j wave Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The J wave is a positive convex deflection that occurs at the junction of the QRS complex and ST segment, the J-point. (Human Phenotype Ontology, HP_0012272)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012272
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Genes

1 genes associated with the j wave phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit