{
    "uniprot_canonical_ac": "M9PC80-1",
    "uniprot_ac": "M9PC80",
    "uniprot_id": "M9PC80_DROME",
    "mass": {
        "chemical_mass": 66759.0,
        "monoisotopic_mass": 66759.0
    },
    "refseq": {
        "ac": "NP_648497",
        "name": "dynein, axonemal, intermediate chain 2, isoform B",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_648497"
    },
    "gene_names": [
        {
            "name": "Dnai2",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/M9PC80",
            "id": "M9PC80"
        },
        {
            "name": "CG6053; Dmel\\CG6053",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_648497",
            "id": "NP_648497"
        },
        {
            "name": "CG6053",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/M9PC80",
            "id": "M9PC80"
        },
        {
            "name": "Dmel\\CG6053",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/M9PC80",
            "id": "M9PC80"
        },
        {
            "name": "Dmel_CG6053",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/M9PC80",
            "id": "M9PC80"
        },
        {
            "name": "Dnai2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_648497",
            "id": "NP_648497"
        }
    ],
    "protein_names": [
        {
            "name": "CG6053-PB; Dnai2-PB",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_648497",
            "id": "NP_648497"
        },
        {
            "name": "CG6053-PC; Dnai2-PC",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001261723",
            "id": "NP_001261723"
        },
        {
            "name": "Dynein, axonemal, intermediate chain 2, isoform C",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "M9PC80"
        },
        {
            "name": "dynein, axonemal, intermediate chain 2, isoform B",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_648497",
            "id": "NP_648497"
        },
        {
            "name": "dynein, axonemal, intermediate chain 2, isoform C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001261723",
            "id": "NP_001261723"
        }
    ],
    "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:0110622",
            "recommended_name": {
                "id": "DOID:0110622",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110622",
                "name": "primary ciliary dyskinesia 9",
                "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, neonatal respiratory distress, sinusitis, otitis, bronchiectasis, and variable occurence of laterality defects and has_material_basis_in homozygous mutation in the DNAI2 gene on chromosome 17q25."
            },
            "synonyms": [
                {
                    "id": "DOID:0110622",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110622",
                    "name": "CILD9",
                    "description": ""
                },
                {
                    "id": "DOID:0110622",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110622",
                    "name": "primary ciliary dyskinesia 9 with or without situs inversus",
                    "description": ""
                },
                {
                    "id": "MONDO:0012906",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012906",
                    "name": "primary ciliary dyskinesia 9",
                    "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAI2 gene."
                },
                {
                    "id": "MONDO:0012906",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012906",
                    "name": "CILD9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012906",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012906",
                    "name": "DNAI2 primary ciliary dyskinesia",
                    "description": ""
                },
                {
                    "id": "MONDO:0012906",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012906",
                    "name": "ciliary dyskinesia, primary, type 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012906",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012906",
                    "name": "primary ciliary dyskinesia 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012906",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012906",
                    "name": "primary ciliary dyskinesia 9 with or without situs inversus",
                    "description": ""
                },
                {
                    "id": "MONDO:0012906",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012906",
                    "name": "primary ciliary dyskinesia caused by mutation in DNAI2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012906",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012906",
                    "name": "primary ciliary dyskinesia type 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012906",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012906",
                    "name": "ciliary dyskinesia, primary, 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012906",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012906",
                    "name": "ciliary dyskinesia, primary, 9, with or without situs inversus",
                    "description": ""
                },
                {
                    "id": "MIM:612444",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/612444",
                    "name": "Ciliary dyskinesia, primary, 9",
                    "description": "Ciliary dyskinesia, primary, 9"
                }
            ],
            "evidence": [
                {
                    "id": "0110622",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110622"
                }
            ]
        },
        {
            "disease_id": "DOID:10003",
            "recommended_name": {
                "id": "DOID:10003",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10003",
                "name": "sensorineural hearing loss",
                "description": "An inner ear disease that is characterized by hearing loss resulting from damage to the cochlea, auditory nerve and/or brainstem."
            },
            "synonyms": [
                {
                    "id": "DOID:10003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10003",
                    "name": "High Frequency Hearing Loss",
                    "description": ""
                },
                {
                    "id": "DOID:10003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10003",
                    "name": "High frequency deafness",
                    "description": ""
                },
                {
                    "id": "DOID:10003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10003",
                    "name": "Perceptive deafness",
                    "description": ""
                },
                {
                    "id": "DOID:10003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10003",
                    "name": "Perceptive hearing loss",
                    "description": ""
                },
                {
                    "id": "DOID:10003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10003",
                    "name": "Perceptive hearing loss or deafness",
                    "description": ""
                },
                {
                    "id": "DOID:10003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10003",
                    "name": "Sensorineural Deafness",
                    "description": ""
                },
                {
                    "id": "DOID:10003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10003",
                    "name": "Sensory hearing loss",
                    "description": ""
                },
                {
                    "id": "DOID:10003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10003",
                    "name": "central hearing loss",
                    "description": ""
                },
                {
                    "id": "DOID:10003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10003",
                    "name": "high-frequency hearing loss",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "10003",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:10003"
                }
            ]
        },
        {
            "disease_id": "DOID:9562",
            "recommended_name": {
                "id": "DOID:9562",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:9562",
                "name": "primary ciliary dyskinesia",
                "description": "A ciliopathy that is characterized by impaired function of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) and fallopian tube."
            },
            "synonyms": [
                {
                    "id": "DOID:9562",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9562",
                    "name": "ciliary motility disorder",
                    "description": ""
                },
                {
                    "id": "DOID:9562",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9562",
                    "name": "immotile ciliary syndrome",
                    "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": "9562",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:9562"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Drosophila melanogaster",
            "taxid": 7227,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "M9PC80",
                    "url": "https://www.uniprot.org/uniprot/M9PC80"
                }
            ],
            "common_name": "Fruit fly"
        }
    ],
    "gene": [
        {
            "name": "Dnai2",
            "url": "https://www.uniprot.org/uniprot/M9PC80",
            "locus": {
                "chromosome": "3L",
                "start_pos": 11697126,
                "end_pos": 11699263,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "FBgn0036195",
                        "url": "https://www.ensembl.org/id/FBgn0036195"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "FBgn0036195",
            "url": "https://bgee.org/?page=gene&gene_id=FBgn0036195",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "FBgn0036195",
            "url": "https://flybase.org/reports/FBgn0036195",
            "database": "FlyBase",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "39318",
            "url": "https://www.ncbi.nlm.nih.gov/gene/39318",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "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_CG6053",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG6053",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "WDFFYRQ",
            "url": "https://omabrowser.org/oma/group/WDFFYRQ/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "3990402at2759",
            "url": "http://www.orthodb.org/?query=3990402at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR12442",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR12442",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR12442:SF7",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR12442:SF7",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "NP_001261723",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001261723",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "M9PC80",
            "url": "https://www.uniprot.org/uniprot/M9PC80",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "M9PC80-1",
            "url": "https://www.uniprot.org/uniprot/M9PC80-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q9VTM3",
            "url": "https://www.uniprot.org/uniprot/Q9VTM3",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q9VTM3-1",
            "url": "https://www.uniprot.org/uniprot/Q9VTM3-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MEYIFKKERRSFGARVHFEDKDEVVFTENSNPELVKSYILKNPVDRVTQYAGQTSLSVANTERATYKSTGITHNEGGWPKDINMHDPEQTVRYKRKIEKDENYITQVMNLTKPMEHYIHQNNAVNIYENYFENLDPAPLPEPCKSRTVNVYRDPNPIKVPVKHLSWSPDGGIKMAVSHCDMRFQGDKSNQKCNSYIWEVENPNEPFLTLEPKVPCVCLEYNQKDPTSLVSGMYNGQVAAWDTRHGKLPVMISEREVCHRDPVNSVLWNNSKSGTEFFSGGSDGQVLWWDTRKLTEPLDRLLMDPVKSDDQDLSRSYGISVLEYETTIPTRFMAGTEMGMLFSCNRKGKTPTEKIQIRMMCHLGPVYAITRNPAFVKNFLTVGDWCARIWSEDCRESSIIWTKSSSSMLTDGAWSYTKVSQFFITRMDGVLDTWDLLQQQNEPVLTVKVCDEPLYCVRTNENGKFVSCGSQLGATFLVEVSDNMVMSAKNDKPLLTAMFERENRREKILEAKSRESKLKVKANHGQDQGDTMMVNGKINMAPFEAACEQAASEYFAAVEQERQRRLPGGKQDAEEADVSEAESSKL",
        "length": 585,
        "header": "tr|M9PC80-1|M9PC80_DROME Isoform 1 of Dynein, axonemal, intermediate chain 2, isoform C  OS=Drosophila melanogaster OX=7227 GN=Dnai2 PE=4 SV=1 CANONICAL=M9PC80-1"
    },
    "isoforms": [
        {
            "isoform_ac": "M9PC80-1",
            "url": "",
            "sequence": {
                "sequence": "MEYIFKKERRSFGARVHFEDKDEVVFTENSNPELVKSYILKNPVDRVTQYAGQTSLSVANTERATYKSTGITHNEGGWPKDINMHDPEQTVRYKRKIEKDENYITQVMNLTKPMEHYIHQNNAVNIYENYFENLDPAPLPEPCKSRTVNVYRDPNPIKVPVKHLSWSPDGGIKMAVSHCDMRFQGDKSNQKCNSYIWEVENPNEPFLTLEPKVPCVCLEYNQKDPTSLVSGMYNGQVAAWDTRHGKLPVMISEREVCHRDPVNSVLWNNSKSGTEFFSGGSDGQVLWWDTRKLTEPLDRLLMDPVKSDDQDLSRSYGISVLEYETTIPTRFMAGTEMGMLFSCNRKGKTPTEKIQIRMMCHLGPVYAITRNPAFVKNFLTVGDWCARIWSEDCRESSIIWTKSSSSMLTDGAWSYTKVSQFFITRMDGVLDTWDLLQQQNEPVLTVKVCDEPLYCVRTNENGKFVSCGSQLGATFLVEVSDNMVMSAKNDKPLLTAMFERENRREKILEAKSRESKLKVKANHGQDQGDTMMVNGKINMAPFEAACEQAASEYFAAVEQERQRRLPGGKQDAEEADVSEAESSKL",
                "length": 585,
                "header": "tr|M9PC80-1|M9PC80_DROME Isoform 1 of Dynein, axonemal, intermediate chain 2, isoform C  OS=Drosophila melanogaster OX=7227 GN=Dnai2 PE=4 SV=1 CANONICAL=M9PC80-1"
            },
            "locus": {
                "chromosome": "3L",
                "start_pos": 11699226,
                "end_pos": 11697215,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0332765",
                        "url": "https://www.ensembl.org/id/FBtr0332765"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0305003",
                        "url": "https://www.ensembl.org/id/FBpp0305003"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q9VTM3-1",
            "url": "",
            "sequence": {
                "sequence": "MEYIFKKERRSFGARVHFEDKDEVVFTENSNPELVKSYILKNPVDRVTQYAGQTSLSVANTERATYKSTGITHNEGGWPKDINMHDPEQTVRYKRKIEKDENYITQVMNLTKPMEHYIHQNNAVNIYENYFENLDPAPLPEPCKSRTVNVYRDPNPIKVPVKHLSWSPDGGIKMAVSHCDMRFQGDKSNQKCNSYIWEVENPNEPFLTLEPKVPCVCLEYNQKDPTSLVSGMYNGQVAAWDTRHGKLPVMISEREVCHRDPVNSVLWNNSKSGTEFFSGGSDGQVLWWDTRKLTEPLDRLLMDPVKSDDQDLSRSYGISVLEYETTIPTRFMAGTEMGMLFSCNRKGKTPTEKIQIRMMCHLGPVYAITRNPAFVKNFLTVGDWCARIWSEDCRESSIIWTKSSSSMLTDGAWSYTKVSQFFITRMDGVLDTWDLLQQQNEPVLTVKVCDEPLYCVRTNENGKFVSCGSQLGATFLVEVSDNMVMSAKNDKPLLTAMFERENRREKILEAKSRESKLKVKANHGQDQGDTMMVNGKINMAPFEAACEQAASEYFAAVEQERQRRLPGGKRRGCGGG",
                "length": 576,
                "header": "tr|Q9VTM3-1|M9PC80_DROME Computationally mapped isoform of Dynein, axonemal, intermediate chain 2, isoform C  OS=Drosophila melanogaster OX=7227 GN=Dnai2 PE=4 SV=2 CANONICAL=M9PC80-1"
            },
            "locus": {
                "chromosome": "3L",
                "start_pos": 11699226,
                "end_pos": 11697246,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0301326",
                        "url": "https://www.ensembl.org/id/FBtr0301326"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0290541",
                        "url": "https://www.ensembl.org/id/FBpp0290541"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [
        {
            "title": "The genome sequence of Drosophila melanogaster.",
            "journal": "Science",
            "date": "2000",
            "authors": "Adams MD, Celniker SE, Holt RA, Evans CA, Gocayne JD, Amanatides PG, Scherer SE, Li PW, Hoskins RA, Galle RF, George RA, Lewis SE, Richards S, Ashburner M, Henderson SN, Sutton GG, Wortman JR, Yandell MD, Zhang Q, Chen LX, Brandon RC, Rogers YH, Blazej RG, Champe M, Pfeiffer BD, Wan KH, Doyle C, Baxter EG, Helt G, Nelson CR, Gabor GL, Abril JF, Agbayani A, An HJ, Andrews-Pfannkoch C, Baldwin D, Ballew RM, Basu A, Baxendale J, Bayraktaroglu L, Beasley EM, Beeson KY, Benos PV, Berman BP, Bhandari D, Bolshakov S, Borkova D, Botchan MR, Bouck J, Brokstein P, Brottier P, Burtis KC, Busam DA, Butler H, Cadieu E, Center A, Chandra I, Cherry JM, Cawley S, Dahlke C, Davenport LB, Davies P, de Pablos B, Delcher A, Deng Z, Mays AD, Dew I, Dietz SM, Dodson K, Doup LE, Downes M, Dugan-Rocha S, Dunkov BC, Dunn P, Durbin KJ, Evangelista CC, Ferraz C, Ferriera S, Fleischmann W, Fosler C, Gabrielian AE, Garg NS, Gelbart WM, Glasser K, Glodek A, Gong F, Gorrell JH, Gu Z, Guan P, Harris M, Harris NL, Harvey D, Heiman TJ, Hernandez JR, Houck J, Hostin D, Houston KA, Howland TJ, Wei MH, Ibegwam C, Jalali M, Kalush F, Karpen GH, Ke Z, Kennison JA, Ketchum KA, Kimmel BE, Kodira CD, Kraft C, Kravitz S, Kulp D, Lai Z, Lasko P, Lei Y, Levitsky AA, Li J, Li Z, Liang Y, Lin X, Liu X, Mattei B, McIntosh TC, McLeod MP, McPherson D, Merkulov G, Milshina NV, Mobarry C, Morris J, Moshrefi A, Mount SM, Moy M, Murphy B, Murphy L, Muzny DM, Nelson DL, Nelson DR, Nelson KA, Nixon K, Nusskern DR, Pacleb JM, Palazzolo M, Pittman GS, Pan S, Pollard J, Puri V, Reese MG, Reinert K, Remington K, Saunders RD, Scheeler F, Shen H, Shue BC, Siden-Kiamos I, Simpson M, Skupski MP, Smith T, Spier E, Spradling AC, Stapleton M, Strong R, Sun E, Svirskas R, Tector C, Turner R, Venter E, Wang AH, Wang X, Wang ZY, Wassarman DA, Weinstock GM, Weissenbach J, Williams SM, WoodageT, Worley KC, Wu D, Yang S, Yao QA, Ye J, Yeh RF, Zaveri JS, Zhan M, Zhang G, Zhao Q, Zheng L, Zheng XH, Zhong FN, Zhong W, Zhou X, Zhu S, Zhu X, Smith HO, Gibbs RA, Myers EW, Rubin GM, Venter JC",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q9VTM3",
                    "url": "https://www.uniprot.org/uniprot/Q9VTM3"
                },
                {
                    "database": "UniProtKB",
                    "id": "M9PC80",
                    "url": "https://www.uniprot.org/uniprot/M9PC80"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "10731132",
                    "url": "https://glygen.org/publication/PubMed/10731132"
                }
            ]
        },
        {
            "title": "Finishing a whole-genome shotgun: release 3 of the Drosophila melanogaster euchromatic genome sequence.",
            "journal": "Genome Biol.",
            "date": "2002",
            "authors": "Celniker SE, Wheeler DA, Kronmiller B, Carlson JW, Halpern A, Patel S, Adams M, Champe M, Dugan SP, Frise E, Hodgson A, George RA, Hoskins RA, Laverty T, Muzny DM, Nelson CR, Pacleb JM, Park S, Pfeiffer BD, Richards S, Sodergren EJ, Svirskas R, Tabor PE, Wan K, Stapleton M, Sutton GG, Venter C, Weinstock G, Scherer SE, Myers EW, Gibbs RA, Rubin GM",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q9VTM3",
                    "url": "https://www.uniprot.org/uniprot/Q9VTM3"
                },
                {
                    "database": "UniProtKB",
                    "id": "M9PC80",
                    "url": "https://www.uniprot.org/uniprot/M9PC80"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "12537568",
                    "url": "https://glygen.org/publication/PubMed/12537568"
                }
            ]
        },
        {
            "title": "Annotation of the Drosophila melanogaster euchromatic genome: a systematic review.",
            "journal": "Genome Biol.",
            "date": "2002",
            "authors": "Misra S, Crosby MA, Mungall CJ, Matthews BB, Campbell KS, Hradecky P, Huang Y, Kaminker JS, Millburn GH, Prochnik SE, Smith CD, Tupy JL, Whitfied EJ, Bayraktaroglu L, Berman BP, Bettencourt BR, Celniker SE, de Grey AD, Drysdale RA, Harris NL, Richter J, Russo S, Schroeder AJ, Shu SQ, Stapleton M, Yamada C, Ashburner M, Gelbart WM, Rubin GM, Lewis SE",
            "evidence": [
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                    "url": "https://www.uniprot.org/uniprot/M9PC80"
                }
            ],
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                {
                    "type": "PubMed",
                    "id": "12537572",
                    "url": "https://glygen.org/publication/PubMed/12537572"
                }
            ]
        },
        {
            "title": "The transposable elements of the Drosophila melanogaster euchromatin: a genomics perspective.",
            "journal": "Genome Biol.",
            "date": "2002",
            "authors": "Kaminker JS, Bergman CM, Kronmiller B, Carlson J, Svirskas R, Patel S, Frise E, Wheeler DA, Lewis SE, Rubin GM, Ashburner M, Celniker SE",
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                {
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                    "id": "M9PC80",
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                }
            ],
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                {
                    "type": "PubMed",
                    "id": "12537573",
                    "url": "https://glygen.org/publication/PubMed/12537573"
                }
            ]
        },
        {
            "title": "Heterochromatic sequences in a Drosophila whole-genome shotgun assembly.",
            "journal": "Genome Biol.",
            "date": "2002",
            "authors": "Hoskins RA, Smith CD, Carlson JW, Carvalho AB, Halpern A, Kaminker JS, Kennedy C, Mungall CJ, Sullivan BA, Sutton GG, Yasuhara JC, Wakimoto BT, Myers EW, Celniker SE, Rubin GM, Karpen GH",
            "evidence": [
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                {
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                    "id": "M9PC80",
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                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "12537574",
                    "url": "https://glygen.org/publication/PubMed/12537574"
                }
            ]
        },
        {
            "title": "Combined evidence annotation of transposable elements in genome sequences.",
            "journal": "PLoS Comput. Biol.",
            "date": "2005",
            "authors": "Quesneville H, Bergman CM, Andrieu O, Autard D, Nouaud D, Ashburner M, Anxolabehere D",
            "evidence": [
                {
                    "database": "UniProtKB",
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                },
                {
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                    "id": "M9PC80",
                    "url": "https://www.uniprot.org/uniprot/M9PC80"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "16110336",
                    "url": "https://glygen.org/publication/PubMed/16110336"
                }
            ]
        },
        {
            "title": "The Release 5.1 annotation of Drosophila melanogaster heterochromatin.",
            "journal": "Science",
            "date": "2007",
            "authors": "Smith CD, Shu S, Mungall CJ, Karpen GH",
            "evidence": [
                {
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                    "id": "Q9VTM3",
                    "url": "https://www.uniprot.org/uniprot/Q9VTM3"
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                {
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                    "id": "M9PC80",
                    "url": "https://www.uniprot.org/uniprot/M9PC80"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "17569856",
                    "url": "https://glygen.org/publication/PubMed/17569856"
                }
            ]
        },
        {
            "title": "Sequence finishing and mapping of Drosophila melanogaster heterochromatin.",
            "journal": "Science",
            "date": "2007",
            "authors": "Hoskins RA, Carlson JW, Kennedy C, Acevedo D, Evans-Holm M, Frise E, Wan KH, Park S, Mendez-Lago M, Rossi F, Villasante A, Dimitri P, Karpen GH, Celniker SE",
            "evidence": [
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                {
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                    "id": "M9PC80",
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                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "17569867",
                    "url": "https://glygen.org/publication/PubMed/17569867"
                }
            ]
        }
    ],
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        {
            "id": "dme:Dmel_CG6053",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG6053",
            "resource": "KEGG Pathway"
        }
    ],
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            {
                "name": "Cellular Component",
                "total": 3,
                "go_terms": [
                    {
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                        "id": "GO:0030425",
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