Hyperaldosteronism Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An adrenal gland hyperfunction disease that results in the overproduction of aldosterone by the adrenal glands. (Human Disease Ontology, DOID_446)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006929
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Genes

18 genes/proteins associated with the disease Hyperaldosteronism from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1 2.88009
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2 2.88009
ATP1A1 ATPase, Na+/K+ transporting, alpha 1 polypeptide 2.88009
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit 2.88009
ATP2B3 ATPase, Ca++ transporting, plasma membrane 3 2.88009
REN renin 1.41748
AQP2 aquaporin 2 (collecting duct) 1.18587
CYBB cytochrome b-245, beta polypeptide 1.14064
NPPB natriuretic peptide B 1.13655
SGK1 serum/glucocorticoid regulated kinase 1 1.11431
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 1.09857
ACE angiotensin I converting enzyme 1.09646
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8) 1.07128
NPPA natriuretic peptide A 1.04427
GAS6 growth arrest-specific 6 1.02821
AGTR1 angiotensin II receptor, type 1 1.02077
IL10 interleukin 10 1.01966
MYH7 myosin, heavy chain 7, cardiac muscle, beta 1.01025