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COX11 cytochrome c oxidase copper chaperone COX11

Gene ID: 1353, updated on 3-Nov-2024
Gene type: protein coding
Also known as: COX11P; MC4DN23

Summary

Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be a heme A biosynthetic enzyme involved in COX formation, according to the yeast mutant studies. However, the studies in Rhodobacter sphaeroides suggest that this gene is not required for heme A biosynthesis, but required for stable formation of the Cu(B) and magnesium centers of COX. This human protein is predicted to contain a transmembrane domain localized in the mitochondrial inner membrane. Multiple transcript variants encoding different isoforms have been found for this gene. A related pseudogene has been found on chromosome 6. [provided by RefSeq, Jun 2009]

Associated conditions

See all available tests in GTR for this gene

DescriptionTests
Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
GeneReviews: Not available
Mitochondrial complex IV deficiency, nuclear type 23
MedGen: C5830322OMIM: 620275GeneReviews: Not available
not available

Genomic context

Location:
17q22
Sequence:
Chromosome: 17; NC_000017.11 (54951902..54968785, complement)
Total number of exons:
6

Links

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