increased circulating renin level Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased level of renin (PRO:000013883) in the blood. (Human Phenotype Ontology, HP_0000848)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000848
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Genes

8 genes associated with the increased circulating renin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CASR calcium-sensing receptor
CLCNKB chloride channel, voltage-sensitive Kb
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
NR3C2 nuclear receptor subfamily 3, group C, member 2
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3