absent spongiotrophoblast Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the middle layer of the placenta between the outermost giant cells and the innermost labyrinth layer; it has a structural role and also produces several layer-specific secreted factors (Mammalian Phenotype Ontology, MP_0012100)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012100
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4 gene mutations causing the absent spongiotrophoblast phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASCL2 achaete-scute family bHLH transcription factor 2
ESRRB estrogen-related receptor beta
FOXD3 forkhead box D3
SOCS3 suppressor of cytokine signaling 3