absent placental labyrinth Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the structure where embryonic blood vessels are surrounded by trophoblast cells and maternal blood (Mammalian Phenotype Ontology, MP_0003403)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003403
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Genes

20 gene mutations causing the absent placental labyrinth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNT aryl hydrocarbon receptor nuclear translocator
CHM choroideremia (Rab escort protein 1)
DLX3 distal-less homeobox 3
DNAJB6 DnaJ (Hsp40) homolog, subfamily B, member 6
ERF Ets2 repressor factor
ESRRB estrogen-related receptor beta
FGFR2 fibroblast growth factor receptor 2
GCM1 glial cells missing homolog 1 (Drosophila)
MAPK14 mitogen-activated protein kinase 14
NCOA6 nuclear receptor coactivator 6
NODAL nodal growth differentiation factor
PEG10 paternally expressed 10
PNPLA6 patatin-like phospholipase domain containing 6
SLC34A2 solute carrier family 34 (type II sodium/phosphate cotransporter), member 2
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1
SPINT1 serine peptidase inhibitor, Kunitz type 1
TFAP2C transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma)
TMED2 transmembrane emp24 domain trafficking protein 2
XIST X inactive specific transcript (non-protein coding)
ZFP36L1 ZFP36 ring finger protein-like 1