APOL2 Back

apolipoprotein L, 2

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NCBI Description of APOL2

This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. Two transcript variants encoding the same protein have been found for this gene.

Community Annotation of APOL2 Add / Edit APOL2: 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).


APOL2 is highly significantly mutated in
APOL2 is significantly mutated in
combined cohort
14 patients (0%)
APOL2 is near significance in

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

Data details

Mutation list for APOL2