ATP13A2 Back

ATPase type 13A2

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NCBI Description of ATP13A2
This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.

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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

ATP13A2 is highly significantly mutated in
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ATP13A2 is significantly mutated in
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ATP13A2 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 ATP13A2