abnormal reichert's membrane morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the extraembryonic basement membrane that forms on the inner surface of the trophectoderm during placenta morphogenesis and is secreted by the distal parietal endoderm; required for the maternofetal exchange of nutrients and is important for the postgastrulation development (Mammalian Phenotype Ontology, MP_0003954)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003954
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16 gene mutations causing the abnormal reichert's membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABI1 abl-interactor 1
COL4A1 collagen, type IV, alpha 1
DAD1 defender against cell death 1
DAG1 dystroglycan 1 (dystrophin-associated glycoprotein 1)
FKTN fukutin
HTT huntingtin
LAMA1 laminin, alpha 1
PLOD3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
POFUT2 protein O-fucosyltransferase 2
POMT1 protein-O-mannosyltransferase 1
POMT2 protein-O-mannosyltransferase 2
SLC31A1 solute carrier family 31 (copper transporter), member 1
SMAD4 SMAD family member 4
T T, brachyury homolog (mouse)
TFAP2C transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma)
UGCG UDP-glucose ceramide glucosyltransferase