COA7 Chromosome 1

Cytochrome c oxidase assembly factor 7
9 variants 9 Health Risk

Upload your DNA to see your personal genotypes for variants in COA7.

What This Gene Does
Enables protein-disulfide reductase activity. Involved in respiratory chain complex IV assembly. Located in mitochondrion and nucleoplasm. Is active in mitochondrial intermembrane space. Implicated in spinocerebellar ataxia with axonal neuropathy type 3. [provided by Alliance of Genome Resources, Jul 2025]
Gene Info
Gene Group
Mitochondrial respiratory chain complex assembly factors
Locus Type
gene with protein product
Location
1p32.3
Ensembl
ENSG00000162377
Associated Conditions (3)
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 3
Key Variants
All Variants (9)
RSID Category Clinical Significance Conditions
RS1553254475 Health Risk Likely pathogenic
RS2149904888 Health Risk Likely pathogenic
RS767873164 Health Risk Likely pathogenic Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3
RS780593265 Health Risk Likely pathogenic
RS1197945739 Health Risk Pathogenic Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3
RS1558102448 Health Risk Pathogenic Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3
RS1558102464 Health Risk Pathogenic Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3
RS780572767 Health Risk Pathogenic Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3
RS961876891 Health Risk Pathogenic Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3
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