absent amniotic folds Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description failure of the amnion to form involutions (Mammalian Phenotype Ontology, MP_0001710)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001710
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Genes

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

Symbol Name
ACVR1 activin A receptor, type I
BECN1 beclin 1, autophagy related
BRCA1 breast cancer 1, early onset
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
NODAL nodal growth differentiation factor
PRMT1 protein arginine methyltransferase 1
WNT3 wingless-type MMTV integration site family, member 3