Microvillus Inclusion Disease Gene Set
Genes
18 genes associated with the disease Microvillus Inclusion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ABCB11
|
ATP-binding cassette, sub-family B (MDR/TAP), member 11
|
|
ACTB
|
actin, beta
|
|
AICDA
|
activation-induced cytidine deaminase
|
|
AQP7
|
aquaporin 7
|
|
CDC42
|
cell division cycle 42
|
|
CFTR
|
cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
|
|
EZR
|
ezrin
|
|
FHL5
|
four and a half LIM domains 5
|
|
IMMT
|
inner membrane protein, mitochondrial
|
|
MYO5B
|
myosin VB
|
|
PDK1
|
pyruvate dehydrogenase kinase, isozyme 1
|
|
RAB11A
|
RAB11A, member RAS oncogene family
|
|
RAB8A
|
RAB8A, member RAS oncogene family
|
|
SLC26A3
|
solute carrier family 26 (anion exchanger), member 3
|
|
SLC9A3
|
solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
|
|
STX3
|
syntaxin 3
|
|
STXBP2
|
syntaxin binding protein 2
|
|
VWF
|
von Willebrand factor
|
