abnormal spongiotrophoblast cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of a trophoblast cell that arises in the junctional zone of the placenta (Mammalian Phenotype Ontology, MP_0008959)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008959
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8 gene mutations causing the abnormal spongiotrophoblast cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALKBH1 alkB, alkylation repair homolog 1 (E. coli)
ASCL2 achaete-scute family bHLH transcription factor 2
ELAVL1 ELAV like RNA binding protein 1
HAND1 heart and neural crest derivatives expressed 1
NCOA6 nuclear receptor coactivator 6
PEG10 paternally expressed 10
SOCS3 suppressor of cytokine signaling 3
SP3 Sp3 transcription factor