| WNK1 | 
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| Identifiers | 
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| Aliases | WNK1, HSAN2, HSN2, KDP, PPP1R167, PRKPSK, p65, WNK lysine deficient protein kinase 1 | 
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| External IDs | OMIM: 605232; MGI: 2442092; HomoloGene: 14253; GeneCards: WNK1; OMA:WNK1 - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 6 (mouse) | 
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 |  |  | Band | 6|6 F1 | Start | 119,923,969 bp | 
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 | End | 120,038,672 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | internal globus pallidus
 inferior ganglion of vagus nerve
 subthalamic nucleus
 dorsal motor nucleus of vagus nerve
 external globus pallidus
 optic nerve
 pars reticulata
 trabecular bone
 pars compacta
 inferior olivary nucleus
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 | | Top expressed in |  | endothelial cell of lymphatic vessel
 stroma of bone marrow
 gastrula
 right lung lobe
 vestibular membrane of cochlear duct
 saccule
 primary oocyte
 myocardium of ventricle
 ciliary body
 cardiac muscle tissue of left ventricle
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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WNK (lysine deficient protein kinase 1), also known as WNK1, is an enzyme that is encoded by the WNK1 gene. WNK1 is serine-threonine protein kinase and part of the "with no lysine/K" kinase WNK family. The predominant role of WNK1 is the regulation of cation-Cl− cotransporters (CCCs) such as the sodium chloride cotransporter (NCC), basolateral Na-K-Cl symporter (NKCC1), and potassium chloride cotransporter (KCC1) located within the kidney. CCCs mediate ion homeostasis and modulate blood pressure by transporting ions in and out of the cell. WNK1 mutations as a result have been implicated in blood pressure disorders/diseases; a prime example being familial hyperkalemic hypertension (FHHt).