herniated intestine Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description protrusion of any portion of the intestine from its normal anatomical position (Mammalian Phenotype Ontology, MP_0005155)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005155
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5 gene mutations causing the herniated intestine phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1
PODXL podocalyxin-like
SFN stratifin
SHROOM3 shroom family member 3
SLIT3 slit homolog 3 (Drosophila)