abnormal chorionic plate morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the portion of the chorion from which chorionic villi develop that establish a connection with the endometrium, giving rise to the fetal portion of the mature placenta (Mammalian Phenotype Ontology, MP_0004560)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004560
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Genes

13 gene mutations causing the abnormal chorionic plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNT aryl hydrocarbon receptor nuclear translocator
COMMD1 copper metabolism (Murr1) domain containing 1
CYR61 cysteine-rich, angiogenic inducer, 61
ELAVL1 ELAV like RNA binding protein 1
ENPP2 ectonucleotide pyrophosphatase/phosphodiesterase 2
FOSL1 FOS-like antigen 1
GCM1 glial cells missing homolog 1 (Drosophila)
GJB3 gap junction protein, beta 3, 31kDa
NOTCH2 notch 2
PNPLA6 patatin-like phospholipase domain containing 6
PPARG peroxisome proliferator-activated receptor gamma
SPINT1 serine peptidase inhibitor, Kunitz type 1
SS18 synovial sarcoma translocation, chromosome 18