CPT2 Back

carnitine palmitoyltransferase II

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NCBI Description of CPT2

The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders.

Community Annotation of CPT2 Add / Edit CPT2: 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

CPT2 is highly significantly mutated in
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CPT2 is significantly mutated in
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CPT2 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 CPT2