Villous Atrophy Of Intestine Gene Set
Genes
19 genes associated with the disease Villous Atrophy Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ADAM17
|
ADAM metallopeptidase domain 17
|
|
ALG3
|
ALG3, alpha-1,3- mannosyltransferase
|
|
CIITA
|
class II, major histocompatibility complex, transactivator
|
|
DGAT1
|
diacylglycerol O-acyltransferase 1
|
|
EPCAM
|
epithelial cell adhesion molecule
|
|
FOXP3
|
forkhead box P3
|
|
IL2RA
|
interleukin 2 receptor, alpha
|
|
MPI
|
mannose phosphate isomerase
|
|
MYO5B
|
myosin VB
|
|
PCSK1
|
proprotein convertase subtilisin/kexin type 1
|
|
RFX5
|
regulatory factor X, 5 (influences HLA class II expression)
|
|
RFXANK
|
regulatory factor X-associated ankyrin-containing protein
|
|
RFXAP
|
regulatory factor X-associated protein
|
|
SKIV2L
|
superkiller viralicidic activity 2-like (S. cerevisiae)
|
|
SPINK5
|
serine peptidase inhibitor, Kazal type 5
|
|
STAT1
|
signal transducer and activator of transcription 1, 91kDa
|
|
STX3
|
syntaxin 3
|
|
TTC37
|
tetratricopeptide repeat domain 37
|
|
WNT2B
|
wingless-type MMTV integration site family, member 2B
|
