Trait

Sinus tachycardia

Heart rate of greater than 100 beats per minute.

Also called: Sinus tach, Sinus tachy
Body system: Abnormality of the cardiovascular system

This page as data

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page <- fromJSON(url)
page$trait$name

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33 genes linked to Sinus tachycardia

Changes in these genes cause rare conditions in which Sinus tachycardia is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.

Gene	How often it is seen	Conditions
BANF1barrier to autointegration nuclear assembly factor 1	Always	In 1 condition
DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit	Always	In 1 condition
DSTdystonin	Always	In 1 condition
GAAalpha glucosidase	Always	In 1 condition
IRF4interferon regulatory factor 4	Always	In 1 condition
LDB3LIM domain binding 3	Always	In 1 condition
NRAPnebulin related anchoring protein	Always	In 1 condition
ABCC6ATP binding cassette subfamily C member 6	Often (30–79%)	In 1 condition
ARSBarylsulfatase B	Often (30–79%)	In 1 condition
DLSTdihydrolipoamide S-succinyltransferase	Often (30–79%)	In 1 condition
DNMT3ADNA methyltransferase 3 alpha	Often (30–79%)	In 1 condition
EPAS1endothelial PAS domain protein 1	Often (30–79%)	In 1 condition
FHfumarate hydratase	Often (30–79%)	In 1 condition
KIF1Bkinesin family member 1B	Often (30–79%)	In 1 condition
MAXMYC associated transcriptional regulator X	Often (30–79%)	In 1 condition
MDH2malate dehydrogenase 2	Often (30–79%)	In 1 condition
NF1neurofibromin 1	Often (30–79%)	In 1 condition
RETret proto-oncogene	Often (30–79%)	In 2 conditions
RYR1ryanodine receptor 1	Often (30–79%)	In 1 condition
SDHAsuccinate dehydrogenase complex flavoprotein subunit A	Often (30–79%)	In 1 condition
SDHAF2succinate dehydrogenase complex assembly factor 2	Often (30–79%)	In 1 condition
SDHBsuccinate dehydrogenase complex iron sulfur subunit B	Often (30–79%)	In 2 conditions
SDHCsuccinate dehydrogenase complex subunit C	Often (30–79%)	In 1 condition
SDHDsuccinate dehydrogenase complex subunit D	Often (30–79%)	In 2 conditions
SLC25A11solute carrier family 25 member 11	Often (30–79%)	In 1 condition
TMEM127transmembrane protein 127	Often (30–79%)	In 1 condition
VHLvon Hippel-Lindau tumor suppressor	Often (30–79%)	In 2 conditions
ALPK3alpha kinase 3	Sometimes (5–29%)	In 1 condition
MYH7myosin heavy chain 7	Sometimes (5–29%)	In 1 condition
MYPNmyopalladin	Sometimes (5–29%)	In 1 condition
PEX5peroxisomal biogenesis factor 5	Sometimes (5–29%)	In 1 condition
TPM2tropomyosin 2	Sometimes (5–29%)	In 1 condition
TPM3tropomyosin 3	Sometimes (5–29%)	In 1 condition

How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.

Broader traits

Abnormal electrophysiology of sinoatrial node origin Elevated heart rate

Where this comes from

The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
Data release 2026.10.16-c6eea6bf.

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