absent amniotic cavity Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the closed space between the embryo and the amnion which contains the amniotic fluid and is formed by the fusion of the parts of the anterior and posterior amniotic folds (Mammalian Phenotype Ontology, MP_0012142)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012142
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Genes

3 gene mutations causing the absent amniotic cavity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EXOC4 exocyst complex component 4
NR5A2 nuclear receptor subfamily 5, group A, member 2
RAD51 RAD51 recombinase