HCCS wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human HCCS wild-type allele is located in the vicinity of Xp22.2 and is approximately 12 kb in length. This allele, which encodes holocytochrome c-type synthase protein, may play a role in electron transport. Mutations in the gene are associated with syndromic microphthalmia 7.

**Synonyms:** - CCHL - DKFZp779I1858 - Holocytochrome C Synthase (Cytochrome C Heme-Lyase) wt Allele - MCOPS7