bradycardia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A slower than normal heart rate (in adults, slower than 60 beats per minute). (Human Phenotype Ontology, HP_0001662)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001662
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Genes

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

Symbol Name
ANK2 ankyrin 2, neuronal
BRAT1 BRCA1-associated ATM activator 1
C10ORF2 chromosome 10 open reading frame 2
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
DST dystonin
EFEMP2 EGF containing fibulin-like extracellular matrix protein 2
GLUL glutamate-ammonia ligase
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
LMNA lamin A/C
NPPA natriuretic peptide A
PAX8 paired box 8
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
PTRF polymerase I and transcript release factor
SCN5A sodium channel, voltage gated, type V alpha subunit
SCN9A sodium channel, voltage gated, type IX alpha subunit
SLC25A20 solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
TLL1 tolloid-like 1
TMEM43 transmembrane protein 43
TRPM4 transient receptor potential cation channel, subfamily M, member 4
TSPYL1 TSPY-like 1