ANO10 Back

anoctamin 10

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NCBI Description of ANO10

The transmembrane protein encoded by this gene is a member of a family of calcium-activated chloride channels. Defects in this gene may be a cause of autosomal recessive spinocerebellar ataxia-10. Several transcript variants encoding different isoforms have been found for this gene.

Community Annotation of ANO10 Add / Edit ANO10: 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).


ANO10 is highly significantly mutated in
ANO10 is significantly mutated in
ANO10 is near significance in

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

Data details

Mutation list for ANO10