abnormal adrenocorticotropin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the level of the pituitary hormone that stimulates the secretion of adrenal cortical steroids and induces growth of the adrenal cortex (Mammalian Phenotype Ontology, MP_0003966)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003966
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Genes

37 gene mutations causing the abnormal 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
AVPR1B arginine vasopressin receptor 1B
CNR1 cannabinoid receptor 1 (brain)
CORT cortistatin
CPE carboxypeptidase E
CRH corticotropin releasing hormone
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
DDX20 DEAD (Asp-Glu-Ala-Asp) box polypeptide 20
DRD2 dopamine receptor D2
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GRID2 glutamate receptor, ionotropic, delta 2
INSM1 insulinoma-associated 1
LEP leptin
LHX3 LIM homeobox 3
LIF leukemia inhibitory factor
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
NOS2 nitric oxide synthase 2, inducible
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
OGN osteoglycin
PAX6 paired box 6
PCSK1 proprotein convertase subtilisin/kexin type 1
PDE8B phosphodiesterase 8B
POMC proopiomelanocortin
PTGER1 prostaglandin E receptor 1 (subtype EP1), 42kDa
PTGER3 prostaglandin E receptor 3 (subtype EP3)
SCG5 secretogranin V
SERPINA6 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6
SOX2 SRY (sex determining region Y)-box 2
SSTR2 somatostatin receptor 2
STAR steroidogenic acute regulatory protein
TBX19 T-box 19
TLR2 toll-like receptor 2
UCN2 urocortin 2