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]
Accession: | NM_001012227 |
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基因名称: | Xk |
基因描述: | Rattus norvegicus X-linked Kx blood group (McLeod syndrome) (Xk), mRNA. |
种属: | Rat |
CDS区长度: | 1338 (查看编码区序列) |
翻译后氨基酸长度: | 445 (查看氨基酸序列) |
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]