barrett esophagus Gene Set

Dataset	GWASdb SNP-Phenotype 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://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0100580
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Genes

17 genes associated with the barrett esophagus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol	Name	Standardized Value
CRTC1	CREB regulated transcription coactivator 1	1.38847
BARX1	BARX homeobox 1	1.35521
PTPDC1	protein tyrosine phosphatase domain containing 1	1.17285
ALDH1A2	aldehyde dehydrogenase 1 family, member A2	1.09906
GRID1	glutamate receptor, ionotropic, delta 1	0.899912
AGBL1	ATP/GTP binding protein-like 1	0.899912
FRMD3	FERM domain containing 3	0.842167
MFHAS1	malignant fibrous histiocytoma amplified sequence 1	0.686028
LECT1	leukocyte cell derived chemotaxin 1	0.621876
KHDRBS2	KH domain containing, RNA binding, signal transduction associated 2	0.605862
EPHB1	EPH receptor B1	0.54245
OSBPL10	oxysterol binding protein-like 10	0.522995
OTX2-AS1	OTX2 antisense RNA 1 (head to head)	0.510802
DSG3	desmoglein 3	0.506461
CAMTA1	calmodulin binding transcription activator 1	0.490196
HECW1	HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1	0.4797
MIR99AHG	mir-99a-let-7c cluster host gene	0.425078