abnormal jejunum morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the portion of the small intestine that extends from the duodenum to the ileum (Mammalian Phenotype Ontology, MP_0004002)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004002
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11 gene mutations causing the abnormal jejunum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BCAM basal cell adhesion molecule (Lutheran blood group)
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CLDN15 claudin 15
EPCAM epithelial cell adhesion molecule
FOXL1 forkhead box L1
ID2 inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
LIPA lipase A, lysosomal acid, cholesterol esterase
NKX2-3 NK2 homeobox 3
PTK6 protein tyrosine kinase 6
SMTN smoothelin