increased adrenocorticotropin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased concentration of adrenocorticotropic hormone (Mammalian Phenotype Ontology, MP_0005129)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005129
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Genes

19 gene mutations causing the increased adrenocorticotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACD adrenocortical dysplasia homolog (mouse)
AGTR2 angiotensin II receptor, type 2
ANXA1 annexin A1
CNR1 cannabinoid receptor 1 (brain)
CORT cortistatin
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
DRD2 dopamine receptor D2
GRID2 glutamate receptor, ionotropic, delta 2
LEP leptin
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
SCG5 secretogranin V
SERPINA6 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6
SSTR2 somatostatin receptor 2
STAR steroidogenic acute regulatory protein
TLR2 toll-like receptor 2
UCN2 urocortin 2