dilated allantois Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	an expansion in the volume of the fetal membrane which contributes to the formation of the umbilical cord and placental blood vessels, as by stretching or distention (Mammalian Phenotype Ontology, MP_0004557)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004557
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Genes

7 gene mutations causing the dilated allantois phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
ENPP2	ectonucleotide pyrophosphatase/phosphodiesterase 2
GTF2I	general transcription factor IIi
GTF2IRD1	GTF2I repeat domain containing 1
HGS	hepatocyte growth factor-regulated tyrosine kinase substrate
ITGA4	integrin, alpha 4 (antigen CD49D, alpha 4 subunit of VLA-4 receptor)
LHX1	LIM homeobox 1
VCAM1	vascular cell adhesion molecule 1