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180441 sel-12

180441

sel-12

Presenilin sel-12

protein-coding

Caenorhabditis elegans

基因描述

Type Description
Definition Presenilin sel-12

研究结论

Date Results Publications
2019-03-02 10:34:00 Mutations in the C. elegans gene encoding a PSEN homolog, sel-12 result in mitochondrial metabolic defects that promote neurodegeneration as a result of oxidative stress. 29989545
2016-09-17 10:12:00 mutations in sel-12 result in defects in calcium homeostasis, leading to mitochondrial dysfunction 26500256
2010-01-21 00:00:00 Data report the cloning and characterization of spr-3 and spr-4, which encode large basic zinc-finger proteins which act as transcriptional repressors for sel-12 [spr-3 and spr-4]. 12668626
2010-01-21 00:00:00 A genetic null allele mutant, sel-12(ar171), showed resistance to oxidative stress and prevented mitochondrial dysfunction-induced apoptosis. 12556527
2010-01-21 00:00:00 spr-2 mutations do not suppress sel-12 by affecting nonsense mediated decay, and increase the levels of sel-12 transcripts with premature translation termination codons. 19302704

名称对应

Type IDs
Gene
UniProtKB-ID: PSN_CAEEL
UniprotKB: P52166
UniParc: UPI00001327DF
EMBL: AF171064, BX284606, U35660
EnsemblGenome: WBGene00004769
KO: cel:CELE_F35H12.3
Nucleutide sequences
EMBL-CDS: AAD50991.1, AAA85511.1, CCD70617.1
Gene_ORFName: F35H12.3
EnsemblGenome_TRS: F35H12.3.1
Protein sequencees
EnsemblGenome_PRO: F35H12.3.1
RefSeq: NP_508175.1
Others
UniRef100: UniRef100_P52166
UniRef90: UniRef90_P52166
UniRef50: UniRef50_P52166
UniGene: Cel.19557

全选

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