absent foregut Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the anterior portion of the primitive digestive tube of the embryo that lies cephalic to the junction of the yolk stalk, consists of endodermal tissue, and gives rise to the pharynx, lower respiratory system, esophagus, stomach, duodenum proximal to the biliary tract, liver, pancreas, biliary tract, and gall bladder (Mammalian Phenotype Ontology, MP_0012083)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012083
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5 gene mutations causing the absent foregut phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GATA4 GATA binding protein 4
HGS hepatocyte growth factor-regulated tyrosine kinase substrate
NODAL nodal growth differentiation factor
OTX2 orthodenticle homeobox 2
SMAD2 SMAD family member 2