pituitary intermediate lobe 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 thin boundary between the adenohypophysis and neurohypophysis of the pituitary that produces melanocyte stimulating hormone (MSH); this area is small or absent in mammalian adults (Mammalian Phenotype Ontology, MP_0008371)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008371
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Genes

3 gene mutations causing the pituitary intermediate lobe hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
DRD2 dopamine receptor D2
TPX2 TPX2, microtubule-associated