XB-FEAT-5797750: Difference between revisions
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Human name has changed for Entrez Gene: 6005. From Rh-associated glycoprotein to Rh associated glycoprotein | Human name has changed for Entrez Gene: 6005. From Rh-associated glycoprotein to Rh associated glycoprotein | ||
This genepage renamed to rhagl = rhag like on 5/20/2019 by KAB. This appears to be a retrotranscribed version of rhag inserted into a new locus. Linking to human rhag is still appropriate, but there is a true orthologue genepage, and that genepage retains the name rhag | |||
=summary from NCBI= | =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] | 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] | ||
Revision as of 06:40, 20 May 2019
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 This genepage renamed to rhagl = rhag like on 5/20/2019 by KAB. This appears to be a retrotranscribed version of rhag inserted into a new locus. Linking to human rhag is still appropriate, but there is a true orthologue genepage, and that genepage retains the name rhag
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]