RGS9 Back

regulator of G-protein signaling 9

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NCBI Description of RGS9
This gene encodes a member of the RGS family of GTPase activating proteins that function in various signaling pathways by accelerating the deactivation of G proteins. This protein is anchored to photoreceptor membranes in retinal cells and deactivates G proteins in the rod and cone phototransduction cascades. Mutations in this gene result in bradyopsia. Multiple transcript variants encoding different isoforms have been found for this gene.

Community Annotation of RGS9 Add / Edit RGS9: 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

RGS9 is highly significantly mutated in
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RGS9 is significantly mutated in
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RGS9 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 RGS9