This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| XK-20-RE | 20 (40 μL) | 200 μL |  |
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| XK-20-OR | 20 (40 μL) | 200 μL |  |
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| XK-20-GO | 20 (40 μL) | 200 μL |  |
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| XK-20-GR | 20 (40 μL) | 200 μL |  |
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| XK-20-AQ | 20 (40 μL) | 200 μL |  |
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This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. [provided by RefSeq, Jul 2008]
Gene Symbol : XK
Gene Name : X-linked Kx blood group
Chromosome : CHR X: 376,857,65-377,321,29
Locus : Xp21.1
Alt. Genes : ZNF263
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