COX6A1 Chromosome 12

Cytochrome c oxidase subunit 6A1
3 variants 3 Health Risk

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What This Gene Does
Cytochrome c oxidase (COX), the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. It 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 the electron transfer and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes polypeptide 1 (liver isoform) of subunit VIa, and polypeptide 1 is found in all non-muscle tissues. Polypeptide 2 (heart/muscle isoform) of subunit VIa is encoded by a different gene, and is present only in striated muscles. These two polypeptides share 66% amino acid sequence identity. It has been reported that there may be several pseudogenes on chromosomes 1, 6, 7q21, 7q31-32 and 12. However, only one pseudogene (COX6A1P) on chromosome 1p31.1 has been documented. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Mitochondrial complex IV: cytochrome c oxidase subunits
Locus Type
gene with protein product
Location
12q24.31
Ensembl
ENSG00000111775
Associated Conditions (1)
Charcot-Marie-Tooth disease recessive intermediate D
Key Variants
All Variants (3)
RSID Category Clinical Significance Conditions
RS2137030876 Health Risk Conflicting classifications of pathogenicity
RS61739965 Health Risk Conflicting classifications of pathogenicity Charcot-Marie-Tooth disease recessive intermediate D, Charcot-Marie-Tooth disease recessive intermediate D
RS587777783 Health Risk Pathogenic Charcot-Marie-Tooth disease recessive intermediate D, Charcot-Marie-Tooth disease recessive intermediate D
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