{ "uniprot_canonical_ac": "Q9W3F1-1", "uniprot_ac": "Q9W3F1", "uniprot_id": "Q9W3F1_DROME", "mass": { "chemical_mass": 31013.0, "monoisotopic_mass": 31013.0 }, "refseq": { "ac": "NP_572481", "name": "uncharacterized protein", "summary": "", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572481" }, "gene_names": [ { "name": "144701_at", "resource": "UniProtKB", "type": "recommended", "url": "https://www.uniprot.org/uniprot/Q9W3F1", "id": "Q9W3F1" }, { "name": "144701_at; Dmel\\CG12116", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572481", "id": "NP_572481" }, { "name": "CG12116", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572481", "id": "NP_572481" }, { "name": "CG12116", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q9W3F1", "id": "Q9W3F1" }, { "name": "Dmel\\CG12116", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q9W3F1", "id": "Q9W3F1" }, { "name": "Dmel_CG12116", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q9W3F1", "id": "Q9W3F1" } ], "protein_names": [ { "name": "CG12116-PA", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572481", "id": "NP_572481" }, { "name": "RE21057p", "resource": "UniProtKB", "type": "synonym", "url": "", "id": "Q9W3F1" }, { "name": "uncharacterized protein", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572481", "id": "NP_572481" } ], "function": [], "disease": [ { "disease_id": "DOID:0111168", "recommended_name": { "id": "DOID:0111168", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0111168", "name": "sepiapterin reductase deficiency", "description": "A dystonia characterized by sustained muscle contractions with diurnal fluctuations, axial hypotonia, oculogyric crises, delays in motor and cognitive development and severe dopamine and serotonin deficiencies that has_material_basis_in mutation in the SPR gene on chromosome 2p resulting in sepiapterin reductase deficiency." }, "synonyms": [ { "id": "DOID:0111168", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0111168", "name": "DRD due to SRD", "description": "" }, { "id": "DOID:0111168", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0111168", "name": "dopa-responsive dystonia due to sepiapterin reductase deficiency", "description": "" }, { "id": "DOID:0111168", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0111168", "name": "SPR deficiency", "description": "" }, { "id": "DOID:0111168", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0111168", "name": "SRD", "description": "" }, { "id": "MONDO:0012994", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012994", "name": "dopa-responsive dystonia due to sepiapterin reductase deficiency", "description": "Dopa responsive dystonia (DRD) due to sepiapterin reductase deficiency (SRD) is a very rare neurometabolic disorder characterized by dystonia with diurnal fluctuations, axial hypotonia, oculogyric crises, and delays in motor and cognitive development." }, { "id": "MONDO:0012994", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012994", "name": "DRD due to SRD", "description": "" }, { "id": "MONDO:0012994", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012994", "name": "DYT-SPR", "description": "" }, { "id": "MONDO:0012994", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012994", "name": "SPR deficiency", "description": "" }, { "id": "MONDO:0012994", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012994", "name": "SRD", "description": "" }, { "id": "MONDO:0012994", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012994", "name": "autosomal recessive sepiapterin reductase-deficient DRD", "description": "" }, { "id": "MONDO:0012994", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012994", "name": "dopa-responsive dystonia due to sepiapterin reductase deficiency", "description": "" }, { "id": "MONDO:0012994", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012994", "name": "sepiapterin reductase deficiency", "description": "" }, { "id": "MONDO:0012994", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012994", "name": "dystonia, DOPA-responsive, due to sepiapterin reductase deficiency", "description": "" }, { "id": "MIM:612716", "resource": "MIM", "url": "https://www.omim.org/entry/612716", "name": "Dystonia, DOPA-responsive, due to sepiapterin reductase deficiency", "description": "Dystonia, DOPA-responsive, due to sepiapterin reductase deficiency" } ], "evidence": [ { "id": "0111168", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:0111168" } ] }, { "disease_id": "DOID:14330", "recommended_name": { "id": "DOID:14330", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:14330", "name": "Parkinson's disease", "description": "A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions." }, "synonyms": [ { "id": "DOID:14330", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:14330", "name": "Parkinson disease", "description": "" }, { "id": "DOID:14330", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:14330", "name": "paralysis agitans", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "late-onset Parkinson disease", "description": "A Parkinson disease that begins after around the age of 50." }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "LOPD", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "PARK", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "PD", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "Parkinson disease, age of onset, modifier, Multifactorial", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "Parkinson disease, late-onset", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "Parkinson disease, late-onset, susceptibility to, Multifactorial", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "Parkinson disease, susceptibility to, Multifactorial", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "autosomal dominant late-onset Parkinson disease", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "hereditary late onset Parkinson disease", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "hereditary late-onset Parkinson disease", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "late onset Parkinson disease", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "late onset Parkinson's disease", "description": "" }, { "id": "MONDO:0008199", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008199", "name": "late-onset Parkinson disease", "description": "" }, { "id": "MIM:168600", "resource": "MIM", "url": "https://www.omim.org/entry/168600", "name": "Parkinson disease", "description": "Parkinson disease" } ], "evidence": [ { "id": "14330", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:14330" } ] }, { "disease_id": "DOID:543", "recommended_name": { "id": "DOID:543", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:543", "name": "dystonia", "description": "A movement disease that is characterized by involuntary muscle contractions causing repetitive or twisting movements." }, "synonyms": [ { "id": "DOID:543", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:543", "name": "dystonic disease", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "early-onset generalized limb-onset dystonia", "description": "A rare movement disorder characterized by involuntary, repetitive, sustained muscle contractions or postures involving one or more sites of the body." }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "DYT-TOR1A", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "DYT1", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "EOTD", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "Oppenheim dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "Oppenheim's dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "dystonia musculorum deformans", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "dystonia-1, torsion", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "early onset primary dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "early onset torsion dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "early-onset generalised torsion dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "early-onset generalized limb-onset dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "early-onset generalized torsion dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "early-onset primary dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "early-onset torsion dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "idiopathic dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "torsion dystonia type 1", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "DYT-TOR1A dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "Dyt1", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "Early-onset Primary dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "Early-onset torsion dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "Primary torsion dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "dystonia 1", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "dystonia 1, torsion, Autosomal dominant", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "dystonia 1, torsion, autosomal dominant", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "dystonia musculorum deformans 1", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "idiopathic dystonia DYT1", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "idiopathic torsion dystonia", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "torsion dystonia 1", "description": "" }, { "id": "MONDO:0007492", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007492", "name": "torsion dystonia 1, autosomal dominant", "description": "" }, { "id": "MIM:128100", "resource": "MIM", "url": "https://www.omim.org/entry/128100", "name": "Dystonia 1, torsion, autosomal dominant", "description": "Dystonia 1, torsion, autosomal dominant" } ], "evidence": [ { "id": "543", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:543" } ] } ], "snv": [], "mutagenesis": [], "expression_tissue": [], "expression_disease": [], "species": [ { "name": "Drosophila melanogaster", "taxid": 7227, "evidence": [ { "database": "UniProtKB", "id": "Q9W3F1", "url": "https://www.uniprot.org/uniprot/Q9W3F1" } ], "common_name": "Fruit fly" } ], "gene": [ { "name": "144701_at", "url": "https://www.uniprot.org/uniprot/Q9W3F1", "locus": { "chromosome": "X", "start_pos": 8467443, "end_pos": 8469012, "strand": "+", "evidence": [ { "database": "Ensembl Gene", "id": "FBgn0030041", "url": "https://www.ensembl.org/id/FBgn0030041" } ] } } ], "crossref": [ { "id": "FBgn0030041", "url": "https://bgee.org/?page=gene&gene_id=FBgn0030041", "database": "Bgee", "categories": [ "Gene Expression" ] }, { "id": "cd05367", "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd05367", "database": "CDD", "categories": [ "Protein Classification" ] }, { "id": "FBgn0030041", "url": "https://flybase.org/reports/FBgn0030041", "database": "FlyBase", "categories": [ "Organism-specific" ] }, { "id": "31782", "url": "https://www.ncbi.nlm.nih.gov/gene/31782", "database": "GeneID", "categories": [ "Genome Annotation" ] }, { "id": "Q9W3F1", "url": "https://www.ebi.ac.uk/intact/interactors/id:Q9W3F1*", "database": "IntAct", "categories": [ "Other" ] }, { "id": "IPR002347", "url": "https://www.ebi.ac.uk/interpro/entry/IPR002347", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR036291", "url": "https://www.ebi.ac.uk/interpro/entry/IPR036291", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "dme:Dmel_CG12116", "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG12116", "database": "KEGG Pathway", "categories": [ "Enzyme and Pathway" ] }, { "id": "YVQHQLY", "url": "https://omabrowser.org/oma/group/YVQHQLY/", "database": "OMA", "categories": [ "Protein Classification" ] }, { "id": "64672at2759", "url": "http://www.orthodb.org/?query=64672at2759", "database": "OrthoDB", "categories": [ "Protein Classification" ] }, { "id": "PTHR44085", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR44085", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PTHR44085:SF2", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR44085:SF2", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PF00106", "url": "http://pfam.xfam.org/family/PF00106", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "NP_572481", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572481", "database": "RefSeq", "categories": [ "Protein" ] }, { "id": "Q9W3F1", "url": "https://www.uniprot.org/uniprot/Q9W3F1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q9W3F1-1", "url": "https://www.uniprot.org/uniprot/Q9W3F1-1", "database": "UniProtKB", "categories": [ "Protein" ] } ], "sequence": { "sequence": "MAAKRMDLNRRTFLVLSGSSNPLGQSLALEFCRRLATGSLALILDEDQEQLRELENHLRSELKTENVKVTIGKLDKDHSNGVQLMEQALMDNFMADKDNQRFERSIILHNEGKAATHMLLEPQSDDDWKAYVQQQLYAPVALNQTWLQSKHLERVEKLAVNVTSSLMVRPLVHAGLLCSCKRARDMYFRAMAAEEYRFGVHVLSFSPGLMDTHEGQCDVNGNRITPADLIATKQLLQLPRIKPCQATLKLINILEEISFVSGHDVDYYDTFVL", "length": 273, "header": "tr|Q9W3F1-1|Q9W3F1_DROME Isoform 1 of RE21057p OS=Drosophila melanogaster OX=7227 GN=144701_at PE=2 SV=1 CANONICAL=Q9W3F1-1" }, "isoforms": [ { "isoform_ac": "Q9W3F1-1", "url": "", "sequence": { "sequence": "MAAKRMDLNRRTFLVLSGSSNPLGQSLALEFCRRLATGSLALILDEDQEQLRELENHLRSELKTENVKVTIGKLDKDHSNGVQLMEQALMDNFMADKDNQRFERSIILHNEGKAATHMLLEPQSDDDWKAYVQQQLYAPVALNQTWLQSKHLERVEKLAVNVTSSLMVRPLVHAGLLCSCKRARDMYFRAMAAEEYRFGVHVLSFSPGLMDTHEGQCDVNGNRITPADLIATKQLLQLPRIKPCQATLKLINILEEISFVSGHDVDYYDTFVL", "length": 273, "header": "tr|Q9W3F1-1|Q9W3F1_DROME Isoform 1 of RE21057p OS=Drosophila melanogaster OX=7227 GN=144701_at PE=2 SV=1 CANONICAL=Q9W3F1-1" }, "locus": { "chromosome": "X", "start_pos": 8468754, "end_pos": 8467936, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "FBtr0071240", "url": "https://www.ensembl.org/id/FBtr0071240" }, { "database": "Ensembl Peptide", "id": "FBpp0071183", "url": "https://www.ensembl.org/id/FBpp0071183" } ] } } ], "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": "Q9W3F1", "url": "https://www.uniprot.org/uniprot/Q9W3F1" } ], "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": "Q9W3F1", "url": 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