absent conotruncal ridges Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the pair of spiral mesenchymal swellings in the primordial ventricular outflow tract, that eventually fuse to form the conotruncal septum, dividing the subvalvular outflow tract and contributing to the membranous interventricular septum (Mammalian Phenotype Ontology, MP_0010586)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010586
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3 gene mutations causing the absent conotruncal ridges phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP10 bone morphogenetic protein 10
HSPG2 heparan sulfate proteoglycan 2
VCAN versican