HCCS Back

holocytochrome c synthase (cytochrome c heme-lyase)

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NCBI Description of HCCS
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.

Community Annotation of HCCS Add / Edit HCCS: Annotations

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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

HCCS is highly significantly mutated in
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HCCS is significantly mutated in
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HCCS is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for HCCS