The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene.
Immunogen Information
Immunogen
Fusion protein of human HCCS
Swissprot
P53701
Synonyms
CCHLCCHLcytochrome c heme-lyaseCytochrome c-type heme lyaseDKFZp779I1858EC 4.4.1.17HccsHolocytochrome c synthase (cytochrome c heme lyase)Holocytochrome c synthaseHolocytochrome c type synthaseHolocytochrome c-type synthaseMCOPS7OTTHUMP0000002