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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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