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32142 ATP7

32142

ATP7

ATP7

protein-coding

Drosophila melanogaster

基因描述

Type Description
Definition ATP7

研究结论

Date Results Publications
2017-07-29 12:39:00 ATP7 Mutation is associated with Menkes and Wilson Diseases, Motor Neuropathy, and Susceptibility to Alzheimer's Disease. 28119449
2016-08-27 11:57:00 This study showed ATP7A mutations impair copper metabolism resulting in neurodegeneration and neurodevelopmental defects in Menkes disease. 25583185
2013-12-14 12:02:00 Using a model of HD, we found that altered expression of Ctr1B or ATP7 in the brain, or modulation of dietary copper availability, significantly modified the phenotypes caused by human Htt exon1-polyQ expression. 23980182
2012-12-29 10:26:00 -regulation of ATP7 specifically in the SIFamide-expressing neurons resulted in male-male courtship behavior 22981378
2010-11-27 10:11:00 These results demonstrate DmATP7 is able to functionally compensate for the absence of ATP7A, with important trafficking motifs conserved in these distantly related orthologues. 20372979

名称对应

Type IDs
Synonymous CG1886, DmATP7, Dmel\CG1886, dmATP7, lincRNA.S9122
Gene
UniProtKB-ID: Q9VYT4_DROME
UniprotKB: Q9VYT4
UniParc: UPI0001914A42
EMBL: AE014298
EnsemblGenome: FBgn0030343
KO: dme:Dmel_CG1886
Nucleutide sequences
EMBL-CDS: AAF48104.3, AGB95309.1
Gene_ORFName: CG1886, Dmel_CG1886
EnsemblGenome_TRS: FBtr0334454, FBtr0273257
Protein sequencees
EnsemblGenome_PRO: FBpp0271765, FBpp0306530
RefSeq: NP_572756.3, NP_001259466.1
Others
UniRef100: UniRef100_Q9VYT4
UniRef90: UniRef90_Q9VYT4
UniRef50: UniRef50_Q9VYT4
UniGene: Dm.18759

全选

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研究热度

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