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RHAG, Rh associated glycoprotein

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RHAG, Rh associated glycoprotein

  • 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]

  • 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)
  • UNIPROT ID#>>Q96E98
    UNIPROT ID#>>Q02094
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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