increased circulating corticosterone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than the normal amount of an adrenocortical steroid that induces glycogen deposition and regulates sodium conservation and potassium secretion (Mammalian Phenotype Ontology, MP_0001745)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001745
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Genes

42 gene mutations causing the increased circulating corticosterone 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