esophagus 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 of the esophagus (Mammalian Phenotype Ontology, MP_0004546)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004546
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Genes

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

Symbol Name
CHUK conserved helix-loop-helix ubiquitous kinase
IP6K2 inositol hexakisphosphate kinase 2
PDGFRA platelet-derived growth factor receptor, alpha polypeptide