| Gene Symbol | Xk |
| Entrez Gene ID | 497078 |
| Full Name | X-linked Kx blood group |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Rattus norvegicus(Norway rat) |
| Genome | |
| Summary | human homolog is a red cell membrane protein whose deficiency causes the McLeod syndrome, a disorder characterized by blood group, neuromuscular and hematopoietic abnormalities [RGD, Feb 2006]. |







































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