Familial Glucocorticoid Deficiency Gene Set
Genes
13 genes associated with the disease Familial Glucocorticoid Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
AAAS
|
achalasia, adrenocortical insufficiency, alacrimia
|
|
ACD
|
adrenocortical dysplasia homolog (mouse)
|
|
FGD1
|
FYVE, RhoGEF and PH domain containing 1
|
|
IGF1
|
insulin-like growth factor 1 (somatomedin C)
|
|
MC1R
|
melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
|
|
MC2R
|
melanocortin 2 receptor (adrenocorticotropic hormone)
|
|
MRAP
|
melanocortin 2 receptor accessory protein
|
|
NNT
|
nicotinamide nucleotide transhydrogenase
|
|
POMC
|
proopiomelanocortin
|
|
RASGRF1
|
Ras protein-specific guanine nucleotide-releasing factor 1
|
|
SOS1
|
son of sevenless homolog 1 (Drosophila)
|
|
STAR
|
steroidogenic acute regulatory protein
|
|
TXNRD2
|
thioredoxin reductase 2
|
