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Pain syndromes

Gene: WNK1

Green List (high evidence)
WNK1 (WNK lysine deficient protein kinase 1)
EnsemblGeneIds (GRCh38): ENSG00000060237
EnsemblGeneIds (GRCh37): ENSG00000060237
OMIM: 605232, Gene2Phenotype
WNK1 is in 10 panels

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Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Neuropathy, hereditary sensory and autonomic, type II, 201300
  • HSAN 2
  • Hereditary sensory and autonomic neuropathy type IIA
OMIM
605232
Clinvar variants
Variants in WNK1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

1 Apr 2020, Gel status: 3

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Added phenotypes Neuropathy, hereditary sensory and autonomic, type II, 201300; HSAN 2; Hereditary sensory and autonomic neuropathy type IIA for gene: WNK1

1 Apr 2020, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: WNK1 was added gene: WNK1 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green Mode of inheritance for gene: WNK1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: WNK1 were set to 15911806; 16636245; 16946995; 21625937; 15455397; 18521183; 15060842 Phenotypes for gene: WNK1 were set to Neuropathy, hereditary sensory and autonomic, type II, 201300; HSAN 2; Hereditary sensory and autonomic neuropathy type IIA