intestinal edema Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	Accumulation of cell free, noninflammatony fluid within the wall of the intestinal tract producing uniform thickening of the mucosal folds. (Human Phenotype Ontology, HP_0005225)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003288
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Genes

9 gene mutations causing the intestinal edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
BCR	breakpoint cluster region
CALCRL	calcitonin receptor-like
CLEC1B	C-type lectin domain family 1, member B
EPCAM	epithelial cell adhesion molecule
NLRP6	NLR family, pyrin domain containing 6
PDPN	podoplanin
PLVAP	plasmalemma vesicle associated protein
PTGS2	prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
TIE1	tyrosine kinase with immunoglobulin-like and EGF-like domains 1