Cushing Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An adrenal gland hyperfunction that is caused by overactivity of the adrenal cortex caused by a tumor of the pituitary gland. (Human Disease Ontology, DOID_12252)
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23 genes/proteins associated with the disease Cushing Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
POMC proopiomelanocortin 2.88009
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha 2.88009
CRH corticotropin releasing hormone 2.88009
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) 1.7448
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2 1.62736
TAT tyrosine aminotransferase 1.45194
NR3C2 nuclear receptor subfamily 3, group C, member 2 1.4313
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.3931
AR androgen receptor 1.35502
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1 1.3484
HSD11B1 hydroxysteroid (11-beta) dehydrogenase 1 1.2059
PRL prolactin 1.19542
TNF tumor necrosis factor 1.18026
TGFB1 transforming growth factor, beta 1 1.10282
FSHB follicle stimulating hormone, beta polypeptide 1.10104
IL5 interleukin 5 1.08975
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2 1.08726
VEGFA vascular endothelial growth factor A 1.0766
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD) 1.06952
STAR steroidogenic acute regulatory protein 1.06771
GSTA2 glutathione S-transferase alpha 2 1.04088
IL1B interleukin 1, beta 1.02077
CCL2 chemokine (C-C motif) ligand 2 1.01663