placental labyrinth hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, of the placental labyrinth, the structure where embryonic blood vessels are surrounded by trophoblast cells and maternal blood (Mammalian Phenotype Ontology, MP_0001715)
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15 gene mutations causing the placental labyrinth hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGO2 argonaute RISC catalytic component 2
CDH1 cadherin 1, type 1, E-cadherin (epithelial)
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
DDX11 DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11
DLK1 delta-like 1 homolog (Drosophila)
EGFR epidermal growth factor receptor
ELAVL1 ELAV like RNA binding protein 1
FZR1 fizzy/cell division cycle 20 related 1 (Drosophila)
GAB1 GRB2-associated binding protein 1
HOXA13 homeobox A13
MYC v-myc avian myelocytomatosis viral oncogene homolog
PAXIP1 PAX interacting (with transcription-activation domain) protein 1
PPARG peroxisome proliferator-activated receptor gamma
TTPA tocopherol (alpha) transfer protein
ZFP36L1 ZFP36 ring finger protein-like 1