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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RHAG-20-RE | 20 (40 μL) | 200 μL |  |
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| RHAG-20-OR | 20 (40 μL) | 200 μL |  |
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| RHAG-20-GO | 20 (40 μL) | 200 μL |  |
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| RHAG-20-GR | 20 (40 μL) | 200 μL |  |
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| RHAG-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : RHAG
Gene Name : Rh associated glycoprotein
Chromosome : CHR 6: 496,368,73-496,051,74
Locus : 6p12.3
Alt. Genes : ZNF263
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