| Protein Name | holocytochrome c synthase |
|---|---|
| Organism | Homo sapiens |
| Gene ID | 3052 |
| Gene Symbol | HCCS |
| UniProt | P53701 (CCHL_HUMAN), A0A024RBY9 (A0A024RBY9_HUMAN) |
| Relationships |
Total Number of functionally related compound(s) :
90
Total Number of Articles : 99 |
Description |
holocytochrome c synthase |
| Gene 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] |
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| Properties | |