(Q21100866)

English

cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10

mammalian protein found in Homo sapiens

cytochrome c oxidase assembly protein
heme A: farnesyltransferase
cytochrome c oxidase assembly homolog 10
heme O synthase
cytochrome c oxidase subunit X
COX10
COX10, heme A:farnesyltransferase cytochrome c oxidase assembly factor
protoheme IX farnesyltransferase, mitochondrial
COX10 homolog, cytochrome c oxidase assembly protein, heme A: farnesyltransferase

In more languages

Statements

1 reference

13 November 2019

UniProt protein ID

Protohaem IX farnesyltransferase, mitochondria

1 reference

InterPro Release 71.0

http://www.ebi.ac.uk/interpro/protein/Q12887

UbiA prenyltransferase conserved site, protein family

1 reference

based on heuristic

inferred from protein domain or family

1 reference

13 November 2019

UniProt protein ID

1 reference

13 November 2019

UniProt protein ID

molecular function

transferase activity

determination method

1 reference

8 April 2019

UniProt protein ID

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

farnesyltranstransferase activity

determination method

1 reference

8 April 2019

Isolation of a human cDNA for heme A:farnesyltransferase by functional complementation of a yeast cox10 mutant

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

cytochrome-c oxidase activity

determination method

1 reference

8 April 2019

Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency

HUGO Gene Nomenclature Committee

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

transferase activity, transferring alkyl or aryl (other than methyl) groups

determination method

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

determination method

1 reference

8 April 2019

UniProt protein ID

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

cytochrome complex

determination method

1 reference

8 April 2019

Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency

British Heart Foundation

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

mitochondrial inner membrane

determination method

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

determination method

1 reference

8 April 2019

Human Protein Atlas

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

determination method

5 references

8 April 2019

UniProt protein ID

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

8 April 2019

Ensembl genome database project

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

8 April 2019

Human Protein Atlas

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

8 April 2019

Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1

HUGO Gene Nomenclature Committee

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

8 April 2019

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

determination method

1 reference

8 April 2019

Human Protein Atlas

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

biological process

cytochrome complex assembly

determination method

1 reference

8 April 2019

Ensembl genome database project

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

mitochondrial fission

determination method

1 reference

8 April 2019

Ensembl genome database project

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

mitochondrion organization

determination method

1 reference

8 April 2019

Ensembl genome database project

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

aerobic respiration

determination method

1 reference

8 April 2019

Ensembl genome database project

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

mitochondrial electron transport, cytochrome c to oxygen

determination method

1 reference

8 April 2019

Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency

HUGO Gene Nomenclature Committee

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

respiratory chain complex IV assembly

determination method

1 reference

8 April 2019

Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1

HUGO Gene Nomenclature Committee

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

cellular respiration

determination method

1 reference

27 March 2018

A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency

HUGO Gene Nomenclature Committee

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q12887&geneProductId=UniProtKB:Q12887

determination method

heme O biosynthetic process

determination method

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

proton transmembrane transport

determination method

1 reference

8 April 2019

Gene Ontology Consortium

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887

determination method

UbiA prenyltransferase conserved site

1 reference

InterPro Release 71.0

http://www.ebi.ac.uk/interpro/protein/Q12887

Identifiers

RefSeq protein ID

1 reference

30 May 2020

UniProt protein ID

1 reference

13 November 2019

UniProt protein ID

Ensembl protein ID

ENSP00000261643

1 reference

Ensembl Release 99

Ensembl protein ID

ENSP00000261643

ENSP00000397750

1 reference

Ensembl Release 99

Ensembl protein ID

ENSP00000397750

ENSP00000462190

1 reference

Ensembl Release 99

Ensembl protein ID

ENSP00000462190

ENSP00000462512

1 reference

Ensembl Release 99

Ensembl protein ID

ENSP00000462512

ENSP00000499396

1 reference

Ensembl Release 99

Ensembl protein ID

ENSP00000499396

ENSP00000499450

1 reference

Ensembl Release 99

Ensembl protein ID

ENSP00000499450

0 references

Sitelinks

Wikipedia(3 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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