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Gene entry

COX15

cytochrome c oxidase assembly factor COX15

Chromosome
10
Cytoband
10q24.2
Variants (rsID)
13

COX15 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q24.2). Its official name is “cytochrome c oxidase assembly factor COX15”. The reference table lists 13 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs2281636Benignsingle nucleotide variantLeigh syndrome
  • rs777532861Conflicting interpretationssingle nucleotide variantLeigh syndrome
  • rs79410539Conflicting interpretationssingle nucleotide variantLeigh syndrome
  • rs397514662Likely pathogenicsingle nucleotide variantCardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
  • rs28939711Pathogenicsingle nucleotide variantCardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
  • rs76530337Uncertain significancesingle nucleotide variantLeigh syndrome

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.