Barrett Esophagus Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:D001471
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Genes

14 genes/proteins associated with the disease Barrett Esophagus from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
MCL1	myeloid cell leukemia 1	2.88009
NR1I2	nuclear receptor subfamily 1, group I, member 2	2.88009
GAST	gastrin	2.88009
PPARG	peroxisome proliferator-activated receptor gamma	2.88009
HGF	hepatocyte growth factor (hepapoietin A; scatter factor)	2.88009
CXCL8	chemokine (C-X-C motif) ligand 8	2.88009
CYP26A1	cytochrome P450, family 26, subfamily A, polypeptide 1	2.88009
PTGS2	prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)	2.88009
RPRM	reprimo, TP53 dependent G2 arrest mediator candidate	2.88009
CDH13	cadherin 13	2.88009
SST	somatostatin	2.88009
RELA	v-rel avian reticuloendotheliosis viral oncogene homolog A	2.88009
SLC9A1	solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1	2.88009
MPO	myeloperoxidase	1.03084