Sinus Tachycardia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Inappropriate sinus tachycardia is a nonparoxysmal tachyarrhythmia characterized by an increased resting heart rate (HR) and/or an exaggerated HR response to minimal exertion or a change in body posture. HR is constantly above the physiological range with no appropriate relation to metabolic or physiological demands. (Human Phenotype Ontology, HP_0011703)
External Link https://www.disgenet.org/browser/0/1/0/C0039239
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Genes

28 genes associated with the disease Sinus Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BANF1 barrier to autointegration factor 1
CPT2 carnitine palmitoyltransferase 2
CRP C-reactive protein, pentraxin-related
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
DLST dihydrolipoamide S-succinyltransferase (E2 component of 2-oxo-glutarate complex)
EHMT1 euchromatic histone-lysine N-methyltransferase 1
FH fumarate hydratase
GCG glucagon
KIAA0195 KIAA0195
KIF1B kinesin family member 1B
KMT2B lysine (K)-specific methyltransferase 2B
LMNA lamin A/C
MAX MYC associated factor X
MDH2 malate dehydrogenase 2, NAD (mitochondrial)
MYPN myopalladin
PEX5 peroxisomal biogenesis factor 5
RET ret proto-oncogene
SDHA succinate dehydrogenase complex, subunit A, flavoprotein (Fp)
SDHAF2 succinate dehydrogenase complex assembly factor 2
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
SLC25A11 solute carrier family 25 (mitochondrial carrier; oxoglutarate carrier), member 11
TMEM127 transmembrane protein 127
TPM2 tropomyosin 2 (beta)
TPM3 tropomyosin 3
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
ZMPSTE24 zinc metallopeptidase STE24