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HCCS

Official Full Name
holocytochrome c synthase
Organism
Homo sapiens
GeneID
3052
Background
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. [provided by RefSeq, Jan 2010]
Synonyms
MLS; CCHL; MCOPS7; LSDMCA1;

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