decreased circulating glucocorticoid level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than normal blood concentration of the corticosteroids regulating carbohydrate metabolism and exhibiting anti-inflammatory activity (Mammalian Phenotype Ontology, MP_0003368)
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31 gene mutations causing the decreased circulating glucocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACD adrenocortical dysplasia homolog (mouse)
AVPR1B arginine vasopressin receptor 1B
CLOCK clock circadian regulator
CRH corticotropin releasing hormone
CRHR1 corticotropin releasing hormone receptor 1
CRTC2 CREB regulated transcription coactivator 2
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
FKBP5 FK506 binding protein 5
GAL galanin/GMAP prepropeptide
H6PD hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)
HMGN1 high mobility group nucleosome binding domain 1
HMGN3 high mobility group nucleosomal binding domain 3
HSD11B1 hydroxysteroid (11-beta) dehydrogenase 1
IFITM1 interferon induced transmembrane protein 1
IL1B interleukin 1, beta
LDLR low density lipoprotein receptor
LIPC lipase, hepatic
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
NMU neuromedin U
NPY2R neuropeptide Y receptor Y2
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
POMC proopiomelanocortin
PRLHR prolactin releasing hormone receptor
SELM selenoprotein M
SLC23A2 solute carrier family 23 (ascorbic acid transporter), member 2
STAR steroidogenic acute regulatory protein
TACR1 tachykinin receptor 1
TBX19 T-box 19
TLR2 toll-like receptor 2