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Trait
Elevated heart rate
Clinical name: Tachycardia
A rapid heartrate that exceeds the range of the normal resting heartrate for age.
Summary
- Also called
- Fast heart rate, Heart racing, Increased heart rate, Racing heart, Rapid heart beat
- Body system
- Abnormality of the cardiovascular system
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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/tachycardia.json"
page <- fromJSON(url)
page$trait$nameElevated heart rateHP:0001649
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Get my Genome Test86 genes linked to Elevated heart rate
Changes in these genes cause rare conditions in which Elevated heart rate 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 |
|---|---|---|
| ECE1endothelin converting enzyme 1 | Always | In 1 condition |
| LMOD2leiomodin 2 | Always | In 1 condition |
| NEXNnexilin F-actin binding protein | Always | In 1 condition |
| RFC4replication factor C subunit 4 | Always | In 1 condition |
| TSHRthyroid stimulating hormone receptor | Always | In 2 conditions |
| HNF4Ahepatocyte nuclear factor 4 alpha | Very often (80–99%) | In 1 condition |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Very often (80–99%) | In 1 condition |
| MT-CYBmitochondrially encoded cytochrome b | Very often (80–99%) | In 1 condition |
| PLXND1plexin D1 | Very often (80–99%) | In 1 condition |
| THRBthyroid hormone receptor beta | Very often (80–99%) | In 1 condition |
| ABCC8ATP binding cassette subfamily C member 8 | Often (30–79%) | In 1 condition |
| DSTdystonin | Often (30–79%) | In 1 condition |
| HMBShydroxymethylbilane synthase | Often (30–79%) | In 2 conditions |
| HNF1AHNF1 homeobox A | Often (30–79%) | In 1 condition |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Often (30–79%) | In 1 condition |
| KYNUkynureninase | Often (30–79%) | In 1 condition |
| MMACHCmetabolism of cobalamin associated C | Often (30–79%) | In 1 condition |
| MYRFmyelin regulatory factor | Often (30–79%) | In 1 condition |
| PGM1phosphoglucomutase 1 | Often (30–79%) | In 1 condition |
| PRDX1peroxiredoxin 1 | Often (30–79%) | In 1 condition |
| PRNPprion protein (Kanno blood group) | Often (30–79%) | In 1 condition |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | 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 2 conditions |
| SLC16A2solute carrier family 16 member 2 | Often (30–79%) | In 1 condition |
| UCP2uncoupling protein 2 | Often (30–79%) | In 1 condition |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | Often (30–79%) | In 1 condition |
| ABCA3ATP binding cassette subfamily A member 3 | Sometimes (5–29%) | In 1 condition |
| ABCC9ATP binding cassette subfamily C member 9 | Sometimes (5–29%) | In 1 condition |
| AKAP9A-kinase anchoring protein 9 | Sometimes (5–29%) | In 1 condition |
| AMNamnion associated transmembrane protein | Sometimes (5–29%) | In 1 condition |
| ASXL1ASXL transcriptional regulator 1 | Sometimes (5–29%) | In 1 condition |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Sometimes (5–29%) | In 1 condition |
| CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1 | Sometimes (5–29%) | In 1 condition |
| CACNB2calcium voltage-gated channel auxiliary subunit beta 2 | Sometimes (5–29%) | In 1 condition |
| CPOXcoproporphyrinogen oxidase | Sometimes (5–29%) | In 2 conditions |
| CSF2RAcolony stimulating factor 2 receptor subunit alpha | Sometimes (5–29%) | In 1 condition |
| CSF2RBcolony stimulating factor 2 receptor subunit beta | Sometimes (5–29%) | In 1 condition |
| CUBNcubilin | Sometimes (5–29%) | In 1 condition |
| ELP1elongator acetyltransferase complex subunit 1 | Sometimes (5–29%) | In 2 conditions |
Show 46 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| FBP1fructose-bisphosphatase 1 | Sometimes (5–29%) | In 2 conditions |
| GPD1Lglycerol-3-phosphate dehydrogenase 1 like | Sometimes (5–29%) | In 1 condition |
| HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4 | Sometimes (5–29%) | In 1 condition |
| KCND3potassium voltage-gated channel subfamily D member 3 | Sometimes (5–29%) | In 1 condition |
| KCNE3potassium voltage-gated channel subfamily E regulatory subunit 3 | Sometimes (5–29%) | In 1 condition |
| KCNE5potassium voltage-gated channel subfamily E regulatory subunit 5 | Sometimes (5–29%) | In 1 condition |
| KCNJ8potassium inwardly rectifying channel subfamily J member 8 | Sometimes (5–29%) | In 1 condition |
| KITKIT proto-oncogene, receptor tyrosine kinase | Sometimes (5–29%) | In 1 condition |
| NAXDNAD(P)HX dehydratase | Sometimes (5–29%) | In 1 condition |
| PKP2plakophilin 2 | Sometimes (5–29%) | In 1 condition |
| PPOXprotoporphyrinogen oxidase | Sometimes (5–29%) | In 2 conditions |
| PRORPprotein only RNase P catalytic subunit | Sometimes (5–29%) | In 1 condition |
| PYGMglycogen phosphorylase, muscle associated | Sometimes (5–29%) | In 1 condition |
| RANGRFRAN guanine nucleotide release factor | Sometimes (5–29%) | In 1 condition |
| RHAGRh associated glycoprotein | Sometimes (5–29%) | In 1 condition |
| RHCERh blood group CcEe antigens | Sometimes (5–29%) | In 1 condition |
| RHDRh blood group D antigen | Sometimes (5–29%) | In 1 condition |
| SCN10Asodium voltage-gated channel alpha subunit 10 | Sometimes (5–29%) | In 1 condition |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Sometimes (5–29%) | In 1 condition |
| SCN2Bsodium voltage-gated channel beta subunit 2 | Sometimes (5–29%) | In 1 condition |
| SCN3Bsodium voltage-gated channel beta subunit 3 | Sometimes (5–29%) | In 1 condition |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Sometimes (5–29%) | In 2 conditions |
| SCNN1Asodium channel epithelial 1 subunit alpha | Sometimes (5–29%) | In 1 condition |
| SEMA3Asemaphorin 3A | Sometimes (5–29%) | In 1 condition |
| SFTPBsurfactant protein B | Sometimes (5–29%) | In 1 condition |
| SFTPCsurfactant protein C | Sometimes (5–29%) | In 1 condition |
| SLMAPsarcolemma associated protein | Sometimes (5–29%) | In 1 condition |
| SRSF2serine and arginine rich splicing factor 2 | Sometimes (5–29%) | In 1 condition |
| SRYsex determining region Y | Sometimes (5–29%) | In 1 condition |
| TET2tet methylcytosine dioxygenase 2 | Sometimes (5–29%) | In 1 condition |
| TRPM4transient receptor potential cation channel subfamily M member 4 | Sometimes (5–29%) | In 1 condition |
| ZNF699zinc finger protein 699 | Sometimes (5–29%) | In 1 condition |
| ACADVLacyl-CoA dehydrogenase very long chain | Rarely (1–4%) | In 1 condition |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Not recorded | In 2 conditions |
| CAVIN1caveolae associated protein 1 | Not recorded | In 1 condition |
| CNBPCCHC-type zinc finger nucleic acid binding protein | Not recorded | In 1 condition |
| FMO3flavin containing dimethylaniline monoxygenase 3 | Not recorded | In 1 condition |
| KIF1Bkinesin family member 1B | Not recorded | In 1 condition |
| MAXMYC associated transcriptional regulator X | Not recorded | In 1 condition |
| RETret proto-oncogene | Not recorded | In 1 condition |
| RYR1ryanodine receptor 1 | Not recorded | In 1 condition |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Not recorded | In 1 condition |
| SDHDsuccinate dehydrogenase complex subunit D | Not recorded | In 1 condition |
| TMEM127transmembrane protein 127 | Not recorded | In 1 condition |
| TNNI3KTNNI3 interacting kinase | Not recorded | In 1 condition |
| VHLvon Hippel-Lindau tumor suppressor | Not recorded | 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.
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Broader traits
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 2026.10.17-8666dff2.
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