decreased circulating growth hormone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than the expected blood concentration of the hormone that promotes body growth, fat mobilization, and inhibition of glucose utilization (Mammalian Phenotype Ontology, MP_0005120)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005120
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Genes

16 gene mutations causing the decreased circulating growth hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BRS3 bombesin-like receptor 3
DRD2 dopamine receptor D2
FGF21 fibroblast growth factor 21
GHRHR growth hormone releasing hormone receptor
HMX2 H6 family homeobox 2
HMX3 H6 family homeobox 3
IGF1 insulin-like growth factor 1 (somatomedin C)
JUND jun D proto-oncogene
LATS1 large tumor suppressor kinase 1
MBOAT4 membrane bound O-acyltransferase domain containing 4
PAX6 paired box 6
PCSK1 proprotein convertase subtilisin/kexin type 1
PROP1 PROP paired-like homeobox 1
RIMS2 regulating synaptic membrane exocytosis 2
SERP1 stress-associated endoplasmic reticulum protein 1
SOCS2 suppressor of cytokine signaling 2