decreased growth hormone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than the expected concentration of the hormone that promotes body growth, fat mobilization, and inhibition of glucose utilization (Mammalian Phenotype Ontology, MP_0005136)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005136
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Genes

28 gene mutations causing the decreased 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
EGR1 early growth response 1
FGF21 fibroblast growth factor 21
GHRH growth hormone releasing hormone
GHRHR growth hormone releasing hormone receptor
HMX2 H6 family homeobox 2
HMX3 H6 family homeobox 3
IGF1 insulin-like growth factor 1 (somatomedin C)
INSM1 insulinoma-associated 1
JUND jun D proto-oncogene
LATS1 large tumor suppressor kinase 1
LHX3 LIM homeobox 3
LHX4 LIM homeobox 4
MBD5 methyl-CpG binding domain protein 5
MBOAT4 membrane bound O-acyltransferase domain containing 4
PAX6 paired box 6
PCSK1 proprotein convertase subtilisin/kexin type 1
POU1F1 POU class 1 homeobox 1
PROP1 PROP paired-like homeobox 1
RASGRF1 Ras protein-specific guanine nucleotide-releasing factor 1
RIMS2 regulating synaptic membrane exocytosis 2
SERP1 stress-associated endoplasmic reticulum protein 1
SOCS2 suppressor of cytokine signaling 2
SOX2 SRY (sex determining region Y)-box 2
SOX3 SRY (sex determining region Y)-box 3
SST somatostatin
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)