barrett esophagus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Metaplasia of the lower esophagus that is characterized by replacement of squamous epithelium with columnar epithelium, occurs especially as a result of chronic gastroesophageal reflux, and is associated with an increased risk for esophageal carcinoma. (BRENDA Tissue and Enzyme Source Ontology, BTO_0003427)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100580
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Genes

3 genes associated with the barrett esophagus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASCC1 activating signal cointegrator 1 complex subunit 1
CTHRC1 collagen triple helix repeat containing 1
MSR1 macrophage scavenger receptor 1