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RHAG

Official Full Name
Rh associated glycoprotein
Organism
Homo sapiens
GeneID
6005
Background
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]
Synonyms
OHS; RH2; OHST; RHNR; Rh50; CD241; RH50A; Rh50GP; SLC42A1;

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