decreased adrenocorticotropin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decreased concentration of adrenocorticotropic hormone (Mammalian Phenotype Ontology, MP_0005128)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005128
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Genes

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

Symbol Name
AVPR1B arginine vasopressin receptor 1B
CPE carboxypeptidase E
DDX20 DEAD (Asp-Glu-Ala-Asp) box polypeptide 20
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
INSM1 insulinoma-associated 1
LHX3 LIM homeobox 3
LIF leukemia inhibitory factor
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
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)
SOX2 SRY (sex determining region Y)-box 2
TBX19 T-box 19