hyperkalemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally increased potassium concentration in the blood. (Human Phenotype Ontology, HP_0002153)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002153
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Genes

14 genes associated with the hyperkalemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CA12 carbonic anhydrase XII
CUL3 cullin 3
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
INVS inversin
KLHL3 kelch-like family member 3
LPIN1 lipin 1
NR3C2 nuclear receptor subfamily 3, group C, member 2
RYR1 ryanodine receptor 1 (skeletal)
SCN4A sodium channel, voltage gated, type IV alpha subunit
SCNN1A sodium channel, non voltage gated 1 alpha subunit
SCNN1B sodium channel, non voltage gated 1 beta subunit
SCNN1G sodium channel, non voltage gated 1 gamma subunit
WNK1 WNK lysine deficient protein kinase 1
WNK4 WNK lysine deficient protein kinase 4