increased circulating glucocorticoid level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than normal blood concentration of the corticosteroids regulating carbohydrate metabolism and exhibiting anti-inflammatory activity (Mammalian Phenotype Ontology, MP_0003367)
External Link
Similar Terms
Downloads & Tools


42 gene mutations causing the increased circulating glucocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCYAP1 adenylate cyclase activating polypeptide 1 (pituitary)
AGTR2 angiotensin II receptor, type 2
APOE apolipoprotein E
ATP1A1 ATPase, Na+/K+ transporting, alpha 1 polypeptide
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CNR1 cannabinoid receptor 1 (brain)
CRH corticotropin releasing hormone
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
DFNB31 deafness, autosomal recessive 31
DHCR7 7-dehydrocholesterol reductase
DLG4 discs, large homolog 4 (Drosophila)
DRD2 dopamine receptor D2
GHR growth hormone receptor
GRID2 glutamate receptor, ionotropic, delta 2
GTF2IRD1 GTF2I repeat domain containing 1
LEP leptin
LEPR leptin receptor
MCHR1 melanin-concentrating hormone receptor 1
MEN1 multiple endocrine neoplasia I
NPY1R neuropeptide Y receptor Y1
NPY2R neuropeptide Y receptor Y2
NPY5R neuropeptide Y receptor Y5
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PCMT1 protein-L-isoaspartate (D-aspartate) O-methyltransferase
PDYN prodynorphin
PITPNA phosphatidylinositol transfer protein, alpha
PLA2G10 phospholipase A2, group X
PLAT plasminogen activator, tissue
POMC proopiomelanocortin
PRLHR prolactin releasing hormone receptor
PROP1 PROP paired-like homeobox 1
RAI1 retinoic acid induced 1
SCG5 secretogranin V
SST somatostatin
TGFB1 transforming growth factor, beta 1
TRAF3 TNF receptor-associated factor 3
UCN urocortin
UCN2 urocortin 2
VGF VGF nerve growth factor inducible
WFS1 Wolfram syndrome 1 (wolframin)
ZEB1 zinc finger E-box binding homeobox 1