abnormal conotruncal ridge morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly 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_0010585)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010585
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14 gene mutations causing the abnormal conotruncal ridge morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
BMP10 bone morphogenetic protein 10
FGFR2 fibroblast growth factor receptor 2
FOXP1 forkhead box P1
GATA4 GATA binding protein 4
HHEX hematopoietically expressed homeobox
HSPG2 heparan sulfate proteoglycan 2
PKD1 polycystic kidney disease 1 (autosomal dominant)
RXRA retinoid X receptor, alpha
SOX4 SRY (sex determining region Y)-box 4
SSR1 signal sequence receptor, alpha
TBX2 T-box 2
TLL1 tolloid-like 1
VCAN versican