gastrointestinal ulcer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any lesion on the mucosal surface of the gastrointestinal tract, usually produced by the sloughing of inflammatory necrotic tissue (Mammalian Phenotype Ontology, MP_0003300)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003300
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Genes

27 gene mutations causing the gastrointestinal 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
CYLD cylindromatosis (turban tumor syndrome)
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
IL6ST interleukin 6 signal transducer
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
KITLG KIT ligand
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
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
PLG plasminogen
RC3H1 ring finger and CCCH-type domains 1
SOX2 SRY (sex determining region Y)-box 2
TGFB1 transforming growth factor, beta 1
TP53 tumor protein p53
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor