- Gene Overview
- Interaction Network
- Sequence Verification
RHAG, Rh associated glycoprotein
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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]
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Gene Synonyms (ammonium transporter Rh type A, Rh 50 glycoprotein, Rhesus associated polypeptide, 50-KD, Rhesus blood group-associated glycoprotein, erythrocyte membrane glycoprotein Rh50, erythrocyte plasma membrane 50 kDa glycoprotein, mutant Rh associated glycoprotein, rh family type A glycoprotein, rh type A glycoprotein, rhesus blood group family type A glycoprotein, rhesus blood group-associated ammonia channel, truncated Rh-associated glycoprotein, truncated RhAG glycoprotein, CD241, OHS, OHST, RH2, RH50A, RHNR, Rh50, Rh50GP, SLC42A1,)
- NCBI Gene ID:
6005
- Species:
Homo sapiens (Human)
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UNIPROT ID#>>Q96E98
UNIPROT ID#>>Q02094
- View the NCBI Database
for this Gene »
Gene products are often involved in multiple pathways and networks within a living
cell. Learn more about other interacting partners.
Rh associated glycoprotein interacts with:
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this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see
how a sequence matches to an experimentally-validated ORF clone.
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