esophageal epithelium hyperplasia Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	overdevelopment or increased size, usually due an increased number of cells in the epithelial layer lining the luminal space of the esophagus (Mammalian Phenotype Ontology, MP_0000466)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000466
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Genes

4 gene mutations causing the esophageal epithelium hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
ATP2A2	ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
KRT4	keratin 4, type II
RAB25	RAB25, member RAS oncogene family
SLC9A3	solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3