embryonic-extraembryonic boundary constriction Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description an invagination or pinching in the visceral endoderm that is centered at the boundary between embryonic and extra-embryonic regions of the developing embryo, often resulting in physical separation of embryonic and extraembryonic ectoderm (Mammalian Phenotype Ontology, MP_0012135)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012135
Similar Terms
Downloads & Tools

Genes

14 gene mutations causing the embryonic-extraembryonic boundary constriction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
FOXA2 forkhead box A2
FOXH1 forkhead box H1
GDF3 growth differentiation factor 3
HIRA histone cell cycle regulator
HTT huntingtin
LDB1 LIM domain binding 1
LHX1 LIM homeobox 1
NODAL nodal growth differentiation factor
OTX2 orthodenticle homeobox 2
PPAP2B phosphatidic acid phosphatase type 2B
RAC1 ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1)
TLN1 talin 1
YAP1 Yes-associated protein 1