conotruncal ridge hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description overdevelopment or increased size 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_0010588)
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3 gene mutations causing the conotruncal ridge hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXP1 forkhead box P1
HHEX hematopoietically expressed homeobox
HSPG2 heparan sulfate proteoglycan 2