KCNJ12 Back

potassium inwardly-rectifying channel, subfamily J, member 12

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NCBI Description of KCNJ12
This gene encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith-Magenis syndrome region on chromosome 17.

Community Annotation of KCNJ12 Add / Edit KCNJ12: 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

KCNJ12 is highly significantly mutated in
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KCNJ12 is significantly mutated in
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KCNJ12 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 KCNJ12