abnormal pituitary gland physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of this unpaired compound gland suspended from the base of the hypothalamus by a short extension of the infundibulum, the infundibular or pituitary stalk (Mammalian Phenotype Ontology, MP_0005646)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005646
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Genes

20 gene mutations causing the abnormal pituitary gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
ARNT2 aryl-hydrocarbon receptor nuclear translocator 2
DDO D-aspartate oxidase
DRD2 dopamine receptor D2
EGR1 early growth response 1
ESR1 estrogen receptor 1
GAL galanin/GMAP prepropeptide
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GSX1 GS homeobox 1
KALRN kalirin, RhoGEF kinase
NOG noggin
OTX1 orthodenticle homeobox 1
POU1F1 POU class 1 homeobox 1
PRL prolactin
PROP1 PROP paired-like homeobox 1
RASGRF1 Ras protein-specific guanine nucleotide-releasing factor 1
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SYTL4 synaptotagmin-like 4
THRB thyroid hormone receptor, beta
WWOX WW domain containing oxidoreductase