XB-FEAT-5797750: Difference between revisions
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=rhag= | =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 | 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] | |||
Revision as of 06:42, 26 September 2017
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]