abnormal fetal atrioventricular canal septation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the process by which the dorsal and ventral endocardial cushions develop in the walls of the common atrioventricular canal, grow toward each other and fuse, dividing the common atrioventricular canal into right and left atrioventricular canals and the atrioventricular septum (Mammalian Phenotype Ontology, MP_0010599)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010599
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7 gene mutations causing the abnormal fetal atrioventricular canal septation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CYR61 cysteine-rich, angiogenic inducer, 61
NRG1 neuregulin 1
PITX2 paired-like homeodomain 2
PKD1 polycystic kidney disease 1 (autosomal dominant)
RXRA retinoid X receptor, alpha
TGFB2 transforming growth factor, beta 2
TLL1 tolloid-like 1