abnormal embryonic-extraembryonic boundary morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the delineating tissue and the segregation between the embryo proper and extraembryonic tissues (Mammalian Phenotype Ontology, MP_0003890)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003890
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Genes

30 gene mutations causing the abnormal embryonic-extraembryonic boundary morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
ARC activity-regulated cytoskeleton-associated protein
BMPR1A bone morphogenetic protein receptor, type IA
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)
BRCA1 breast cancer 1, early onset
FGFR1 fibroblast growth factor receptor 1
FOXA2 forkhead box A2
FOXH1 forkhead box H1
GCLC glutamate-cysteine ligase, catalytic subunit
GDF3 growth differentiation factor 3
HIRA histone cell cycle regulator
HSD17B12 hydroxysteroid (17-beta) dehydrogenase 12
HSP90B1 heat shock protein 90kDa beta (Grp94), member 1
HTT huntingtin
LDB1 LIM domain binding 1
LHX1 LIM homeobox 1
MAX MYC associated factor X
NODAL nodal growth differentiation factor
OTX2 orthodenticle homeobox 2
PALB2 partner and localizer of BRCA2
POU2F1 POU class 2 homeobox 1
PPAP2B phosphatidic acid phosphatase type 2B
RAC1 ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1)
SMAD2 SMAD family member 2
SMAD4 SMAD family member 4
TFAP2C transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma)
TLN1 talin 1
TRIM33 tripartite motif containing 33
TSG101 tumor susceptibility 101
YAP1 Yes-associated protein 1