pituitary gland hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description overdevelopment or increased size, usually due to increased cell number, of the pituitary gland (Mammalian Phenotype Ontology, MP_0000635)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000635
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Genes

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

Symbol Name
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
PRL prolactin