abnormal pituitary intermediate lobe morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly 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_0008130)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008130
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Genes

8 gene mutations causing the abnormal pituitary intermediate lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
DRD2 dopamine receptor D2
IRS2 insulin receptor substrate 2
LHX3 LIM homeobox 3
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
TCF7L2 transcription factor 7-like 2 (T-cell specific, HMG-box)
TPX2 TPX2, microtubule-associated