abnormal small intestinal microvillus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the additional extensions of the villi of the small intestine which protrude from the apical surface of the epithelial cells lining the villi; the microvilli increase the absorptive surface area of the small intestine by approximately 600-fold (Mammalian Phenotype Ontology, MP_0008109)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008109
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7 gene mutations causing the abnormal small intestinal microvillus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CRB3 crumbs family member 3
EZR ezrin
HR hair growth associated
IGF2BP1 insulin-like growth factor 2 mRNA binding protein 1
RAB8A RAB8A, member RAS oncogene family
SAV1 salvador family WW domain containing protein 1
WASF1 WAS protein family, member 1