Entrez gene ID | | 497078 |
Official gene symbol | | Xk |
Full name | | X-linked Kx blood group (McLeod syndrome) homolog |
Aliases | | - |
Gene 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] |
Location | | Chromosome: 0 Locus: Xq13 |
Gene position | | 25591151 - 25624912 Map Viewer |
Gene orientation | | minus |
Gene size | | 33762 bp |
Gene sequence |
| |