abnormality of renin-angiotensin system Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the renin-angiotensin system. (Human Phenotype Ontology, HP_0000847)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000847
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Genes

17 genes associated with the abnormality of renin-angiotensin system 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
CASR calcium-sensing receptor
CLCNKB chloride channel, voltage-sensitive Kb
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
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
NR3C2 nuclear receptor subfamily 3, group C, member 2
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
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