Glucocorticoid Deficiency With Achalasia Gene Set
Genes
17 genes associated with the disease Glucocorticoid Deficiency With Achalasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
AAAS
|
achalasia, adrenocortical insufficiency, alacrimia
|
|
AGFG2
|
ArfGAP with FG repeats 2
|
|
FTH1
|
ferritin, heavy polypeptide 1
|
|
GH1
|
growth hormone 1
|
|
GMPPA
|
GDP-mannose pyrophosphorylase A
|
|
IGFALS
|
insulin-like growth factor binding protein, acid labile subunit
|
|
MC2R
|
melanocortin 2 receptor (adrenocorticotropic hormone)
|
|
MRAP
|
melanocortin 2 receptor accessory protein
|
|
NR5A1
|
nuclear receptor subfamily 5, group A, member 1
|
|
POMC
|
proopiomelanocortin
|
|
RGPD2
|
RANBP2-like and GRIP domain containing 2
|
|
SGPL1
|
sphingosine-1-phosphate lyase 1
|
|
SMARCD1
|
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1
|
|
SOD1
|
superoxide dismutase 1, soluble
|
|
TMEM206
|
transmembrane protein 206
|
|
TRAPPC11
|
trafficking protein particle complex 11
|
|
TSHR
|
thyroid stimulating hormone receptor
|
