decreased circulating corticosterone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than the normal blood amount of an adrenocortical steroid that induces glycogen deposition and regulates sodium conservation and potassium secretion (Mammalian Phenotype Ontology, MP_0002665)
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30 gene mutations causing the decreased circulating corticosterone 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
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