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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