| Gene Symbol | HCCS |
| Entrez Gene ID | 3052 |
| Full Name | holocytochrome c synthase |
| Synonyms | CCHL,LSDMCA1,MCOPS7,MLS |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | 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]. |
| Disorder MIM: | |
| Disorder Html: | Linear skin defects with multiple congenital anomalies 1, 309801 (3) |
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