KCNK9 Back

potassium channel, subfamily K, member 9

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NCBI Description of KCNK9
This gene encodes a member of the superfamily of potassium channel proteins containing two pore-forming P domains, and is highly expressed in the cerebellum. Amplification and overexpression of this gene has been observed in several types of human carcinomas, notably in breast cancer. This gene is imprinted in fetal brain, with preferential expression from the maternal allele.

Community Annotation of KCNK9 Add / Edit KCNK9: 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

KCNK9 is highly significantly mutated in
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KCNK9 is significantly mutated in
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KCNK9 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 KCNK9