{
    "uniprot_canonical_ac": "A0A0C4DHM8-1",
    "uniprot_ac": "A0A0C4DHM8",
    "uniprot_id": "A0A0C4DHM8_DROME",
    "mass": {
        "chemical_mass": 97237.0,
        "monoisotopic_mass": 97237.0
    },
    "refseq": {
        "ac": "NP_001015352",
        "name": "uncharacterized protein, isoform C",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001015352"
    },
    "gene_names": [
        {
            "name": "CG40260",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8",
            "id": "A0A0C4DHM8"
        },
        {
            "name": "Dmel\\CG17684",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8",
            "id": "A0A0C4DHM8"
        },
        {
            "name": "CG17684",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001263157",
            "id": "NP_001263157"
        },
        {
            "name": "CG17684",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8",
            "id": "A0A0C4DHM8"
        },
        {
            "name": "CG40072; CG40260; Dmel\\CG17684",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001263157",
            "id": "NP_001263157"
        },
        {
            "name": "CG40072",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8",
            "id": "A0A0C4DHM8"
        },
        {
            "name": "CG40260",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8",
            "id": "A0A0C4DHM8"
        },
        {
            "name": "Dmel\\CG17684",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8",
            "id": "A0A0C4DHM8"
        },
        {
            "name": "Dmel_CG17684",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8",
            "id": "A0A0C4DHM8"
        }
    ],
    "protein_names": [
        {
            "name": "CG17684-PC",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001015352",
            "id": "NP_001015352"
        },
        {
            "name": "CG17684-PD",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001263157",
            "id": "NP_001263157"
        },
        {
            "name": "Uncharacterized protein, isoform C",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A0C4DHM8"
        },
        {
            "name": "uncharacterized protein, isoform C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001015352",
            "id": "NP_001015352"
        },
        {
            "name": "uncharacterized protein, isoform D",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001263157",
            "id": "NP_001263157"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0070063",
            "recommended_name": {
                "id": "DOID:0070063",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0070063",
                "name": "autosomal dominant intellectual developmental disorder 33",
                "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DPP6 gene on chromosome 7q36.2."
            },
            "synonyms": [
                {
                    "id": "DOID:0070063",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0070063",
                    "name": "autosomal dominant non-syndromic intellectual disability 33",
                    "description": ""
                },
                {
                    "id": "DOID:0070063",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0070063",
                    "name": "MRD33",
                    "description": ""
                },
                {
                    "id": "DOID:0070063",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0070063",
                    "name": "autosomal dominant mental retardation 33",
                    "description": ""
                },
                {
                    "id": "MONDO:0014580",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014580",
                    "name": "intellectual disability, autosomal dominant 33",
                    "description": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DPP6 gene."
                },
                {
                    "id": "MONDO:0014580",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014580",
                    "name": "DPP6 autosomal dominant non-syndromic intellectual disability",
                    "description": ""
                },
                {
                    "id": "MONDO:0014580",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014580",
                    "name": "MRD33",
                    "description": ""
                },
                {
                    "id": "MONDO:0014580",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014580",
                    "name": "autosomal dominant intellectual disability 33",
                    "description": ""
                },
                {
                    "id": "MONDO:0014580",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014580",
                    "name": "autosomal dominant mental retardation 33",
                    "description": ""
                },
                {
                    "id": "MONDO:0014580",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014580",
                    "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in DPP6",
                    "description": ""
                },
                {
                    "id": "MONDO:0014580",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014580",
                    "name": "intellectual disability, autosomal dominant 33",
                    "description": ""
                },
                {
                    "id": "MONDO:0014580",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014580",
                    "name": "intellectual disability, autosomal dominant type 33",
                    "description": ""
                },
                {
                    "id": "MONDO:0014580",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014580",
                    "name": "mental retardation, autosomal dominant type 33",
                    "description": ""
                },
                {
                    "id": "MONDO:0014580",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014580",
                    "name": "autosomal dominant non-syndromic intellectual disability 33",
                    "description": ""
                },
                {
                    "id": "MONDO:0014580",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014580",
                    "name": "mental retardation, autosomal dominant 33",
                    "description": ""
                },
                {
                    "id": "MIM:616311",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/616311",
                    "name": "Intellectual developmental disorder, autosomal dominant 33",
                    "description": "Intellectual developmental disorder, autosomal dominant 33"
                }
            ],
            "evidence": [
                {
                    "id": "0070063",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0070063"
                }
            ]
        },
        {
            "disease_id": "DOID:12377",
            "recommended_name": {
                "id": "DOID:12377",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/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."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "12377",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:12377"
                }
            ]
        },
        {
            "disease_id": "DOID:2841",
            "recommended_name": {
                "id": "DOID:2841",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing."
            },
            "synonyms": [
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "Exercise induced asthma",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "bronchial hyperreactivity",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "chronic obstructive asthma",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "chronic obstructive asthma with acute exacerbation",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "chronic obstructive asthma with status asthmaticus",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "exercise-induced asthma",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "inherited susceptibility to asthma",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, nocturnal, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, bronchial",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, diminished response to Antileukotriene treatment 1N",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, protection against",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma-related traits, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MIM:600807",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/600807",
                    "name": "Asthma",
                    "description": "Asthma"
                }
            ],
            "evidence": [
                {
                    "id": "2841",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2841"
                }
            ]
        },
        {
            "disease_id": "DOID:332",
            "recommended_name": {
                "id": "DOID:332",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/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."
            },
            "synonyms": [
                {
                    "id": "DOID:332",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:332",
                    "name": "ALS",
                    "description": ""
                },
                {
                    "id": "DOID:332",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:332",
                    "name": "Lou Gehrig's disease",
                    "description": ""
                },
                {
                    "id": "DOID:332",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:332",
                    "name": "motor neuron disease, bulbar",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "ALS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "FALS",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, autosomal dominant amyotrophic lateral sclerosis 1, autosomal recessive, included",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, familial",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, familial",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, sporadic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, sporadic, included",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MIM:105400",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/105400",
                    "name": "Amyotrophic lateral sclerosis 1",
                    "description": "Amyotrophic lateral sclerosis 1"
                }
            ],
            "evidence": [
                {
                    "id": "332",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:332"
                }
            ]
        },
        {
            "disease_id": "DOID:3748",
            "recommended_name": {
                "id": "DOID:3748",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3748",
                "name": "esophagus squamous cell carcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus."
            },
            "synonyms": [
                {
                    "id": "DOID:3748",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3748",
                    "name": "SCC of esophagus",
                    "description": ""
                },
                {
                    "id": "DOID:3748",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3748",
                    "name": "SCC of oesophagus",
                    "description": ""
                },
                {
                    "id": "DOID:3748",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3748",
                    "name": "oesophagus squamous cell carcinoma",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "3748",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3748"
                }
            ]
        },
        {
            "disease_id": "DOID:3907",
            "recommended_name": {
                "id": "DOID:3907",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3907",
                "name": "lung squamous cell carcinoma",
                "description": "A non-small cell lung carcinoma that has_material_basis_in the squamous cell."
            },
            "synonyms": [
                {
                    "id": "DOID:3907",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3907",
                    "name": "Epidermoid cell carcinoma of the lung",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "3907",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3907"
                }
            ]
        },
        {
            "disease_id": "DOID:3908",
            "recommended_name": {
                "id": "DOID:3908",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/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."
            },
            "synonyms": [
                {
                    "id": "DOID:3908",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3908",
                    "name": "NSCLC",
                    "description": ""
                },
                {
                    "id": "DOID:3908",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3908",
                    "name": "Non-small cell lung cancer",
                    "description": ""
                },
                {
                    "id": "DOID:3908",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3908",
                    "name": "non-small cell lung carcinoma",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "3908",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3908"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Drosophila melanogaster",
            "taxid": 7227,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0C4DHM8",
                    "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8"
                }
            ],
            "common_name": "Fruit fly"
        }
    ],
    "gene": [
        {
            "name": "Dmel\\CG17684",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8",
            "locus": {
                "chromosome": "2R",
                "start_pos": 1866080,
                "end_pos": 2262115,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "FBgn0263780",
                        "url": "https://www.ensembl.org/id/FBgn0263780"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "FBgn0263780",
            "url": "https://bgee.org/?page=gene&gene_id=FBgn0263780",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "FBgn0263780",
            "url": "https://flybase.org/reports/FBgn0263780",
            "database": "FlyBase",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "3355066",
            "url": "https://www.ncbi.nlm.nih.gov/gene/3355066",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "IPR001375",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001375",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR002469",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR002469",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR029058",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR029058",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "dme:Dmel_CG17684",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG17684",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "DNDHHMP",
            "url": "https://omabrowser.org/oma/group/DNDHHMP/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "2876738at2759",
            "url": "http://www.orthodb.org/?query=2876738at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR11731",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR11731",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR11731:SF187",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR11731:SF187",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF00326",
            "url": "http://pfam.xfam.org/family/PF00326",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF00930",
            "url": "http://pfam.xfam.org/family/PF00930",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "NP_001015352",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001015352",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0C4DHM8",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0C4DHM8-1",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0C4DHN5",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHN5",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0C4DHN5-1",
            "url": "https://www.uniprot.org/uniprot/A0A0C4DHN5-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MHTNMTSDRSGGGGGSWRLPPDETLQVQDPKQKDHDFDFDEGHNWRSIILSLLVISFVVSGIVTAIYLLGYVDELLYWSGRRMILDEYLQGDLIPRRLPSSWVTTQKYVFQSDDGSLAVLDTTTNLVKVLVTNHTLRQLNVRRYLCSSDLKYVLFTHNVKKNFQKSFTAFYTIYDVTNDHHTPVKLKDTLKVQRTRLQYASWLGNTTAIIFVVKNDIFIRQSPLVEEDIRITSSGHENHIYNGVPDWLYQEEIFETPEAIWTSSDGTHFMYALFNDTNVGMMTYPWLSSGALFSGSGIFSGSIFPETKMVRFPTPGTTNPEVELWAVDITNLSDIQKFNIKPPATIYGQDYYLTSAGWISDSNCQVSVVYMGRSQNYSVISLCSKEEDWKCLEVHSERAPEDEWLDIFPHPVFSSDGSSFLFLANIQESENYQFTHIKHVMISQRRISVISHGRYEVTKILCWDTINHKVYFMATQDKKPGQRHLYSVQDPIHDDIRKVEPQCITCDLGDDLWSSRYYYTNCTHFEAFITPSLGVATNYGIEFYILECQGPGLPVSGVHMQTTHSLVKILYDTRPFYTERLQKLALPTQRSFEVPLPHGGRAQVQLLLPPSWREELRDAAFPVIVEVNGRPGSESVSEKFKIDWGTYMSSRNDVVYIRLDVRGSKGQSKKTLYRHLGGVEVLDQISVIGYLLDTIGFLDETRVGMWGWGYGGYVTSMALGTQQDVFKCGIAVSPTADWLYSTFTERILGLPAENFKGYVEADATQRARLIKSNSYFLIHGLADTTAPFVHGVQLAKSLTSANILFRYQTYADEGHDLSGVLEHVYSSMEQYFAECLSLDPDDTKPEVDNSIVPAE",
        "length": 855,
        "header": "tr|A0A0C4DHM8-1|A0A0C4DHM8_DROME Isoform 1 of Uncharacterized protein, isoform C  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG17684 PE=4 SV=1 CANONICAL=A0A0C4DHM8-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A0C4DHM8-1",
            "url": "",
            "sequence": {
                "sequence": "MHTNMTSDRSGGGGGSWRLPPDETLQVQDPKQKDHDFDFDEGHNWRSIILSLLVISFVVSGIVTAIYLLGYVDELLYWSGRRMILDEYLQGDLIPRRLPSSWVTTQKYVFQSDDGSLAVLDTTTNLVKVLVTNHTLRQLNVRRYLCSSDLKYVLFTHNVKKNFQKSFTAFYTIYDVTNDHHTPVKLKDTLKVQRTRLQYASWLGNTTAIIFVVKNDIFIRQSPLVEEDIRITSSGHENHIYNGVPDWLYQEEIFETPEAIWTSSDGTHFMYALFNDTNVGMMTYPWLSSGALFSGSGIFSGSIFPETKMVRFPTPGTTNPEVELWAVDITNLSDIQKFNIKPPATIYGQDYYLTSAGWISDSNCQVSVVYMGRSQNYSVISLCSKEEDWKCLEVHSERAPEDEWLDIFPHPVFSSDGSSFLFLANIQESENYQFTHIKHVMISQRRISVISHGRYEVTKILCWDTINHKVYFMATQDKKPGQRHLYSVQDPIHDDIRKVEPQCITCDLGDDLWSSRYYYTNCTHFEAFITPSLGVATNYGIEFYILECQGPGLPVSGVHMQTTHSLVKILYDTRPFYTERLQKLALPTQRSFEVPLPHGGRAQVQLLLPPSWREELRDAAFPVIVEVNGRPGSESVSEKFKIDWGTYMSSRNDVVYIRLDVRGSKGQSKKTLYRHLGGVEVLDQISVIGYLLDTIGFLDETRVGMWGWGYGGYVTSMALGTQQDVFKCGIAVSPTADWLYSTFTERILGLPAENFKGYVEADATQRARLIKSNSYFLIHGLADTTAPFVHGVQLAKSLTSANILFRYQTYADEGHDLSGVLEHVYSSMEQYFAECLSLDPDDTKPEVDNSIVPAE",
                "length": 855,
                "header": "tr|A0A0C4DHM8-1|A0A0C4DHM8_DROME Isoform 1 of Uncharacterized protein, isoform C  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG17684 PE=4 SV=1 CANONICAL=A0A0C4DHM8-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 2119185,
                "end_pos": 1866163,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0300103",
                        "url": "https://www.ensembl.org/id/FBtr0300103"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0289380",
                        "url": "https://www.ensembl.org/id/FBpp0289380"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A0C4DHN5-1",
            "url": "",
            "sequence": {
                "sequence": "MHTNMTSDRSGGGGGSWRLPPDETLQVQDPKQKDHDFDFDEGHNWRSIILSLLVISFVVSGIVTAIYLLGYVDELLYWSGRRMILDEYLQGDLIPRRLPSSWVTTQKYVFQSDDGSLAVLDTTTNLVKVLVTNHTLRQLNVRRYLCSSDLKYVLFTHNVKKNFQKSFTAFYTIYDVTNDHHTPVKLKDTLKVQRTRLQYASWLGNTTAIIFVVKNDIFIRQSPLVEEDIRITSSGHENHIYNGVPDWLYQEEIFETPEAIWTSSDGTHFMYALFNDTNVGMMTYPWLSSGALFSGSGIFSGSIFPETKMVRFPTPGTTNPEVELWAVDITNLSDIQKFNIKPPATIYGQDYYLTSAGWISDSNCQVSVVYMGRSQNYSVISLCSKEEDWKCLEVHSERAPEDEWLDIFPHPVFSSDGSSFLFLANIQESENYQFTHIKHVMISQRRISVISHGRYELLISANKMLHRCDKYKIRKRMNIERPN",
                "length": 483,
                "header": "tr|A0A0C4DHN5-1|A0A0C4DHM8_DROME Computationally mapped isoform of Uncharacterized protein, isoform C  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG17684 PE=4 SV=1 CANONICAL=A0A0C4DHM8-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 2119185,
                "end_pos": 1994818,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0334734",
                        "url": "https://www.ensembl.org/id/FBtr0334734"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0306782",
                        "url": "https://www.ensembl.org/id/FBpp0306782"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "dme:Dmel_CG17684",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG17684",
            "resource": "KEGG Pathway"
        }
    ],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Molecular Function",
                "total": 2,
                "go_terms": [
                    {
                        "name": "dipeptidyl-peptidase activity",
                        "id": "GO:0008239",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008239",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0C4DHM8",
                                "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "serine-type peptidase activity",
                        "id": "GO:0008236",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008236",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0C4DHM8",
                                "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 1,
                "go_terms": [
                    {
                        "name": "plasma membrane",
                        "id": "GO:0005886",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0C4DHM8",
                                "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Biological Process",
                "total": 1,
                "go_terms": [
                    {
                        "name": "proteolysis",
                        "id": "GO:0006508",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0C4DHM8",
                                "url": "https://www.uniprot.org/uniprot/A0A0C4DHM8"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 133,
            "end_pos": 135,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 205,
            "end_pos": 207,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 275,
            "end_pos": 277,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 331,
            "end_pos": 333,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 376,
            "end_pos": 378,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 4,
            "end_pos": 6,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 521,
            "end_pos": 523,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
        }
    ],
    "section_stats": [
        {
            "table_id": "glycosylation",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
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                {
                    "field": "total_sites",
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                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
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                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported",
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        {
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        {
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        {
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}