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1351 COX8A

1351

COX8A

cytochrome c oxidase subunit 8A

protein-coding

Homo sapiens

基因描述

Type Description
Definition cytochrome c oxidase subunit 8A

研究结论

Date Results Publications
2016-07-02 11:47:00 COX8A is indispensable for function of human complex IV and its mutation causes Leigh-like syndrome and epilepsy. 26685157
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 20877624

名称对应

Type IDs
Synonymous COX, COX8, COX8-2, COX8L, VIII, VIII-L
Gene
UniProtKB-ID: COX8A_HUMAN, Q53XN1_HUMAN
UniprotKB: P10176, Q53XN1
UniParc: UPI000004CF5F
EMBL: CH471076, CR407687, AK311934, J04823, BC063025, BT009803
Ensembl: ENSG00000176340
KO: hsa:1351
Nucleutide sequences
EMBL-CDS: AAH63025.1, AAA99313.1, BAG34875.1, EAW74186.1, CAG28615.1, AAP88805.1
Gene_ORFName: hCG_27157
Ensembl_TRS: ENST00000314133
Protein sequencees
Ensembl_PRO: ENSP00000321260
RefSeq: NP_004065.1
Others
UniRef100: UniRef100_P10176
UniRef90: UniRef90_P10176
UniRef50: UniRef50_P10176
UniGene: Hs.743989
CCDS: CCDS8054.1

全选

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研究热度

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