                    {
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                ],
                "pmid": ""
            },
            {
                "name": "transcription initiation at RNA polymerase I promoter",
                "id": "GO:0006361",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006361",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9M6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9M6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleolar large rRNA transcription by RNA polymerase I",
                "id": "GO:0042790",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042790",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9V9M6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "female germ-line stem cell population maintenance",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9M6",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "RNA polymerase I general transcription initiation factor activity",
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                    {
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                "pmid": ""
            },
            {
                "name": "RNA polymerase I core binding",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9M6",
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                    }
                ],
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            }
        ],
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                    {
                        "glytoucan_ac": "",
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                            {
                                "label": "isoglyp",
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                            }
                        ],
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                        "site_category_dict": {
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                        },
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                            }
                        ]
                    }
                ]
            }
        ],
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    {
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                ],
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        ],
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                "name": "cytoplasm",
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                    {
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                ],
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            },
            {
                "name": "Cul4-RING E3 ubiquitin ligase complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0080008",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "negative regulation of fatty acid biosynthetic process",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9T1",
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
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                "name": "Drosophila melanogaster",
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                "evidence": [
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                        "id": "Q9V9U1",
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                    }
                ],
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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            {
                "disease_id": "DOID:0050328",
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                "url": "https://disease-ontology.org/term/DOID:0050328",
                "evidence": [
                    {
                        "id": "0050328",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0050328"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0112185",
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                "url": "https://disease-ontology.org/term/DOID:0112185",
                "evidence": [
                    {
                        "id": "0112185",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112185"
                    }
                ],
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            }
        ],
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            {
                "name": "D-glucose:sodium symporter activity",
                "id": "GO:0005412",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9U1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9U1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "symporter activity",
                "id": "GO:0015293",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015293",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "apical plasma membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016324",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9U1",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "glucose homeostasis",
                "id": "GO:0042593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042593",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9U1",
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                    }
                ],
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            },
            {
                "name": "sodium ion transport",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006814",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9U1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9U1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "D-glucose import across plasma membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098708",
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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                ],
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        ],
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            {
                "name": "acetyl-CoA hydrolase activity",
                "id": "GO:0003986",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9V9W4"
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            },
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                "name": "fatty acyl-CoA hydrolase activity",
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                        "id": "Q9V9W4",
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                    }
                ],
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        ],
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                "name": "mitochondrion",
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                ],
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            },
            {
                "name": "mitochondrial matrix",
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                ],
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                "name": "acyl-CoA metabolic process",
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                ],
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        ],
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                    }
                ],
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        ],
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                "disease_id": "DOID:0070239",
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                "evidence": [
                    {
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                    }
                ],
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        ],
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                "name": "mitochondrion",
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                ],
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            },
            {
                "name": "mitochondrial inner membrane",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "heterotetrameric polyprenyl diphosphate synthase complex",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
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                    }
                ],
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            },
            {
                "name": "polyprenyl diphosphate synthase complex",
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                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
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                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "prenyltransferase activity",
                "id": "GO:0004659",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004659",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "all-trans-decaprenyl-diphosphate synthase activity",
                "id": "GO:0097269",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097269",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "prenyl diphosphate synthase activity",
                "id": "GO:0120531",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0120531",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "ubiquinone biosynthetic process",
                "id": "GO:0006744",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006744",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "isoprenoid biosynthetic process",
                "id": "GO:0008299",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008299",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "pheromone biosynthetic process",
                "id": "GO:0042811",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042811",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9V9Z3-1"
    },
    {
        "uniprot_canonical_ac": "Q9V9Z5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 116,
        "chemical_mass": 13388.0,
        "gene_names": "Dmel\\CG15563;CG15563;Dmel\\CG15563;Dmel_CG15563",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9V9Z5-1"
    },
    {
        "uniprot_canonical_ac": "Q9VA09-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 787,
        "chemical_mass": 86850.0,
        "gene_names": "Gycbeta100B;CG1470;Dgc beta 1;Dgcbeta1;Dmel\\CG1470;Dmel_CG1470;Gbeta100B;Gyc-beta-100B;Gycbeta-100B;Gycbeta100B;dgcb1;dgcbeta1;gyc beta;gycbeta100B;sGC-beta;sGCbeta100B;sGCbeta1",
        "protein_name": "Guanylate cyclase soluble subunit beta-1",
        "disease": [
            {
                "disease_id": "DOID:0060001",
                "name": "withdrawal disorder",
                "description": "A substance-related disorder that occurs upon the abrupt discontinuation/separation or a decrease in dosage of the intake of medications, recreational drugs, and alcohol.",
                "url": "https://disease-ontology.org/term/DOID:0060001",
                "evidence": [
                    {
                        "id": "0060001",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060001"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "guanylate cyclase activity",
                "id": "GO:0004383",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004383",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "GTP binding",
                "id": "GO:0005525",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005525",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "heme binding",
                "id": "GO:0020037",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0020037",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cGMP biosynthetic process",
                "id": "GO:0006182",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006182",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular signal transduction",
                "id": "GO:0035556",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035556",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to oxygen levels",
                "id": "GO:0070482",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070482",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "guanylate cyclase complex, soluble",
                "id": "GO:0008074",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008074",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9VA09-1",
                "start_pos": "750",
                "end_pos": "750",
                "site_lbl": "Thr750",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 750,
                        "start_aa": "Thr",
                        "end_pos": 750,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr750",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "Q9VA09-1"
    },
    {
        "uniprot_canonical_ac": "Q9VA17-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 529,
        "chemical_mass": 57069.0,
        "gene_names": "Sox100B;CG12098;CG15552;CG18674;CT6009;Dmel\\CG15552;Dmel_CG15552;SOX100B;SOXE;Sox100B;Sox100;Sox9;SoxB;dSox9",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050463",
                "name": "campomelic dysplasia",
                "description": "An osteochondrodysplasia that has_material_basis_in heterozygous mutation in the SOX9 gene on chromosome 17q24 and that is characterized by congenital shortness and bowing of long tubular bones, especially in the lower extremities, as well as by hypoplastic scapulae, narrow iliac wings, and nonmineralized thoracic pedicles.",
                "url": "https://disease-ontology.org/term/DOID:0050463",
                "evidence": [
                    {
                        "id": "0050463",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050463"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0090111",
                "name": "PCWH syndrome",
                "description": "A syndrome that is characterized by the association of the features of Waardenburg-Shah syndrome (sensorineural hearing loss, pigmentary abnormalities and Hirschsprung disease; see this term) with neurological features, including: neonatal hypotonia, intellectual deficit (of variable severity), nystagmus, progressive spasticity, ataxia and epilepsy, and has_material_basis_in heterozygous mutation in the SRY-box 10 (SOX10) gene on chromosome 22q13.",
                "url": "https://disease-ontology.org/term/DOID:0090111",
                "evidence": [
                    {
                        "id": "0090111",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0090111"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110955",
                "name": "Waardenburg syndrome type 4C",
                "description": "A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and Hirschsprung disease that has_material_basis_in heterozygous mutation in the SOX10 gene on chromosome 22q13.",
                "url": "https://disease-ontology.org/term/DOID:0110955",
                "evidence": [
                    {
                        "id": "0110955",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110955"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110956",
                "name": "Waardenburg syndrome type 2E",
                "description": "A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in heterozygous mutations in the SOX10 gene on chromosome 22q13.",
                "url": "https://disease-ontology.org/term/DOID:0110956",
                "evidence": [
                    {
                        "id": "0110956",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110956"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111763",
                "name": "46,XX sex reversal 2",
                "description": "A 46,XX sex reversal that has_material_basis_in heterozygous duplication or triplication of a 68-kb regulatory region -584 to -516 kb upstream of the SOX9 gene on chromosome 17q24.",
                "url": "https://disease-ontology.org/term/DOID:0111763",
                "evidence": [
                    {
                        "id": "0111763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111775",
                "name": "46,XY sex reversal 10",
                "description": "A 46 XY sex reversal characterized by an XY karyotype, phenotypically female genitalia and failure to develop secondary sexual characteristics at puberty including menstruation that has_material_basis_in heterozygous deletion of a region upstream of the SOX9 gene on chromosome 17q24.",
                "url": "https://disease-ontology.org/term/DOID:0111775",
                "evidence": [
                    {
                        "id": "0111775",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111775"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10487",
                "name": "Hirschsprung's disease",
                "description": "A megacolon that is characterized by a blockage of the large intestine due to improper muscle movement in the bowel.",
                "url": "https://disease-ontology.org/term/DOID:10487",
                "evidence": [
                    {
                        "id": "10487",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10487"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3614",
                "name": "Kallmann syndrome",
                "description": "A hypogonadotropic hypogonadism with a defective sense of smell (anosmia or hyposmia).",
                "url": "https://disease-ontology.org/term/DOID:3614",
                "evidence": [
                    {
                        "id": "3614",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3614"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3905",
                "name": "lung carcinoma",
                "description": "A lung cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells and is located_in the lungs and has_symptom cough and has_symptom chest discomfort or pain and has_symptom weight loss and has_symptom hemoptysis.",
                "url": "https://disease-ontology.org/term/DOID:3905",
                "evidence": [
                    {
                        "id": "3905",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3905"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9258",
                "name": "Waardenburg syndrome",
                "description": "A syndrome characterized by varying degrees of deafness, minor defects in structures arising from the neural crest and pigmentation anomalies of the hair, the skin and/or the iris of both eyes.",
                "url": "https://disease-ontology.org/term/DOID:9258",
                "evidence": [
                    {
                        "id": "9258",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9258"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "male gonad development",
                "id": "GO:0008584",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008584",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
                "id": "GO:0000978",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000978",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-binding transcription factor activity, RNA polymerase II-specific",
                "id": "GO:0000981",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000981",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VA17-1"
    },
    {
        "uniprot_canonical_ac": "Q9VA23-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA23",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA23"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 814,
        "chemical_mass": 94753.0,
        "gene_names": "Dmel\\CG15548;CG15548;Dmel\\CG15548;Dmel_CG15548",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VA23-1"
    },
    {
        "uniprot_canonical_ac": "Q9VA48-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA48",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA48"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 649,
        "chemical_mass": 72745.0,
        "gene_names": "Spn100A;CG1342;Dmel\\CG1342;Dmel_CG1342;Spn100A;Spn100",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA48",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA48"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of immune response",
                "id": "GO:0050776",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050776",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA48",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA48"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mating",
                "id": "GO:0007618",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007618",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA48",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA48"
                    }
                ],
                "pmid": ""
            }
        ],
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                "name": "tRNA nucleoside ribose methylation",
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                "name": "cytoskeleton",
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                "name": "retinitis pigmentosa",
                "description": "A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss.",
                "url": "https://disease-ontology.org/term/DOID:10584",
                "evidence": [
                    {
                        "id": "10584",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10584"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11054",
                "name": "urinary bladder cancer",
                "description": "An urinary system cancer that results_in malignant growth located_in the urinary bladder.",
                "url": "https://disease-ontology.org/term/DOID:11054",
                "evidence": [
                    {
                        "id": "11054",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11054"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2043",
                "name": "hepatitis B",
                "description": "A viral hepatitis that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus (Orthohepadnavirus hominoidei), which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice.",
                "url": "https://disease-ontology.org/term/DOID:2043",
                "evidence": [
                    {
                        "id": "2043",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2043"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:234",
                "name": "colon adenocarcinoma",
                "description": "A colon carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:234",
                "evidence": [
                    {
                        "id": "234",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:234"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2671",
                "name": "transitional cell carcinoma",
                "description": "A carcinoma that derives_from transitional epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:2671",
                "evidence": [
                    {
                        "id": "2671",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2671"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3459",
                "name": "breast carcinoma",
                "description": "A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:3459",
                "evidence": [
                    {
                        "id": "3459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3748",
                "name": "esophagus squamous cell carcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus.",
                "url": "https://disease-ontology.org/term/DOID:3748",
                "evidence": [
                    {
                        "id": "3748",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3748"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "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.",
                "url": "https://disease-ontology.org/term/DOID:3883",
                "evidence": [
                    {
                        "id": "3883",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3883"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
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                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
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            },
            {
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                "name": "renal cell carcinoma",
                "description": "A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney.",
                "url": "https://disease-ontology.org/term/DOID:4450",
                "evidence": [
                    {
                        "id": "4450",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4450"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5015",
                "name": "fibrolamellar carcinoma",
                "description": "A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers.",
                "url": "https://disease-ontology.org/term/DOID:5015",
                "evidence": [
                    {
                        "id": "5015",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5015"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB76",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB76"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB76",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB76"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "carbonate dehydratase activity",
                "id": "GO:0004089",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004089",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB76",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB76"
                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VB76-1"
    },
    {
        "uniprot_canonical_ac": "Q9VB80-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB80",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB80"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 29156.0,
        "gene_names": "Dmel\\CG14258;CG14258;Dmel\\CG14258;Dmel_CG14258",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB80",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB80"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "circadian rhythm",
                "id": "GO:0007623",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007623",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB80",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB80"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
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    },
    {
        "uniprot_canonical_ac": "Q9VB89-1",
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            {
                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VB89",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB89"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 341,
        "chemical_mass": 37167.0,
        "gene_names": "DmelL2;CG6277;DmelL2;Dmel\\CG6277;Dmel_CG6277",
        "protein_name": "Lipase domain-containing protein",
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            {
                "disease_id": "DOID:9970",
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                "description": "An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness.",
                "url": "https://disease-ontology.org/term/DOID:9970",
                "evidence": [
                    {
                        "id": "9970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9970"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB89",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB89"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "lipase activity",
                "id": "GO:0016298",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016298",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB89",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB89"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "triacylglycerol lipase activity",
                "id": "GO:0004806",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004806",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB89",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB89"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "lipid catabolic process",
                "id": "GO:0016042",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016042",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB89",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB89"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VB89-1"
    },
    {
        "uniprot_canonical_ac": "Q9VB95-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB95",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB95"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 360,
        "chemical_mass": 39484.0,
        "gene_names": "TwdlC;CG14254;Dmel\\CG14254;Dmel_CG14254;TwdlC",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular matrix",
                "id": "GO:0031012",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031012",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB95",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB95"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chitin-based extracellular matrix",
                "id": "GO:0062129",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0062129",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB95",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB95"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "structural constituent of chitin-based cuticle",
                "id": "GO:0005214",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005214",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB95",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB95"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "structural constituent of chitin-based larval cuticle",
                "id": "GO:0008010",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008010",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB95",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB95"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "chitin-based cuticle development",
                "id": "GO:0040003",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040003",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB95",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB95"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9VB95-1",
                "start_pos": "89",
                "end_pos": "89",
                "site_lbl": "Thr89",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 89,
                        "start_aa": "Thr",
                        "end_pos": 89,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr89",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "Q9VB95-1"
    },
    {
        "uniprot_canonical_ac": "Q9VBA1-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBA1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBA1"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 469,
        "chemical_mass": 53825.0,
        "gene_names": "Spag1;CG18472;Dmel\\CG18472;Dmel_CG18472;Spag1",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0110607",
                "name": "primary ciliary dyskinesia 28",
                "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer and inner dynein arm defect, recurrent upper and lower airway disease, bronchiectasis, and decreased fertility and has_material_basis_in homozygous or compound heterozygous mutation in the SPAG1 gene on chromosome 8q22.",
                "url": "https://disease-ontology.org/term/DOID:0110607",
                "evidence": [
                    {
                        "id": "0110607",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110607"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBA1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBA1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBA1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBA1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein folding chaperone complex",
                "id": "GO:0101031",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0101031",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBA1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBA1"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "heat shock protein binding",
                "id": "GO:0031072",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031072",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBA1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBA1"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein targeting to mitochondrion",
                "id": "GO:0006626",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006626",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBA1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBA1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axonemal dynein complex assembly",
                "id": "GO:0070286",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070286",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBA1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBA1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "Q9VBA1-1"
    },
    {
        "uniprot_canonical_ac": "Q9VBA2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBA2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBA2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 405,
        "chemical_mass": 47215.0,
        "gene_names": "Dmel\\CG14252;CG14252;Dmel\\CG14252;Dmel_CG14252",
        "protein_name": "Myb/SANT-like DNA-binding domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "nuclear body",
                "id": "GO:0016604",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016604",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBA2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBA2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "positive regulation of DNA-templated transcription",
                "id": "GO:0045893",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045893",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBA2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBA2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q9VBA2-1"
    },
    {
        "uniprot_canonical_ac": "Q9VBD5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBD5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBD5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 309,
        "chemical_mass": 30854.0,
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                "disease_id": "DOID:0080350",
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                "description": "A retinitis pigmentosa that has_material_basis_in mutation in the REEP6 gene on chromosome 19p13.",
                "url": "https://disease-ontology.org/term/DOID:0080350",
                "evidence": [
                    {
                        "id": "0080350",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080350"
                    }
                ],
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            },
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                "disease_id": "DOID:0110782",
                "name": "hereditary spastic paraplegia 31",
                "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11.",
                "url": "https://disease-ontology.org/term/DOID:0110782",
                "evidence": [
                    {
                        "id": "0110782",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110782"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "endoplasmic reticulum membrane",
                "id": "GO:0005789",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005789",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBM3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBM3"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
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            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
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                        "id": "Q9VBM5",
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                ],
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        ],
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        "gene_names": "CG17195-PA;CG17195-PA;CG17195;Dmel\\CG17195;Dmel_CG17195",
        "protein_name": "Palmitoyltransferase",
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        "cellular_component": [
            {
                "name": "endoplasmic reticulum",
                "id": "GO:0005783",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005783",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VBM5",
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                    }
                ],
                "pmid": ""
            },
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                "name": "Golgi apparatus",
                "id": "GO:0005794",
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                    {
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                        "id": "Q9VBM5",
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                    }
                ],
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            },
            {
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                        "id": "Q9VBM5",
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                    }
                ],
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            }
        ],
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            {
                "name": "protein targeting to membrane",
                "id": "GO:0006612",
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            }
        ],
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            {
                "name": "protein-cysteine S-palmitoyltransferase activity",
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                    {
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                ],
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                        "id": "0111893",
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            {
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                ],
                "pmid": ""
            },
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                "name": "cytosolic large ribosomal subunit",
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                    {
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                        "id": "Q9VBN5",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cytoplasmic translation",
                "id": "GO:0002181",
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                    {
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                        "id": "Q9VBN5",
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                    }
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            }
        ],
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            {
                "name": "structural constituent of ribosome",
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                    {
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                        "id": "Q9VBN5",
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                    }
                ],
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            }
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            }
        ],
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                "url": "https://disease-ontology.org/term/DOID:0050763",
                "evidence": [
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                        "id": "0050763",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0050763"
                    }
                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:0070221",
                "evidence": [
                    {
                        "id": "0070221",
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                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:0080954",
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                "url": "https://disease-ontology.org/term/DOID:0080954",
                "evidence": [
                    {
                        "id": "0080954",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0080954"
                    }
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            },
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                "url": "https://disease-ontology.org/term/DOID:0111353",
                "evidence": [
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                        "id": "0111353",
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                    }
                ],
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            },
            {
                "disease_id": "DOID:13580",
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                "url": "https://disease-ontology.org/term/DOID:13580",
                "evidence": [
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                        "id": "13580",
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                    }
                ],
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            },
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                    {
                        "id": "557",
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                    }
                ],
                "weight": 0.0
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                        "database": "UniProtKB",
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                    }
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                "pmid": ""
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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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            },
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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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            },
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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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            }
        ],
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            {
                "name": "ecdysteroid 22-kinase activity",
                "id": "GO:0106389",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBS8",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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                ],
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            }
        ],
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        "protein_name": "CHK kinase-like domain-containing protein",
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            {
                "name": "xenobiotic metabolic process",
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                    }
                ],
                "pmid": ""
            },
            {
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                    }
                ],
                "pmid": ""
            },
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                    }
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            }
        ],
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                    }
                ],
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            }
        ],
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    },
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                "name": "Drosophila melanogaster",
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                        "id": "Q9VC06",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC06"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "Dmel\\CG11771;CG11771;Dmel\\CG11771;Dmel_CG11771;anon-EST:Posey100",
        "protein_name": "Peptidase M3A/M3B catalytic domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "mitochondrial intermembrane space",
                "id": "GO:0005758",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005758",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC06",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC06"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC06",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC06"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "hydrolase activity",
                "id": "GO:0016787",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016787",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC06",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC06"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC06",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "Q9VC08-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC08",
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                    }
                ],
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                "reference_species": "Drosophila melanogaster [7227]"
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            {
                "name": "DNA binding",
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        ],
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            {
                "name": "nucleus",
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            },
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                ],
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                "name": "establishment of mitotic spindle localization",
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                "name": "mitochondrion",
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            {
                "name": "extracellular region",
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            {
                "name": "cellular process involved in reproduction in multicellular organism",
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                ],
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            {
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                "url": "https://disease-ontology.org/term/DOID:0090094",
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                    }
                ],
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            },
            {
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                "evidence": [
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                    }
                ],
                "pmid": ""
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        ],
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                "name": "neuron differentiation",
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        ],
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        ],
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                "name": "mRNA processing",
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                ],
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                "name": "male mating behavior",
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                        "id": "Q9VCJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCJ5"
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            },
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VCJ5"
                    }
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            {
                "name": "aminergic neurotransmitter loading into synaptic vesicle",
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                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VCJ5"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "terminal bouton",
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            {
                "name": "synaptic vesicle membrane",
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                    {
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                ],
                "pmid": ""
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        ],
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                "name": "serotonin:sodium:chloride symporter activity",
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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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                ],
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        ],
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            {
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                    {
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                        "id": "Q9VCQ8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VCQ8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
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                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cytoplasm",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "amino acid metabolic process",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006520",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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                "name": "aminoacylase activity",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
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                ],
                "pmid": ""
            }
        ],
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                "name": "cytoplasm",
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "amino acid metabolic process",
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                    }
                ],
                "pmid": ""
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        ],
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    {
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                ],
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        ],
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    {
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                "name": "Drosophila melanogaster",
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                ],
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        ],
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            {
                "name": "motile cilium",
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                    }
                ],
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            },
            {
                "name": "acrosomal vesicle",
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "flagellated sperm motility",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cilium assembly",
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                    {
                        "database": "UniProtKB",
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                ],
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        ],
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    {
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                ],
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        ],
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            {
                "disease_id": "DOID:0111077",
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                "url": "https://disease-ontology.org/term/DOID:0111077",
                "evidence": [
                    {
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                    }
                ],
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            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
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                    {
                        "id": "10763",
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                    }
                ],
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            },
            {
                "disease_id": "DOID:12365",
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                "url": "https://disease-ontology.org/term/DOID:12365",
                "evidence": [
                    {
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                "name": "magnesium ion binding",
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                    {
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                ],
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            },
            {
                "name": "ATP binding",
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                    }
                ],
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            },
            {
                "name": "kinase activity",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VD23"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "potassium ion binding",
                "id": "GO:0030955",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030955",
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                    {
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                ],
                "pmid": ""
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        ],
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            {
                "name": "cytoplasm",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                ],
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            {
                "name": "cytosol",
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                ],
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                "name": "plasma membrane",
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                ],
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        ],
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                "name": "glycolytic process",
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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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                "name": "system development",
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                "name": "intracellular protein transport",
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                "name": "vesicle-mediated transport",
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                ],
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        ],
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                "name": "GTPase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003924",
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                    {
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                ],
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            {
                "name": "GTP binding",
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                ],
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            },
            {
                "name": "metal ion binding",
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                ],
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        ],
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                "name": "cytoplasm",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                ],
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                "name": "protein targeting to ER",
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            {
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]
