abnormal pituitary secretion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the production and/or release of biologically active substances from pituitary tissue (Mammalian Phenotype Ontology, MP_0001746)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001746
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12 gene mutations causing the abnormal pituitary secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
ARNT2 aryl-hydrocarbon receptor nuclear translocator 2
EGR1 early growth response 1
GAL galanin/GMAP prepropeptide
GSX1 GS homeobox 1
KALRN kalirin, RhoGEF kinase
OTX1 orthodenticle 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