abnormal visceral endoderm physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the primitive endoderm-derived tissue which remains in contact with and surrounds the extra-embryonic ectoderm and the epiblast and provides signals for the differentiation and patterning of the epiblast; a small number of visceral endoderm cells also contribute to the endoderm of the embryonic gut (Mammalian Phenotype Ontology, MP_0012028)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012028
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8 gene mutations causing the abnormal visceral endoderm physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AMOT angiomotin
FOXD3 forkhead box D3
GDF3 growth differentiation factor 3
NCKAP1 NCK-associated protein 1
PIKFYVE phosphoinositide kinase, FYVE finger containing
PRICKLE1 prickle homolog 1 (Drosophila)
RAC1 ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1)
RAX retina and anterior neural fold homeobox