Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10
P688
A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiencyCytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiencyIsolation of a human cDNA for heme A:farnesyltransferase by functional complementation of a yeast cox10 mutant
P921
Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
COX10
@uk
Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10
@en
Protohäm-IX-Farnesyltransferase
@de
type
label
COX10
@uk
Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10
@en
Protohäm-IX-Farnesyltransferase
@de
altLabel
COX10 homolog, cytochrome c oxidase assembly protein, heme A: farnesyltransferase
@en
COX10
@en
COX10, heme A:farnesyltransferase cytochrome c oxidase assembly factor
@en
cytochrome c oxidase assembly homolog 10
@en
cytochrome c oxidase assembly protein
@en
cytochrome c oxidase subunit X
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heme A: farnesyltransferase
@en
heme O synthase
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protoheme IX farnesyltransferase, mitochondrial
@en
prefLabel
COX10
@uk
Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10
@en
Protohäm-IX-Farnesyltransferase
@de
P680
P681
P682
P705
P352
P637
P31
P352
P637
P680
P681
P682
P702
P703
P705
ENSP00000261643
ENSP00000397750
ENSP00000462190
ENSP00000462512
ENSP00000499396
ENSP00000499450