ostium secundum atrial septal defect Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A kind of atrial septum defect arising from an enlarged foramen ovale, inadequate growth of the septum secundum, or excessive absorption of the septum primum. (Human Phenotype Ontology, HP_0001684)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010405
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9 gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DNAH5 dynein, axonemal, heavy chain 5
FBLN1 fibulin 1
HEY2 hes-related family bHLH transcription factor with YRPW motif 2
NOS3 nitric oxide synthase 3 (endothelial cell)
NTF3 neurotrophin 3
NTRK3 neurotrophic tyrosine kinase, receptor, type 3
PDS5B PDS5 cohesin associated factor B
RYR1 ryanodine receptor 1 (skeletal)
SOS1 son of sevenless homolog 1 (Drosophila)