abnormal spongiotrophoblast size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the size 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_0012097)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012097
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Genes

25 gene mutations causing the abnormal spongiotrophoblast size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
AKT1 v-akt murine thymoma viral oncogene homolog 1
ARID1A AT rich interactive domain 1A (SWI-like)
C3 complement component 3
CITED1 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 1
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
EGFR epidermal growth factor receptor
ELAVL1 ELAV like RNA binding protein 1
ERF Ets2 repressor factor
GJB3 gap junction protein, beta 3, 31kDa
HSD17B2 hydroxysteroid (17-beta) dehydrogenase 2
HSF1 heat shock transcription factor 1
JUP junction plakoglobin
MAPK14 mitogen-activated protein kinase 14
NCOA6 nuclear receptor coactivator 6
NODAL nodal growth differentiation factor
NRK Nik related kinase
PHLDA2 pleckstrin homology-like domain, family A, member 2
PLAC1 placenta-specific 1
PTP4A2 protein tyrosine phosphatase type IVA, member 2
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RBPJ recombination signal binding protein for immunoglobulin kappa J region
SENP2 SUMO1/sentrin/SMT3 specific peptidase 2
SOCS3 suppressor of cytokine signaling 3
SP3 Sp3 transcription factor
Funding