CYP4V2 Back

cytochrome P450, family 4, subfamily V, polypeptide 2

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NCBI Description of CYP4V2

This gene encodes a member of the cytochrome P450 hemethiolate protein superfamily which are involved in oxidizing various substrates in the metabolic pathway. It is implicated in the metabolism of fatty acid precursors into n-3 polyunsaturated fatty acids. Mutations in this gene result in Bietti crystalline corneoretinal dystrophy.

Community Annotation of CYP4V2 Add / Edit CYP4V2: 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).


CYP4V2 is highly significantly mutated in
CYP4V2 is significantly mutated in
CYP4V2 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for CYP4V2