hypokalemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002900
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Genes

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

Symbol Name
AIP aryl hydrocarbon receptor interacting protein
BMPR1A bone morphogenetic protein receptor, type IA
BSND barttin CLCNK-type chloride channel accessory beta subunit
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CASR calcium-sensing receptor
CLCNKA chloride channel, voltage-sensitive Ka
CLCNKB chloride channel, voltage-sensitive Kb
COL3A1 collagen, type III, alpha 1
CTNS cystinosin, lysosomal cystine transporter
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
OCRL oculocerebrorenal syndrome of Lowe
SCN4A sodium channel, voltage gated, type IV alpha subunit
SCNN1B sodium channel, non voltage gated 1 beta subunit
SCNN1G sodium channel, non voltage gated 1 gamma subunit
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC26A3 solute carrier family 26 (anion exchanger), member 3
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2
SMAD4 SMAD family member 4