cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10

Preferred Label : cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10;

Approved symbol HGNC : COX10;

Name synonyms HGNC : heme O synthase; mitochondrial; protoheme IX farnesyltransferase;

Chromosome HGNC : 17p12;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000006695;

Details

Origin ID

HGNC:2260;

UMLS CUI

C1413629;

Automatic exact mappings (from CISMeF team)
- Cytochrome C oxidase assembly factor cox10 [OMIM gene]
- Mitochondrial inheritance [HPO term]
- Mitochondrion [NCIt concept]
- Muscular Dystrophy Secondary to Mitochondrial Disorder [NCIt concept]
- NADH:ubiquinone oxidoreductase core subunit S3 [ORDO Gene]
- cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 [ORDO Gene]
OMIM gene
- Cytochrome C oxidase assembly factor cox10 [OMIM gene]
Orphanet gene
- cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- COX10 gene [LOINC component]
- Cytochrome C oxidase assembly factor cox10 [OMIM gene]

Keyword's position in hierarchy(ies) :

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