abnormal circulating renin Gene Set
Genes
8 genes associated with the abnormal circulating renin 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
|
