enlarged pituitary gland Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally increased size of the pituitary gland. (Human Phenotype Ontology, HP_0012505)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000636
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11 gene mutations causing the enlarged pituitary gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AES amino-terminal enhancer of split
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
DRD2 dopamine receptor D2
MEN1 multiple endocrine neoplasia I
PRL prolactin
TCF7L2 transcription factor 7-like 2 (T-cell specific, HMG-box)
THRB thyroid hormone receptor, beta
WWOX WW domain containing oxidoreductase