XB-FEAT-5797750

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Revision as of 07:42, 26 September 2017 by imported>Xenbase (→‎rhag)
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rhag

This is the community wiki page for the gene rhag please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.

nomenclature changes

09/24/2017 Human name has changed for Entrez Gene: 6005. From Rh-associated glycoprotein to Rh associated glycoprotein

summary from NCBI

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.[provided by RefSeq, Mar 2009]