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)
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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