{ "uniprot_canonical_ac": "Q961K6-1", "uniprot_ac": "Q961K6", "uniprot_id": "Q961K6_DROME", "mass": { "chemical_mass": 67175.0, "monoisotopic_mass": 67175.0 }, "refseq": { "ac": "NP_001286874", "name": "uncharacterized protein, isoform B", "summary": "", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286874" }, "gene_names": [ { "name": "Dmel\\CG3829", "resource": "UniProtKB", "type": "recommended", "url": "https://www.uniprot.org/uniprot/Q961K6", "id": "Q961K6" }, { "name": "CG3829", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286874", "id": "NP_001286874" }, { "name": "CG3829", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q961K6", "id": "Q961K6" }, { "name": "Dmel\\CG3829", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286874", "id": "NP_001286874" }, { "name": "Dmel_CG3829", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q961K6", "id": "Q961K6" } ], "protein_names": [ { "name": "CG3829-PB", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286874", "id": "NP_001286874" }, { "name": "GH19047p", "resource": "UniProtKB", "type": "synonym", "url": "", "id": "Q961K6" }, { "name": "Uncharacterized protein, isoform A", "resource": "UniProtKB", "type": "synonym", "url": "", "id": "Q961K6" }, { "name": "Uncharacterized protein, isoform B", "resource": "UniProtKB", "type": "synonym", "url": "", "id": "Q961K6" }, { "name": "uncharacterized protein, isoform B", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286874", "id": "NP_001286874" } ], "function": [], "disease": [ { "disease_id": "DOID:0111444", "recommended_name": { "id": "DOID:0111444", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0111444", "name": "progressive myoclonus epilepsy 4", "description": "A progressive myoclonus epilepsy characterized by progressive myoclonic epilepsy often associated with renal failure that has_material_basis_in homozygous or compound heterozygous of mutation in the SCARB2 gene on chromosome 4q21.1." }, "synonyms": [ { "id": "DOID:0111444", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0111444", "name": "AMRF", "description": "" }, { "id": "DOID:0111444", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0111444", "name": "EPM4", "description": "" }, { "id": "DOID:0111444", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0111444", "name": "Myoclonus-nephropathy syndrome", "description": "" }, { "id": "DOID:0111444", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0111444", "name": "action myoclonus-renal failure syndrome", "description": "" }, { "id": "MONDO:0009699", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009699", "name": "action myoclonus-renal failure syndrome", "description": "Action myoclonus-renal failure syndrome (AMRF) is a rare epilepsy syndrome characterized by progressive myoclonus epilepsy in association with primary glomerular disease. Patients present with neurologic symptoms (including tremor, action myoclonus, tonic-clonic seizures, later ataxia and dysarthria) that may precede, occur simultaneously or be followed by renal manifestations including proteinuria that progresses to nephrotic syndrome and end-stage renal disease. In some patients, sensorimotor peripheral neuropathy, sensorineural hearing loss and dilated cardiomyopathy are associated symptoms." }, { "id": "MONDO:0009699", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009699", "name": "AMRF", "description": "" }, { "id": "MONDO:0009699", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009699", "name": "EPM4", "description": "" }, { "id": "MONDO:0009699", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009699", "name": "action myoclonus-renal failure syndrome", "description": "" }, { "id": "MONDO:0009699", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009699", "name": "epilepsy, progressive myoclonic 4, with or without renal failure", "description": "" }, { "id": "MONDO:0009699", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009699", "name": "epilepsy, progressive myoclonic, 4, with or without renal failure", "description": "" }, { "id": "MONDO:0009699", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009699", "name": "myoclonus-nephropathy syndrome", "description": "" }, { "id": "MONDO:0009699", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009699", "name": "progressive myoclonic epilepsy type 4", "description": "" }, { "id": "MIM:254900", "resource": "MIM", "url": "https://www.omim.org/entry/254900", "name": "Epilepsy, progressive myoclonic 4, with or without renal failure", "description": "Epilepsy, progressive myoclonic 4, with or without renal failure" } ], "evidence": [ { "id": "0111444", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:0111444" } ] }, { "disease_id": "DOID:891", "recommended_name": { "id": "DOID:891", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:891", "name": "progressive myoclonus epilepsy", "description": "A variable age at onset electroclinical syndrome characterised by a relentlessly progressive disease course until death." }, "synonyms": [ { "id": "DOID:891", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:891", "name": "PME", "description": "" }, { "id": "DOID:891", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:891", "name": "progressive myoclonic epilepsy", "description": "" }, { "id": "MONDO:0010682", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010682", "name": "obsolete myoclonic epilepsy, progressive, X-linked", "description": "" }, { "id": "MONDO:0010682", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010682", "name": "myoclonic epilepsy, progressive", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "Unverricht-Lundborg syndrome", "description": "Unverricht-Lundborg disease (ULD) is a rare progressive myoclonic epilepsy disorder characterized by action- and stimulus-sensitive myoclonus, and tonic-clonic seizures with ataxia, but with only a mild cognitive decline over time." }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "PME type 1", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "ULD", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "Unverricht - Lundborg disease", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "Unverricht's disease", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "Unverricht-Lundborg disease", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "Unverricht-Lundborg syndrome", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "progressive myoclonic epilepsy type 1", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "progressive myoclonus epilepsy type 1", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "Baltic myoclonic epilepsy", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "EPM1", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "Uld", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "epilepsy, progressive myoclonic type 1", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "epilepsy, progressive myoclonic, 1", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "epilepsy, progressive myoclonic, 1A", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "epilepsy, progressive myoclonus 1", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "myoclonic epilepsy of Unverricht and Lundborg", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "myoclonus progressive epilepsy of Unverricht and Lundborg", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "progressive myoclonic epilepsy", "description": "" }, { "id": "MONDO:0009698", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009698", "name": "progressive myoclonus epilepsy Baltic myoclonic epilepsy", "description": "" }, { "id": "MIM:254800", "resource": "MIM", "url": "https://www.omim.org/entry/254800", "name": "Epilepsy, progressive myoclonic 1", "description": "Epilepsy, progressive myoclonic 1" } ], "evidence": [ { "id": "891", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:891" } ] } ], "snv": [], "mutagenesis": [], "expression_tissue": [], "expression_disease": [], "species": [ { "name": "Drosophila melanogaster", "taxid": 7227, "evidence": [ { "database": "UniProtKB", "id": "Q961K6", "url": "https://www.uniprot.org/uniprot/Q961K6" } ], "common_name": "Fruit fly" } ], "gene": [ { "name": "Dmel\\CG3829", "url": "https://www.uniprot.org/uniprot/Q961K6", "locus": { "chromosome": "2R", "start_pos": 24990489, "end_pos": 24986044, "strand": "-", "evidence": [ { "database": "Ensembl Gene", "id": "FBgn0035091", "url": "https://www.ensembl.org/id/FBgn0035091" } ] } } ], "crossref": [ { "id": "FBgn0035091", "url": "https://bgee.org/?page=gene&gene_id=FBgn0035091", "database": "Bgee", "categories": [ "Gene Expression" ] }, { "id": "FBgn0035091", "url": "https://flybase.org/reports/FBgn0035091", "database": "FlyBase", "categories": [ "Organism-specific" ] }, { "id": "38000", "url": "https://www.ncbi.nlm.nih.gov/gene/38000", "database": "GeneID", "categories": [ "Genome Annotation" ] }, { "id": "Q961K6", "url": "https://www.ebi.ac.uk/intact/interactors/id:Q961K6*", "database": "IntAct", "categories": [ "Other" ] }, { "id": "IPR002159", "url": "https://www.ebi.ac.uk/interpro/entry/IPR002159", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "dme:Dmel_CG3829", "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG3829", "database": "KEGG Pathway", "categories": [ "Enzyme and Pathway" ] }, { "id": "LNPRQED", "url": "https://omabrowser.org/oma/group/LNPRQED/", "database": "OMA", "categories": [ "Protein Classification" ] }, { "id": "315994at2759", "url": "http://www.orthodb.org/?query=315994at2759", "database": "OrthoDB", "categories": [ "Protein Classification" ] }, { "id": "PTHR11923", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR11923", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PTHR11923:SF50", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR11923:SF50", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PF01130", "url": "http://pfam.xfam.org/family/PF01130", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "PR_Q961K6", "url": "http://purl.obolibrary.org/obo/PR_Q961K6", "database": "PRO", "categories": [ "Protein" ] }, { "id": "R-DME-114608", "url": "https://www.reactome.org/PathwayBrowser/#R-DME-114608", "database": "Reactome", "categories": [ "Protein Classification" ] }, { "id": "R-DME-1236973", "url": "https://www.reactome.org/PathwayBrowser/#R-DME-1236973", "database": "Reactome", "categories": [ "Protein Classification" ] }, { "id": "R-DME-434313", "url": "https://www.reactome.org/PathwayBrowser/#R-DME-434313", "database": "Reactome", "categories": [ "Protein Classification" ] }, { "id": "R-DME-6798695", "url": "https://www.reactome.org/PathwayBrowser/#R-DME-6798695", "database": "Reactome", "categories": [ "Protein Classification" ] }, { "id": "NP_001286874", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286874", "database": "RefSeq", "categories": [ "Protein" ] }, { "id": "Q961K6", "url": "https://www.uniprot.org/uniprot/Q961K6", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q961K6-1", "url": "https://www.uniprot.org/uniprot/Q961K6-1", "database": "UniProtKB", "categories": [ "Protein" ] } ], "sequence": { "sequence": "MSHTKDAEMSMPARQESDRTSAPSVTKSLTLNSTRSGVGTGNFGGYGMTNGAEKPSVLHMIMEALGLRNQAQNREPTSKDIGTLIMLGVMFLLFVISVTGFFVMWFTEYYNNTILENLILAENSDTANSWLNPDPKYDTLLKAHIFHYPNIDDYLAGRADKIKVVDVGPLTYQEHTVKDEVSFNKNFTVSFRDRKSYKFLPEKSSIGEHEVVRVPNVPLISAAGPVKRMKAFERLAVSTWIKQFKEPLFKNLTVSEYLWGYEDSIIKLKSLGRGRRRFGLLMSRNGTSVDSVQLNTGEDDITKFSIITQFNGMPQLDYWEGDECNRIDGSEPSMFSPHLLQDRSTVNVFLQVLCRKVPLHFEKEVTIYNDIDVLRYRTPMDVFSHPSKNPANQCYCQNTELCLPSGVINATKCYGDAPIFPSFPHFFTGDPVLYQDFEGIEPDAAVHQTYADIHPRFGFPISGASRVQINIMLDKTPILRNQGDRLKNTTILPLMWIEITSGDFSEEVLHTLYLSTFGLNAIQQTLKYGTLLISVTSFSLIVAGVYYLNSRREQQLQESKTSAELEALNGGENVIVVHHIDMPVPLPVQDGGIHQGT", "length": 597, "header": "tr|Q961K6-1|Q961K6_DROME Isoform 1 of GH19047p OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG3829 PE=2 SV=1 CANONICAL=Q961K6-1" }, "isoforms": [ { "isoform_ac": "Q961K6-1", "url": "", "sequence": { "sequence": "MSHTKDAEMSMPARQESDRTSAPSVTKSLTLNSTRSGVGTGNFGGYGMTNGAEKPSVLHMIMEALGLRNQAQNREPTSKDIGTLIMLGVMFLLFVISVTGFFVMWFTEYYNNTILENLILAENSDTANSWLNPDPKYDTLLKAHIFHYPNIDDYLAGRADKIKVVDVGPLTYQEHTVKDEVSFNKNFTVSFRDRKSYKFLPEKSSIGEHEVVRVPNVPLISAAGPVKRMKAFERLAVSTWIKQFKEPLFKNLTVSEYLWGYEDSIIKLKSLGRGRRRFGLLMSRNGTSVDSVQLNTGEDDITKFSIITQFNGMPQLDYWEGDECNRIDGSEPSMFSPHLLQDRSTVNVFLQVLCRKVPLHFEKEVTIYNDIDVLRYRTPMDVFSHPSKNPANQCYCQNTELCLPSGVINATKCYGDAPIFPSFPHFFTGDPVLYQDFEGIEPDAAVHQTYADIHPRFGFPISGASRVQINIMLDKTPILRNQGDRLKNTTILPLMWIEITSGDFSEEVLHTLYLSTFGLNAIQQTLKYGTLLISVTSFSLIVAGVYYLNSRREQQLQESKTSAELEALNGGENVIVVHHIDMPVPLPVQDGGIHQGT", "length": 597, "header": "tr|Q961K6-1|Q961K6_DROME Isoform 1 of GH19047p OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG3829 PE=2 SV=1 CANONICAL=Q961K6-1" }, "locus": { "chromosome": "2R", "start_pos": 24990292, "end_pos": 24988215, "strand": "-", "evidence": [ { "database": "Ensembl Transcript", "id": "FBtr0343506", "url": "https://www.ensembl.org/id/FBtr0343506" }, { "database": "Ensembl Peptide", "id": "FBpp0310111", "url": "https://www.ensembl.org/id/FBpp0310111" } ] } } ], "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": "Q961K6", "url": "https://www.uniprot.org/uniprot/Q961K6" } ], "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": "Q961K6", "url": "https://www.uniprot.org/uniprot/Q961K6" } ], "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": [ { "database": "UniProtKB", "id": "Q961K6", "url": "https://www.uniprot.org/uniprot/Q961K6" } ], "reference": [ { "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", "evidence": [ { "database": "UniProtKB", "id": "Q961K6", "url": "https://www.uniprot.org/uniprot/Q961K6" } ], "reference": [ { "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": [ { "database": "UniProtKB", "id": "Q961K6", "url": "https://www.uniprot.org/uniprot/Q961K6" } ], "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. 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