small amniotic cavity Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size 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_0012104)
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7 gene mutations causing the small amniotic cavity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AXIN1 axin 1
CRB2 crumbs family member 2
HTT huntingtin
PRKCI protein kinase C, iota
PTK2 protein tyrosine kinase 2
TLN1 talin 1
TSIX TSIX transcript, XIST antisense RNA