RHAG Back

Rh-associated glycoprotein

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NCBI Description of RHAG
The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.

Community Annotation of RHAG Add / Edit RHAG: 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

RHAG is highly significantly mutated in
(none)
RHAG is significantly mutated in
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RHAG 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 RHAG