Genes in panel

Fetal anomalies

Gene: CPOX

Amber List (moderate evidence)

CPOX (coproporphyrinogen oxidase)
EnsemblGeneIds (GRCh38): ENSG00000080819
EnsemblGeneIds (GRCh37): ENSG00000080819
OMIM: 612732, Gene2Phenotype
CPOX is in 10 panels

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History Filter Activity

9 Mar 2026, Gel status: 2

Created, Added New Source, Set mode of inheritance

Arina Puzriakova (Genomics England Curator)

gene: CPOX was added gene: CPOX was added to Fetal anomalies. Sources: Expert Review Amber Mode of inheritance for gene: CPOX was set to BIALLELIC, autosomal or pseudoautosomal