stomach inflammation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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26 gene mutations causing the stomach inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
A4GNT alpha-1,4-N-acetylglucosaminyltransferase
AIRE autoimmune regulator
FOXP3 forkhead box P3
GAST gastrin
IFNG interferon, gamma
IL18 interleukin 18
IL4 interleukin 4
IL6ST interleukin 6 signal transducer
KITLG KIT ligand
OCLN occludin
OLFM4 olfactomedin 4
PRKDC protein kinase, DNA-activated, catalytic polypeptide
RELB v-rel avian reticuloendotheliosis viral oncogene homolog B
RUNX3 runt-related transcription factor 3
SH3BP2 SH3-domain binding protein 2
SHARPIN SHANK-associated RH domain interactor
SLC9A2 solute carrier family 9, subfamily A (NHE2, cation proton antiporter 2), member 2
SLC9A4 solute carrier family 9, subfamily A (NHE4, cation proton antiporter 4), member 4
SMAD3 SMAD family member 3
SOX2 SRY (sex determining region Y)-box 2
SPDEF SAM pointed domain containing ETS transcription factor
TGFB1 transforming growth factor, beta 1
TOP3B topoisomerase (DNA) III beta
TREX1 three prime repair exonuclease 1
TTC7A tetratricopeptide repeat domain 7A
XCL1 chemokine (C motif) ligand 1