abnormal ectoplacental cone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the thickened trophoblast of the blastocyst in rodents that becomes the fetal portion of the placenta (Mammalian Phenotype Ontology, MP_0005032)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005032
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34 gene mutations causing the abnormal ectoplacental cone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATAD3A ATPase family, AAA domain containing 3A
AURKB aurora kinase B
BPTF bromodomain PHD finger transcription factor
CHM choroideremia (Rab escort protein 1)
CR1L complement component (3b/4b) receptor 1-like
CXXC1 CXXC finger protein 1
DHX9 DEAH (Asp-Glu-Ala-His) box helicase 9
DNMT3L DNA (cytosine-5-)-methyltransferase 3-like
ERF Ets2 repressor factor
ETS2 v-ets avian erythroblastosis virus E26 oncogene homolog 2
FBXL5 F-box and leucine-rich repeat protein 5
GNPNAT1 glucosamine-phosphate N-acetyltransferase 1
HAND1 heart and neural crest derivatives expressed 1
LAMA1 laminin, alpha 1
MAP2K1 mitogen-activated protein kinase kinase 1
MAPK1 mitogen-activated protein kinase 1
MTOR mechanistic target of rapamycin (serine/threonine kinase)
N6AMT1 N-6 adenine-specific DNA methyltransferase 1 (putative)
NF2 neurofibromin 2 (merlin)
NODAL nodal growth differentiation factor
PNPLA6 patatin-like phospholipase domain containing 6
POU2F1 POU class 2 homeobox 1
PPP1R8 protein phosphatase 1, regulatory subunit 8
RANGAP1 Ran GTPase activating protein 1
RTEL1 regulator of telomere elongation helicase 1
SMAD2 SMAD family member 2
SMAD4 SMAD family member 4
SOX2 SRY (sex determining region Y)-box 2
T T, brachyury homolog (mouse)
TERF1 telomeric repeat binding factor (NIMA-interacting) 1
TFAP2C transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma)
TFDP1 transcription factor Dp-1
THBD thrombomodulin
TSIX TSIX transcript, XIST antisense RNA