abnormality of small intestinal villus morphology Gene Set
Genes
14 genes associated with the abnormality of small intestinal villus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ADAM17
|
ADAM metallopeptidase domain 17
|
|
ALG3
|
ALG3, alpha-1,3- mannosyltransferase
|
|
CIITA
|
class II, major histocompatibility complex, transactivator
|
|
EPCAM
|
epithelial cell adhesion molecule
|
|
FOXP3
|
forkhead box P3
|
|
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
|
|
TTC37
|
tetratricopeptide repeat domain 37
|
