Hypoaldosteronism Gene Set
Genes
18 genes associated with the disease Hypoaldosteronism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
CHD7
|
chromodomain helicase DNA binding protein 7
|
|
CYP11B2
|
cytochrome P450, family 11, subfamily B, polypeptide 2
|
|
CYP17A1
|
cytochrome P450, family 17, subfamily A, polypeptide 1
|
|
CYP21A2
|
cytochrome P450, family 21, subfamily A, polypeptide 2
|
|
CYP2C19
|
cytochrome P450, family 2, subfamily C, polypeptide 19
|
|
GGCT
|
gamma-glutamylcyclotransferase
|
|
HSD3B2
|
hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2
|
|
MC2R
|
melanocortin 2 receptor (adrenocorticotropic hormone)
|
|
NR0B1
|
nuclear receptor subfamily 0, group B, member 1
|
|
NR3C2
|
nuclear receptor subfamily 3, group C, member 2
|
|
POMC
|
proopiomelanocortin
|
|
PTH
|
parathyroid hormone
|
|
REN
|
renin
|
|
RHCG
|
Rh family, C glycoprotein
|
|
SCNN1G
|
sodium channel, non voltage gated 1 gamma subunit
|
|
SLC30A10
|
solute carrier family 30, member 10
|
|
SLC30A8
|
solute carrier family 30 (zinc transporter), member 8
|
|
TPO
|
thyroid peroxidase
|
