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1352 COX10

1352

COX10

cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10

protein-coding

Homo sapiens

基因描述

Type Description
Definition cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10

研究结论

Date Results Publications
2021-02-06 13:51:00 A Novel COX10 Deletion Polymorphism as a Susceptibility Factor for Sudden Cardiac Death Risk in Chinese Populations. 33180568
2015-12-05 10:59:00 On the basis of its pivotal role in regulating cell death upon COX dysfunction, CerS6 might potentially represent a novel target for therapeutic intervention in mitochondrial diseases caused by COX dysfunction. 25766330
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 20877624
2010-08-23 11:43:00 ISCU and COX10 are target genes of miR-210 related to mitochondrial metabolism 20498629
2010-04-12 11:04:00 COX 15 mRNA was significantly more abundant in the cerebral tissue of Alzheimer's disease (AD) patients and COX10 and COX15 SNP were significantly less represented in the patient group, suggesting a possible protective role toward the risk for AD 19826901

名称对应

Type IDs
Gene
UniProtKB-ID: COX10_HUMAN
UniprotKB: Q12887
UniParc: UPI00017A7114, UPI000013D1C8
EMBL: U82007, BC006394, U82008, AK295925, BT006985, U82010, U82006, U82004, BC000060, U82005, AC005389, U82009, AC005224, U09466, AK312718
Ensembl: ENSG00000006695
KO: hsa:1352
Nucleutide sequences
EMBL-CDS: AAA21148.1, AAC51330.1, AAH00060.1, BAG35592.1, BAG58712.1, AAP35631.1, AAH06394.1
Ensembl_TRS: ENST00000261643, ENST00000664217
Protein sequencees
Ensembl_PRO: ENSP00000261643, ENSP00000499396
RefSeq: NP_001294.2
Others
UniRef100: UniRef100_Q12887
UniRef90: UniRef90_Q12887
UniRef50: UniRef50_Q12887
UniGene: Hs.462278
CCDS: CCDS11166.1

全选

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