thick embryonic epiblast Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased thickness of the transient structure derived from the inner cell mass which lies above the hypoblast; the epiblast tissue gives rise to the three primary germ layers (ectoderm, definitive endoderm, and mesoderm) and to the extraembryonic mesoderm of the visceral yolk sac, the allantois, and the amnion (Mammalian Phenotype Ontology, MP_0011190)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011190
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Genes

6 gene mutations causing the thick embryonic epiblast phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I
BMPR1A bone morphogenetic protein receptor, type IA
BPTF bromodomain PHD finger transcription factor
ECSIT ECSIT signalling integrator
PRKCI protein kinase C, iota
RAC1 ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1)