abnormal corticosterone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalous blood or tissue amount of an adrenocortical steroid that induces glycogen deposition and regulates sodium conservation and potassium secretion (Mammalian Phenotype Ontology, MP_0003963)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003963
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Genes

76 gene mutations causing the abnormal corticosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACD adrenocortical dysplasia homolog (mouse)
ADCY8 adenylate cyclase 8 (brain)
ADCYAP1 adenylate cyclase activating polypeptide 1 (pituitary)
AGTR2 angiotensin II receptor, type 2
APOE apolipoprotein E
ATP1A1 ATPase, Na+/K+ transporting, alpha 1 polypeptide
AVPR1A arginine vasopressin receptor 1A
AVPR1B arginine vasopressin receptor 1B
C12ORF10 chromosome 12 open reading frame 10
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CHGA chromogranin A
CLOCK clock circadian regulator
CNR1 cannabinoid receptor 1 (brain)
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
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
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
FKBP5 FK506 binding protein 5
GHR growth hormone receptor
GRID2 glutamate receptor, ionotropic, delta 2
GTF2IRD1 GTF2I repeat domain containing 1
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
LEP leptin
LEPR leptin receptor
LIPC lipase, hepatic
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
MCHR1 melanin-concentrating hormone receptor 1
MEN1 multiple endocrine neoplasia I
NMU neuromedin U
NPY1R neuropeptide Y receptor Y1
NPY2R neuropeptide Y receptor Y2
NPY5R neuropeptide Y receptor Y5
NPY6R neuropeptide Y receptor Y6 (pseudogene)
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NR5A1 nuclear receptor subfamily 5, group A, member 1
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PCMT1 protein-L-isoaspartate (D-aspartate) O-methyltransferase
PDE8B phosphodiesterase 8B
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
SELM selenoprotein M
SERPINA6 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6
SLC18A2 solute carrier family 18 (vesicular monoamine transporter), member 2
SLC23A2 solute carrier family 23 (ascorbic acid transporter), member 2
SST somatostatin
STAR steroidogenic acute regulatory protein
TACR1 tachykinin receptor 1
TBX19 T-box 19
TGFB1 transforming growth factor, beta 1
TLR2 toll-like receptor 2
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