palpitations Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A sensation that the heart is pounding or racing, which is a non-specific sign but may be a manifestation of arrhythmia. (Human Phenotype Ontology, HP_0001962)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001962
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Genes

16 genes associated with the palpitations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CNBP CCHC-type zinc finger, nucleic acid binding protein
DSC2 desmocollin 2
DSG2 desmoglein 2
ISCU iron-sulfur cluster assembly enzyme
JPH2 junctophilin 2
KCNA5 potassium channel, voltage gated shaker related subfamily A, member 5
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
PKP2 plakophilin 2
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SCN9A sodium channel, voltage gated, type IX alpha subunit
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
TMEM43 transmembrane protein 43