WNK1

WNK1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesWNK1, HSAN2, HSN2, KDP, PPP1R167, PRKPSK, p65, WNK lysine deficient protein kinase 1
External IDsOMIM: 605232; MGI: 2442092; HomoloGene: 14253; GeneCards: WNK1; OMA:WNK1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

65125

232341

Ensembl

ENSG00000060237

ENSMUSG00000045962

UniProt

Q9H4A3

P83741

RefSeq (mRNA)

NM_001184985
NM_014823
NM_018979
NM_213655

RefSeq (protein)

NP_001171914
NP_055638
NP_061852
NP_998820

NP_001171949
NP_001171950
NP_001186012
NP_001186013
NP_941992

Location (UCSC)Chr 12: 0.75 – 0.91 MbChr 6: 119.92 – 120.04 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

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).