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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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