Familial Hyperaldosteronism Gene Set
Genes
18 genes associated with the disease Familial Hyperaldosteronism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
AGT
|
angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
|
|
ATP1A1
|
ATPase, Na+/K+ transporting, alpha 1 polypeptide
|
|
ATP2B3
|
ATPase, Ca++ transporting, plasma membrane 3
|
|
CACNA1D
|
calcium channel, voltage-dependent, L type, alpha 1D subunit
|
|
CLCN2
|
chloride channel, voltage-sensitive 2
|
|
CYP11B1
|
cytochrome P450, family 11, subfamily B, polypeptide 1
|
|
CYP11B2
|
cytochrome P450, family 11, subfamily B, polypeptide 2
|
|
ENPEP
|
glutamyl aminopeptidase (aminopeptidase A)
|
|
FLNB
|
filamin B, beta
|
|
GNA12
|
guanine nucleotide binding protein (G protein) alpha 12
|
|
KCNJ5
|
potassium channel, inwardly rectifying subfamily J, member 5
|
|
LGALS14
|
lectin, galactoside-binding, soluble, 14
|
|
NR3C2
|
nuclear receptor subfamily 3, group C, member 2
|
|
PMS2
|
PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
|
|
POMC
|
proopiomelanocortin
|
|
PPP1R2P9
|
protein phosphatase 1, regulatory (inhibitor) subunit 2 pseudogene 9
|
|
REN
|
renin
|
|
S100A6
|
S100 calcium binding protein A6
|
