Hyperaldosteronism Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An adrenal gland hyperfunction disease that results in the overproduction of aldosterone by the adrenal glands. (Human Disease Ontology, DOID_446)
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Genes

19 genes associated with the Hyperaldosteronism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ADD1 adducin 1 (alpha)
ADIPOQ adiponectin, C1Q and collagen domain containing
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
ARHGAP9 Rho GTPase activating protein 9
ATP1A1 ATPase, Na+/K+ transporting, alpha 1 polypeptide
ATP2B3 ATPase, Ca++ transporting, plasma membrane 3
BDKRB2 bradykinin receptor B2
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
FZD4 frizzled class receptor 4
HSD3B1 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1
HSD3B2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2
KCNJ3 potassium channel, inwardly rectifying subfamily J, member 3
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
KDM5C lysine (K)-specific demethylase 5C
LRP1B low density lipoprotein receptor-related protein 1B
REN renin
ZFP37 ZFP37 zinc finger protein