disorganized placental labyrinth Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description derangement of the placental layers where embryonic blood vessels are surrounded by trophoblast cells and maternal blood (Mammalian Phenotype Ontology, MP_0011527)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011527
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7 gene mutations causing the disorganized placental labyrinth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CITED1 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 1
CUL4B cullin 4B
FGFRL1 fibroblast growth factor receptor-like 1
GAB1 GRB2-associated binding protein 1
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
HSD17B2 hydroxysteroid (17-beta) dehydrogenase 2
NSDHL NAD(P) dependent steroid dehydrogenase-like