abnormal parietal endoderm morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the primitive endoderm-derived tissue that lines the luminal surface of the mural trophectoderm (Mammalian Phenotype Ontology, MP_0011187)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011187
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23 gene mutations causing the abnormal parietal endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABI1 abl-interactor 1
BRCA1 breast cancer 1, early onset
COL4A1 collagen, type IV, alpha 1
CTDNEP1 CTD nuclear envelope phosphatase 1
DAD1 defender against cell death 1
DAG1 dystroglycan 1 (dystrophin-associated glycoprotein 1)
DHX9 DEAH (Asp-Glu-Ala-His) box helicase 9
FKTN fukutin
HNF1B HNF1 homeobox B
HTT huntingtin
LAMA1 laminin, alpha 1
LAMB1 laminin, beta 1
MESDC2 mesoderm development candidate 2
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)
TSG101 tumor susceptibility 101
UGCG UDP-glucose ceramide glucosyltransferase