CHRNA9 Back

cholinergic receptor, nicotinic, alpha 9

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NCBI Description of CHRNA9

This gene is a member of the ligand-gated ionic channel family and nicotinic acetylcholine receptor gene superfamily. It encodes a plasma membrane protein that forms homo- or hetero-oligomeric divalent cation channels. This protein is involved in cochlea hair cell development and is also expressed in the outer hair cells (OHCs) of the adult cochlea.

Community Annotation of CHRNA9 Add / Edit CHRNA9: Annotations

No community annotations yet for CHRNA9.
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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

CHRNA9 is highly significantly mutated in
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CHRNA9 is significantly mutated in
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CHRNA9 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 CHRNA9