Type | Description |
---|---|
Definition | ATP7 |
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 |
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
|
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Refseq |
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