pituitary intermediate lobe hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced 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_0008369)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008369
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Genes

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

Symbol Name
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3