renal potassium wasting Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description High urine potassium in the presence of hypokalemia. (Human Phenotype Ontology, HP_0000128)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000128
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Genes

5 genes associated with the renal potassium wasting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CLCNKB chloride channel, voltage-sensitive Kb
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3