Gene entry
CPOX
coproporphyrinogen oxidase
- Chromosome
- 3
- Cytoband
- 3q11.2
- Variants (rsID)
- 13
CPOX is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q11.2). Its official name is “coproporphyrinogen oxidase”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs1131857Benignsingle nucleotide variantHereditary coproporphyria|Acute intermittent porphyria
- rs11921054Benignsingle nucleotide variantHereditary coproporphyria
- rs1729995Benignsingle nucleotide variantHereditary coproporphyria
- rs7103Benignsingle nucleotide variantHereditary coproporphyria
- rs121917868Pathogenicsingle nucleotide variantHarderoporphyria
- rs28931603Uncertain significancesingle nucleotide variantCoproporphyria|Hereditary coproporphyria
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.