small intestinal inflammation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description local accumulation of fluid, plasma proteins, and leukocytes in the small intestine (Mammalian Phenotype Ontology, MP_0003306)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003306
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Genes

17 gene mutations causing the small intestinal inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCC4 ATP-binding cassette, sub-family C (CFTR/MRP), member 4
AGR2 anterior gradient 2
CBFA2T2 core-binding factor, runt domain, alpha subunit 2; translocated to, 2
EFS embryonal Fyn-associated substrate
EPCAM epithelial cell adhesion molecule
FERMT1 fermitin family member 1
IL10 interleukin 10
IL13 interleukin 13
IL4 interleukin 4
INPP5D inositol polyphosphate-5-phosphatase, 145kDa
MUC2 mucin 2, oligomeric mucus/gel-forming
RC3H1 ring finger and CCCH-type domains 1
RUNX3 runt-related transcription factor 3
SMAD3 SMAD family member 3
SPDEF SAM pointed domain containing ETS transcription factor
TGFB1 transforming growth factor, beta 1
TNF tumor necrosis factor