Esophageal Dysplasia Gene Set
Genes
12 genes associated with the disease Esophageal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ADH1B
|
alcohol dehydrogenase 1B (class I), beta polypeptide
|
|
CDX2
|
caudal type homeobox 2
|
|
CXCR4
|
chemokine (C-X-C motif) receptor 4
|
|
EPHX1
|
epoxide hydrolase 1, microsomal (xenobiotic)
|
|
IL1B
|
interleukin 1, beta
|
|
KCNH2
|
potassium channel, voltage gated eag related subfamily H, member 2
|
|
MPO
|
myeloperoxidase
|
|
MTHFR
|
methylenetetrahydrofolate reductase (NAD(P)H)
|
|
SLC10A2
|
solute carrier family 10 (sodium/bile acid cotransporter), member 2
|
|
SLC30A7
|
solute carrier family 30 (zinc transporter), member 7
|
|
TP53
|
tumor protein p53
|
|
VDR
|
vitamin D (1,25- dihydroxyvitamin D3) receptor
|
