Adrenal Insufficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Insufficient production of steroid hormones (primarily cortisol) by the adrenal glands as a result of a primary defect in the glands themselves. (Human Phenotype Ontology, HP_0000846)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D000309
Similar Terms
Downloads & Tools

Genes

25 genes/proteins associated with the disease Adrenal Insufficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1 2.88009
NR5A1 nuclear receptor subfamily 5, group A, member 1 2.88009
VEGFA vascular endothelial growth factor A 1.37676
AKT1 v-akt murine thymoma viral oncogene homolog 1 1.34256
POMC proopiomelanocortin 1.29843
IL4 interleukin 4 1.20163
CCL2 chemokine (C-C motif) ligand 2 1.18587
CCL11 chemokine (C-C motif) ligand 11 1.16799
PRL prolactin 1.16666
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.14919
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2 1.13075
GH1 growth hormone 1 1.1198
KRT8 keratin 8, type II 1.11606
AR androgen receptor 1.11466
CTSD cathepsin D 1.07947
ACTG2 actin, gamma 2, smooth muscle, enteric 1.07875
FAS Fas cell surface death receptor 1.07625
IFNG interferon, gamma 1.06297
MAPK1 mitogen-activated protein kinase 1 1.05126
TNF tumor necrosis factor 1.04757
MAP2K1 mitogen-activated protein kinase kinase 1 1.04465
PER1 period circadian clock 1 1.04014
IL5 interleukin 5 1.03567
ABCC3 ATP-binding cassette, sub-family C (CFTR/MRP), member 3 1.03345
TAT tyrosine aminotransferase 1.01928