Source:http://linkedlifedata.com/resource/umls/id/C2697531
NCI: Human HCCS wild-type allele is located in the vicinity of Xp22.3 and is approximately 12 kb in length. This allele, which encodes cytochrome c-type heme lyase protein, may play a role in electron transport. Mutations in the gene are associated with syndromic microphthalmia 7.