absent parietal endoderm Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the primitive endoderm-derived tissue that lines the luminal surface of the mural trophectoderm (Mammalian Phenotype Ontology, MP_0012162)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012162
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Genes

1 gene mutations causing the absent parietal endoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
HNF1B HNF1 homeobox B