thin placenta labyrinth Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decrease in the width of the structure where embryonic blood vessels are surrounded by trophoblast cells and maternal blood (Mammalian Phenotype Ontology, MP_0011523)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011523
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Genes

9 gene mutations causing the thin placenta labyrinth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHM choroideremia (Rab escort protein 1)
GAB1 GRB2-associated binding protein 1
ITGB8 integrin, beta 8
MAPK1 mitogen-activated protein kinase 1
MYH9 myosin, heavy chain 9, non-muscle
NODAL nodal growth differentiation factor
NSDHL NAD(P) dependent steroid dehydrogenase-like
NUMB numb homolog (Drosophila)
UBR4 ubiquitin protein ligase E3 component n-recognin 4