# cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21100866](https://www.wikidata.org/wiki/Q21100866)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/COX10)  
**Source**: https://4ort.xyz/entity/cytochrome-c-oxidase-assembly-factor-heme-a-farnesyltransferase-cox10


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q12887)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887)
5. [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)
6. [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](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887)
7. [Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887)
8. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887)
9. [A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q12887&geneProductId=UniProtKB:Q12887)
10. [A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q12887)
11. Ensembl Release 99