absent ectoplacental cone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing the thickened trophoblast of the blastocyst in rodents that becomes the fetal portion of the placenta (Mammalian Phenotype Ontology, MP_0001717)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001717
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8 gene mutations causing the absent ectoplacental cone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATAD3A ATPase family, AAA domain containing 3A
CXXC1 CXXC finger protein 1
MAP2K1 mitogen-activated protein kinase kinase 1
MAPK1 mitogen-activated protein kinase 1
POU2F1 POU class 2 homeobox 1
PPP1R8 protein phosphatase 1, regulatory subunit 8
SOX2 SRY (sex determining region Y)-box 2
TFAP2C transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma)