靶标：
HCCS
产品别名：
CCHL； LSDMCA1； MCOPS7； MLS； HCCS； holocytochrome c synthase； holocytochrome c synthase； holocytochrome c-type synthase； cytochrome c heme-lyase； cytochrome c-type heme lyase； holocytochrome-c synthetase； microphthalamia with linear skin defects； microphthalmia with linear skin defects； 全细胞色素C合成酶； 全细胞色素C合酶(HCCS)；
背景信息：
holocytochrome c synthase(HCCS) Homo sapiens 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],
