intestinal ulcer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description lesions in the mucous lining of the intestine (Mammalian Phenotype Ontology, MP_0000512)
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20 gene mutations causing the intestinal ulcer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
B3GNT6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CGN cingulin
FADS2 fatty acid desaturase 2
FPR2 formyl peptide receptor 2
GNAI2 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 2
IL2 interleukin 2
LTBP4 latent transforming growth factor beta binding protein 4
MMP7 matrix metallopeptidase 7
MUC2 mucin 2, oligomeric mucus/gel-forming
NFIL3 nuclear factor, interleukin 3 regulated
NLRP6 NLR family, pyrin domain containing 6
PGLYRP1 peptidoglycan recognition protein 1
PGLYRP2 peptidoglycan recognition protein 2
PGLYRP3 peptidoglycan recognition protein 3
PGLYRP4 peptidoglycan recognition protein 4
PLG plasminogen
RC3H1 ring finger and CCCH-type domains 1
TP53 tumor protein p53
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor