Acth Deficiency, Isolated Gene Set
Genes
10 genes associated with the disease Acth Deficiency, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
CHRNA4
|
cholinergic receptor, nicotinic, alpha 4 (neuronal)
|
|
CRH
|
corticotropin releasing hormone
|
|
HLA-C
|
major histocompatibility complex, class I, C
|
|
NFKB2
|
nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
|
|
POMC
|
proopiomelanocortin
|
|
POU1F1
|
POU class 1 homeobox 1
|
|
RPE65
|
retinal pigment epithelium-specific protein 65kDa
|
|
SERPINA6
|
serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6
|
|
SLC20A1
|
solute carrier family 20 (phosphate transporter), member 1
|
|
TBX19
|
T-box 19
|
