Official Full Name
holocytochrome c synthase
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.
HCCS; holocytochrome c synthase; holocytochrome c synthase (cytochrome c heme lyase); cytochrome c-type heme lyase; CCHL; cytochrome c heme lyase; OTTHUMP00000022904; OTTHUMP00000022905; DKFZp779I1858; EC 184.108.40.206; Holocytochrome c type synthase; MCOPS7; OTTHUMP00000022903; OTTMUSP00000021173; OTTMUSP00000021174; RGD1563855; RP23-37L2.1; cytochrome c heme-lyase; holocytochrome c-type synthase; holocytochrome c synthase (cytochrome c heme-lyase)