{
    "uniprot_canonical_ac": "A0A0B4LG18-1",
    "uniprot_ac": "A0A0B4LG18",
    "uniprot_id": "A0A0B4LG18_DROME",
    "mass": {
        "chemical_mass": 83339.0,
        "monoisotopic_mass": 83339.0
    },
    "refseq": {
        "ac": "NP_001286656",
        "name": "uncharacterized protein, isoform C",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286656"
    },
    "gene_names": [
        {
            "name": "Dmel\\CG9313",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LG18",
            "id": "A0A0B4LG18"
        },
        {
            "name": "CG9313",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286657",
            "id": "NP_001286657"
        },
        {
            "name": "CG9313",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LG18",
            "id": "A0A0B4LG18"
        },
        {
            "name": "Dmel\\CG9313",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286657",
            "id": "NP_001286657"
        },
        {
            "name": "Dmel_CG9313",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LG18",
            "id": "A0A0B4LG18"
        }
    ],
    "protein_names": [
        {
            "name": "CG9313-PB",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286657",
            "id": "NP_001286657"
        },
        {
            "name": "CG9313-PC",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286656",
            "id": "NP_001286656"
        },
        {
            "name": "Uncharacterized protein, isoform B",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A0B4LG18"
        },
        {
            "name": "uncharacterized protein, isoform B",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286657",
            "id": "NP_001286657"
        },
        {
            "name": "uncharacterized protein, isoform C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286656",
            "id": "NP_001286656"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0050144",
            "recommended_name": {
                "id": "DOID:0050144",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/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."
            },
            "synonyms": [
                {
                    "id": "DOID:0050144",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050144",
                    "name": "Kartagener's syndrome",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "0050144",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050144"
                }
            ]
        },
        {
            "disease_id": "DOID:0050545",
            "recommended_name": {
                "id": "DOID:0050545",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050545",
                "name": "visceral heterotaxy",
                "description": "A physical disorder characterized by the abnormal distribution of the major visceral organs within the chest and abdomen."
            },
            "synonyms": [
                {
                    "id": "DOID:0050545",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050545",
                    "name": "heterotaxia",
                    "description": ""
                },
                {
                    "id": "DOID:0050545",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050545",
                    "name": "situs ambiguus",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "heterotaxy, visceral, 2, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "DTGA2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "heterotaxy, visceral, 2, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "transposition of the great arteries, dextro-looped 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "HTX2",
                    "description": ""
                },
                {
                    "id": "MONDO:0011546",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011546",
                    "name": "Htx",
                    "description": ""
                },
                {
                    "id": "MONDO:0011659",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011659",
                    "name": "heterotaxy, visceral, 3, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0011659",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011659",
                    "name": "HTX3",
                    "description": ""
                },
                {
                    "id": "MONDO:0011659",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011659",
                    "name": "heterotaxy, visceral, 3, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, 1, X-linked",
                    "description": "X-linked visceral heterotaxy type 1 is a very rare form of heterotaxy that has only been reported in a few families. Heterotaxy is the right/left transposition of thoracic and/or abdominal organs. This condition is caused by mutations in the ZIC3 gene, is inherited in an X-linked recessive fashion, and is usually seen in males. Physical features include heart abnormalities such as dextrocardia, transposition of great vessels, ventricular septal defect, patent ductus arteriosus, pulmonic stenosis ; situs inversus, and missing (asplenia) and/or extra spleens (polysplenia).Affected individualscan also experience abnormalities in the development of the midline of the body, which can cause holoprosencephaly, myelomeningocele, urological anomalies, widely spaced eyes (hypertelorism), cleft palate, and abnormalities of the sacral spine and anus. Heterotaxia with recurrent respiratory infections are called primary ciliary dyskinesia."
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "ZIC3 visceral heterotaxy",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "congenital heart defects, nonsyndromic, 1, X-linked, X-linked recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, 1, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, 1, X-linked, X-linked recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "visceral heterotaxy caused by mutation in ZIC3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "HTX1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "X-linked visceral heterotaxy 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "congenital heart defects, multiple types, 1, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "dextrocardia with Other Cardiac malformations",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "heterotaxy, visceral, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "laterality, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0010607",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010607",
                    "name": "situs inversus, Complex Cardiac defects, and splenic defects, X-linked",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "heterotaxy, visceral, 6, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "heterotaxy, visceral, 6, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "heterotaxy, visceral, 6, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0013887",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013887",
                    "name": "HTX6",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "heterotaxy, visceral, 4, autosomal",
                    "description": "Any visceral heterotaxy in which the cause of the disease is a mutation in the ACVR2B gene."
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "ACVR2B visceral heterotaxy",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "heterotaxy, visceral, 4, autosomal",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "visceral heterotaxy caused by mutation in ACVR2B",
                    "description": ""
                },
                {
                    "id": "MONDO:0013403",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013403",
                    "name": "HTX4",
                    "description": ""
                },
                {
                    "id": "MIM:605376",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/605376",
                    "name": "Heterotaxy, visceral, 2, autosomal",
                    "description": "Heterotaxy, visceral, 2, autosomal"
                },
                {
                    "id": "MIM:306955",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/306955",
                    "name": "Heterotaxy, visceral, 1, X-linked",
                    "description": "Heterotaxy, visceral, 1, X-linked"
                },
                {
                    "id": "MIM:614779",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/614779",
                    "name": "Heterotaxy, visceral, 6, autosomal",
                    "description": "Heterotaxy, visceral, 6, autosomal"
                },
                {
                    "id": "MIM:613751",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/613751",
                    "name": "Heterotaxy, visceral, 4, autosomal",
                    "description": "Heterotaxy, visceral, 4, autosomal"
                }
            ],
            "evidence": [
                {
                    "id": "0050545",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050545"
                }
            ]
        },
        {
            "disease_id": "DOID:0110594",
            "recommended_name": {
                "id": "DOID:0110594",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110594",
                "name": "primary ciliary dyskinesia 1",
                "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect and in about half of patients situs inversus and has_material_basis_in compound heterozygous mutation in the DNAI1 gene on chromosome 9p13."
            },
            "synonyms": [
                {
                    "id": "DOID:0110594",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110594",
                    "name": "CILD1",
                    "description": ""
                },
                {
                    "id": "DOID:0110594",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110594",
                    "name": "primary ciliary dyskinesia 1 with or without situs inversus",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "primary ciliary dyskinesia 1",
                    "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAI1 gene."
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "CILD1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "DNAI1 primary ciliary dyskinesia",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "ciliary dyskinesia, primary, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "primary ciliary dyskinesia 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "primary ciliary dyskinesia 1 with or without situs inversus",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "primary ciliary dyskinesia caused by mutation in DNAI1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "primary ciliary dyskinesia type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "Kartagener syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "PCD",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "Polynesian bronchiectasis",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "Siewert syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "ciliary dyskinesia, primary, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "ciliary dyskinesia, primary, 1, with or without situs inversus",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "dextrocardia, bronchiectasis, and sinusitis",
                    "description": ""
                },
                {
                    "id": "MONDO:0009484",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009484",
                    "name": "immotile cilia syndrome",
                    "description": ""
                },
                {
                    "id": "MIM:244400",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/244400",
                    "name": "Kartagener syndrome",
                    "description": "Kartagener syndrome"
                }
            ],
            "evidence": [
                {
                    "id": "0110594",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110594"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Drosophila melanogaster",
            "taxid": 7227,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0B4LG18",
                    "url": "https://www.uniprot.org/uniprot/A0A0B4LG18"
                }
            ],
            "common_name": "Fruit fly"
        }
    ],
    "gene": [
        {
            "name": "Dmel\\CG9313",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LG18",
            "locus": {
                "chromosome": "2R",
                "start_pos": 20984043,
                "end_pos": 20978901,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "FBgn0034566",
                        "url": "https://www.ensembl.org/id/FBgn0034566"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "FBgn0034566",
            "url": "https://bgee.org/?page=gene&gene_id=FBgn0034566",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "FBgn0034566",
            "url": "https://flybase.org/reports/FBgn0034566",
            "database": "FlyBase",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "37374",
            "url": "https://www.ncbi.nlm.nih.gov/gene/37374",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "Q8MSJ9",
            "url": "https://www.ebi.ac.uk/intact/interactors/id:Q8MSJ9*",
            "database": "IntAct",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "IPR001680",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001680",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR015943",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR015943",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR036322",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR036322",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "dme:Dmel_CG9313",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG9313",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "FNYCERA",
            "url": "https://omabrowser.org/oma/group/FNYCERA/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "3088529at2759",
            "url": "http://www.orthodb.org/?query=3088529at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR12442",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR12442",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR12442:SF11",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR12442:SF11",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "NP_001286657",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286657",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0B4LG18",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LG18",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0B4LG18-1",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LG18-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q8MSJ9",
            "url": "https://www.uniprot.org/uniprot/Q8MSJ9",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q8MSJ9-1",
            "url": "https://www.uniprot.org/uniprot/Q8MSJ9-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MATKPGKGDGKQVKGKLRTSKNKTDGPGGGGGDADDFDAWMKSRQLLKPDDQLDLTEAELGEEITKVLTPTNTNIVRNLVVYSFKEGEFVPAPLPGNTVTLIAFAGNSLHVDSDEGRRQIEESDEIGYPLPMPNYTVVEQRETDNVDGEEGEGEEDDDGATAKDAAVEDEDVEEEDDEEAKGTEGDEGEGEGEGEGAAARQEDDEPAHQAAAVSSKKRKLINQFNYCERGALTYTNPKRNVDTQTIPPPRSQFGANVLQWVIYDSYMENFAESQKDGTKKEERKRGKREKKFRDKSAIAEQLNKKYLKCWQILERMINQNIYDDIAHDYRYWEDPADEFREGEGNLLPLWKFQYDKTKKMNVTDILFNPSYYDLFAVCFGSHDFMKQTNEGYLCLFTVKNPSFPDYIIQTDCGVMCCDIHPTYPFLAVIGLYDGNVAVYNLREDCKEPLYVSRGVNCKHGECVWQIKWGLDMADGEVNFFSVSSDGRVFNWILMQNKLWVTTIITLYRENGLVDGPDGTKVTLKSGGSCMVFHPVDNKIFLVGTECGYIYKCSTAFSSKYLMTYYAHNMSVYRIDFNRFNSNIFVSCGADWMVKVWEDMRPDPLFIFDLGAAVGDVKWAPYSSTVFAAVTTEGKVHVFDLNVNKYKAICIQAVVPKRKNKLTRLSFNEKLAFIVVGDEKGVTTSLKLSPNLRMMVKPPKKQLYLDQNTLQIGKLEKLLSLVRELPEGSTAVPDAATTVRS",
        "length": 740,
        "header": "tr|A0A0B4LG18-1|A0A0B4LG18_DROME Isoform 1 of Uncharacterized protein, isoform B  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG9313 PE=4 SV=1 CANONICAL=A0A0B4LG18-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A0B4LG18-1",
            "url": "",
            "sequence": {
                "sequence": "MATKPGKGDGKQVKGKLRTSKNKTDGPGGGGGDADDFDAWMKSRQLLKPDDQLDLTEAELGEEITKVLTPTNTNIVRNLVVYSFKEGEFVPAPLPGNTVTLIAFAGNSLHVDSDEGRRQIEESDEIGYPLPMPNYTVVEQRETDNVDGEEGEGEEDDDGATAKDAAVEDEDVEEEDDEEAKGTEGDEGEGEGEGEGAAARQEDDEPAHQAAAVSSKKRKLINQFNYCERGALTYTNPKRNVDTQTIPPPRSQFGANVLQWVIYDSYMENFAESQKDGTKKEERKRGKREKKFRDKSAIAEQLNKKYLKCWQILERMINQNIYDDIAHDYRYWEDPADEFREGEGNLLPLWKFQYDKTKKMNVTDILFNPSYYDLFAVCFGSHDFMKQTNEGYLCLFTVKNPSFPDYIIQTDCGVMCCDIHPTYPFLAVIGLYDGNVAVYNLREDCKEPLYVSRGVNCKHGECVWQIKWGLDMADGEVNFFSVSSDGRVFNWILMQNKLWVTTIITLYRENGLVDGPDGTKVTLKSGGSCMVFHPVDNKIFLVGTECGYIYKCSTAFSSKYLMTYYAHNMSVYRIDFNRFNSNIFVSCGADWMVKVWEDMRPDPLFIFDLGAAVGDVKWAPYSSTVFAAVTTEGKVHVFDLNVNKYKAICIQAVVPKRKNKLTRLSFNEKLAFIVVGDEKGVTTSLKLSPNLRMMVKPPKKQLYLDQNTLQIGKLEKLLSLVRELPEGSTAVPDAATTVRS",
                "length": 740,
                "header": "tr|A0A0B4LG18-1|A0A0B4LG18_DROME Isoform 1 of Uncharacterized protein, isoform B  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG9313 PE=4 SV=1 CANONICAL=A0A0B4LG18-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 20983796,
                "end_pos": 20979506,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0342788",
                        "url": "https://www.ensembl.org/id/FBtr0342788"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0309629",
                        "url": "https://www.ensembl.org/id/FBpp0309629"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q8MSJ9-1",
            "url": "",
            "sequence": {
                "sequence": "MATKPGKGDGKQVKGKRTSKNKTDGPGGGGGDADDFDAWMKSRQLLKPDDQLDLTEAELGEEITKVLTPTNTNIVRNLVVYSFKEGEFVPAPLPGNTVTLIAFAGNSLHVDSDEGRRQIEESDEIGYPLPMPNYTVVEQRETDNVDGEEGEGEEDDDGATAKDAAVEDEDVEEEDDEEAKGTEGDEGEGEGEGEGAAARQEDDEPAHQAAAVSSKKRKLINQFNYCERGALTYTNPKRNVDTQTIPPPRSQFGANVLQWVIYDSYMENFAESQKDGTKKEERKRGKREKKFRDKSAIAEQLNKKYLKCWQILERMINQNIYDDIAHDYRYWEDPADEFREGEGNLLPLWKFQYDKTKKMNVTDILFNPSYYDLFAVCFGSHDFMKQTNEGYLCLFTVKNPSFPDYIIQTDCGVMCCDIHPTYPFLAVIGLYDGNVAVYNLREDCKEPLYVSRGVNCKHGECVWQIKWGLDMADGEVNFFSVSSDGRVFNWILMQNKLWVTTIITLYRENGLVDGPDGTKVTLKSGGSCMVFHPVDNKIFLVGTECGYIYKCSTAFSSKYLMTYYAHNMSVYRIDFNRFNSNIFVSCGADWMVKVWEDMRPDPLFIFDLGAAVGDVKWAPYSSTVFAAVTTEGKVHVFDLNVNKYKAICIQAVVPKRKNKLTRLSFNEKLAFIVVGDEKGVTTSLKLSPNLRMMVKPPKKQLYLDQNTLQIGKLEKLLSLVRELPEGSTAVPDAATTVRS",
                "length": 739,
                "header": "tr|Q8MSJ9-1|A0A0B4LG18_DROME Computationally mapped isoform of Uncharacterized protein, isoform B  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG9313 PE=4 SV=1 CANONICAL=A0A0B4LG18-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 20983796,
                "end_pos": 20979506,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0071521",
                        "url": "https://www.ensembl.org/id/FBtr0071521"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0071450",
                        "url": "https://www.ensembl.org/id/FBpp0071450"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "dme:Dmel_CG9313",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG9313",
            "resource": "KEGG Pathway"
        }
    ],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Biological Process",
                "total": 3,
                "go_terms": [
                    {
                        "name": "sensory perception of sound",
                        "id": "GO:0007605",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007605",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LG18",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LG18"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cilium movement",
                        "id": "GO:0003341",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003341",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LG18",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LG18"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "outer dynein arm assembly",
                        "id": "GO:0036158",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036158",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LG18",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LG18"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 2,
                "go_terms": [
                    {
                        "name": "dynein light chain binding",
                        "id": "GO:0045503",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045503",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LG18",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LG18"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "dynein heavy chain binding",
                        "id": "GO:0045504",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045504",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LG18",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LG18"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 1,
                "go_terms": [
                    {
                        "name": "outer dynein arm",
                        "id": "GO:0036157",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036157",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LG18",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LG18"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 134,
            "end_pos": 136,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 22,
            "end_pos": 24,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 361,
            "end_pos": 363,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 568,
            "end_pos": 570,
            "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
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported",
            "table_stats": [
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                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
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                {
                    "field": "n_linked_glycans",
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                {
                    "field": "n_linked_glycan_sites",
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                },
                {
                    "field": "o_linked_glycans",
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                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported_with_glycan",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
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                {
                    "field": "n_linked_glycans",
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                {
                    "field": "n_linked_glycan_sites",
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                {
                    "field": "o_linked_glycans",
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                {
                    "field": "o_linked_glycan_sites",
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                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_predicted",
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                    "field": "total",
                    "count": 0
                },
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                    "field": "total_sites",
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                    "field": "n_linked_glycans",
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                {
                    "field": "n_linked_glycan_sites",
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                {
                    "field": "o_linked_glycans",
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                {
                    "field": "o_linked_glycan_sites",
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                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_automatic_literature_mining",
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                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
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                    "field": "n_linked_glycans",
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                {
                    "field": "n_linked_glycan_sites",
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                    "field": "o_linked_glycans",
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                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "phosphorylation",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
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            ],
            "sort_fields": []
        },
        {
            "table_id": "snv",
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        {
            "table_id": "snv_disease",
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                    "field": "total",
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        {
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    ]
}