small pituitary gland Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally decreased size of the pituitary gland. (Human Phenotype Ontology, HP_0012506)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005361
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Genes

22 gene mutations causing the small pituitary gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CSHL1 chorionic somatomammotropin hormone-like 1
DDR2 discoidin domain receptor tyrosine kinase 2
DISP1 dispatched homolog 1 (Drosophila)
GHR growth hormone receptor
GHRH growth hormone releasing hormone
GHRHR growth hormone releasing hormone receptor
GSX1 GS homeobox 1
HES1 hes family bHLH transcription factor 1
HMX2 H6 family homeobox 2
HMX3 H6 family homeobox 3
INSM1 insulinoma-associated 1
IRS2 insulin receptor substrate 2
MARK2 MAP/microtubule affinity-regulating kinase 2
MBD5 methyl-CpG binding domain protein 5
NDST1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
PITX2 paired-like homeodomain 2
PROP1 PROP paired-like homeobox 1
PTPRS protein tyrosine phosphatase, receptor type, S
SERP1 stress-associated endoplasmic reticulum protein 1
SIM1 single-minded family bHLH transcription factor 1
SIX6 SIX homeobox 6
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3