decreased circulating renin level Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An decreased level of renin (PRO:000013883) in the blood. (Human Phenotype Ontology, HP_0003351)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003351
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Genes

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

Symbol Name
AVPR2 arginine vasopressin receptor 2
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
NR3C2 nuclear receptor subfamily 3, group C, member 2
SCNN1B sodium channel, non voltage gated 1 beta subunit
SCNN1G sodium channel, non voltage gated 1 gamma subunit