abnormal small intestinal crypt cell physiology Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	any functional anomaly of the cells that make up the tubular intestinal glands found in the mucosal membranes of the small intestine (Mammalian Phenotype Ontology, MP_0010156)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010156
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Genes

7 gene mutations causing the abnormal small intestinal crypt cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
CFTR	cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CTNNB1	catenin (cadherin-associated protein), beta 1, 88kDa
GLP2R	glucagon-like peptide 2 receptor
PRKDC	protein kinase, DNA-activated, catalytic polypeptide
PTGS1	prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
TERT	telomerase reverse transcriptase
TIGAR	TP53 induced glycolysis regulatory phosphatase