esophagus hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or decreased size of the esophagus, usually due a reduced number of cells (Mammalian Phenotype Ontology, MP_0010881)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010881
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Genes

2 gene mutations causing the esophagus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GLI2 GLI family zinc finger 2
IFT172 intraflagellar transport 172