WNK4 Chromosome 17

WNK lysine deficient protein kinase 4
42 variants 42 Health Risk

Upload your DNA to see your personal genotypes for variants in WNK4.

What This Gene Does
This gene encodes a member of the WNK family of serine-threonine protein kinases. The kinase is part of the tight junction complex in kidney cells, and regulates the balance between NaCl reabsorption and K(+) secretion. The kinase regulates the activities of several types of ion channels, cotransporters, and exchangers involved in electrolyte flux in epithelial cells. Mutations in this gene result in pseudohypoaldosteronism type IIB.[provided by RefSeq, Sep 2009]
Gene Info
Gene Group
WNK lysine deficient protein kinases
Locus Type
gene with protein product
Location
17q21.2
Ensembl
ENSG00000126562
Associated Conditions (4)
Pseudohypoaldosteronism type 2B
Inborn genetic diseases
WNK4-related disorder
Renal tubulopathies
Key Variants
RS137853095
Conflicting classifications of pathogenicity
Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
Health Risk
RS140897013
Conflicting classifications of pathogenicity
Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
Health Risk
RS141615112
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS145020225
Conflicting classifications of pathogenicity
Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
Health Risk
RS146190504
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS146216767
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS199712166
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS199775692
Conflicting classifications of pathogenicity
Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
Health Risk
RS200182836
Conflicting classifications of pathogenicity
Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
Health Risk
RS200438705
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS200593980
Conflicting classifications of pathogenicity
Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
Health Risk
RS200640984
Conflicting classifications of pathogenicity
WNK4-related disorder, Pseudohypoaldosteronism type 2B, WNK4-related disorder
Health Risk
All Variants (42)
RSID Category Clinical Significance Conditions
RS137853095 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS140897013 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
RS141615112 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS145020225 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
RS146190504 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS146216767 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS199712166 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS199775692 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
RS200182836 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
RS200438705 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200593980 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS200640984 Health Risk Conflicting classifications of pathogenicity WNK4-related disorder, Pseudohypoaldosteronism type 2B, WNK4-related disorder
RS202060087 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Pseudohypoaldosteronism type 2B, Inborn genetic diseases
RS369221665 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
RS370770635 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
RS373427674 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS374889836 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS387907562 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS545588214 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
RS61755595 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS61755600 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS61755602 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS61755607 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS61755628 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
RS748879947 Health Risk Conflicting classifications of pathogenicity
RS752469952 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Pseudohypoaldosteronism type 2B, Inborn genetic diseases
RS754495845 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS757050478 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS758058076 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Pseudohypoaldosteronism type 2B, Inborn genetic diseases
RS761294614 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
RS765644398 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS769815091 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
RS772583212 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS773898452 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Inborn genetic diseases, Pseudohypoaldosteronism type 2B
RS778394259 Health Risk Conflicting classifications of pathogenicity Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS778501298 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS137853093 Health Risk Likely pathogenic Pseudohypoaldosteronism type 2B, Renal tubulopathies, Pseudohypoaldosteronism type 2B
RS2144087861 Health Risk Likely pathogenic Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS2544005779 Health Risk Likely pathogenic WNK4-related disorder, WNK4-related disorder
RS137853092 Health Risk Pathogenic Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS137853094 Health Risk Pathogenic Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
RS2143987485 Health Risk Pathogenic Pseudohypoaldosteronism type 2B, Pseudohypoaldosteronism type 2B
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