absent trophectoderm Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the outermost layer of cells in the blastodermic vesicle, which will develop into the trophoblast layer and then contact the endometrium and take part in establishing the embryo's means of nutrition (Mammalian Phenotype Ontology, MP_0012102)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012102
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7 gene mutations causing the absent trophectoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDH1 cadherin 1, type 1, E-cadherin (epithelial)
EOMES eomesodermin
EVX1 even-skipped homeobox 1
GMNN geminin, DNA replication inhibitor
GNL3 guanine nucleotide binding protein-like 3 (nucleolar)
RYBP RING1 and YY1 binding protein
TEAD4 TEA domain family member 4