This gene encodes a member of the WNK subfamily of serine/threonine protein kinases. The encoded protein may be a key regulator of blood pressure by controlling the transport of sodium and chloride ions. Mutations in this gene have been associated with pseudohypoaldosteronism type II and hereditary sensory neuropathy type II. Alternatively spliced transcript variants encoding different isoforms have been described but the full-length nature of all of them has yet to be determined.[provided by RefSeq, May 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| WNK1-20-RE | 20 (40 μL) | 200 μL |  |
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| WNK1-20-OR | 20 (40 μL) | 200 μL |  |
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| WNK1-20-GO | 20 (40 μL) | 200 μL |  |
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| WNK1-20-GR | 20 (40 μL) | 200 μL |  |
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| WNK1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the WNK subfamily of serine/threonine protein kinases. The encoded protein may be a key regulator of blood pressure by controlling the transport of sodium and chloride ions. Mutations in this gene have been associated with pseudohypoaldosteronism type II and hereditary sensory neuropathy type II. Alternatively spliced transcript variants encoding different isoforms have been described but the full-length nature of all of them has yet to be determined.[provided by RefSeq, May 2010]
Gene Symbol : WNK1
Gene Name : WNK lysine deficient protein kinase 1
Chromosome : CHR 12: 752,551-911,451
Locus : 12p13.33
Alt. Genes : ATP6AP2
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